@article { ISI:000347373500003,
	title = {Simple method for the preparation of ultra-small palladium nanoparticles and their utilization for the hydrogenation of terminal alkyne groups to alkanes},
	journal = {Nanoscale},
	volume = {7},
	number = {3},
	year = {2015},
	month = {NOV},
	pages = {872-876},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>A simple and convenient method for the preparation of ultra-small palladium nanoparticles (Pd-NPs) by a modified digestive ripening method is described. These nanoparticles catalyse the hydrogenation of the terminal alkyne groups to alkanes selectively, and show no effect on other labile protecting and internal alkyne or internal/external alkene groups present in the molecule.</p>},
	issn = {2040-3364},
	doi = {10.1039/c4nr04239e},
	author = {Seth, Jhumur and Kona, Chandrababu Naidu and Das, Shyamsundar and Bhagavatula L. V. Prasad}
}
@article {47605,
	title = {Synthesis of four diastereomers of notoryne and their C-13 NMR chemical shifts analysis},
	journal = {Journal of Chemical Sciences},
	volume = {133},
	year = {2021},
	month = {SEP},
	pages = {76},
	type = {Article},
	abstract = {In this manuscript we document the details of the synthesis of four diastereomers of notoryne. The synthesis of one of the diastereomer having a similar relative stereochemistry of substituents on the both THF rings like notoryne, however, being the relative stereochemistry between the bridging carbon of these two THF units is changed from anti to syn has been executed mainly to learn how the ring carbon chemical shifts vary with this change. Interestingly, the deviations are found mainly for the carbons of THF ring that bears the Br-group. In addition to this isomer, three more diastereomers having the relative stereochemistry of substituents on either of the THF rings varied have been also synthesized. All four diastereomers have been subjected for extensive NMR studies and their C-13 NMR chemical shifts have been compared with notoryne and laurendecumenyne B. In addition, chemical shifts for the four diastereomers along with these natural products were calculated with the help of DFT calculations and compared to the experimentally obtained chemical shift values.},
	issn = {0974-3626},
	doi = {10.1007/s12039-021-01929-y},
	author = {Senapati, Sibadatta and Das, Shyamsundar and Dixit, Ruchi and Vanka, Kumar and Ramana, V, Chepuri}
}
