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SYNTHETIC STUDIES ON AMBRUTICIN: DETERMINATION OF THE ABSOLUTE STEREOCHEMISTRY BY A CHIRAL SYNTHESIS OF THE CYCLOPROPANE RING

DOI: 10.1016/S0040-4039(01)90430-7

Source and publish data:

Tetrahedron Letters p. 1751 - 1754 (1981)

Update date:2022-09-26

Topics:

Authors:

Barnes, Nigel J.Barnes, Nigel J.

Davidson, Alan H.Davidson, Alan H.

Hughes, Leslie R.Hughes, Leslie R.

Procter, GarryProcter, Garry

Rajcoomar, VeedianandRajcoomar, Veedianand

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Article abstract of DOI:10.1016/S0040-4039(01)90430-7

We report the highly stereoselective synthesis of the cyclopropane (3) and its conversion to a degradation product of ambruticin.

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Full text of DOI:10.1016/S0040-4039(01)90430-7

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Product name:(+/-)-3-methyl-cyclopropane-1r,2t-dicarboxylic acid

Cas No:1074-33-5

1074-33-5

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