@article {47658,
	title = {Synthesis of anisotropic rod-like gold nanostructures in organic media},
	journal = {Journal of Chemical Sciences},
	volume = {133},
	year = {2021},
	month = {DEC},
	pages = {106},
	type = {Article},
	abstract = {Synthesis of anisotropic rod-like gold nanostructures was carried out in chloroform employing a modified ascorbic acid derivative as a reducing agent in the presence and absence of seed particles. The seed particles and/or the chloroaurate ions were phase transferred to the organic media using n-octadecyl amine. High-resolution transmission electron microscopy analysis clearly revealed that the anisotropic structures are single crystalline in nature. The stabilization of certain crystallographic faces of anisotropic gold nanostructures by amines is invoked to explain the formation of these structures.},
	issn = {0974-3626},
	doi = {10.1007/s12039-021-01952-z},
	author = {Prasad, V, Bhagavatula L. and Sivasankaran, Prathap Chandran and Patel, Pitambar and Malekar, V, Pushpa and Maya, V, K. and Ramana, V, Chepuri}
}
@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}
}
