STEREOSELECTIVITE ET REGIOSELECTIVITE DE LA REDUCTION DES CYCLOPROPENES-2,3 ET METHYLENE-2 CYCLOPROPANES FONCTIONALISES EN POSITION 1

DOI: 10.1016/S0040-4020(01)88652-X

Source and publish data:

Tetrahedron p. 4281 - 4290 (1983)

Update date:2022-07-29

Topics:

Authors:

Vincens, M.

Dumont, C.

Vidal, M.

Domnin, I. N.

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Article abstract of DOI:10.1016/S0040-4020(01)88652-X

Reduction of 2 cyclopropenyl esters and alcohols with lithium aluminium hydride is selective; at low temperatures (0 deg C) the double bond is not reduced, but at higher temperatures (65 deg C) the reduction is complete and only the cyclopropylmethanol is

Full text of DOI:10.1016/S0040-4020(01)88652-X

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