| Literature DB >> 15917905 |
Jon-Paul Griffiths1, Hui Nie, R James Brown, Peter Day, John D Wallis.
Abstract
Syntheses of enantiopure organosulfur donors by three different strategies requiring only four-six steps are reported. The key step involves either double substitution of an enantiopure cyclic sulfate ester by a dithiolate, attachment of a chiral diol as a ketal, or completely diastereoselective cycloaddition of 1,3-dithiole-2,4,5-trithione to an enantiopure alkene.Entities:
Mesh：
Substances：
Year: 2005 PMID： 15917905 DOI： 10.1039/b502437d
Source DB: PubMed Journal: Org Biomol Chem ISSN： 1477-0520 Impact factor: 3.876