@article { ISI:000227107500022,
	title = {Synthesis, structure, electrochemistry and ROMP-activity of new ferrocenyl analog of Grubbs{\textquoteright} metathesis catalyst},
	journal = {Journal of Organometallic Chemistry},
	volume = {690},
	number = {4},
	year = {2005},
	month = {FEB},
	pages = {1018-1027},
	publisher = {ELSEVIER SCIENCE SA},
	address = {PO BOX 564, 1001 LAUSANNE, SWITZERLAND},
	abstract = {<p>Treatment of [(PCy3)(2)Cl2Ru=CH-Ph] (1) with vinylferrocene 1 and 1-ferrocenyl-1,3-butadiene 2 yielded solid products. These new complexes were characterized by H-1 NMR, P-31 NMR and C-13 NMR spectroscopy. X-ray crystal structures of both the complexes have been solved. The crystal structure of II confirmed the assigned structure and revealed existence of two sets of intermolecular C-H-Cl(M) type interactions, viz. (Ru)Cl-H-C(ferrocene) and (Ru)Cl-H-CHCl2. The air-stable, dark solid II is all efficient catalyst for ring-opening metathesis polymerization (ROMP) of cyclopentene, norbornene and cycloocta-1,5-diene. Electrochemical behavior of the complexes clearly reflects electronic communication between two metal centers. (C) 2004 Elsevier B.V. All rights reserved.</p>},
	keywords = {Electrochemistry, ferrocene, Metathesis, non-covalent interactions, ring-opening metathesis polymerization, ruthenium carbene},
	issn = {0022-328X},
	doi = {10.1016/j.jorganchem.2004.11.012},
	author = {Maishal, T. K. and Mondal, Biplab and Puranik, Vedavati G. and Wadgaonkar, P. P. and Lahiri, Goutam Kumar and Sarkar, A.}
}
@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.}
}
