@article { ISI:000297732400016,
	title = {Enantioselective total syntheses of (-)-isonitramine, (-)-sibirine, and (+)-nitramine by ring-closing metathesis},
	journal = {European Journal of Organic Chemistry},
	number = {36},
	year = {2011},
	month = {DEC},
	pages = {7372-7377},
	publisher = {WILEY-V C H VERLAG GMBH},
	address = {PO BOX 10 11 61, D-69451 WEINHEIM, GERMANY},
	abstract = {<p>Concise enantioselective total syntheses of naturally occurring 2-azaspiro[5,5]undecan-7-ol (Nitraria) alkaloids viz. ()-isonitramine, ()-sibirine, and (+)-nitramine are accomplished in 42, 38, and 25?\% overall yield, respectively, in six steps starting from enantiomerically pure (S)-methyl 3-allyl-2-oxo-1,2,3,6-tetrahydropyridine-3-carboxylate (\&gt;99?\%?ee). The key feature of the syntheses involves diastereoselective HosomiSakurai allylation followed by ring-closing metathesis.</p>},
	keywords = {Alk-aloids, Allylation, Amino alcohols, Metathesis, Total synthesis},
	issn = {1434-193X},
	doi = {10.1002/ejoc.201101256},
	author = {Pandey, Ganesh and Kumara, Prasanna C. and Burugu, Shiva Kumar and Puranik, Vedavati G.}
}
@article { ISI:000325943800011,
	title = {Dimethyl [(2R,3R,5S)-5-phenylmorpholine-2,3-diyl]diacetate as a designer substrate in the syntheses of important heterocyclic scaffolds},
	journal = {Asian Journal of Organic Chemistry},
	volume = {1},
	number = {1},
	year = {2012},
	month = {SEP},
	pages = {65-70},
	publisher = {WILEY-V C H VERLAG GMBH},
	address = {BOSCHSTRASSE 12, D-69469 WEINHEIM, GERMANY},
	abstract = {<p>Designed scaffold dimethyl [(2R,3R,5S)-5-phenylmorpholine-2,3-diyl]diacetate was synthesized in optically pure form by photoinduced one-electron reductive beta-activation of an alpha,beta-unsaturated carbonyl moiety for stereoselective C-C bond formation. Use of the morpholine derivative as a {\textquoteleft}{\textquoteleft}chemical multitalent{\textquoteright}{\textquoteright} is demonstrated by its easy transformation to valuable heterocyclic building blocks such as methyl [(2R,3S)-3-hydroxy-5-oxopyrrolidin-2-yl]acetate, methyl [(2R,3S)-3-amino-5-oxotetrahydrofuran-2-yl]acetate, (3R,4S)-4-aminohexane-1,3,6-triol, and 2-[(2R,3S)-3-aminotetrahydrofuran-2-yl]ethanol.</p>},
	keywords = {Amino alcohols, butyrolactams, butyrolactones, morpholines, photoinduced electron transfer reactions},
	issn = {2193-5807},
	doi = {10.1002/ajoc.201200033},
	author = {Pandey, Ganesh and Gaikwad, Amrut L. and Gadre, Smita R.}
}
