A Useful Synthesis of Chiral Glyoxylates-Reference-Cited by-同舟云学术

A Useful Synthesis of Chiral Glyoxylates

Published:1990-09 Issue:18 Volume:20 Page:2837-2847
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Fernández Franco,García Gerardo,Rodríguez José E.

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/00397919008051497

Reference25 articles.

1. Synthesis and Reactivity of 2-Azabicyclo[2.2.1]heptanes, Heptenes and Heptadienes

2. The unexpected formation of trans-β-lactams in the reaction of α-iminoesters (RNC(H)C(O)OR′) with diethylzinc. Crystal structure of trans -1-(N -t -butyl)-3-(N-t -butyl-N-ethylamino)-4- methoxycarbonylazetidin-2-one

3. The acid chloride–iminoester condensation: a direct approach to PS-5 and PS-6 intermediates and related compounds

4. .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid. Configuration by asymmetric synthesis

5. Isolation of anhydrous menthyl glyoxylate requires distillation, and its separation from tin co-products is not very sharp, thus lowering the yield of the desired product

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