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Preparation of Enantiomerically Pure 5‐Palladatricyclo[4.1.0.0 2, 4 ]heptanes and Conversion into Enantiomerically Pure Complexes with Helical Chirality at Palladium
Author(s) -
Hashmi A. Stephen K.,
Naumann Frank,
Probst Ralf,
Bats Jan W.
Publication year - 1997
Publication title -
angewandte chemie international edition in english
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 0570-0833
DOI - 10.1002/anie.199701041
Subject(s) - palladium , chirality (physics) , denticity , planar chirality , planar , chemistry , stereochemistry , crystallography , catalysis , enantioselective synthesis , organic chemistry , crystal structure , chiral symmetry , physics , computer graphics (images) , quantum mechanics , computer science , nambu–jona lasinio model , quark
A dramatic deviation from square‐planar coordination for Pd II complexes: the CPdC and PPdPlanes in the helical chiral complexes 2 (∪ = 1,1′‐ferrocenediyl) are unexpectedly tipped toward each other by as much as 30°. These complexes are prepared from the appropriate bidentate phosphane ligands and the bishomopalladole 1 , which is remarkably stable and availalbe in enantiomerically pure form in good yields. E = CO 2 Me.
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