Synthetic Access to the Mandelalide Family of Macrolides: Development of an Anion Relay Chemistry Strategy-Reference-Cited by-同舟云学术

Synthetic Access to the Mandelalide Family of Macrolides: Development of an Anion Relay Chemistry Strategy

Published:2018-02-26 Issue:8 Volume:83 Page:4287-4306
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Nguyen Minh H.¹^ORCID,Imanishi Masashi¹,Kurogi Taichi¹,Wan Xuemei²,Ishmael Jane E.²,McPhail Kerry L.²^ORCID,Smith Amos B.¹^ORCID

Affiliation:

1. Department of Chemistry, Laboratory for Research on the Structure of Matter, and Monell Chemical Senses Center, University of Pennsylvania, Philadelphia, Pennsylvania 19104, United States

2. Department of Pharmaceutical Sciences, Oregon State University, Corvallis, Oregon 97331, United States

Funder

National Cancer Institute

Japan Society for the Promotion of Science

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b00268

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2. Evolution of multi-component anion relay chemistry (ARC): construction of architecturally complex natural and unnatural products

3. The Spongistatins: Architecturally Complex Natural Products-Part One: A Formal Synthesis of (+)-Spongistatin 1 by Construction of an Advanced ABCD Fragment

4. The Spongistatins: Architecturally Complex Natural Products-Part Two: Synthesis of the C(29-51) Subunit, Fragment Assembly, and Final Elaboration to (+)-Spongistatin 2

5. Spongipyran synthetic studies. Evolution of a scalable total synthesis of (+)-spongistatin 1

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