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Photochemical Reactions Via Zwitterionic Intermediates

 

Marketed By :  Scholars' Press   Sold By :  Kamal Books International  
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  • Product Description
 

The research focuses on the design of photoremovable protecting groups that can be used to deprotect biological substrates of an organic compound by photolysis. The deprotection of the protecting group via photolysis requires heterolysis of a bond to the substrate. Heterolysis of a C-O or C-S ?-bonds in a zwitterionic intermediate is proposed. The photochemical electrocyclic reactions studied involve acrylanilides, benzothiophene carboxanilides, and N-(9-oxothioxanthenyl) benzothiophene carboxamides. The most efficient photochemical electrocyclic ring closure and leaving group expulsion found thus far occurs with benzothiophene carboxanilides, which has considerable potential for use as cage compounds.

Product Specifications
SKU :COC61212
AuthorMajher I. Sarker and Tasnuva Shahrin
LanguageEnglish
BindingPaperback
Number of Pages280
Publishing Year10.02.2014
ISBN9783639708783
Edition1 st
Book TypeOrganic chemistry
Country of ManufactureIndia
Product BrandScholars' Press
Product Packaging InfoBox
In The Box1 Piece
Product First Available On ClickOnCare.com2015-08-05 00:00:00
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