�ݺ�ߣshows by User: RoshenRejiIdiculla

�ݺ�ߣshows by User: RoshenRejiIdiculla / http://www.slideshare.net/images/logo.gif �ݺ�ߣshows by User: RoshenRejiIdiculla / Mon, 06 Jan 2020 17:35:17 GMT �ݺ�ߣShare feed for �ݺ�ߣshows by User: RoshenRejiIdiculla 100 named reactions /slideshow/100-named-reactions/216051450 100namedreactions-200106173517
100 named reactions with examples of total syntheses which utilized these reactions, with reaction conditions. with included references for each syntheses.]]>
100 named reactions with examples of total syntheses which utilized these reactions, with reaction conditions. with included references for each syntheses.]]> Mon, 06 Jan 2020 17:35:17 GMT /slideshow/100-named-reactions/216051450 RoshenRejiIdiculla@slideshare.net(RoshenRejiIdiculla) 100 named reactions RoshenRejiIdiculla 100 named reactions with examples of total syntheses which utilized these reactions, with reaction conditions. with included references for each syntheses. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/100namedreactions-200106173517-thumbnail.jpg?width=120&height=120&fit=bounds" /> 100 named reactions with examples of total syntheses which utilized these reactions, with reaction conditions. with included references for each syntheses.

100 named reactions from Roshen Reji Idiculla

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0 Ion exchange chromatography /slideshow/ion-exchange-chromatography-216048395/216048395 ion-exchangechromatography-200106173010
Principles of Ion -exchange chromatography, High performance liquid chromatography (HPLC) , chromatography generally stands for a technique which separates mixtures based on different dynamic sharing of their components between two distinct physio-chemical environments called mobile and stationary phase by repeated absorption/desorption steps. Ion chromatography (IC) is a member of large family of liquid phase chromatographic methods (that is a mobile phase is a liquid and a stationary phase is a solid).]]>
Principles of Ion -exchange chromatography, High performance liquid chromatography (HPLC) , chromatography generally stands for a technique which separates mixtures based on different dynamic sharing of their components between two distinct physio-chemical environments called mobile and stationary phase by repeated absorption/desorption steps. Ion chromatography (IC) is a member of large family of liquid phase chromatographic methods (that is a mobile phase is a liquid and a stationary phase is a solid).]]> Mon, 06 Jan 2020 17:30:10 GMT /slideshow/ion-exchange-chromatography-216048395/216048395 RoshenRejiIdiculla@slideshare.net(RoshenRejiIdiculla) Ion exchange chromatography RoshenRejiIdiculla Principles of Ion -exchange chromatography, High performance liquid chromatography (HPLC) , chromatography generally stands for a technique which separates mixtures based on different dynamic sharing of their components between two distinct physio-chemical environments called mobile and stationary phase by repeated absorption/desorption steps. Ion chromatography (IC) is a member of large family of liquid phase chromatographic methods (that is a mobile phase is a liquid and a stationary phase is a solid). <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/ion-exchangechromatography-200106173010-thumbnail.jpg?width=120&height=120&fit=bounds" /> Principles of Ion -exchange chromatography, High performance liquid chromatography (HPLC) , chromatography generally stands for a technique which separates mixtures based on different dynamic sharing of their components between two distinct physio-chemical environments called mobile and stationary phase by repeated absorption/desorption steps. Ion chromatography (IC) is a member of large family of liquid phase chromatographic methods (that is a mobile phase is a liquid and a stationary phase is a solid).

Ion exchange chromatography from Roshen Reji Idiculla

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0 Ion exchange chromatography2 /slideshow/ion-exchange-chromatography2/216046935 ionexchangechromatography2-200106172739
Ion exchange chromatography, Principles of Ion -exchange chromatographyHigh performance liquid chromatography (HPLC), Isocratic and Gradient Elution , The Ion Exchanger (Matrix)]]>
Ion exchange chromatography, Principles of Ion -exchange chromatographyHigh performance liquid chromatography (HPLC), Isocratic and Gradient Elution , The Ion Exchanger (Matrix)]]> Mon, 06 Jan 2020 17:27:39 GMT /slideshow/ion-exchange-chromatography2/216046935 RoshenRejiIdiculla@slideshare.net(RoshenRejiIdiculla) Ion exchange chromatography2 RoshenRejiIdiculla Ion exchange chromatography, Principles of Ion -exchange chromatographyHigh performance liquid chromatography (HPLC), Isocratic and Gradient Elution , The Ion Exchanger (Matrix) <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/ionexchangechromatography2-200106172739-thumbnail.jpg?width=120&height=120&fit=bounds" /> Ion exchange chromatography, Principles of Ion -exchange chromatographyHigh performance liquid chromatography (HPLC), Isocratic and Gradient Elution , The Ion Exchanger (Matrix)

