Synthesis of a des-B-Ring Bryostatin Analogue Leads to an Unexpected Ring Expansion of the Bryolactone Core-Reference-Cited by-同舟云学术

Synthesis of a des-B-Ring Bryostatin Analogue Leads to an Unexpected Ring Expansion of the Bryolactone Core

Published:2014-09-10 Issue:38 Volume:136 Page:13202-13208
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Kraft Matthew B.¹,Poudel Yam B.¹,Kedei Noemi²,Lewin Nancy E.²,Peach Megan L.³,Blumberg Peter M.²,Keck Gary E.¹

Affiliation:

1. Department of Chemistry, University of Utah, Salt Lake City, Utah 84112, United States

2. Laboratory of Cancer Biology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892-4255, United States

3. Basic Science Program, Leidos Biomedical Research, Inc., Chemical Biology Laboratory, Frederick National Laboratory for Cancer Research, Frederick, Maryland 21702, United States

Funder

National Institutes of Health

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja5078188

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4. Identification of Sibling Species of the Bryozoan Bugula neritina That Produce Different Anticancer Bryostatins and Harbor Distinct Strains of the Bacterial Symbiont "Candidatus Endobugula sertula"

5. Small-subunit rRNA genes and in situ hybridization with oligonucleotides specific for the bacterial symbionts in the larvae of the bryozoan Bugula neritina and proposal of "Candidatus endobugula sertula"

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