Aziridine-Mediated Ligation at Phenylalanine and Tryptophan Sites

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DC Field	Value	Language
dc.contributor.author	Sakhuja, Rajeev	-
dc.contributor.author	Bajaj, Kiran	-
dc.date.accessioned	2021-11-11T10:59:22Z	-
dc.date.available	2021-11-11T10:59:22Z	-
dc.date.issued	2017-05-23	-
dc.identifier.uri	https://onlinelibrary.wiley.com/doi/10.1002/asia.201700538	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3358	-
dc.description.abstract	An efficient approach towards peptide synthesis that allows easy access to variety of small peptides via one-pot aziridine-mediated ligation/desulfurization strategy has been described. The protocol afforded a library of phenylalanine- and tryptophan-containing α-peptides in good yields by regioselective ring-opening of aziridine-3-aryl-2-carboxylates with peptide thioacids, followed by desulfurization.	en_US
dc.language.iso	en	en_US
dc.publisher	Wiley	en_US
dc.subject	Chemistry	en_US
dc.subject	Aziridine-Mediated	en_US
dc.subject	Phenylalanine	en_US
dc.subject	Tryptophan	en_US
dc.title	Aziridine-Mediated Ligation at Phenylalanine and Tryptophan Sites	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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