Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/62027
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSama, Gopal Reddy-
dc.date.accessioned2023-06-15T06:08:28Z-
dc.date.available2023-06-15T06:08:28Z-
dc.date.issued2023-06-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/62027-
dc.description662-672en_US
dc.description.abstractPhotolabile protecting groups (PPGs) are invaluable tools for protecting a variety of functionalities and serve as alternatives to protecting groups that need chemical cleavage. PPGs are mainly classified into 3 categories namely, 2-nitrobenzyl type PPGs, coumarin-based PPGs, and benzyl type PPGs which have been designed by Wang and co-workers based on the meta effect and computational study observations. This work describes the design and synthesis of a julolidinebased benzyl type PPG 4 and the analysis of its reaction intermediates. The julolidine PPG 4 is applied for the protection of alcohols as carbonates, amines as carbamates, carboxylic acids as esters, and hydroxamic acid. Analysis of the photolyzed samples by HPLC has also been conducted.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.62(06) [June 2023]en_US
dc.subjectBenzyl type PPGsen_US
dc.subjectJulolidine-based PPGen_US
dc.subjectMild conditionen_US
dc.subjectDeprotectionen_US
dc.titleDesign and application of a new julolidine-based photolabile protecting groupen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v62i6.2570en_US
Appears in Collections:IJC Vol.62(06) [June 2023]

Files in This Item:
File Description SizeFormat 
IJC 62 (06) 662-672.pdf8.81 MBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.