A HIGHLY STEREOSELECTIVE SYNTHESIS OF SUBSTITUTED BUTADIENES AND CONJUGATED POLYENES

DOI: 10.1016/S0040-4039(00)77721-5

Source and publish data:

Tetrahedron Letters p. 809 - 812 (1992)

Update date:2022-09-26

Topics:

Authors:

Patro, Balaram

Ila, Hiriyakkanavar

Junjappa, Hiriyakkanavar

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Article abstract of DOI:10.1016/S0040-4039(00)77721-5

A highly stereoselective synthesis of 1,3-butadienes and its higher enyl analogs has been developed through thermal dehydrative ring opening of cyclopropyl carbinols in dimethylsulphoxide.

Full text of DOI:10.1016/S0040-4039(00)77721-5

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Product name:[2-(6-Methoxy-3,4-dihydro-naphthalen-2-yl)-cyclopropyl]-phenyl-methanol

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