Ruthenium‐Catalyzed Butadiene‐Mediated Crotylation and Oxazaborolidine‐Catalyzed Vinylogous Mukaiyama Aldol Reaction for The Synthesis of C1–C19 and C23–C35 of Neaumycin B-Reference-Cited by-同舟云学术

Ruthenium‐Catalyzed Butadiene‐Mediated Crotylation and Oxazaborolidine‐Catalyzed Vinylogous Mukaiyama Aldol Reaction for The Synthesis of C1–C19 and C23–C35 of Neaumycin B

Published:2022-11-23 Issue:52 Volume:61 Page:
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew Chem Int Ed

Author:

Liang Xinting¹,Yoo Minjin¹,Schempp Tabitha¹,Maejima Saki¹,Krische Michael J.¹^ORCID

Affiliation:

1. University of Texas at Austin Department of Chemistry 105 E 24th St. (A5300) Austin TX 78712-1167 USA

Funder

Welch Foundation

National Institutes of Health

Uehara Memorial Foundation

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.202214786

Reference67 articles.

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3. Additional congeners of the macrolide neaumycin: structure revision and biological activity

4. Integration of Genomic Data with NMR Analysis Enables Assignment of the Full Stereostructure of Neaumycin B, a Potent Inhibitor of Glioblastoma from a Marine-Derived Micromonospora

5. Stereoselective Synthesis of the Southern Hemisphere Acyclic Domain of Neaumycin B

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