Properties and reactions of substituted 1,2-thiazetidine 1,1-dioxides: Acylation of β-sultams at C-4, reduction of 4-acyl-β-sultams, and stereochemistry of 4-(α-hydroxyalkyl)-β-sultams-Reference-Cited by-同舟云学术

Properties and reactions of substituted 1,2-thiazetidine 1,1-dioxides: Acylation of β-sultams at C-4, reduction of 4-acyl-β-sultams, and stereochemistry of 4-(α-hydroxyalkyl)-β-sultams

Published:1991-02-12 Issue:2 Volume:1991 Page:171-178
ISSN:0170-2041
Container-title:Liebigs Annalen der Chemie
language:de
Short-container-title:Liebigs Ann. Chem.

Author:

Müller Martin,Otto Hans-Hartwig

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Reference30 articles.

1. The penems, a new class of .beta.-lactam antibiotics. 5. Total synthesis of racemic 6-.alpha.-hydroxyethylpenemcarboxylic acids

2. Synthesis of 6-(1-hydroxyethyl)-1,1-dimethyl-1-carba-2-penem derivatives via dieckmann-type cyclization

3. 1-(Dialkylaminomethyl)-azetidin-2-ones. Intermediates in a highly stereoselective preparation of trans-3,4-disubstituted azetidin-2-ones

4. A stereocontrolled synthesis of (+)-thienamycin

5. Metallation of N-Substituted β-Lactams. A Method for the Introduction of 3-Substituents into β-Lactams

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