Ion exchange chromatography2 from Roshen Reji Idiculla

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0 Learning new reactions by solving total syntheses merged /slideshow/learning-new-reactions-by-solving-total-syntheses-merged-216042150/216042150 learningnewreactionsbysolvingtotalsyntheses-merged-200106171904
Total synthesis of Sterpurenone New, Total Synthesis of (훽)-Cyperolone, Protecting Group-Free Total Synthesis of (−)-Lannotinidine B, Enantiospecific Total Synthesis of the (−)-Presilphiperfolan-8-ol, Enantioselective Total Synthesis of (−)-Pavidolide B, total synthesis of Eupalinilide E]]>
Total synthesis of Sterpurenone New, Total Synthesis of (훽)-Cyperolone, Protecting Group-Free Total Synthesis of (−)-Lannotinidine B, Enantiospecific Total Synthesis of the (−)-Presilphiperfolan-8-ol, Enantioselective Total Synthesis of (−)-Pavidolide B, total synthesis of Eupalinilide E]]> Mon, 06 Jan 2020 17:19:04 GMT /slideshow/learning-new-reactions-by-solving-total-syntheses-merged-216042150/216042150 RoshenRejiIdiculla@slideshare.net(RoshenRejiIdiculla) Learning new reactions by solving total syntheses merged RoshenRejiIdiculla Total synthesis of Sterpurenone New, Total Synthesis of (훽)-Cyperolone, Protecting Group-Free Total Synthesis of (−)-Lannotinidine B, Enantiospecific Total Synthesis of the (−)-Presilphiperfolan-8-ol, Enantioselective Total Synthesis of (−)-Pavidolide B, total synthesis of Eupalinilide E <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/learningnewreactionsbysolvingtotalsyntheses-merged-200106171904-thumbnail.jpg?width=120&height=120&fit=bounds" /> Total synthesis of Sterpurenone New, Total Synthesis of (훽)-Cyperolone, Protecting Group-Free Total Synthesis of (−)-Lannotinidine B, Enantiospecific Total Synthesis of the (−)-Presilphiperfolan-8-ol, Enantioselective Total Synthesis of (−)-Pavidolide B, total synthesis of Eupalinilide E

Learning new reactions by solving total syntheses merged from Roshen Reji Idiculla

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0 chemistry question - 5 questions /slideshow/chemistry-question-5-questions/216008783 stereochemistryquestion-200106161652
5 questions in chemistry ; 5 questions in chemistry ; 5 questions in chemistry ; 5 questions in chemistry ]]>
5 questions in chemistry ; 5 questions in chemistry ; 5 questions in chemistry ; 5 questions in chemistry ]]> Mon, 06 Jan 2020 16:16:52 GMT /slideshow/chemistry-question-5-questions/216008783 RoshenRejiIdiculla@slideshare.net(RoshenRejiIdiculla) chemistry question - 5 questions RoshenRejiIdiculla 5 questions in chemistry ; 5 questions in chemistry ; 5 questions in chemistry ; 5 questions in chemistry <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/stereochemistryquestion-200106161652-thumbnail.jpg?width=120&height=120&fit=bounds" /> 5 questions in chemistry ; 5 questions in chemistry ; 5 questions in chemistry ; 5 questions in chemistry

chemistry question - 5 questions from Roshen Reji Idiculla

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0 Questions for you /slideshow/questions-for-you-216006863/216006863 questionsforyou-200106161252
Questions for youQuestions for youQuestions for youQuestions for youQuestions for youQuestions for youQuestions for you]]>
Questions for youQuestions for youQuestions for youQuestions for youQuestions for youQuestions for youQuestions for you]]> Mon, 06 Jan 2020 16:12:52 GMT /slideshow/questions-for-you-216006863/216006863 RoshenRejiIdiculla@slideshare.net(RoshenRejiIdiculla) Questions for you RoshenRejiIdiculla Questions for youQuestions for youQuestions for youQuestions for youQuestions for youQuestions for youQuestions for you <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/questionsforyou-200106161252-thumbnail.jpg?width=120&height=120&fit=bounds" /> Questions for youQuestions for youQuestions for youQuestions for youQuestions for youQuestions for youQuestions for you

