Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Arun Raj Kizhakkayil Mangadan"'
Publikováno v:
ACS Catalysis. 11:14842-14847
A simple procedure for the intermolecular enantioselective palladium-catalyzed decarboxylative allylation of β-ketoacids is described. This method, inspired by a stoichiometric control experiment p...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96197dab1f533b801664146ec412d552
https://doi.org/10.1021/acscatal.1c04546
https://doi.org/10.1021/acscatal.1c04546
Publikováno v:
Angewandte Chemie. 133:22398-22403
Asymmetric allylic alkylation (AAA) is a powerful method for the formation of highly useful, non-racemic allylic compounds. Here we present a complementary enantioselective process that generates allylic lactones via π-acid catalysis. More specifica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12cde43a0f9f8c4227b3136e9cba2de2
https://doi.org/10.1002/ange.202108336
https://doi.org/10.1002/ange.202108336
Autor:
Pravin Kumar, Arun Raj Kizhakkayil Mangadan, Gaurav Saini, Manmohan Kapur, Gangam Srikanth Kumar
Publikováno v:
Organic letters. 20(2)
A diverse array of isoquinolines and phenanthridines have been accessed by developing a two-step, one-pot method constituting regioselective palladium-catalyzed Kuwajima–Urabe α-arylation of silylenol ethers and acid-mediated deprotection, annulat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6bf13dc2435a8119e9c512be401fcb8
https://pubmed.ncbi.nlm.nih.gov/29313688
https://pubmed.ncbi.nlm.nih.gov/29313688
Publikováno v:
ChemInform. 46
A new unified strategy has been developed for the synthesis of substituted 2-alkenylindoles and carbazoles. The strategy uses palladium-catalyzed α-arylation of TES-enol ethers of enones as the key step. The method is highly regioselective, provides
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0a9b10c70f354e211b6329df9458466
https://doi.org/10.1002/chin.201529073
https://doi.org/10.1002/chin.201529073
Publikováno v:
Organic letters. 17(5)
A new unified strategy has been developed for the synthesis of substituted 2-alkenylindoles and carbazoles. The strategy uses palladium-catalyzed α-arylation of TES-enol ethers of enones as the key step. The method is highly regioselective, provides
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0379e83ec0cccbd6032e195ee24dcf53
https://pubmed.ncbi.nlm.nih.gov/25706978
https://pubmed.ncbi.nlm.nih.gov/25706978