Isomer selectivity in stereocontrolled Payne rearrangement–epoxide cleavage of 2,3-epoxy alcohols in aprotic solvents: application to an enantioselective total synthesis of (+)-exo-brevicomin-Reference-Cited by-同舟云学术

Isomer selectivity in stereocontrolled Payne rearrangement–epoxide cleavage of 2,3-epoxy alcohols in aprotic solvents: application to an enantioselective total synthesis of (+)-exo-brevicomin

Published:1990 Issue:5 Volume: Page:1375-1382
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Page Philip C. Bulman,Rayner Christopher M.,Sutherland Ian O.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1990/P1/P19900001375

Reference30 articles.

1. Epoxide Migrations with α,β-Epoxy Alcohols

2. J. G. Buchanan and H. Z.Sable, in ‘Selective Organic Transformations’, vol. 25, ed. B. S. Thyagarajan, Wiley, New York, 1972, 109.

3. B. E. Rossiter , in ‘Asymmetric Synthesis,’ vol. 5, ed. J. D. Morrison, Academic Press, New York, 1985, ch. 7.

4. 728. Cyclitols. Part VII. Anhydroinositols and the “epoxide migration.”

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