Allylic Alcohol Transposition by Ortho Ester-Initiated Carbonate Extension. Synthesis of the Vasodilator 11(R),12(S),15(S)-Trihydroxyeicosa- 5(Z),8(Z),13(E)-trienoic Acid-Reference-Cited by-同舟云学术

Allylic Alcohol Transposition by Ortho Ester-Initiated Carbonate Extension. Synthesis of the Vasodilator 11(R),12(S),15(S)-Trihydroxyeicosa- 5(Z),8(Z),13(E)-trienoic Acid

Published:2006-05-01 Issue:11 Volume:8 Page:2441-2443
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Conrow Raymond E.¹

Affiliation:

1. Alcon Research, Ltd., Chemical Preparations Research, 6201 South Freeway, R8-6, Fort Worth, Texas 76134

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol0608808

Reference30 articles.

1. Asymmetric synthesis of the stereoisomers of 11,12,15(S)-trihydroxyeicosa-5(Z),8(Z),13(E)-trienoic acid, a potent endothelium-derived vasodilator

2. Transformation of 15-hete to 14,15-dihydroxyeicosatrienoic acid and 11,14,15- and 13,14,15-trihydroxyeicosatrienoic acid

3. 2-Substituted tetrahydrofurans of known absolute stereochemistry by ScN' chirality transfer

4. Synthesis of Cryptophycin 52 Using the Sharpless Asymmetric Dihydroxylation: Diol to Epoxide Transformation Optimized for a Base-Sensitive Substrate

5. Stereospecific Synthesis of Cryptophycin 1

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