Questions for you from Roshen Reji Idiculla

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0 Funny creative questions for you /slideshow/funny-creative-questions-for-you/216004670 funnycreativequestionsforyou-200106160832
Funny creative questions for you; Funny creative questions for you; Funny creative questions for you; Funny creative questions for you; ]]>
Funny creative questions for you; Funny creative questions for you; Funny creative questions for you; Funny creative questions for you; ]]> Mon, 06 Jan 2020 16:08:32 GMT /slideshow/funny-creative-questions-for-you/216004670 RoshenRejiIdiculla@slideshare.net(RoshenRejiIdiculla) Funny creative questions for you RoshenRejiIdiculla Funny creative questions for you; Funny creative questions for you; Funny creative questions for you; Funny creative questions for you; <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/funnycreativequestionsforyou-200106160832-thumbnail.jpg?width=120&height=120&fit=bounds" /> Funny creative questions for you; Funny creative questions for you; Funny creative questions for you; Funny creative questions for you;

Funny creative questions for you from Roshen Reji Idiculla

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0 Carbon acid modified /slideshow/carbon-acid-modified/216001136 carbonacidmodified-200106160144
acid base indicators, carbon acid, pH scale., carbanions, acids and conjugate bases, reactions of carbon acids, phosphonium ions as carbon acids , Carbon acids in synthesis, Super acid, ]]>
acid base indicators, carbon acid, pH scale., carbanions, acids and conjugate bases, reactions of carbon acids, phosphonium ions as carbon acids , Carbon acids in synthesis, Super acid, ]]> Mon, 06 Jan 2020 16:01:44 GMT /slideshow/carbon-acid-modified/216001136 RoshenRejiIdiculla@slideshare.net(RoshenRejiIdiculla) Carbon acid modified RoshenRejiIdiculla acid base indicators, carbon acid, pH scale., carbanions, acids and conjugate bases, reactions of carbon acids, phosphonium ions as carbon acids , Carbon acids in synthesis, Super acid, <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/carbonacidmodified-200106160144-thumbnail.jpg?width=120&height=120&fit=bounds" /> acid base indicators, carbon acid, pH scale., carbanions, acids and conjugate bases, reactions of carbon acids, phosphonium ions as carbon acids , Carbon acids in synthesis, Super acid,

Carbon acid modified from Roshen Reji Idiculla

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0 Maillard reaction - a very brief overiew /slideshow/maillard-reaction-a-very-brief-overiew/215995750 maillardreaction-200106155232
Maillard reaction, Amadori product , furfurals, hydromethylfurfural, reductones , strecker aldehydes ]]>
Maillard reaction, Amadori product , furfurals, hydromethylfurfural, reductones , strecker aldehydes ]]> Mon, 06 Jan 2020 15:52:32 GMT /slideshow/maillard-reaction-a-very-brief-overiew/215995750 RoshenRejiIdiculla@slideshare.net(RoshenRejiIdiculla) Maillard reaction - a very brief overiew RoshenRejiIdiculla Maillard reaction, Amadori product , furfurals, hydromethylfurfural, reductones , strecker aldehydes <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/maillardreaction-200106155232-thumbnail.jpg?width=120&height=120&fit=bounds" /> Maillard reaction, Amadori product , furfurals, hydromethylfurfural, reductones , strecker aldehydes

Maillard reaction - a very brief overiew from Roshen Reji Idiculla

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0 chemistry of making chapati /RoshenRejiIdiculla/chemistry-of-making-chapati glutin-200106154841
Gluten, Gliadin, Glutenins , role of oil, butter ; role of yeast, aromatic compounds in chapati]]>
Gluten, Gliadin, Glutenins , role of oil, butter ; role of yeast, aromatic compounds in chapati]]> Mon, 06 Jan 2020 15:48:41 GMT /RoshenRejiIdiculla/chemistry-of-making-chapati RoshenRejiIdiculla@slideshare.net(RoshenRejiIdiculla) chemistry of making chapati RoshenRejiIdiculla Gluten, Gliadin, Glutenins , role of oil, butter ; role of yeast, aromatic compounds in chapati <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/glutin-200106154841-thumbnail.jpg?width=120&height=120&fit=bounds" /> Gluten, Gliadin, Glutenins , role of oil, butter ; role of yeast, aromatic compounds in chapati

