Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Shobhan Mondal"'
Publikováno v:
JACS Au, Vol 4, Iss 8, Pp 2832-2837 (2024)
Externí odkaz:
https://doaj.org/article/5102f3ca0f4b4e8da1b7fd49eddf3538
Our group has reported several one-pot protocols for the synthesis of diaryliodonium salts, which have been recognized as attractive multi-purpose reagents in areas ranging from organic synthesis to materials chemistry. Over the years, we have identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51200368d2400c2cf927124d07b8c712
https://doi.org/10.26434/chemrxiv-2023-q88sc
https://doi.org/10.26434/chemrxiv-2023-q88sc
Publikováno v:
Angewandte Chemie. 135
Efficient protocols for accessing iodo-implanted diaryl and aryl(vinyl) sulfides have been developed using iodonium salts as reactive electrophilic arylation and vinylation reagents. The reactions take place under transition metal-free conditions, em
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65e452648ea14be49582893acc8b84f6
https://doi.org/10.1002/ange.202216296
https://doi.org/10.1002/ange.202216296
Efficient protocols for accessing iodo-implanted diaryl and aryl(vinyl) thioethers have been developed using iodonium salts as reactive electrophilic arylation and vinylation reagents. The reactions take place under transition metal-free, thiol-free,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aba2373b07882897f0fa02d27b360f81
https://doi.org/10.26434/chemrxiv-2022-c1bt4
https://doi.org/10.26434/chemrxiv-2022-c1bt4
Publikováno v:
Angewandte Chemie. 133:5752-5756
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed15033068472e14b1d72dd89eb06041
https://doi.org/10.1002/ange.202015249
https://doi.org/10.1002/ange.202015249
Publikováno v:
Angewandte Chemie. 131:15183-15187
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::addc7e4ba015ac879dec4b6f312bc7bb
https://doi.org/10.1002/ange.201907269
https://doi.org/10.1002/ange.201907269
Publikováno v:
Angewandte Chemie International Edition. 58:7117-7121
Herein, we report the redox-neutral, intermolecular, and highly branch-selective amidation of allylic C-H bonds enabled by Cp*IrIII catalysis. A variety of readily available carboxylic acids were converted into the corresponding dioxazolones and effi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b1b03a7e514ddb8e85ba6c257a492c1
https://doi.org/10.1002/anie.201901733
https://doi.org/10.1002/anie.201901733
Publikováno v:
Chemical Science
Herein we describe an unprecedented RuII-catalyzed site-selective and regiospecific annulation of benzoic acids with propargylic carbonates. The weakly coordinating carboxylic acid moiety outperformed other typically used directing groups in C–H ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::474e0cf5c9df97f57775fba35c59f2a4
https://doi.org/10.1039/c9sc01703h
https://doi.org/10.1039/c9sc01703h
Publikováno v:
Angewandte Chemie (International ed. in English). 60(11)
Herein, we report a Cp*Ir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a19a88a8b178776ce7469f7162146f09
https://pubmed.ncbi.nlm.nih.gov/33400853
https://pubmed.ncbi.nlm.nih.gov/33400853
Publikováno v:
The Journal of Organic Chemistry. 83:14553-14567
A highly efficient and stereoselective route to access 1,3-disubstituted 1,2,3,4-tetrahydropyrazino[1,2-a]indoles and 3,4-dihydro-1H-[1,4]oxazino[4,3-a]indoles with excellent stereoselectivity (de, ee >99%) via base mediated ring opening of aziridine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dc82f2c5d03a16e1ba07d466de22fe3
https://doi.org/10.1021/acs.joc.8b02339
https://doi.org/10.1021/acs.joc.8b02339