Diastereoselective Synthesis of Enantiomeric Tertiary Alcohols via Nucleophilic Additions to Protected D- and L-Erythrulose Derivatives

DOI: 10.1016/S0957-4166(00)86047-4

Source and publish data:

Tetrahedron Asymmetry p. 1511 - 1514 (1992)

Update date:2022-07-30

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Authors:

Carda, Miguel

Gonzales, Florenzi

Rodriguez, Santiago

Marco, J. Alberto

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Article abstract of DOI:10.1016/S0957-4166(00)86047-4

The diastereoselectivity of the addition of several organometallic reagents to the carbonyl group of protected D- and L-erythrulose derivatives has been investigated.Tertiary alcohols are stereoselectively formed, the diastereomeric ratio being markedly d

Full text of DOI:10.1016/S0957-4166(00)86047-4

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