A practical route to both enantiomers of bicyclo[3.3.0]oct-2-en-7-one and their use for the synthesis of key trisubstituted cyclopentanes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. Substrate non-enantiospecific and product enantioselective reduction of bicyclo[3.2.0]hept-2-en-6-one using yeast
2. Resolution of bicyclo[3.2.0]hept-2-en-6-ols and bicyclo[4.2.0]oct-2-en-endo-7-ol using lipases
3. Reduction of bicyclo [3.2.0] hept-2-en-6-one with dehydrogenase enzymes in whole cell preparations of some fungi and yeasts
4. Reduction of 7-chlorobicyclo[3.2.0]hept-2-en-6-ones catalysed by 3α, 20β-hydroxysteroiddehydrogenase
5. Highly enantioselective elimination of meso-compounds
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1. Adducts of dichloroketene with 1,3-cyclopentadienes in the synthesis of bioactive cyclopentanoids;Russian Chemical Bulletin;2021-01
2. Total Syntheses of the Tetracyclic Cyclopiane Diterpenes Conidiogenone, Conidiogenol, and Conidiogenone B;Angewandte Chemie International Edition;2016-03-03
3. Total Syntheses of the Tetracyclic Cyclopiane Diterpenes Conidiogenone, Conidiogenol, and Conidiogenone B;Angewandte Chemie;2016-03-03
4. Synthesis of Novel, Chiral Bicyclo[3.1.0]hex-2-ene Amino Acid Derivatives as Useful Synthons in Medicinal Chemistry;Helvetica Chimica Acta;2015-09
5. An efficient procedure for synthesis of 2-formylcyclopent-2-enecarboxylic acid;Research on Chemical Intermediates;2014-06-24
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