chemistry of making chapati from Roshen Reji Idiculla

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0 Crispine- 12 paths to travel /slideshow/crispine-12-paths-to-travel/215991345 crispine-200106154507
Garinor Ruano Stereoselective Synthesis in 2013, Bischler Napieralski cyclisation accelerated by microwave irradiation, . Racemic crispine A from 6,7-dimethoxy-1,2,3,4 tetrahydroisoquinoline]]>
Garinor Ruano Stereoselective Synthesis in 2013, Bischler Napieralski cyclisation accelerated by microwave irradiation, . Racemic crispine A from 6,7-dimethoxy-1,2,3,4 tetrahydroisoquinoline]]> Mon, 06 Jan 2020 15:45:07 GMT /slideshow/crispine-12-paths-to-travel/215991345 RoshenRejiIdiculla@slideshare.net(RoshenRejiIdiculla) Crispine- 12 paths to travel RoshenRejiIdiculla Garinor Ruano Stereoselective Synthesis in 2013, Bischler Napieralski cyclisation accelerated by microwave irradiation, . Racemic crispine A from 6,7-dimethoxy-1,2,3,4 tetrahydroisoquinoline <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/crispine-200106154507-thumbnail.jpg?width=120&height=120&fit=bounds" /> Garinor Ruano Stereoselective Synthesis in 2013, Bischler Napieralski cyclisation accelerated by microwave irradiation, . Racemic crispine A from 6,7-dimethoxy-1,2,3,4 tetrahydroisoquinoline

Crispine- 12 paths to travel from Roshen Reji Idiculla

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0 Chemistry of cooking a brief view /slideshow/chemistry-of-cooking-a-brief-view/215987635 chemistryofcookingabriefview-200106153825
Food as a heterogeneous mixture, types of cooking, types of oils, chemistry of rancidity, uses of cooking , starch gelatinization in cooking rice, Maillard reaction, caramelisation]]>
Food as a heterogeneous mixture, types of cooking, types of oils, chemistry of rancidity, uses of cooking , starch gelatinization in cooking rice, Maillard reaction, caramelisation]]> Mon, 06 Jan 2020 15:38:25 GMT /slideshow/chemistry-of-cooking-a-brief-view/215987635 RoshenRejiIdiculla@slideshare.net(RoshenRejiIdiculla) Chemistry of cooking a brief view RoshenRejiIdiculla Food as a heterogeneous mixture, types of cooking, types of oils, chemistry of rancidity, uses of cooking , starch gelatinization in cooking rice, Maillard reaction, caramelisation <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/chemistryofcookingabriefview-200106153825-thumbnail.jpg?width=120&height=120&fit=bounds" /> Food as a heterogeneous mixture, types of cooking, types of oils, chemistry of rancidity, uses of cooking , starch gelatinization in cooking rice, Maillard reaction, caramelisation

Chemistry of cooking a brief view from Roshen Reji Idiculla

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0 Carbenes - octet defying molecules /slideshow/carbenes-octet-defying-molecules/215985127 carbenes-200106153330
Carbenes- octet defying molecules, its fate, reactions, synthesis of carbenoids,spin multiplicity of carbenes triplet, singlet carbenes, Fischer and Schrock carbenes]]>
Carbenes- octet defying molecules, its fate, reactions, synthesis of carbenoids,spin multiplicity of carbenes triplet, singlet carbenes, Fischer and Schrock carbenes]]> Mon, 06 Jan 2020 15:33:30 GMT /slideshow/carbenes-octet-defying-molecules/215985127 RoshenRejiIdiculla@slideshare.net(RoshenRejiIdiculla) Carbenes - octet defying molecules RoshenRejiIdiculla Carbenes- octet defying molecules, its fate, reactions, synthesis of carbenoids,spin multiplicity of carbenes triplet, singlet carbenes, Fischer and Schrock carbenes <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/carbenes-200106153330-thumbnail.jpg?width=120&height=120&fit=bounds" /> Carbenes- octet defying molecules, its fate, reactions, synthesis of carbenoids,spin multiplicity of carbenes triplet, singlet carbenes, Fischer and Schrock carbenes

