Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Jayaraman, Dhineshkumar"'
Publikováno v:
ACS Omega, Vol 2, Iss 8, Pp 4885-4893 (2017)
Externí odkaz:
https://doaj.org/article/5268396ccff349d38646838af3912ab1
Autor:
Ji Zhang, Niels R. M. Reintjens, Jayaraman Dhineshkumar, Martin D. Witte, Adriaan J. Minnaard
Publikováno v:
Organic letters, 24(29), 5339-5344. AMER CHEMICAL SOC INC
To circumvent protecting groups, the site-selective modification of unprotected glycosides is intensively studied. We show that site-selective oxidation, followed by treatment of the corresponding trityl hydrazone with tert-butyl hypochlorite and a H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::258648faaf2da00241692ad17f6ead3c
https://doi.org/10.1021/acs.orglett.2c01992
https://doi.org/10.1021/acs.orglett.2c01992
Publikováno v:
Advanced Synthesis & Catalysis. 362:2466-2473
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0853f24ab1fd8dcf73c904121fbc23e
https://doi.org/10.1002/adsc.202000347
https://doi.org/10.1002/adsc.202000347
Akademický článek
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Autor:
Yogesh Siddaraju, Kiran R. Bettadapur, Kandikere Ramaiah Prabhu, Kaliyamoorthy Alagiri, Jayaraman Dhineshkumar, Begur Vasanthkumar Varun
Publikováno v:
Tetrahedron Letters. 58:803-824
A significant number of reactions have appeared in the literature regarding cross dehydrogenative coupling (CDC) reactions over the years. This review aims to cover the advances in the area of C C bond formations via CDC reactions in the last six yea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23ed0a2e1b7044b3e1df7576f64ac15c
https://doi.org/10.1016/j.tetlet.2017.01.035
https://doi.org/10.1016/j.tetlet.2017.01.035
Publikováno v:
ChemistrySelect. 1:1033-1038
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b8c465879500843d9654a7edece48e6
https://doi.org/10.1002/slct.201600292
https://doi.org/10.1002/slct.201600292
Publikováno v:
European Journal of Organic Chemistry. 2016:447-452
An efficient azidation of 1,3-dicarbonyl compounds led to tertiary azides in the presence of tetrabutylammonium iodide (TBAI). TBAI is used as a pre-catalyst along with aq. tert-butyl hydroperoxide (TBHP) as an oxidant in aqueous medium. This operati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e344d0a9f63388abd7060caa1ec03e0
https://doi.org/10.1002/ejoc.201501374
https://doi.org/10.1002/ejoc.201501374
Publikováno v:
The Journal of organic chemistry. 83(1)
Azidation of indoles using iodine and copper bromide as catalysts under ambient reaction conditions is presented. The regioselectivity is directed by the substituent at the C3-position of indole. A radical stabilizing group such as an ester or ketone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::865904c9226961bfd7fd1fffbb93205e
https://pubmed.ncbi.nlm.nih.gov/29205046
https://pubmed.ncbi.nlm.nih.gov/29205046
Publikováno v:
ChemInform. 47
Dearomatizative azidation and peroxidation of β-naphthols have been explored using copper bromide as a catalyst. These reactions lead to highly valuable naphthalenone derivatives such as quaternary azide derivatives and quaternary peroxide derivativ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24dd4a6a417e337eace4e19a3490d6b9
https://doi.org/10.1002/chin.201652181
https://doi.org/10.1002/chin.201652181
Publikováno v:
Organic Letters. 15:1092-1095
A versatile aerobic catalytic system (I(2) and O(2)/TBHP) for C-H functionalization is reported. This CDC (cross-dehydrogentive coupling) reaction is compatible with a large number of nucleophiles and is performed under ambient reaction conditions. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::945efc840c1492ade912e8f7167e186b
https://doi.org/10.1021/ol4001153
https://doi.org/10.1021/ol4001153