Synthetic Aspects of Homochiral β-Lactams Derived from N-Protected α-Aminoimines Via Asymmetric [2+2] Cycloaddition Reaction-Reference-Cited by-同舟云学术

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Synthetic Aspects of Homochiral β-Lactams Derived from N-Protected α-Aminoimines Via Asymmetric [2+2] Cycloaddition Reaction

Published:2010-09-01 Issue:7 Volume:101 Page:541-554
ISSN:0037-9646
Container-title:Bulletin des Sociétés Chimiques Belges
language:en
Short-container-title:Bull. Soc. Chim. Belges

Author:

Palomo Claudio,Cossío Fernando P.,Cuevas Carmen,Ontoria Jesús M.,Odriozola José M.,Munt Simon

Publisher

Wiley

Subject

General Chemistry

Reference66 articles.

1. Zur Kenntniss der Ketene. Diphenylketen

2. Chiral control of the Staudinger reaction

3. Syntheses of 3-amino-2-azetidinones: A literature survey

4. An Enantioselective ?-Lactam Synthesis Starting fromL-(S)-Glyceraldehyde Acetonide

Cited by 12 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Asymmetric Synthesis of β-Lactams by the Staudinger Reaction;Organic Reactions;2018-04-04

2. Ketenes as Privileged Synthons in the Syntheses of Heterocyclic Compounds. Part 1;Advances in Heterocyclic Chemistry;2014

3. Asymmetric Synthesis of β-Lactams via the Staudinger Reaction;Amino Acids, Peptides and Proteins in Organic Chemistry;2011-04-07

4. Highly Stereoselective Synthesis of β-Lactams Utilizing α-Chloroimines as New and Powerful Chiral Inductors;Chemistry - A European Journal;2008-06-11

5. Asymmetric synthesis of 3-amino-4-hydroxy-2-(hydroxymethyl)pyrrolidines as potential glycosidase inhibitors;Organic & Biomolecular Chemistry;2007

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