An improved synthesis of the (E,Z)-dienoate precursor of (+)-damavaricin D via a vinylogous Horner-Wadsworth-Emmons reaction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. Total Synthesis of (+)-Damavaricin D
2. Direct synthesis of Z-unsaturated esters. A useful modification of the horner-emmons olefination.
3. Horner-wadsworth-emmons reaction: Use of lithium chloride and an amine for base-sensitive compounds
4. Asymmetric synthesis of the benzoquinoid ansamycin antitumor antibiotics: total synthesis of (+)-macbecin
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1. Still–Gennari Olefination and its Applications in Organic Synthesis;Advanced Synthesis & Catalysis;2020-06-08
2. Preparation of Macrocyclic Z-Enoates and (E,Z)- or (Z,E)-Dienoates through Catalytic Stereoselective Ring-Closing Metathesis;Journal of the American Chemical Society;2014-11-17
3. Simple and Advantageneous Stereoselective Synthesis of (Z)-Allyl Phosphonates Starting from Baylis–Hillman Adducts;Synthetic Communications;2012-09
4. ChemInform Abstract: An Improved Synthesis of the (E,Z)-Dienoate Precursor of (+)-Damavaricin D via a Vinylogous Horner-Wadsworth-Emmons Reaction.;ChemInform;2010-06-16
5. Synthesis of 4-Methyldienoates Using a Vinylogous Horner−Wadsworth−Emmons Reagent. Application to the Synthesis of Trichostatic Acid;The Journal of Organic Chemistry;2010-02-16
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