Progress toward the Total Synthesis of Bafilomycin A1: Stereoselective Synthesis of the C15−C25 Subunit by Additions of Nonracemic Allenylzinc Reagents to Aldehydes-Reference-Cited by-同舟云学术

Progress toward the Total Synthesis of Bafilomycin A1: Stereoselective Synthesis of the C15−C25 Subunit by Additions of Nonracemic Allenylzinc Reagents to Aldehydes

Published:2000-08-10 Issue:18 Volume:2 Page:2897-2900
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Marshall James A.¹,Adams Nicholas D.¹

Affiliation:

1. Department of Chemistry, McCormick Road, P.O. Box 400319, University of Virginia, Charlottesville, Virginia 22904

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol006344b

Reference21 articles.

1. Metabolic products of microorganisms. 224. Bafilomycins, a new group of macrolide antibiotics. Production, isolation, chemical structure and biological activity.

2. Alkaline degradation products of concanamycin a

3. The structure and absolute configuration of the 18-membered macrolide lactone antibiotic X-4357B (concanamycin A).

4. The isolation and structures of hygrolidin amide and defumarylhygrolidin.

5. Stereochemistry of the hygrolidins

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