Stereoselective synthesis of the enantiomer of the key fragment of crocacin
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 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. Total Synthesis of (+)-Crocacin C
4. Total synthesis of (+)-crocacin C
5. Total synthesis of (+)-crocacin C
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1. Diastereoselective synthesis of an advanced intermediate of the crocacin family using asymmetric transfer hydrogenation-DKR and Marshall allenylation as key reactions;Tetrahedron;2015-11
2. Asymmetric Synthesis of Stigmatellin and Crocacin C;Bulletin of the Chemical Society of Japan;2015-02-15
3. Enantioselective Synthesis of (+)-Crocacin C. An Example of a Highly Challenging Mismatched Double Asymmetric δ-Stannylcrotylboration Reaction;Organic Letters;2012-03-12
4. The Synthesis of Long-Chain α-Alkyl-β-Hydroxy Esters Using Allylic Halides in a Fráter-Seebach Alkylation;European Journal of Organic Chemistry;2011-12-16
5. Total Synthesis of Aculeatins A and B from L-Malic Acid;Helvetica Chimica Acta;2010-12
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