Synthesis and configurational assignment of (R) and (S)-2-bromohexadecanoic acids

DOI: 10.1016/0957-4166(95)00305-9

Source and publish data:

Tetrahedron Asymmetry p. 2291 - 2298 (1995)

Update date:2022-08-05

Topics:

Authors:

Hernanz Hernanz

Camps Camps

Guerrero

Delgado Delgado

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Article abstract of DOI:10.1016/0957-4166(95)00305-9

Synthesis of both enantiomers of 2-bromohexadecanoic acid is described by diastereoselective bromination of esters (+) and (-)-3 followed by removal of the chiral auxiliary. The absolute configuration of the acids is confirmed by an independent chemical s

Full text of DOI:10.1016/0957-4166(95)00305-9

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Product name:(1S,2R,4R)-(+)-1-dicyclohexylsulfamoylmethyl-7,7-dimethylbicyclo<2.2.1>hept-2-yl hexadecanoate

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