‘Hidden’ axial chirality as a stereodirecting element in reactions involving enol(ate) intermediates. Part 1. Cyclisation reactions of methyl (4R)-3-(2-diazo-3-oxobutanoyl)thiazolidine-4-carboxylate and related compounds-Reference-Cited by-同舟云学术

‘Hidden’ axial chirality as a stereodirecting element in reactions involving enol(ate) intermediates. Part 1. Cyclisation reactions of methyl (4R)-3-(2-diazo-3-oxobutanoyl)thiazolidine-4-carboxylate and related compounds

Published:1993 Issue:15 Volume: Page:1761-1770
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Beagley Brian,Betts Michael J.,Pritchard Robin G.,Schofield Anthony,Stoodley Richard J.,Vohra Shaheen

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1993/P1/P19930001761

Reference25 articles.

1. A cyclisation reaction of methyl (4R)-3-(2-diazo-3-oxobutanoyl)thiazolidine-4-carboxylate which proceeds with retention of configuration, probably via a planar ester enolate intermediate possessing axial chirality

2. Synthesis and catalytic reactions of chiral N-(diazoacetyl)oxazolidones

3. 3-(3-Pyrrolyl)thiopyrrolidones as precursors of benzo[1,2-b:4,3-b']dipyrroles. Synthesis of structures related to the phosphodiesterase inhibitors PDE-I and PDE-II

4. The Action of Formaldehyde upon Cysteine

5. Direct introduction of the diazo function in organic synthesis

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