First asymmetric total synthesis of aspergillide D-Reference-Cited by-同舟云学术

First asymmetric total synthesis of aspergillide D

Published:2017 Issue:8 Volume:15 Page:1863-1871
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Jena Bighnanshu K.¹²³⁴,Reddy G. Sudhakar¹²³⁴,Mohapatra Debendra K.¹²³⁴^ORCID

Affiliation:

1. Natural Products Chemistry Division

2. CSIR-Indian Institute of Chemical Technology

3. Hyderabad 500 007

4. India

Abstract

The first asymmetric total synthesis of aspergillide D was achieved in a longest linear sequence of 18 steps following Sharpless resolution, Yamaguchi esterification, RCM reaction and Shiina macrolactonization.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/OB/C6OB02435A

Reference35 articles.

1. (-)-Semivioxanthin, A New Abscisic Active Compound against Hinoki Cypress Leaves Isolated from Cryptosporiopsis abietina

2. Antibacterial phenolic components from Eriocaulon buergerianum

3. New cytotoxic sesquiterpenoid nitrobenzoyl esters from a marine isolate of the fungus Aspergillus versicolor

4. Azonazine, a Novel Dipeptide from a Hawaiian Marine Sediment-Derived Fungus, Aspergillus insulicola

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