@article { ISI:000243703200018,
	title = {Total synthesis of pachastrissamine (jaspine B) enantiomers from D-glucose},
	journal = {Tetrahedron Letters},
	volume = {48},
	number = {2},
	year = {2007},
	month = {JAN},
	pages = {265-268},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>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. (c) 2006 Published by Elsevier Ltd.</p>},
	keywords = {4-furanose, chiron approach, Ohira-Bestmann reaction, pachastrissamine/jaspine B, pentodialdo-1, ring isomerization},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2006.11.048},
	author = {Ramana, C. V. and Giri, Awadut G. and Suryawanshi, Sharad B. and Gonnade, Rajesh G.}
}
