ASYMMETRIC REDUCTION OF KETONE REDUCTIVE CLEAVAGE OF CHIRAL ACETALS USING ORGANOALUMINIUM REAGENTS

DOI: 10.1016/S0040-4039(00)85961-4

Source and publish data:

Tetrahedron Letters p. 4581 - 4584 (1983)

Update date:2022-07-29

Topics:

Authors:

Mori, Atsunori

Fujiwara, Junya

Maruoka, Keiji

Yamamoto, Hisashi

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Article abstract of DOI:10.1016/S0040-4039(00)85961-4

Some chiral acetals are cleaved by organoaluminium reagents.The products are formed diastereoselectively, and the removal of the chiral auxiliary affords optically active alcohols.

Full text of DOI:10.1016/S0040-4039(00)85961-4

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