Carbenes - octet defying molecules from Roshen Reji Idiculla

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0 Electromagnetic spectrum, interaction with matter /RoshenRejiIdiculla/electromagnetic-spectrum-interaction-with-matter electromagneticspectrum-200106150619
what is light, how is it useful in spectroscopy, what are the different ways it can interact with matter]]>
what is light, how is it useful in spectroscopy, what are the different ways it can interact with matter]]> Mon, 06 Jan 2020 15:06:19 GMT /RoshenRejiIdiculla/electromagnetic-spectrum-interaction-with-matter RoshenRejiIdiculla@slideshare.net(RoshenRejiIdiculla) Electromagnetic spectrum, interaction with matter RoshenRejiIdiculla what is light, how is it useful in spectroscopy, what are the different ways it can interact with matter <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/electromagneticspectrum-200106150619-thumbnail.jpg?width=120&height=120&fit=bounds" /> what is light, how is it useful in spectroscopy, what are the different ways it can interact with matter

Electromagnetic spectrum, interaction with matter from Roshen Reji Idiculla

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0 Protecting groups and their deprotection /slideshow/protecting-groups-and-their-deprotection/84361422 work-171218121251
Protecting group (PG) is a small molecule, to mask temporarily the a specific functional group of a molecule from undergoing reaction, allowing the rest of the functional groups present in the molecule to react without affecting the original reactivity and leave from the host molecule without affecting the rest of the functional groups. The addition of protecting groups to functional groups is termed ‘protection’ and removal of protecting group is ‘deprotection’. ]]>
Protecting group (PG) is a small molecule, to mask temporarily the a specific functional group of a molecule from undergoing reaction, allowing the rest of the functional groups present in the molecule to react without affecting the original reactivity and leave from the host molecule without affecting the rest of the functional groups. The addition of protecting groups to functional groups is termed ‘protection’ and removal of protecting group is ‘deprotection’. ]]> Mon, 18 Dec 2017 12:12:51 GMT /slideshow/protecting-groups-and-their-deprotection/84361422 RoshenRejiIdiculla@slideshare.net(RoshenRejiIdiculla) Protecting groups and their deprotection RoshenRejiIdiculla Protecting group (PG) is a small molecule, to mask temporarily the a specific functional group of a molecule from undergoing reaction, allowing the rest of the functional groups present in the molecule to react without affecting the original reactivity and leave from the host molecule without affecting the rest of the functional groups. The addition of protecting groups to functional groups is termed ‘protection’ and removal of protecting group is ‘deprotection’. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/work-171218121251-thumbnail.jpg?width=120&height=120&fit=bounds" /> Protecting group (PG) is a small molecule, to mask temporarily the a specific functional group of a molecule from undergoing reaction, allowing the rest of the functional groups present in the molecule to react without affecting the original reactivity and leave from the host molecule without affecting the rest of the functional groups. The addition of protecting groups to functional groups is termed ‘protection’ and removal of protecting group is ‘deprotection’.

Protecting groups and their deprotection from Roshen Reji Idiculla

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0 Chiral catalysts /slideshow/chiral-catalysts-82146610/82146610 chiralcatalysts-171116073205
this presentation describes ways to enantiomeric product synthesis, hence introducing to chiral catalysts. the temperature effects are discussed with relation to soai autocatalysis. it shows introduction to stereocartography.]]>
this presentation describes ways to enantiomeric product synthesis, hence introducing to chiral catalysts. the temperature effects are discussed with relation to soai autocatalysis. it shows introduction to stereocartography.]]> Thu, 16 Nov 2017 07:32:05 GMT /slideshow/chiral-catalysts-82146610/82146610 RoshenRejiIdiculla@slideshare.net(RoshenRejiIdiculla) Chiral catalysts RoshenRejiIdiculla this presentation describes ways to enantiomeric product synthesis, hence introducing to chiral catalysts. the temperature effects are discussed with relation to soai autocatalysis. it shows introduction to stereocartography. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/chiralcatalysts-171116073205-thumbnail.jpg?width=120&height=120&fit=bounds" /> this presentation describes ways to enantiomeric product synthesis, hence introducing to chiral catalysts. the temperature effects are discussed with relation to soai autocatalysis. it shows introduction to stereocartography.

Chiral catalysts from Roshen Reji Idiculla

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0 Chiral catalysts /slideshow/chiral-catalysts/82146363 chiralcatalysts-171116072547
this presentation describes ways to enantiomeric product synthesis, hence introducing to chiral catalysts. the temperature effects are discussed with relation to soai autocatalysis. it shows introduction to stereocartography.]]>
this presentation describes ways to enantiomeric product synthesis, hence introducing to chiral catalysts. the temperature effects are discussed with relation to soai autocatalysis. it shows introduction to stereocartography.]]> Thu, 16 Nov 2017 07:25:47 GMT /slideshow/chiral-catalysts/82146363 RoshenRejiIdiculla@slideshare.net(RoshenRejiIdiculla) Chiral catalysts RoshenRejiIdiculla this presentation describes ways to enantiomeric product synthesis, hence introducing to chiral catalysts. the temperature effects are discussed with relation to soai autocatalysis. it shows introduction to stereocartography. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/chiralcatalysts-171116072547-thumbnail.jpg?width=120&height=120&fit=bounds" /> this presentation describes ways to enantiomeric product synthesis, hence introducing to chiral catalysts. the temperature effects are discussed with relation to soai autocatalysis. it shows introduction to stereocartography.

