@article { ISI:000250183300024,
	title = {Carbohydrate based approach towards the synthesis of aspercyclide C},
	journal = {Tetrahedron Letter},
	volume = {48},
	number = {42},
	year = {2007},
	month = {OCT},
	pages = {7524-7527},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A formal total synthesis of aspercyclide C (3) is described in which D-ribose is employed as a chiral pool material. The key step is a ring closing metathesis. (C) 2007 Elsevier Ltd. All rights reserved.</p>},
	keywords = {chiron approach, D-ribose, Mukaiyama reagent, ring closing metathesis (RCM), Ullmann coupling},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2007.08.050},
	author = {Ramana, C. V. and Mondal, Mohabul A. and Puranik, Vedavati G. and Gurjar, Mukund K.}
}
@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.}
}
