Chemo-enzymatic Preparations of (R)- and (S)-3-Iodocyclohex-2-en-1-yl Acetate
Author:
Affiliation:
1. a Laboratoire des Carbocycles (Associé au CNRS) , Institut de Chimie Moléculaire et des Matériaux d'Orsay , Université de Paris-Sud , Orsay, France
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1081/SCC-120021839
Reference13 articles.
1. Synthesis of optically active forms of seudenol, the pheromone of douglas fir beetle
2. Enantioselective synthesis of cyclic dialkyl (3-hydroxy-1-alkenyl) phosphonates by baker's yeast-mediated reduction of the corresponding enones
3. Chemo-enzymatic preparation of optically active endo-bicyclo[4.1.0]heptan-2-ols
4. Enantiomeric excesses of (R)- and (S)-3-iodocyclohex-2-en-1-ol were determined after transformation to 3-methylcyclohex-2-en-1-ol (Seudenol), by1H-NMR of the corresponding α-methoxy α-trifluoromethylphenylacetate and from its chiroptical properties
5. An Enantioselective Approach to the Taxanes: Direct access to functionalizedcis-tricyclo[9.3.1.03,8]pentadecanesvia ?-hydroxy ketone andWagner-Meerwein rearrangements
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