Search Results - "Cheeseman, Matt"
-
1
A temporary stereocentre approach for the asymmetric synthesis of chiral cyclopropane-carboxaldehydes
Published in Organic & biomolecular chemistry (01-01-2009)“…A novel way of combining chiral auxiliaries and substrate directable reactions is described that employs a three-step sequence of…”
Get more information
Journal Article -
2
Asymmetric Synthesis of Chiral δ-Lactones Containing Multiple Contiguous Stereocenters
Published in Organic letters (15-07-2011)“…A versatile methodology for the asymmetric synthesis of chiral δ-lactones containing multiple contiguous stereocenters has been developed that relies on a…”
Get full text
Journal Article -
3
Efficient Asymmetric Synthesis of Chiral Hydroxy-γ-butyrolactones
Published in Organic letters (02-07-2009)“…Treatment of β-vinyl-β-hydroxy-N-acyloxazolidin-2-ones with VO(acac)2 and tert-butyl hydroperoxide results in formation of unstable epoxides that are…”
Get full text
Journal Article -
4
An efficient asymmetric synthesis of grenadamide
Published in Tetrahedron letters (14-11-2005)“…The cyclopropane containing natural product grenadamide has been prepared in six steps using ( R)-5,5-dimethyl-oxazolidin-2-one as a chiral auxiliary for…”
Get full text
Journal Article -
5
An efficient synthesis of semiplenamide C
Published in Tetrahedron letters (15-08-2005)“…Semiplenamides are anandamide-like fatty acid amide metabolites previously isolated from a marine cyanobacterium that display a range of biological activity…”
Get full text
Journal Article -
6
A novel strategy for the asymmetric synthesis of chiral cyclopropane carboxaldehydes
Published in Chemical communications (Cambridge, England) (14-05-2005)“…A new way of combining chiral auxiliaries and substrate-directable reactions for asymmetric synthesis is described that employs a three-step sequence of…”
Get more information
Journal Article -
7
Stereoselective synthesis of (E)-trisubstituted alpha,beta-unsaturated amides and acids
Published in Organic & biomolecular chemistry (21-08-2005)“…Potassium alkoxides of N-acyl-oxazolidin-2-one-syn-aldols undergo stereoselective elimination reactions to afford a range of trisubstituted…”
Get more information
Journal Article