Synthesis, resolution and absolute configuration determination of (S)- and (R)-4-formyl-5-hydroxy [2.2]paracyclophane and its application in the asymmetric synthesis of α-amino acids-Reference-Cited by-同舟云学术

Synthesis, resolution and absolute configuration determination of (S)- and (R)-4-formyl-5-hydroxy [2.2]paracyclophane and its application in the asymmetric synthesis of α-amino acids

Published:1995 Issue:14 Volume: Page:1873-1879
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Antonov Dmitri Yu.,Belokon Yuri N.,Ikonnikov Nikolai S.,Orlova Svetlana A.,Pisarevsky Aleksander P.,Raevski Nikolai I.,Rozenberg Valeria I.,Sergeeva Elena V.,Struchkov Yuri T.,Tararov Vitali I.,Vorontsov Evgeni V.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1995/P1/P19950001873

Reference32 articles.

1. The chiral pool as a source of enantioselective catalysts and auxiliaries

2. R. Noyori , Asymmetric Catalysis in Organic Synthesis, Wiley, New York, 1994.

3. Asymmetric synthesis catalyzed by chiral ferrocenylphosphine-transition metal complexes. 2. Nickel- and palladium-catalyzed asymmetric Grignard cross-coupling

4. Asymmetric synthesis catalyzed by chiral ferrocenylphosphine-metal complexes

5. Chiral cooperativity: the nature of the diastereoselective and enantioselective step in the gold(I)-catalyzed aldol reaction utilizing chiral ferrocenylamine ligands

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