29780-95-8Relevant articles and documents
A straightforward synthesis of perbenzylated conduritols from alditols by ring closing olefin metathesis
Gallos, John K.,Koftis, Theocharis V.,Sarli, Vassiliki C.,Litinas, Konstantinos E.
, p. 3075 - 3077 (1999)
The synthesis of perbenzylated conduritols A, E and F has been achieved in six steps by formal conversion of galactitol, D-mannitol and D-glucitol into the respective terminal dienes, followed by ring closing olefin metathesis. The Royal Society of Chemistry 1999.
Improved stereochemical analysis of conformationally flexible diamines by binding to a bisporphyrin molecular clip
Norrehed, Sara,Johansson, Henrik,Grennberg, Helena,Gogoll, Adolf
supporting information, p. 14631 - 14638 (2013/11/06)
The relative stereochemistry of acyclic diamines with several stereogenic centers has been analyzed by NMR spectroscopy in combination with conformational deconvolution. Binding to a bisporphyrin molecular clip improves the stereochemical assignment signi
Asymmetric synthesis using reactions with modest group selectivity
Ward, Dale E.,Liu, YaDong,Rhee, Chung K.
, p. 1429 - 1446 (2007/10/02)
The isomeric purity of products from certain group-selective reactions can be significantly amplified when reactions can occur sequentially.The theoretical basis for a strategy that exploits reactions with modest enantiotopic group selectivity for asymmet