The First Stable Enantiomerically Pure Chiral N−H Oxaziridines: Synthesis and Reactivity-Reference-Cited by-同舟云学术

The First Stable Enantiomerically Pure Chiral N−H Oxaziridines: Synthesis and Reactivity

Published:2000-06-01 Issue:13 Volume:65 Page:4204-4207
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Page Philip C. Bulman¹,Murrell Victor L.¹,Limousin Corinne¹,Laffan David D. P.¹,Bethell Donald¹,Slawin Alexandra M. Z.¹,Smith Timothy A. D.¹

Affiliation:

1. Department of Chemistry, Loughborough University, Loughborough, Leicestershire, LE11 3TU, England, Astra Zeneca Pharmaceuticals, Silk Road Business Park, Macclesfield, Cheshire, SK10 2NA, U.K., Robert Robinson Laboratories, Department of Chemistry, University of Liverpool, Oxford Street, Liverpool L69 3BX, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo000176j

Reference24 articles.

1. Oxaziridinyl free radicals

2. The asymmetric synthesis of .alpha.-amino acids. Electrophilic azidation of chiral imide enolates, a practical approach to the synthesis of (R)- and (S)-.alpha.-azido carboxylic acids

3. The nonplanar amide group in N-acylaziridines: conformational behavior and chiroptical properties

4. Oxaziridine, V. Herstellung und Umlagerung von 2‐Acyl‐oxaziridinen

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