First stereoselective total synthesis of brevipolide M-Reference-Cited by-同舟云学术

First stereoselective total synthesis of brevipolide M

Published:2017 Issue:30 Volume:15 Page:6393-6400
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Shiva Raju Kasa¹²³⁴,Sabitha Gowravaram¹²³⁴^ORCID

Affiliation:

1. Natural Products Chemistry Division

2. CSIR-Indian Institute of Chemical Technology

3. Hyderabad 500 007

4. India

Abstract

The first stereoselective total synthesis of a cytotoxic brevipolide M, which shares a pyrone framework bearing a tetrahydrofuran moiety and a cinnamate group with the readily available (−)-DET, is described.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/OB/C7OB01438D

Reference34 articles.

1. Bioactive 5,6-Dihydro-α-pyrone Derivatives from Hyptis brevipes

2. Absolute Configuration and Conformational Analysis of Brevipolides, Bioactive 5,6-Dihydro-α-pyrones from Hyptis brevipes

3. Antibacterial and antifungal activity of Indonesian ethnomedical plants

4. Three new compounds from the plant Lippia alva as inhibitors of chemokine receptor 5 (CCR5)

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