Total synthesis of pachastrissamine (jaspine B) enantiomers from D-glucose

Ramana, C. V. ; Giri, Awadut G. ; Suryawanshi, Sharad B. ; Gonnade, Rajesh G. (2007) Total synthesis of pachastrissamine (jaspine B) enantiomers from D-glucose Tetrahedron Letters, 48 (2). pp. 265-268. ISSN 0040-4039

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Official URL: http://www.sciencedirect.com/science/article/pii/S...

Related URL: http://dx.doi.org/10.1016/j.tetlet.2006.11.048

Abstract

Synthesis of both enantiomers of pachastrissamine is described from a common chiral template. The stereoselective construction of the central tetrahydrofuran units was based on the pseudodesymmetrization of a pentodialdo-1,4-furanose derivative taking advantage of the latent symmetry present.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Chiron Approach; Pachastrissamine/Jaspine B; Pentodialdo-1,4-Furanose; Ohira–Bestmann Reaction; Ring Isomerization
ID Code:106155
Deposited On:01 Feb 2018 16:56
Last Modified:01 Feb 2018 16:56

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