An Entry to the Optically Pure β-Lactam Skeleton Based on 1,3-Dipolar Cycloaddition of Nitrones to 4,6-Di-O-Acetyl-2,3-Dideoxy-D-Threo-Hex-2-Enono-1,5-Lactone-Reference-Cited by-同舟云学术

An Entry to the Optically Pure β-Lactam Skeleton Based on 1,3-Dipolar Cycloaddition of Nitrones to 4,6-Di-O-Acetyl-2,3-Dideoxy-D-Threo-Hex-2-Enono-1,5-Lactone

Published:1987-09 Issue:3 Volume:6 Page:463-470
ISSN:0732-8303
Container-title:Journal of Carbohydrate Chemistry
language:en
Short-container-title:Journal of Carbohydrate Chemistry

Author:

Panfil Irma,Belzecki CzesLaw,Chmielewski Marek

Publisher

Informa UK Limited

Subject

Organic Chemistry,Biochemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/10256018808623883

Reference9 articles.

1. Synthesis of b-Lactams from a,b-Unsaturated Sugar d-Lactones

2. The asymmetric synthesis of β-lactam antibiotics -II. The first enantioselective synthesis of the carbacephalosporin nucleus.

3. Studies on v-triazoles. Part 4. The 4-methoxybenzyl group, a versatile N-protecting group for the synthesis of N-unsubstituted v-triazoles

4. Cycloaddition of nitrones and α,β-unsaturated sugar lactones

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5. 1,3-Dipolar Cycloadditions in the Synthesis of Carbohydrate Mimics. Part 2: Nitrones and Oximes;Current Organic Chemistry;2003-04-01