Diastereoselective synthesis of an advanced intermediate of the crocacin family using asymmetric transfer hydrogenation-DKR and Marshall allenylation as key reactions-Reference-Cited by-同舟云学术

Diastereoselective synthesis of an advanced intermediate of the crocacin family using asymmetric transfer hydrogenation-DKR and Marshall allenylation as key reactions

Published:2015-11 Issue:47 Volume:71 Page:8960-8964
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Kumaraswamy Gullapalli,Narayanarao Vykunthapu,Shanigaram Prakash,Balakishan Guniganti

Funder

DST, New Delhi

Council of Scientific and Industrial Research

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference33 articles.

1. Crocacin, a new electron transport inhibitor from Chondromyces cracatus (myxobacteria). Production, isolation, physico-chemical and biological properties.

2. The Crocacins, Novel Antifungal and Cytotoxic Antibiotics fromChondromyces crocatus andChondromyces pediculatus (Myxobacteria): Isolation and Structure Elucidation

3. The Crocacins: Novel Natural Products as Leads for Agricultural Fungicides

4. The role of molecular modeling in the design of analogues of the fungicidal natural products crocacins A and D

5. Total Synthesis of (+)-Crocacin C

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