Efficient Syntheses of Thiadiazole Peptides

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DC Field	Value	Language
dc.contributor.author	Bajaj, Kiran	-
dc.date.accessioned	2021-11-11T11:23:44Z	-
dc.date.available	2021-11-11T11:23:44Z	-
dc.date.issued	2010-08-09	-
dc.identifier.uri	https://pubs.acs.org/doi/abs/10.1021/jo100922c	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3507	-
dc.description.abstract	Novel N-(Cbz-aminoacyl)thiosemicarbazides 3a−c were cyclized by treatment with sulfuric acid to give 1,3,4-thiadiazoles 4a−c. Compounds 4a−c reacted with N-(Cbz-aminoacyl)- and -dipeptidoylbenzotriazoles to afford chirally pure 1,3,4-thiadiazol-2-yl-substituted amino acids 6a−c and dipeptides 7a−c.	en_US
dc.language.iso	en	en_US
dc.publisher	ACS	en_US
dc.subject	Chemistry	en_US
dc.subject	High-performance liquid chromatography	en_US
dc.subject	Peptides and proteins	en_US
dc.subject	Electromagnetic radiation	en_US
dc.title	Efficient Syntheses of Thiadiazole Peptides	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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