Efficient, large-scale preparation of (R)- and (S)-1-(2,4,6-triisopropylphenyl)ethanol, versatile chiral auxiliary for cyclopentenone, γ-butyrolactone, and γ-butyrolactam synthesis-Reference-Cited by-同舟云学术

Efficient, large-scale preparation of (R)- and (S)-1-(2,4,6-triisopropylphenyl)ethanol, versatile chiral auxiliary for cyclopentenone, γ-butyrolactone, and γ-butyrolactam synthesis

Published:1996-09 Issue:9 Volume:7 Page:2707-2710
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Delair Philippe,Kanazawa Alice M.,de Azevedo Mariangela B.M.,Greene Andrew E.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference24 articles.

1. Asymmetric induction in the cycloaddition reaction of dichloroketene with chiral enol ethers. A versatile approach to optically active cyclopentenone derivatives.

2. Enantioselective ring construction through asymmetric olefin-ketene cycloaddition. A highly enantiocontrolled approach to (-)-.alpha.-cuparenone and (+)-.beta.-cuparenone

3. Novel, enantioselective lactone construction. First synthesis of methylenolactocin, antitumor antibiotic from Penicillium sp

4. Synthesis and absolute stereochemistry of (-)-protolichesterinic acid, antitumor antibiotic lactone from Cetraria islandica

5. Asymmetric Diels-Alder cycloadditions using chiral alkyl vinyl ethers and a dienyl sulfone

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