AN EFFICIENT PROCEDURE FOR THE SYNTHESIS AND ISOLATION OF (+)-(2R,3R,11R,12R)-AND (-)-(2S,3S,11S,12S)-TETRAPHENYL-18-CROWN-6

DOI: 10.1016/S0040-4039(01)80675-4

Source and publish data:

Tetrahedron Letters p. 3849 - 3852 (1989)

Update date:2022-08-02

Topics:

Authors:

Crosby, John

Fakley, Martin E.

Gemmell, Colin

Martin, Kelth

Quick, Andrew

et al. et al.

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Article abstract of DOI:10.1016/S0040-4039(01)80675-4

The enantiomers of the chiral 2,3-diphenyl- and 2,3,11,12-tetraphenyl-1,4,7,10,13,16-hexaoxacyclooctadecanes have been prepared in single step reactions from the readily-available chiral precursors, (RR)- and (SS)-hydrobenzoins, followed by bulk isolation

Full text of DOI:10.1016/S0040-4039(01)80675-4

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Product name:(2R,3R)-2,3-Diphenyl-1,4,7,10,13,16-hexaoxa-cyclooctadecane

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