Organolithium-Mediated Conversion of β-Alkoxy Aziridines into Allylic Sulfonamides: Effect of the N-Sulfonyl Group and a Formal Synthesis of (±)-Perhydrohistrionicotoxin-Reference-Cited by-同舟云学术

Organolithium-Mediated Conversion of β-Alkoxy Aziridines into Allylic Sulfonamides: Effect of the N-Sulfonyl Group and a Formal Synthesis of (±)-Perhydrohistrionicotoxin

Published:2008-09-09 Issue:19 Volume:73 Page:7852-7855
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Coote Susannah C.¹,Moore Stephen P.¹,O’Brien Peter¹,Whitwood Adrian C.¹,Gilday John¹

Affiliation:

1. Department of Chemistry, University of York, Heslington, York YO10 5DD, U.K., and Process R & D, AstraZeneca Avlon Works, Severn Road, Hallen, Bristol BS10 7ZE, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo801586h

Reference28 articles.

1. Oxiranyl Anions and Aziridinyl Anions

2. Expanding the Utility of Lithiated Epoxides and Aziridines in Synthesis

3. cFor a special issue ofTetrahedronon “oxiranyl and aziridinyl anions”, see:Tetrahedron 2003, 59, 9693−9847

4. New Route to Azaspirocycles via the Organolithium-Mediated Conversion of β-Alkoxy Aziridines into Cyclopentenyl Amines

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