Total Synthesis of (+)-Prunustatin A: Utility of Organotrifluoroborate-Mediated Prenylation and Shiina MNBA Esterification and Macrolactonization To Avoid a Competing Thorpe–Ingold Effect Accelerated Transesterification-Reference-Cited by-同舟云学术

Total Synthesis of (+)-Prunustatin A: Utility of Organotrifluoroborate-Mediated Prenylation and Shiina MNBA Esterification and Macrolactonization To Avoid a Competing Thorpe–Ingold Effect Accelerated Transesterification

Published:2018-08-30 Issue:18 Volume:20 Page:5671-5675
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Chojnacka Maja W.¹,Batey Robert A.¹^ORCID

Affiliation:

1. Davenport Research Laboratories, Department of Chemistry, University of Toronto, 80 St. George Street, Toronto ON, Canada M5S 3H6

Funder

Ministry of Advanced Education

Natural Sciences and Engineering Research Council of Canada

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.8b02396

Reference34 articles.

1. Prunustatin A, a Novel GRP78 Molecular Chaperone Down-regulator Isolated from Streptomyces violaceoniger

2. bToru, N.; Shin-ya, K. PCT Int. Appl. WO 2006101073A1, 2006. (+)-Prunustatin A absolute sterochemistry:

3. Absolute Structure of Prunustatin A, a Novel GRP78 Molecular Chaperone Down-Regulator

4. Novel GRP78 Molecular Chaperone Expression Down-regulators JBIR-04 and -05 Isolated from Streptomyces violaceoniger

5. A Novel Antimycin-like Compound, JBIR-06, from Streptomyces sp. ML55

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