@article { ISI:000230685900019,
	title = {Stereoselective synthesis of spiroannulated cyclopentenones by the Pauson-Khand reaction on carbohydrate derived enynes},
	journal = {Tetrahedron Letters},
	volume = {46},
	number = {32},
	year = {2005},
	month = {AUG},
	pages = {5329-5332},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>The stereoselective synthesis of spiroannulated cyclopentenones by the Pauson-Khand reactions on hexose and pentose derived enynes was achieved under carbon monoxide free conditions using a stoichiometric quantity of Co-2(CO)(8). The cobalt complex of the alkyne was cleaved using dimethoxyethane-acetonitrile at 85 degrees C to furnish spiroarmulated cyclopentenones in 75-94\% yields. (c) 2005 Elsevier Ltd. All rights reserved.</p>},
	keywords = {carbohydrates, cyclopentenone, diversity oriented synthesis, Pauson-Khand reaction},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2005.06.013},
	author = {Hotha, Srinivas and Maurya, S. K. and Gurjar, M. K.}
}
@article { ISI:000236986000027,
	title = {Synthesis of spiroannulated dihydroisobenzofuranylated monosaccharides},
	journal = {Tetrahedron Letters},
	volume = {47},
	number = {19},
	year = {2006},
	month = {MAY},
	pages = {3307-3310},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>An efficient synthesis of spiroannulated dihydroisobenzofurans is achieved using easily accessible carbohydrate-derived furanyl propargyl ethers via an AuCl3 promoted intramolecular Diels-Alder (IMDA) reaction. The scope of the spiroannulation protocol was demonstrated using a diverse range of pentofuranosyl, hexofuransoyl and hexopyranosyl derived substrates in order to synthesize spiroannulated dihydroisobenzofurans. The reaction is high yielding, moisture tolerant, fast and uses only a catalytic amount of AuCl3. (c) 2006 Elsevier Ltd. All rights reserved.</p>},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2006.03.016},
	author = {Maurya, S. K. and Hotha, Srinivas}
}
