Synthesis of Homoallylic Chiral Tertiary Alcohols via Chelation-Controlled Diastereoselective Nucleophilic Addition on α-Alkoxyketones: Application for the Synthesis of the C1−C11 Subunit of 8-epi-Fostriecin-Reference-Cited by-同舟云学术

Synthesis of Homoallylic Chiral Tertiary Alcohols via Chelation-Controlled Diastereoselective Nucleophilic Addition on α-Alkoxyketones: Application for the Synthesis of the C1−C11 Subunit of 8-epi-Fostriecin

Published:2003-09-06 Issue:20 Volume:5 Page:3755-3757
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Ramachandran P. Veeraraghavan¹,Liu Haipeng¹,Ram Reddy M. Venkat¹,Brown Herbert C.¹

Affiliation:

1. Herbert C. Brown Center for Borane Research, 560 Oval Drive, Department of Chemistry, Purdue University, West Lafayette, Indiana 47907-2084

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol035516c

Reference37 articles.

1. Acyclic stereocontrol via allylic organometallic compounds

2. Selective reactions using allylic metals

3. α-Chiral allylboronates: reagents for asymmetric synthesis

4. (b) Roush, W. R. ACS Symposium Series 386; American Chemical Society: Washington, DC, 1989; p 242.

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