Staudinger/aza-Wittig reaction to accessNβ-protected amino alkyl isothiocyanates-Reference-Cited by-同舟云学术

Staudinger/aza-Wittig reaction to accessNβ-protected amino alkyl isothiocyanates

Published:2018 Issue:26 Volume:16 Page:4874-4880
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Santhosh L.¹²,Durgamma S.¹²,Shekharappa Shekharappa¹²,Sureshbabu Vommina V.¹²^ORCID

Affiliation:

1. Bangalore

2. India

Abstract

General strategy of the Staudinger/aza-Wittig reaction has been effectively employed as anad hocapproach for accessingN^β-protected alkyl isothiocyanates fromN^β-protected alkyl azides.

Funder

Science and Engineering Research Board

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB01061G

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5. Synthesis and structure–activity relationships of aliphatic isothiocyanate analogs as antibiotic agents

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