STEREOSELECTION IN THE REACTION OF ACID HALIDES AND VINYLOGOUS URETHANES

DOI: 10.1016/S0040-4039(00)96744-3

Source and publish data:

Tetrahedron Letters p. 5423 - 5426 (1987)

Update date:2022-08-02

Topics:

Authors:

Schlessinger, Richard H.

Tata, James R.

Springer, James P.

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Article abstract of DOI:10.1016/S0040-4039(00)96744-3

Acid halides which carry either an α-phenyl or α-alkoxy residue show fascinatingly high and useful diastereoselection on condensation with the vinylogous urethane derived ketene acetal enamine 3.Optically active halides or this type undergo reaction with

Full text of DOI:10.1016/S0040-4039(00)96744-3

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