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Ruthenium-catalyzed Oppenauer-type oxidation of 3 beta-hydroxy steroids. A highly efficient entry into the steroidal hormones with 4-en-3-one functionality

Almeida, MLS (author)
Uppsala universitet
Kocovsky, P (author)
Uppsala universitet
Backvall, JE (author)
Uppsala universitet
 (creator_code:org_t)
AMER CHEMICAL SOC, 1996
English 6587-6590 s.
In: JOURNAL OF ORGANIC CHEMISTRY. - : AMER CHEMICAL SOC. ; 61:19
  • Other publication (other academic/artistic)
Abstract Subject headings
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  • Oxidation of 5-unsaturated 3 beta-hydroxy steroids 1 to the corresponding 4-en-3-one derivatives 2 can be performed efficiently by acetone at reflux in the presence of a catalytic system consisting of either (PPh(3))(3)RuCl2 (3) and K2CO3 or [(C(4)Ph(4)C

Keyword

AEROBIC OXIDATION; SELECTIVE AROMATIZATION; A-RING; ALCOHOLS; FRAGMENT

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vet (subject category)
ovr (subject category)

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Kocovsky, P
Backvall, JE
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