Study of Chemical Ligation Via 17-, 18- and 19-Membered Cyclic Transition States

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DC Field	Value	Language
dc.contributor.author	Bajaj, Kiran	-
dc.date.accessioned	2021-11-11T11:23:28Z	-
dc.date.available	2021-11-11T11:23:28Z	-
dc.date.issued	2012-09-14	-
dc.identifier.uri	https://onlinelibrary.wiley.com/doi/10.1111/cbdd.12053	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3503	-
dc.description.abstract	Unprotected S-acylated cysteine isopeptides containing α-, β- or γ-amino acid units have been synthesized, and their conversion to native hexapeptides by S- to the N-terminus ligations involving 17-, 18- and 19-membered cyclic transition states have been demonstrated both experimentally and computationally to be more favorable than intermolecular cross-ligations.	en_US
dc.language.iso	en	en_US
dc.publisher	Wiley	en_US
dc.subject	Chemistry	en_US
dc.subject	Chemical Ligation	en_US
dc.subject	19-Membered Cyclic	en_US
dc.title	Study of Chemical Ligation Via 17-, 18- and 19-Membered Cyclic Transition States	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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