Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Sagar Arepally"'
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-8 (2024)
Abstract Electrochemistry offers tunable, cost effective and environmentally friendly alternatives to carry out redox reactions with electrons as traceless reagents. The use of organoiodine compounds as electrocatalysts is largely underdeveloped, des
Externí odkaz:
https://doaj.org/article/c5c221bd87a54b2abce5ce6d69ef90c1
Publikováno v:
Angewandte Chemie.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab20065a89d25d5a18dd29454e4255d5
https://doi.org/10.1002/ange.202303460
https://doi.org/10.1002/ange.202303460
Autor:
Sagar Arepally, Ponnusamy Nandhakumar, Gisela A. González-Montiel, Alina Dzhaparova, Gyeongho Kim, Ahyeon Ma, Ki Min Nam, Haesik Yang, Paul Ha-Yeon Cheong, Jin Kyoon Park
Publikováno v:
ACS Catalysis. 12:6874-6886
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c14b2e69d3ff800ed3c6c4bc6058dd4
https://doi.org/10.1021/acscatal.2c01404
https://doi.org/10.1021/acscatal.2c01404
Publikováno v:
RSC Advances. 10:12599-12603
The direct oxidative cleavage of activated alkynes via hydroamination has been described using organic photocatalyst under visible-light irradiation at room temperature. In this reaction, the single electron oxidation of an in situ formed enamine fol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b30e9f3ece6bbb405f3c685ff702f0a6
https://doi.org/10.1039/c9ra10555g
https://doi.org/10.1039/c9ra10555g
Publikováno v:
European Journal of Organic Chemistry. 2019:1542-1547
A stereoselective aminoiodination of activated alkynes with PhI(OAc)2 and amines via multiple-site functionalization to afford (Z)diethyl 2-(diphenylamino)-3-iodomaleate derivatives with superior yields has been described. The key feature of this rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::462c3c61c101b4fada4d01e293ce4afd
https://doi.org/10.1002/ejoc.201801725
https://doi.org/10.1002/ejoc.201801725
Publikováno v:
European Journal of Organic Chemistry. 2018:5700-5705
PIDA/TBAB-promoted oxidative geminal diazidofunctionalization of alkynes has been described for the first time. The transformation demonstrates a mechanistically distinctive approach to access geminal diazides, in which TBAB plays a crucial role as b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c93dde79c7b2cb7eee2732b255902fe0
https://doi.org/10.1002/ejoc.201801081
https://doi.org/10.1002/ejoc.201801081
Publikováno v:
RSC advances. 10(21)
The direct oxidative cleavage of activated alkynes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::69f48be8ee070bdb3aadf030811ff413
https://pubmed.ncbi.nlm.nih.gov/35497603
https://pubmed.ncbi.nlm.nih.gov/35497603
Publikováno v:
The Journal of Organic Chemistry. 82:331-342
An efficient protocol for the synthesis of quinazoline derivatives through nickel-catalyzed ligand-/base-free oxidative isocyanide insertion under aerobic conditions with intramolecular bis-amine nucleophiles has been developed. A one-pot sequential
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e01b3b4c40c68967cbde4ca2af4431b5
https://doi.org/10.1021/acs.joc.6b02423
https://doi.org/10.1021/acs.joc.6b02423
The direct oxidative cleavage of activated alkynes via hydroamination has been described using organic photocatalyst under visible-light irradiation at room temperature. In this reaction, the single electron oxidation of an insitu formed enamines und
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6bcd2f526227d70a448cea3003444e1
https://doi.org/10.26434/chemrxiv.7322402.v3
https://doi.org/10.26434/chemrxiv.7322402.v3
A stereoselective aminoiodination of activated alkynes with PhI(OAc)2 and amines via multiple-site functionalization to afford (Z)diethyl 2-(diphenylamino)-3-iodomaleate derivatives with superior yields has been described. The key feature of this rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::750341b31988af1e3dc8010abe891a2b
https://doi.org/10.26434/chemrxiv.7315358.v2
https://doi.org/10.26434/chemrxiv.7315358.v2