Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Velayutham Ravikumar"'
Autor:
Koul, Summon, Kurhade, Suresh, Bhosale, Sandeep, Naik, Keshav, Salunkhe, Videsh, Ravula, Sudhir, Punde, Prasad, Velayutham, Ravikumar, Tiwari, Atul, Ahl, Daniela, Malkapuram, Srividya, Mudagala, Vamsi, Raje, Amol, Umrani, Dhananjay, Tambe, Suhas, Patil, Poonam, Singh, Umesh, Bhuniya, Debnath, Hariharan, Narayanan, Mookhtiar, Kasim
Publikováno v:
In Bioorganic & Medicinal Chemistry Letters 15 April 2022 62
Publikováno v:
Supramolecular Chemistry
Supramolecular Chemistry, Vol. 23, No 1 & 2 (2011) pp. 69-73
Supramolecular Chemistry, Vol. 23, No 1 & 2 (2011) pp. 69-73
In this brief essay, one of the most common and least appreciated challenge in the field is addressed. Few chemists, particularly supramolecular chemists, exist who are not all too familiar with solubility problems during the synthesis of new molecul
Publikováno v:
Journal of Chemical Sciences. 120:205-216
A domino enyne cross-metathesis/intramolecular Diels-Alder reaction has been successfully used to synthesize a bicyclo[5.3.1] undecene, corresponding to AB-ring of taxol without the gem dimethyl group.
Publikováno v:
Tetrahedron Letters. 47:981-984
An efficient domino cross-enyne metathesis/intramolecular Diels–Alder reaction is demonstrated for the construction of a bicyclo[5.3.1]undecene.
Publikováno v:
ChemInform. 42
Autor:
Abbas Sanchawala, Debnath Bhuniya, D. Srinivasa Reddy, Velayutham Ravikumar, Kurhade Suresh Eknath
Publikováno v:
Organic letters. 13(14)
The first total synthesis of isofregenedadiol, a bicyclic diterpene isolated from H. Viscosum, is reported starting from a d-(−)-pantolactone chiral pool. A one-pot quadruple reaction sequence comprising an enyne ring-closing metathesis/cross-metat
Autor:
Oksana Kel, Naomi Sakai, Ravuri S. K. Kishore, Eric Vauthey, Velayutham Ravikumar, Rajesh S. Bhosale, Stefan Matile
Publikováno v:
Chemical Science, Vol. 1 (2010) pp. 357-368
The objective of this study was to synthesize multichromophoric donor–acceptor systems with non-halogenated red (RO) naphthalenediimides (NDIs) attached along p-oligophenyl (POP) and oligophenylethynyl (OPE) scaffolds, and to evaluate their usefuln
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::164c220be170dcecd2d63dce12e249e4
https://archive-ouverte.unige.ch/unige:14679
https://archive-ouverte.unige.ch/unige:14679
Autor:
Alberto Gomez-Casado, Pascal Jonkheijm, Alejandro Oscar Perez-Velasco, Ravuri S. K. Kishore, Stefan Matile, Velayutham Ravikumar, Michal Borkovec, Jurriaan Huskens, Naomi Sakai, Eric Vauthey, Plinio Maroni, Oksana Kel, Tomohisa Sawada, Rajesh S. Bhosale
Publikováno v:
Angewandte Chemie (international edition), 48(35), 6461-6464. Wiley
Angewandte Chemie, Vol. 121, No 35 (2009) pp. 6583-6586
Angewandte Chemie: International Edition, Vol. 48, No 35 (2009) pp. 6461-6464
Angewandte Chemie, Vol. 121, No 35 (2009) pp. 6583-6586
Angewandte Chemie: International Edition, Vol. 48, No 35 (2009) pp. 6461-6464
Matching matters when building supramolecular n/p-heterojunction photosystems on solid supports that excel with efficient photocurrent generation, important critical thickness, smooth surfaces, and flawless responsiveness to functional probes for the
Autor:
Velayutham Ravikumar, Alexandre Fürstenberg, Natalie Banerji, Eric Vauthey, Guillaume Bollot, Rajesh S. Bhosale, Sara Marie Butterfield, Ravuri S. K. Kishore, Santanu Maity, Virginie Gorteau, Duy-Hien Tran, Naomi Sakai, Alejandro Oscar Perez-Velasco, Stefan Matile, Federico Mora, Shinya Hagihara, Andreas Hennig, Jiri Mareda
Publikováno v:
Pure and Applied Chemistry, Vol. 80, No 8 (2008) pp. 1873-1882
The objective with synthetic multifunctional nanoarchitecture is to create large suprastructures with interesting functions. For this purpose, lipid bilayer membranes or conducting surfaces have been used as platforms and rigid-rod molecules as shape
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e0dfef80a2abd193608df06a8829649
https://archive-ouverte.unige.ch/unige:8008
https://archive-ouverte.unige.ch/unige:8008
Publikováno v:
ChemInform. 38