Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Subrata Maity"'
Publikováno v:
Journal of the Franklin Institute. 360:5211-5241
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::029d01fdd0bd6ec8ba095f61f944c581
https://doi.org/10.1016/j.jfranklin.2023.03.029
https://doi.org/10.1016/j.jfranklin.2023.03.029
Autor:
Subrata Maity, Alex M. Szpilman
Publikováno v:
Organic Letters. 25:1218-1222
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8193cf1a9336c8e25968de8b84b3453c
https://doi.org/10.1021/acs.orglett.3c00313
https://doi.org/10.1021/acs.orglett.3c00313
Publikováno v:
Clinical Diabetology. 8:116-120
Introduction. Published literature on type 1 diabetes (T1DM) patients from India suggests that a substantial number of them are negative to GAD 65 and IA-2 antibodies. Antibody positivity rates have been linked to dietary and socio-economic factors
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b16bc1bef372f6a46b8ce1174e0c037c
https://doi.org/10.5603/dk.2019.0005
https://doi.org/10.5603/dk.2019.0005
Publikováno v:
European Journal of Organic Chemistry. 2019:969-987
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b548fed724dab92adf30782b421e7152
https://doi.org/10.1002/ejoc.201801524
https://doi.org/10.1002/ejoc.201801524
Publikováno v:
Organicbiomolecular chemistry. 17(33)
An efficient strategy for the construction of both C(3)–N(1′) bisindoles and C(3)–N(1′) diindolylmethane has been explored via proper tuning of the nucleophilicity of indoline/indole to spiro-epoxyoxindole. Lewis acid-catalyzed highly regio-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61fdd5d397503c59eeecaba23e874f7f
https://pubmed.ncbi.nlm.nih.gov/31386749
https://pubmed.ncbi.nlm.nih.gov/31386749
Publikováno v:
The Journal of organic chemistry. 84(4)
A convenient and metal/catalyst-free approach for the reversal of regioselectivity in nucleophilic fluorination of a wide range of spiro-epoxyoxindoles has been reported simply by altering the nucleophilic fluoride reagents. Py·(HF)x-mediated fluori
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8b6eb4411a3672c8a5cc3470a9d4863
https://pubmed.ncbi.nlm.nih.gov/30642178
https://pubmed.ncbi.nlm.nih.gov/30642178
Publikováno v:
Advanced Synthesis & Catalysis. 358:2300-2306
Metal triflate-catalysed intermolecular Friedel–Crafts reactions involving electron-rich benzenoid arenes and spiroepoxyoxindoles at the spiro-centre have been developed for the exclusive regioselective synthesis of 3-aryl-(3-hydroxymethyl)oxindole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aad7b680ab392fc8e02b945577a33007
https://doi.org/10.1002/adsc.201600312
https://doi.org/10.1002/adsc.201600312
Publikováno v:
Organic Letters. 17:3430-3433
An efficient strategy for the synthesis of 3-(3-indolyl)-oxindole-3-methanol has been developed to achieve a Lewis acid catalyzed, highly regioselective ring opening of spiro-epoxyoxindoles with indoles. The method is used for the gram-scale formal t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed450a82f4fd1d529ccb458e1d8fe9a6
https://doi.org/10.1021/acs.orglett.5b01432
https://doi.org/10.1021/acs.orglett.5b01432
Publikováno v:
Organic letters. 19(8)
An effective Lewis acid catalyzed regioselective C3-allylation and a formal [3 + 2]-annulation reaction of spiro-epoxyoxindoles have been developed and can be accessed simply by changing the reaction conditions. This method has been successfully empl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::124b8d3317a3e9b54f2a058c3d67b78b
https://pubmed.ncbi.nlm.nih.gov/28383270
https://pubmed.ncbi.nlm.nih.gov/28383270
Publikováno v:
ChemInform. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5870fe5a0165a01e5e38ab44a3ad5713
https://doi.org/10.1002/chin.201649127
https://doi.org/10.1002/chin.201649127