Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Basab Bijayi Dhar"'
Publikováno v:
ACS Omega, Vol 9, Iss 33, Pp 35458-35462 (2024)
Externí odkaz:
https://doaj.org/article/849d9d4ef9924a97811e9070681c056c
Publikováno v:
ACS Omega, Vol 5, Iss 26, Pp 15962-15972 (2020)
Externí odkaz:
https://doaj.org/article/483b6b77787749508a6b6563eb29dbaa
Autor:
Dennis Kühbeck, Basab Bijayi Dhar, Eva-Maria Schön, Carlos Cativiela, Vicente Gotor-Fernández, David Díaz Díaz
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 1111-1118 (2013)
The activity of gelatin and collagen proteins towards C–C bond formation via Henry (nitroaldol) reaction between aldehydes and nitroalkanes is demonstrated for the first time. Among other variables, protein source, physical state and chemical modif
Externí odkaz:
https://doaj.org/article/c781aff0170846fb9c0635cf38bc894f
Autor:
Susanta Sinha Roy, Debosmita Banerjee, Basab Bijayi Dhar, Gourav Bhattacharya, Sayantan Maity
Publikováno v:
ACS Applied Nano Materials. 5:3548-3557
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82286c623409d3126b4bf79639a97dc6
https://doi.org/10.1021/acsanm.1c04169
https://doi.org/10.1021/acsanm.1c04169
Autor:
Bhawana Nagar, Basab Bijayi Dhar
Publikováno v:
The Journal of Organic Chemistry. 87:3195-3201
In the presence of eosin Y, a visible light-induced one-step procedure (isolated yield of ≥75%) for thiolation of substituted 1,4-naphthoquinones using various aromatic and aliphatic thiols at room temperature is described herein. The rate-determin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68db554f8d8db97a6cf30831aca65ba1
https://doi.org/10.1021/acs.joc.1c02924
https://doi.org/10.1021/acs.joc.1c02924
Publikováno v:
Chemical Communications. 58:4075-4078
Ni(II)-tetradentate amido-quinoline complexes effectively catalysed C-H chlorination of a series of hydrocarbons in the presence of NaOCl and acetic acid. The bond dissociation energy of the C(sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d03d704cb4093252077cbad2b7d59ae6
https://doi.org/10.1039/d2cc00639a
https://doi.org/10.1039/d2cc00639a
Publikováno v:
ChemElectroChem. 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61d420a5af56acbd96812c0eaccb0b3f
https://doi.org/10.1002/celc.202201044
https://doi.org/10.1002/celc.202201044
Publikováno v:
Dalton transactions (Cambridge, England : 2003).
Cu(ii)-tetradentate amido-quinoline complexes effectively catalysed aromatic C–H hydroxylation using H2O2 as an oxidant in the absence of an external base with a high selectivity of around 90% for phenols via the non-radical pathway (TON ≥720).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d51d581bf1b9fb85f6ae04f8860db5e
https://pubmed.ncbi.nlm.nih.gov/36537082
https://pubmed.ncbi.nlm.nih.gov/36537082
Autor:
Bhawana Nagar, Basab Bijayi Dhar
Publikováno v:
ACS omega. 7(36)
A visible-light-mediated C-H arylation of substituted 1,4-napthoquinones (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::198d25bf7f8e15fa8c174b05ad9ca324
https://pubmed.ncbi.nlm.nih.gov/36119980
https://pubmed.ncbi.nlm.nih.gov/36119980
Publikováno v:
Organic Letters. 23:3269-3273
This paper describes an efficient, sustainable, one-step procedure for synthesizing substituted phenazines and phenoxazinones from commercially available ortho-substituted aromatic amines with very good yield (≥80%) in water. The procedure uses eos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0692fa7c1bec996c9844b354c37526b
https://doi.org/10.1021/acs.orglett.1c00725
https://doi.org/10.1021/acs.orglett.1c00725