Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Uttam Dutta"'
Autor:
Debabrata Maiti, Uttam Dutta
Publikováno v:
Accounts of Chemical Research. 55:354-372
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::393b843941660af393f66181f916a0da
https://doi.org/10.1021/acs.accounts.1c00629
https://doi.org/10.1021/acs.accounts.1c00629
Autor:
Sheuli Sasmal, Gaurav Prakash, Uttam Dutta, Ranjini Laskar, Goutam Kumar Lahiri, Debabrata Maiti
Publikováno v:
Chemical Science. 13:5616-5621
An unprecedented report on Rh-catalyzed meta-C–H alkynylation of arenes, aided by a weakly coordinating cyano-based directing template, was developed using bromoalkynes as the coupling partner.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be5cf5182c5b66e6dafe57cff2dd38de
https://doi.org/10.1039/d2sc00982j
https://doi.org/10.1039/d2sc00982j
Autor:
Uttam Dutta, Debabrata Maiti
Publikováno v:
Encyclopedia of Reagents for Organic Synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a0534045b8a261c11e3d73e9341ee82
https://doi.org/10.1002/047084289x.rn02355
https://doi.org/10.1002/047084289x.rn02355
Autor:
Uttam Dutta, Debabrata Maiti
Publikováno v:
Encyclopedia of Reagents for Organic Synthesis. :1-5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1505c7cb5c16e93a400e3a109d0bc70b
https://doi.org/10.1002/047084289x.rn02356
https://doi.org/10.1002/047084289x.rn02356
Publikováno v:
Remote CH Bond Functionalizations. :1-5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8635174959a9293f6b7f07f82bf7a3da
https://doi.org/10.1002/9783527824137.ch1
https://doi.org/10.1002/9783527824137.ch1
Autor:
Uttam Dutta, Debabrata Maiti
Publikováno v:
Remote C-H Bond Functionalizations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65b19e486554380b1026bf0e44285a8e
https://doi.org/10.1002/9783527824137.ch8
https://doi.org/10.1002/9783527824137.ch8
Publikováno v:
Chemistry Letters. 49:1406-1420
In the past few decades, synthetic organic chemistry has been invigorated with the development of transition metal catalyzed directing group assisted regioselective C–H functionalization. Although ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3533a6cdff30e04637ac003c267f2d74
https://doi.org/10.1246/cl.200500
https://doi.org/10.1246/cl.200500
Autor:
Sandeep Pimparkar, Astam Mandal, Adithyaraj Koodan, Jagrit Grover, Uttam Dutta, Sandip Porey, Debabrata Maiti
Publikováno v:
Angewandte Chemie. 132:21017-21022
Biaryl compounds are extremely important structural motifs in natural products, biologically active components and pharmaceuticals. Selective synthesis of biaryls by distinguishing the subtle reactivity difference of distal arene C-H bonds are signif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5dd9e1fe352c304a9847c73fa6d8b224
https://doi.org/10.1002/ange.202005664
https://doi.org/10.1002/ange.202005664
Autor:
Uttam Dutta, Sandip Porey, Sandeep Pimparkar, Astam Mandal, Jagrit Grover, Adithyaraj Koodan, Debabrata Maiti
Publikováno v:
Angewandte Chemie International Edition. 59:20831-20836
Biaryl compounds are extremely important structural motifs in natural products, biologically active components and pharmaceuticals. Selective synthesis of biaryls by distinguishing the subtle reactivity difference of distal arene C-H bonds are signif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33c96c1a87c2b40c5df102a3416db997
https://doi.org/10.1002/anie.202005664
https://doi.org/10.1002/anie.202005664
Autor:
Arun Maji, Uttam Dutta, Ramasamy Jayarajan, Sandeep Pimparkar, Argha Saha, Gang Lu, Debabrata Maiti, Trisha Bhattacharya, David W. Lupton
Publikováno v:
Chemistry – A European Journal. 26:11558-11564
The significance of site selective functionalization stands upon the superior selectivity, easy synthesis and diverse product utility. In this work we demonstrate the para-selective introduction of versatile nitrile moiety, enabled by detachable and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a579a670831e1f734635fdab0bb65038
https://doi.org/10.1002/chem.202001368
https://doi.org/10.1002/chem.202001368