Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Bholanath Maity"'
Autor:
Krishnamoorthy Muralirajan, Rajesh Kancherla, Bholanath Maity, Safakath Karuthedath, Frédéric Laquai, Luigi Cavallo, Magnus Rueping
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-12 (2023)
Abstract Photocatalytic selective C(sp3)–H activation/cross-coupling reactions are appealing in organic synthesis. In this manuscript, we describe the development of photoexcited-state Pd-catalyzed dehydrogenative β-sulfonylation reactions using a
Externí odkaz:
https://doaj.org/article/86fdd31caf2544a69426e6cb4d594158
Modulating stereoselectivity in allylic C(sp3)-H bond arylations via nickel and photoredox catalysis
Autor:
Long Huang, Marcin Szewczyk, Rajesh Kancherla, Bholanath Maity, Chen Zhu, Luigi Cavallo, Magnus Rueping
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-10 (2023)
The selective construction of C-C double bonds in alkenes, which can be one of two isomers, is a fundamental focus of organic chemistry. Here, the authors systematically investigated the stereoselectivity in allylic C(sp3)-H bond arylations and demon
Externí odkaz:
https://doaj.org/article/10b6529edc394b3a945d9b06db6f679c
Autor:
Rajesh Kancherla, Krishnamoorthy Muralirajan, Bholanath Maity, Safakath Karuthedath, Gadde Sathish Kumar, Frédéric Laquai, Luigi Cavallo, Magnus Rueping
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-9 (2022)
Although the combination of photo- and nickel catalysis has garnered intense interest in the preceding years, the mechanisms by which these transformations occur are to some degree unresolved. Here the authors provide computational and spectroscopic
Externí odkaz:
https://doaj.org/article/cd49c2633c5543fa87a7adaa24234737
Autor:
Lin Guo, Watchara Srimontree, Chen Zhu, Bholanath Maity, Xiangqian Liu, Luigi Cavallo, Magnus Rueping
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-6 (2019)
Classical Suzuki-Miyaura couplings require wasteful electrophilic coupling partners and an exogenous base often engaging in side-reactions. Here, the authors report an alternative Suzuki-type synthesis of biaryls, involving the base-free nickel-catal
Externí odkaz:
https://doaj.org/article/1dd80129277045a59ff2d6711c078b3f
Publikováno v:
ACS Catalysis. 13:6249-6260
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f35b4d10545901f5558d24301b2bb5a
https://doi.org/10.1021/acscatal.3c00567
https://doi.org/10.1021/acscatal.3c00567
Publikováno v:
ACS Catalysis. 12:13215-13224
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02960645f7898cc0a1a26e7d4f97954e
https://doi.org/10.1021/acscatal.2c04284
https://doi.org/10.1021/acscatal.2c04284
Publikováno v:
ACS Catalysis. 11:13973-13982
Computational analysis of the arylation of aliphatic Csp3–H bonds catalyzed by decatungstate–nickel validates the reaction mechanism and provides valuable insights into how to accomplish the corres...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf6dc1d34cf66bf96a63ea1465d069f7
https://doi.org/10.1021/acscatal.1c04142
https://doi.org/10.1021/acscatal.1c04142
Publikováno v:
ACS Catalysis. 11:4061-4070
L.C. acknowledges the King Abdullah University of Science and Technology (KAUST) for support and the KAUST Supercomputing Laboratory for providing computational resources of the supercomputer Shaheen II.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63314eafccce42e62c6ea2528c30ccdf
https://doi.org/10.1021/acscatal.0c04856
https://doi.org/10.1021/acscatal.0c04856
Autor:
Munmun Ghosh, Imtiyaz Ahmad Bhat, Bholanath Maity, Mohammed Eddaoudi, Prashant M. Bhatt, Luigi Cavallo, Santanu Chand, Avishek Dey, Niveen M. Khashab, Monerah Altamimy
Publikováno v:
Chemical Communications. 57:9124-9127
The separation of xylene isomers is one of the most challenging tasks in the petrochemical industry. Herein, we developed an efficient adsorptive molecular sieving strategy using crystalline trianglimine macrocycle (1) to separate the elusive m-xylen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b20937fb2162d455cdac20c033f79b1
https://doi.org/10.1039/d1cc03531b
https://doi.org/10.1039/d1cc03531b
Publikováno v:
Journal of the American Chemical Society 142(33), 14286-14294 (2020). doi:10.1021/jacs.0c05917
Journal of the American Chemical Society
Journal of the American Chemical Society
Journal of the American Chemical Society 142(33), 14286-14294 (2020). doi:10.1021/jacs.0c05917
Published by American Chemical Society, Washington, DC
Published by American Chemical Society, Washington, DC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a7280e1b7bbac1f41bfcedd43702bcc
https://doi.org/10.1021/jacs.0c05917
https://doi.org/10.1021/jacs.0c05917