Tetrahedron Letters

Asymmetric synthesis of (+)-passifloricin A and its 6-epimer

S Chandrasekhar, C Rambabu, AS Reddy

Index: Chandrasekhar; Rambabu; Reddy, A. Syamprasad Tetrahedron Letters, 2008 , vol. 49, # 29-30 p. 4476 - 4478

Full Text: HTML

Citation Number: 14

Abstract

Download PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... Stereoselective total syntheses of the antiprotozoal natural product (+)-passifloricin A and its C-6 epimer have been achieved in ∼5% overall yield. The strategy is based on Jacobsen epoxidation, Grubbs' metathesis and an Evans' intramolecular oxa-Michael reaction.

Asymmetric synthesis of (2R)-and (2S)-2-iodohexadecanal, nat...

[Jacoby, Claude; Braekman, Jean-Claude; Daloze, Desire Tetrahedron, 1996 , vol. 52, # 31 p. 10473 - 10484]

Syntheses and interfacial behaviour of neoglycolipid analogu...

[Lafont, Dominique; Bouchu, Marie-Noelle; Girard-Egrot, Agnes; Boullanger, Paul Carbohydrate Research, 2001 , vol. 336, # 3 p. 181 - 194]

Asymmetric synthesis of (2R)-and (2S)-2-iodohexadecanal, nat...

[Jacoby, Claude; Braekman, Jean-Claude; Daloze, Desire Tetrahedron, 1996 , vol. 52, # 31 p. 10473 - 10484]

A convenient resolution of long-chain alkyl epoxides with Ja...

[Savle, Prashant S.; Lamoreaux, Marika J.; Berry, John F.; Gandour, Richard D. Tetrahedron Asymmetry, 1998 , vol. 9, # 11 p. 1843 - 1846]