Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Subhasis Paul"'
Publikováno v:
Journal of the American Chemical Society. 145:2773-2778
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c747cc9f5a569ba6c74603c9f77a9245
https://doi.org/10.1021/jacs.2c12699
https://doi.org/10.1021/jacs.2c12699
Publikováno v:
Organic Letters. 24:8047-8051
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2090992b53fa8f03de4715f8b8620205
https://doi.org/10.1021/acs.orglett.2c03300
https://doi.org/10.1021/acs.orglett.2c03300
Publikováno v:
Handbook of CH-Functionalization. :1-32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e073ec35cb6ee69ab5c0e4602b13673
https://doi.org/10.1002/9783527834242.chf0093
https://doi.org/10.1002/9783527834242.chf0093
Publikováno v:
Organic letters. 24(43)
Herein, we describe a photocatalytic method for the direct incorporation of an oxime functional group at inert C(sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a7bffd2ac8a8845f68ca960c80c60993
https://pubmed.ncbi.nlm.nih.gov/36286621
https://pubmed.ncbi.nlm.nih.gov/36286621
Publikováno v:
Chemistry – An Asian Journal. 14:3154-3160
An aerobic radical approach for the synthesis of unsymmetrical heteroaryl ketones is described herein. The reaction involves cross-dehydrogenative coupling between aldehydes and heteroaromatic bases with molecular oxygen (O2 ). The key aspect of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bb9dc77e4fb68231c37ce832a7b910e
https://doi.org/10.1002/asia.201900857
https://doi.org/10.1002/asia.201900857
Autor:
Subhasis Paul, Joyram Guin
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 27(13)
Herein, an operationally simple, environmentally benign, and effective method for intermolecular radical hydroacylation of unactivated substrates employing photo-induced hydrogen atom transfer (HAT) initiation is described. The use of commercially av
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a2de997525bfed86dface29f9ccf5a2
https://pubmed.ncbi.nlm.nih.gov/33350515
https://pubmed.ncbi.nlm.nih.gov/33350515
The population of the country is growing exponentially day by day. Therefore it is very necessary for the system to manage the economy of the country and also to provide its citizens healthy food. The backbone of the food industry depends on the prod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aea4dc0f0041df7d3996e29de0aca2dd
https://doi.org/10.36375/prepare_u.a79
https://doi.org/10.36375/prepare_u.a79
Publikováno v:
Synlett. 28:1244-1249
3,3-Dialkylated oxindoles (1,3-dihydro-2H-indol-2-ones), particularly those containing C3 quaternary stereogenic centers, occupy an important place in organic synthesis and drug discovery. The radical 1,2-alkylarylation of activated olefins with alky
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9813564e5cc9a39f1546eb6ab0d8f392
https://doi.org/10.1055/s-0036-1588754
https://doi.org/10.1055/s-0036-1588754
Autor:
Subhasis Paul, Joyram Guin
Publikováno v:
Green Chemistry. 19:2530-2534
An efficient radical addition/elimination reaction that enables selective incorporation of alkenyl, alkynyl and allyl functional groups into the C(sp3)–H bond under green reaction conditions is developed. The process is based on the catalytic forma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff335f73a79733eada089015b26522a9
https://doi.org/10.1039/c7gc00840f
https://doi.org/10.1039/c7gc00840f
Publikováno v:
Angewandte Chemie. 128:7887-7891
An efficient method for the aerobic radical-cascade alkylation/cyclization of α,β-unsaturated amides to afford functionalized oxindoles with a C3 quaternary stereocenter is described. The process is based on the generation of valuable alkyl radical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45fa31faf7432ffaa7b47430f7c35d31
https://doi.org/10.1002/ange.201603809
https://doi.org/10.1002/ange.201603809