Chiral catalysts from Roshen Reji Idiculla

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0 Introduction to infrared spectrometry /RoshenRejiIdiculla/introduction-to-infrared-spectrometry ir-170925120153
This is a document presentation of identification of major classes of organic compounds using IR spectroscopy. This is based on the book Wiley: Spectrometric Identification of Organic Compounds, by Robert Silverstein, 8th Edition .]]>
This is a document presentation of identification of major classes of organic compounds using IR spectroscopy. This is based on the book Wiley: Spectrometric Identification of Organic Compounds, by Robert Silverstein, 8th Edition .]]> Mon, 25 Sep 2017 12:01:53 GMT /RoshenRejiIdiculla/introduction-to-infrared-spectrometry RoshenRejiIdiculla@slideshare.net(RoshenRejiIdiculla) Introduction to infrared spectrometry RoshenRejiIdiculla This is a document presentation of identification of major classes of organic compounds using IR spectroscopy. This is based on the book Wiley: Spectrometric Identification of Organic Compounds, by Robert Silverstein, 8th Edition . <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/ir-170925120153-thumbnail.jpg?width=120&height=120&fit=bounds" /> This is a document presentation of identification of major classes of organic compounds using IR spectroscopy. This is based on the book Wiley: Spectrometric Identification of Organic Compounds, by Robert Silverstein, 8th Edition .

Introduction to infrared spectrometry from Roshen Reji Idiculla

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0 Designing synthetic photosynthetic systems /slideshow/designing-synthetic-photosynthetic-systems-80131896/80131896 designingsyntheticphotosyntheticsystems-copy-170925115550
This docx is a part of the the pdf with the same title which I have attached .]]>
This docx is a part of the the pdf with the same title which I have attached .]]> Mon, 25 Sep 2017 11:55:50 GMT /slideshow/designing-synthetic-photosynthetic-systems-80131896/80131896 RoshenRejiIdiculla@slideshare.net(RoshenRejiIdiculla) Designing synthetic photosynthetic systems RoshenRejiIdiculla This docx is a part of the the pdf with the same title which I have attached . <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/designingsyntheticphotosyntheticsystems-copy-170925115550-thumbnail.jpg?width=120&height=120&fit=bounds" /> This docx is a part of the the pdf with the same title which I have attached .

Designing synthetic photosynthetic systems from Roshen Reji Idiculla

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0 Designing synthetic photosynthetic systems /slideshow/designing-synthetic-photosynthetic-systems/80131793 designingsyntheticphotosyntheticsystems-170925115222
this presentation is just an introduction to the vast field of photoelectrochemical cells and it's constituents. ]]>
this presentation is just an introduction to the vast field of photoelectrochemical cells and it's constituents. ]]> Mon, 25 Sep 2017 11:52:22 GMT /slideshow/designing-synthetic-photosynthetic-systems/80131793 RoshenRejiIdiculla@slideshare.net(RoshenRejiIdiculla) Designing synthetic photosynthetic systems RoshenRejiIdiculla this presentation is just an introduction to the vast field of photoelectrochemical cells and it's constituents. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/designingsyntheticphotosyntheticsystems-170925115222-thumbnail.jpg?width=120&height=120&fit=bounds" /> this presentation is just an introduction to the vast field of photoelectrochemical cells and it's constituents.

Designing synthetic photosynthetic systems from Roshen Reji Idiculla

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0 https://public.slidesharecdn.com/v2/images/profile-picture.png https://cdn.slidesharecdn.com/ss_thumbnails/100namedreactions-200106173517-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/100-named-reactions/216051450 100 named reactions https://cdn.slidesharecdn.com/ss_thumbnails/ion-exchangechromatography-200106173010-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/ion-exchange-chromatography-216048395/216048395 Ion exchange chromato... https://cdn.slidesharecdn.com/ss_thumbnails/ionexchangechromatography2-200106172739-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/ion-exchange-chromatography2/216046935 Ion exchange chromatog...