Gold(I)-Mediated Cycloisomerization/Cycloaddition Enables Bioinspired Syntheses of Neonectrolides B

Gold(I)-Mediated Cycloisomerization/Cycloaddition Enables Bioinspired Syntheses of Neonectrolides B–E and Analogues

Published:2019-08-30 Issue:38 Volume:141 Page:15135-15144
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Purgett Thomas J.¹,Dyer Matthew W.¹,Bickel Bryce¹,McNeely James¹,Porco John A.¹^ORCID

Affiliation:

1. Department of Chemistry, Center for Molecular Discovery (BU-CMD), Boston University, 590 Commonwealth Avenue, Boston, Massachusetts 02215, United States

Funder

Boston University

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.9b06355

Reference80 articles.

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5. Neonectrolide A, a New Oxaphenalenone Spiroketal from the Fungus Neonectria sp.

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