Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Tanmay K. Pati"'
Autor:
Ashok Raj Patel, Gurupada Maity, Tanmay K. Pati, Laksmikanta Adak, Christopher L. Cioffi, Subhash Banerjee
Publikováno v:
Frontiers in Chemistry, Vol 12 (2024)
We report the fabrication of a novel spinel-type Pd₀.₁Cu₀.₉Co₂O₄ nano-flake material designed for Mizoroki-Heck and Suzuki coupling-cum-transesterification reactions. The Pd₀.₁Cu₀.₉Co₂O₄ material was synthesized using a simple
Externí odkaz:
https://doaj.org/article/955a855e89374127891fab3205821096
Publikováno v:
The Journal of Organic Chemistry. 85:13272-13279
A metal-free, simultaneous triple C-C coupling cyclization reaction between phenacyl bromides and indoles is discovered in a highly regioselective fashion to furnish 3,5-diarylcarbazoles. DMAP is utilized as the only reagent for the unusual and rapid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbf494c25bdf7e61bae0ea0cf40c7265
https://doi.org/10.1021/acs.joc.0c01670
https://doi.org/10.1021/acs.joc.0c01670
Autor:
Mrinalkanti Kundu, Tanmay K. Pati, Uttam Kumar Khamrai, Deepak Tayde, Dilip K. Maiti, Sk Ajarul
Publikováno v:
The Journal of Organic Chemistry. 85:8563-8579
We have identified different N-substituted 2-pyridones as inbuilt directing groups for selective C–H-activated functionalization instead of deprotecting and/or throwing away the directing groups. A...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85f57710722b77535895252e5dfa67de
https://doi.org/10.1021/acs.joc.0c00941
https://doi.org/10.1021/acs.joc.0c00941
Autor:
Tanmay K, Pati, Sk, Ajarul, Mrinalkanti, Kundu, Deepak, Tayde, Uttam, Khamrai, Dilip K, Maiti
Publikováno v:
The Journal of organic chemistry. 85(13)
We have identified different N-substituted 2-pyridones as inbuilt directing groups for selective C-H-activated functionalization instead of deprotecting and/or throwing away the directing groups. A robust general method for external ligand-free Pd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9dff2904ce6d98f8a7c37bb5ab4bca8b
https://pubmed.ncbi.nlm.nih.gov/32574496
https://pubmed.ncbi.nlm.nih.gov/32574496
Publikováno v:
Chemical communications (Cambridge, England). 56(3)
We demonstrated a highly competitive and selective C–C and N–C cross-coupled 7-, 6- and 5-annulation utilizing 2-ethynylanilides to afford functionalized 1H-benzo[b]azepin-2(5H)-ones, 2-quinolinones, and 3-acylindoles in high yield. ZnCl2 was fou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4058ee5dd26879e132b3aa4f20aa623
https://pubmed.ncbi.nlm.nih.gov/31829322
https://pubmed.ncbi.nlm.nih.gov/31829322
Publikováno v:
Organic Letters. 20:4062-4066
A new bidentate directing group, 3-amino-1-methyl-1H-pyridin-2-one, is introduced to achieve a powerful PdII metallacycle for selective γ-C(sp3)–H activation and arylation of aromatic and aliphatic carboxylic acid derivatives. The versatility of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::470685508e659a32e579be4fe9377ceb
https://doi.org/10.1021/acs.orglett.8b01618
https://doi.org/10.1021/acs.orglett.8b01618
Publikováno v:
Organic letters. 20(13)
A new bidentate directing group, 3-amino-1-methyl-1 H-pyridin-2-one, is introduced to achieve a powerful Pd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6c01e8dbbc1a406f23a5c80331432ed3
https://pubmed.ncbi.nlm.nih.gov/29894193
https://pubmed.ncbi.nlm.nih.gov/29894193