A catalytic asymmetric bioorganic route to enantioenriched tetrahydro- and dihydropyranones.
A conceptually novel approach to hetero Diels-Alder adducts of carbonyl compounds is described using as the key steps an antibody-mediated kinetic resolution of hydroxyenones followed by a ring-closure process. Various beta-hydroxyenones proved to be very good substrates for antibodies 84G3- and 93F...
المؤلفون الرئيسيون: | Baker-Glenn, C, Hodnett, N, Reiter, M, Ropp, S, Ancliff, R, Gouverneur, V |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
2005
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مواد مشابهة
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A biocatalytic route to enantioenriched, sulfanyl aldol products
حسب: Baker-Glenn, C, وآخرون
منشور في: (2004) -
A biocatalytic approach to enantioenriched hetero Diels-Alder adducts from beta-hydroxy ynones
حسب: Reiter, M, وآخرون
منشور في: (2005) -
Palladium-catalyzed oxidative cyclizations: synthesis of dihydropyranones and furanones.
حسب: Reiter, M, وآخرون
منشور في: (2005) -
ORGN 26-Cyclizations of enantioenriched beta-hydroxyynones: Synthetic route to enantioenriched unsaturated pyranones and furanones
حسب: Sawicki, M, وآخرون
منشور في: (2006) -
Catalytic asymmetric radical aminoperfluoroalkylation and aminodifluoromethylation of alkenes to versatile enantioenriched-fluoroalkyl amines
حسب: Jin-Shun Lin, وآخرون
منشور في: (2017-03-01)