@article { ISI:000256839100021,
	title = {Stereoselective synthesis of beta-C-Allyl- and beta-C-propargyl-D-arabinofuranosides},
	journal = {Synthesis-Stuttgart},
	number = {11},
	year = {2008},
	month = {JUN},
	pages = {1783-1787},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>The stereoselective synthesis of beta-configured C-allyl- and C-propargyl-D-arabinofuranosides (4,7-anhydro-1,2,3-deoxy-D-gluco-oct-1-enitols and -oct-1-ynitols) was addressed by employing allylation/propargylation of a dialdofuranose under aqueous Barbier reaction conditions and acid-catalyzed furan ring transposition of 5-O-mesyl-manno-oct-7-eno- or 5-O-mesyl-manno-oct-7-ynofuranoside derivatives.</p>},
	keywords = {Allylation, Barbier reaction, C-glycoside, D-mannose, propargylation, Ring transposition},
	issn = {0039-7881},
	doi = {10.1055/s-2008-1067016},
	author = {Ramana, C. V. and Narute, Sachin B. and Gonnade, Rajesh G. and Patil, Rahul S.}
}
@article {45733,
	title = {Unified approach to fused and spirocyclic oxindoles through lewis-acid-promoted opening of spiroepoxyoxindoles with allylsilanes: application to the formal synthesis of (+/-)-physovenine},
	journal = {European Journal of Organic Chemistry},
	year = {2017},
	month = {MAY },
	pages = {2603-2609},
	type = {Article},
	abstract = {<p>A protocol for the construction of oxindoles containing all-carbon quaternary centres in a highly regioselective manner has been developed. The reaction involves opening of spiroepoxyoxindoles with allylsilanes to give Hosomi-Sakurai-type products as well as new silicon-containing spirocyclic oxindoles. A formal synthesis of (+/-)-physovenine was accomplished in five steps using this protocol.</p>},
	keywords = {alkaloids, Allylation, annulation, Lewis acids, spiro compounds},
	issn = {1434-193X},
	doi = {10.1002/ejoc.201700259},
	author = {Sharma, Brijesh M. and Yadav, Mahesh and Gonnade, Rajesh G. and Kumar, Pradeep}
}
