CONJUGATE ADDITION REACTIONS OF ENANTIOMERICALLY PURE ACYLKETENE ACETALS AND ETHYLLITHIUM. A PRONOUNCED SALT EFFECT.

DOI: 10.1016/S0040-4039(00)79469-X

Source and publish data:

Tetrahedron Letters p. 465 - 466 (1991)

Update date:2022-09-26

Topics:: Authors:

Konopelski, Joseph P.

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Article abstract of DOI:10.1016/S0040-4039(00)79469-X

The order of addition of salt-free ethylithium/benzene solution to enantiomerically pure acylketene acetal 1 dictates the product formed in a chemospecific manner.Introduction of lithium bromide removes the distinction.

Full text of DOI:10.1016/S0040-4039(00)79469-X

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Article Doi

CONJUGATE ADDITION REACTIONS OF ENANTIOMERICALLY PURE ACYLKETENE ACETALS AND ETHYLLITHIUM. A PRONOUNCED SALT EFFECT.

DOI: 10.1016/S0040-4039(00)79469-X

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)79469-X

Full text of DOI:10.1016/S0040-4039(00)79469-X

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