Hydroxy-Directed Diastereoselective Installation of a Methyl Group on Indalone Models and Spiroketal Potential Precursors for the Bafilomycin A1 C15−C25 Subunit-Reference-Cited by-同舟云学术

Hydroxy-Directed Diastereoselective Installation of a Methyl Group on Indalone Models and Spiroketal Potential Precursors for the Bafilomycin A1 C15−C25 Subunit

Published:2002-03-13 Issue:7 Volume:67 Page:2118-2124
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Poupon Jean-Christophe¹,Lopez Roman¹,Prunet Joëlle¹,Férézou Jean-Pierre¹

Affiliation:

1. Laboratoire de Synthèse Organique associé au CNRS, UMR 7652, Ecole Polytechnique, DCSO, 91128 Palaiseau, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo016231l

Reference21 articles.

1. The structure of the bafilomycins, a new group of macrolide antibiotics

2. Bafilomycins: a class of inhibitors of membrane ATPases from microorganisms, animal cells, and plant cells.

3. Diastereoselective aldol reactions of β-silyloxy ethyl ketones. Application to the total synthesis of bafilomycin A1

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