Zobrazeno 1 - 10
of 37
pro vyhledávání: '"C. P. Irfana Jesin"'
Publikováno v:
SynOpen, Vol 06, Iss 04, Pp 319-328 (2022)
The sulfoximine-based tetrazoles have been synthesized via azido-Ugi four-component reactions of sulfoximines, isocyanides, aldehydes, and TMS-azide in MeOH at 70 °C in the presence of InCl3. Replacement of sulfoximines with sulfonimidamides (SIA) h
Externí odkaz:
https://doaj.org/article/7757cdd87063405f995738af2ba574d7
Publikováno v:
Synlett. 34:678-682
A transition-metal-free novel route to access N-(o-halo)arylsulfoximines/sulfonimidamides is achieved by the reaction of sulfoximine/sulfonimidamide, aryne precursor, and CCl4/CBr4 in the presence of KF/18-crown-6. The in situ generated benzyne inter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7978c52fbe38b0591ddafb89ea1413b0
https://doi.org/10.1055/a-1921-0875
https://doi.org/10.1055/a-1921-0875
Publikováno v:
Advanced Synthesis & Catalysis. 364:1144-1149
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a3322e1e717f6ba9e27005571a0f7a5
https://doi.org/10.1002/adsc.202101432
https://doi.org/10.1002/adsc.202101432
Publikováno v:
Organic & Biomolecular Chemistry. 20:7036-7039
Hitherto unknown α-sulfoximinophosphonates are synthesized via the Kabachnik–Fields reaction with imine (sulfoximine) as a nucleophile for the first time.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1176d44ef43724b9deab9af80c60dc8c
https://doi.org/10.1039/d2ob01355j
https://doi.org/10.1039/d2ob01355j
Autor:
C. P. Irfana Jesin, V. R. Padma Priya, Ramesh Kataria, V. Alisha, P. S. Vimalkumar, Anuja G. Joseph, Ganesh Chandra Nandi
Publikováno v:
ChemistrySelect. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2f53d8f631e52f776c33c73f1df1fa6
https://doi.org/10.1002/slct.202202898
https://doi.org/10.1002/slct.202202898
Publikováno v:
Advanced Synthesis & Catalysis. 363:1756-1781
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61017d49934f0aa1fb5522dcdb2d9e0b
https://doi.org/10.1002/adsc.202001372
https://doi.org/10.1002/adsc.202001372
Publikováno v:
Organic & Biomolecular Chemistry. 19:7061-7065
Herein, we disclose a metal-free novel approach for the synthesis of N-(α-substituted)alkyl sulfoximines/sulfonimidamides via one-pot multicomponent Petasis reactions of aryl boronic acids, ortho-hydroxyarylaldehydes and sulfoximines/sulfonimidamide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::490210ee029d3227b5f76a21395444a5
https://doi.org/10.1039/d1ob01181b
https://doi.org/10.1039/d1ob01181b
Autor:
C. P., Irfana Jesin1,2, Nandi, Ganesh Chandra1,2 ganeshnandi@gmail.com
Publikováno v:
Chemistry - A European Journal. 1/14/2019, Vol. 25 Issue 3, p743-749. 7p.
Publikováno v:
ChemistrySelect. 4:14004-14006
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3ba7ec549d2fe63d7793c60024dadcc
https://doi.org/10.1002/slct.201904548
https://doi.org/10.1002/slct.201904548
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 25(3)
Sulfonimidamides (SIAs) are acting both as surrogate amines and nucleophiles depending on the reaction conditions to access propargylamines and N-propargyl SIAs, respectively. The amine part of SIAs has been cleaved in an InCl3 -catalyzed three-compo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3eecc071256746db82c5566e230bd7f3
https://pubmed.ncbi.nlm.nih.gov/30395377
https://pubmed.ncbi.nlm.nih.gov/30395377