Studies on diastereoselective reduction of cyclic β-ketoesters with boron hydrides. Part 4: The reductive profile of functionalized cyclohexanone derivatives-Reference-Cited by-同舟云学术

Studies on diastereoselective reduction of cyclic β-ketoesters with boron hydrides. Part 4: The reductive profile of functionalized cyclohexanone derivatives

Published:2004-03 Issue:12 Volume:60 Page:2745-2755
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Fraga Carlos A.M,Teixeira Lis Helena P,Menezes Carla Maria de S,Sant'Anna Carlos Mauricio R,Ramos Maria da Conceição K.V,Neto Francisco R.de Aquino,Barreiro Eliezer J

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

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3. A formal synthesis of ptaquilosin the aglycon of a potent bracken carcinogen ptaquiloside

4. Enantioselective Total Syntheses of the Nitraria Alkaloids (-)-Nitramine and (+)-Isonitramine

5. Enantiofacial selective reduction of 2-allyl-2-carboethoxy-cyclopentanone mediated by baker's yeast

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