Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Anjali Dahiya"'
Publikováno v:
SynOpen, Vol 05, Iss 03, Pp 232-251 (2021)
The upsurge of interest in the development of methodologies for the construction of sulfur-containing compounds via the use of expedient reagents has established sustainable tools in organic chemistry. This review focuses on sulfonylation reactions u
Externí odkaz:
https://doaj.org/article/4bd90c92ac35486db96cff11f0fc6f90
Autor:
Smit Patel, Jitesh Adwani, Raushan Singh, Debolina Majumdar, Anjali Dahiya, Kumar Sambhav Verma, Lalit Kumar Pandey, Nitesh Singh Rajput, Shweta Kulshreshtha
Publikováno v:
Vegetos. 36:238-248
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08a9e7d4f48770d692b945640404d61a
https://doi.org/10.1007/s42535-023-00588-3
https://doi.org/10.1007/s42535-023-00588-3
Autor:
Nikita Chakraborty, Kamal K. Rajbongshi, Anjali Dahiya, Bubul Das, Akshar Vaishnani, Bhisma K. Patel
Publikováno v:
Chemical Communications. 59:2779-2782
N-Iodosuccinimide catalyzed, visible-light-induced oxidative decarboxylative cross-coupling between cinnamic acids and NH-sulfoximines leading to α-keto-N-acyl sulfoximines is presented.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0216beeafe1a4b8164841c790eaab3a
https://doi.org/10.1039/d3cc00142c
https://doi.org/10.1039/d3cc00142c
Publikováno v:
The Journal of Organic Chemistry. 87:13383-13388
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7abf9ff3a5d682a2d4aaa61c20ff92b8
https://doi.org/10.1021/acs.joc.2c01626
https://doi.org/10.1021/acs.joc.2c01626
Publikováno v:
Organic Letters. 24:1918-1923
An inimitable illustration of the green-light-induced synthesis of thio-functionalized pyrroles has been established using β-ketodinitriles and thiophenols as the reacting partners and eosin Y as the photocatalyst. Large-scale synthesis and some use
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::786f9b8a80cf97555e98362a2fd5220f
https://doi.org/10.1021/acs.orglett.2c00283
https://doi.org/10.1021/acs.orglett.2c00283
Publikováno v:
The Journal of Organic Chemistry. 86:17504-17510
A Cu(II)-promoted synthesis of an aza-fused N-heterocycle having a benz-imidazopyridine scaffold is developed via an addition-cyclization reaction followed by an Ullmann-type C-N coupling between o-iodoanilines and γ-ketodinitriles. This protocol fe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b5579842129536324abb8295d05e9f7
https://doi.org/10.1021/acs.joc.1c02198
https://doi.org/10.1021/acs.joc.1c02198
Publikováno v:
The Journal of Organic Chemistry. 86:11968-11986
An inimitable illustration of a green-light-induced, regioselective difunctionalization of terminal alkynes has been disclosed using sodium arylsulfinates and carboxylic acids in the presence of eosin Y as the photocatalyst. The present methodology i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0556101d929dbdefa2f844497922d224
https://doi.org/10.1021/acs.joc.1c01350
https://doi.org/10.1021/acs.joc.1c01350
Publikováno v:
SynOpen, Vol 05, Iss 03, Pp 232-251 (2021)
The upsurge of interest in the development of methodologies for the construction of sulfur-containing compounds via the use of expedient reagents has established sustainable tools in organic chemistry. This review focuses on sulfonylation reactions u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99faf14433d885d8f1a39bae07fa0837
https://doi.org/10.1055/a-1577-9755
https://doi.org/10.1055/a-1577-9755
Publikováno v:
Organic & Biomolecular Chemistry. 19:6847-6857
A Pd(ii)/Cu(ii) catalysed domino synthesis of tricyanovinylindoles has been achieved using DMSO as a one-carbon synthon. The reaction proceeds via the construction of 2-aryl-3-formyl indole followed by sequential addition of malononitrile and a CN re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3adb96c40e4a357851276ccf1891d51a
https://doi.org/10.1039/d1ob01086g
https://doi.org/10.1039/d1ob01086g
Publikováno v:
Organic Letters. 22:3728-3733
A visible-light-induced synthesis of N-hydroxybenzimidoyl cyanides from aromatic terminal alkenes is achieved by using Eosin Y as an organic photoredox catalyst. The process goes via a radical pathway with successive incorporation of two nitrogen ato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5267afa0db443232a3d7535de132edb6
https://doi.org/10.1021/acs.orglett.0c01235
https://doi.org/10.1021/acs.orglett.0c01235