Catalytic Enantioselective Cr-Mediated Propargylation: Application to Halichondrin Synthesis-Reference-Cited by-同舟云学术

Catalytic Enantioselective Cr-Mediated Propargylation: Application to Halichondrin Synthesis

Published:2009-09-16 Issue:20 Volume:11 Page:4520-4523
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Liu Songbai¹,Kim Joseph T.¹,Dong Cheng-Guo¹,Kishi Yoshito¹

Affiliation:

1. Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol9016595

Reference36 articles.

1. Total synthesis of halichondrin B and norhalichondrin B

2. For isolation and synthesis on the halichondrins, see refs1−3in the preceding paper:Yang, Y.R.; Kim, D.S.; Kishi, Y.Org. Lett.2009,11, (DOI10.1021/ol9016589).

3. For discovery and development of E7389, see ref5in ref2.

4. For reviews on Cr-mediated carbon−carbon bond-forming reactions, see:

5. aSaccomano, N. A.InComprehensive Organic Synthesis;Trost, B. M.; Fleming, I., Eds.Pergamon:Oxford, 1991; Vol. 1, p173.

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