1,2 ASYMMETRIC INDUCTION IN THE CYCLIC HYDROBORATION OF 1,5-DIENES. A SYNTHESIS OF THE PRELOG-DJERASSI LACTONE

DOI: 10.1016/S0040-4039(01)82003-7

Source and publish data:

Tetrahedron Letters p. 3721 - 3724 (1981)

Update date:2022-08-10

Topics:: Authors:

Morgans, David J.

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Article abstract of DOI:10.1016/S0040-4039(01)82003-7

Cyclic hydroboration of an appropriately substituted 1,5-diene yields a 1,5 diol as the major product which can be converted to the racemic Prelog-Djerassi lactone.

Full text of DOI:10.1016/S0040-4039(01)82003-7

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Article Doi

1,2 ASYMMETRIC INDUCTION IN THE CYCLIC HYDROBORATION OF 1,5-DIENES. A SYNTHESIS OF THE PRELOG-DJERASSI LACTONE

DOI: 10.1016/S0040-4039(01)82003-7

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(01)82003-7

Full text of DOI:10.1016/S0040-4039(01)82003-7

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