_tcm18-11397.gif )
Urgent high quality communications from across the chemical sciences.
Subscribers
Free access
Communication
Chem. Commun., 2005, 3927 - 3929, DOI: 10.1039/b507679j
Conformational diastereoisomerism in a chiral pretzelane
Yi Liu, Scott A. Vignon, Xiyun Zhang, K. N. Houk and J. Fraser Stoddart
The introduction of a stereogenic center by a stereospecific synthesis into an optically active, donor–acceptor pretzelane, that exhibits helicity as well as fixed chirality, leads to a marked preference for one conformational diastereoisomer over the other in both acetone and dimethylsulfoxide that can be understood from computational models.
RSS feed
