Highly stereoselective route to aldol products incorporating fluorine containing methyl groups starting from a single D-glucose-derived intermediate

DOI: 10.1016/S0957-4166(97)00120-1

Source and publish data:

Tetrahedron Asymmetry p. 1157 - 1160 (1997)

Update date:2022-07-29

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Authors:

Yamazaki, Takashi

Hiraoka, Shuichi

Kitazume, Tomoya

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Article abstract of DOI:10.1016/S0957-4166(97)00120-1

Chiral aldol structures with fluorine modifications on a methyl group have been realized by utilization of the relatively rigid cyclic intermediates from the very common chiral pool compound, D-glucose, leading to attainment of the high diastereoselectivi

Full text of DOI:10.1016/S0957-4166(97)00120-1

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