A Facile Synthesis of Thioacids from N -Acylbenzotriazoles

Siva S. Panda

doi:10.1055/s-0033-1340292

A Facile Synthesis of Thioacids from N -Acylbenzotriazoles

Siva S. Panda

Chemistry and Biochemistry

Research output: Contribution to journal › Article › peer-review

7 Scopus citations

Abstract

Protected amino/peptide thioacids have been synthesized in pure form in excellent yields and with retention of chirality by using protected aminoacyl- and peptidoylbenzotriazoles as active intermediates.

Original language	English (US)
Article number	ST-2013-S0893-L
Pages (from-to)	247-250
Number of pages	4
Journal	Synlett
Volume	25
Issue number	2
DOIs	https://doi.org/10.1055/s-0033-1340292
State	Published - Jan 2014

Keywords

amino acids
benzotriazole methodology
chirality
peptides
thioacids

ASJC Scopus subject areas

Organic Chemistry

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10.1055/s-0033-1340292

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title = "A Facile Synthesis of Thioacids from N -Acylbenzotriazoles",

abstract = "Protected amino/peptide thioacids have been synthesized in pure form in excellent yields and with retention of chirality by using protected aminoacyl- and peptidoylbenzotriazoles as active intermediates.",

keywords = "amino acids, benzotriazole methodology, chirality, peptides, thioacids",

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year = "2014",

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AB - Protected amino/peptide thioacids have been synthesized in pure form in excellent yields and with retention of chirality by using protected aminoacyl- and peptidoylbenzotriazoles as active intermediates.

KW - amino acids

KW - benzotriazole methodology

KW - chirality

KW - peptides

KW - thioacids

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JF - Synlett

IS - 2

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ER -

A Facile Synthesis of Thioacids from N -Acylbenzotriazoles

Abstract

Keywords

ASJC Scopus subject areas

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