Volume 27, Issue 11
Isocyclic Compounds
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ChemInform Abstract: Control of the Diastereoselectivity of the Allylation and Deuteration of 2-Hydroxyalkyl Aryl Sulfoxides.

P. RENAUD

P. RENAUD

Inst. Chim. Org., Univ. Fribourg, CH-1700 Fribourg, Switz.

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T. BOURQUARD

T. BOURQUARD

Inst. Chim. Org., Univ. Fribourg, CH-1700 Fribourg, Switz.

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First published: March 12, 1996

Abstract

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ChemInform Abstract

Whereas the radical allylation of the syn educts proceeds with moderate diastereoselectivity, good levels of selectivity can be observed for the anti analogues (Ia) and (Ib). The configuration at C( 1) can be inverted by silyl-protecting of the OH group (→ cf. ( Ic)).

chemical structure image

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