Solvolysis of (4,5)-anti-4-Aryl-5-tosyloxy-2(E)-hexenoate Derivatives
Author:
Affiliation:
1. School of Pharmaceutical Sciences, Toho University
2. Tsukuba Research Institute, Novartis Pharma K.K.
Publisher
Pharmaceutical Society of Japan
Subject
Drug Discovery,General Chemistry,General Medicine
Link
http://www.jstage.jst.go.jp/article/cpb/53/10/53_10_1259/_pdf
Reference9 articles.
1. Formal total synthesis of (−)-anisomycin based on the stereoselective nucleophilic substitution along with aryl migration
2. Formal synthesis of (−)-anisomycin based on stereoselective nucleophilic substitution along with 1,2-aryl migration
3. A facile chemoenzymatic route to enantiomerically pure 4,5-disubstituted-2-hexenoate derivatives.
4. A Facile Chemoenzymatic Route to Optically Active 4,5-Disubstituted-2E-hexenoate Derivatives. I.
5. A Facile Chemoenzymatic Route to Optically Active 4,5-Disubstituted-2E-hexenoate Derviatives. II.
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