ISSN:
1572-9001
Keywords:
Chiral bromohydrins
;
syn- andanti-diastereoisomer
;
chemoenzymatic synthesis
;
X-ray crystallography
;
absolute configuration
Source:
Springer Online Journal Archives 1860-2000
Topics:
Chemistry and Pharmacology
Notes:
Abstract The X-ray crystal structures of (−)-syn-4-phenyl-3-bromo-2-butyl camphanate (I) and (+-anti-4-phenyl-3-bromo-2-butyl camphanate (II) have been determined. Thesyn diastereoisomer of bromohydrin has the (2S,3S) absolute configuration whereas theanti diastereoisomer has the (2S,3R) absolute configuration. The crystallized derivatives I and II have been obtained by the reaction of each stereoisomer of bromohydrin, synthesized by reduction with baker's yeast, with (1S)-camphanic chloride. Crystal data: (I) C20H25BrO4:M w: 409.32; orthorhombic,P212121;a=11.245(3),b=12.086(1),c=14.512(4) å; Z=4; finalR=0.053 for 1819 observed reflections. (II) C20H25BrO4;M w=409.32; monoclinic, P21;a=11.352(1),b=6.378(1),c=14.255(2) å,Β=110.38(1)ℴ;Z=2; finalR=0.045 for 1672 observed reflections.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/BF02286447
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