Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Dongen, Lin"'
Publikováno v:
The Journal of Organic Chemistry. 88:5687-5695
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8606154bf00cb53b456849443890372
https://doi.org/10.1021/acs.joc.3c00149
https://doi.org/10.1021/acs.joc.3c00149
Publikováno v:
Organic & Biomolecular Chemistry. 21:3167-3171
The one-step visible light-induced direct alkylation of the C8–H bond for purine derivatives by ethers was developed. Of particular interest is that substrates include purines with various functional groups and even unprotected 9H-purines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f9cbf077f0592322b5f250947f92940
https://doi.org/10.1039/d3ob00147d
https://doi.org/10.1039/d3ob00147d
Publikováno v:
The Journal of Organic Chemistry. 87:11558-11564
A cross-dehydrogenation coupling reaction between purines and alcohols, induced by visible light, using an acridinium photocatalyst and air as the sole oxidant, to synthesize a series of C8-alkoxy purine derivatives was developed. This protocol is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::752a6524ed8b1500479f848e1cf6e0b5
https://doi.org/10.1021/acs.joc.2c01146
https://doi.org/10.1021/acs.joc.2c01146
Publikováno v:
The Journal of Organic Chemistry. 85:2415-2425
The one-step copper-mediated regioselective formation of the C8–S bond for purine derivatives with arylthiols was achieved using air as the green oxidant in the presence of 1.0 equiv of Na2CO3 and ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a94ed51f5db71c7b4d81be0d8ab0341
https://doi.org/10.1021/acs.joc.9b03115
https://doi.org/10.1021/acs.joc.9b03115
Publikováno v:
Chinese Chemical Letters. 34:107467
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26257f7d2f65a5a809639ee363d91b38
https://doi.org/10.1016/j.cclet.2022.04.065
https://doi.org/10.1016/j.cclet.2022.04.065
Publikováno v:
Daxue Huaxue. :2209026
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14823b735a4383120589fe80c79c8949
https://doi.org/10.3866/pku.dxhx202209026
https://doi.org/10.3866/pku.dxhx202209026
Publikováno v:
Organicbiomolecular chemistry. 19(23)
An efficient oxidative functionalization of purine-like substrates with (thio)ethers or methylarenes under mild conditions is described. Using I2 as the catalyst, and TBHP as the oxidant, this protocol provides a valuable synthetic tool for the assem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ecda667d92929f98a89faab8da6968c
https://pubmed.ncbi.nlm.nih.gov/34018534
https://pubmed.ncbi.nlm.nih.gov/34018534
Publikováno v:
The Journal of organic chemistry. 85(4)
The one-step copper-mediated regioselective formation of the C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5f07387ba0c63b4a76870c19c973eb40
https://pubmed.ncbi.nlm.nih.gov/31898455
https://pubmed.ncbi.nlm.nih.gov/31898455
Publikováno v:
Synlett. 28:868-872
A novel method for the selective N9-amidoalkylation of purines using N,N-dialkylamides as alkylation reagents via activation of sp3 C–H bond adjacent to an amide nitrogen atom has been developed in the presence of KI and tert-butyl hydroperoxide (T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::572413df74ddc678696e3ca33b62ac92
https://doi.org/10.1055/s-0036-1588134
https://doi.org/10.1055/s-0036-1588134
Publikováno v:
The Journal of organic chemistry. 83(7)
An oxidative coupling reaction between purines and alkyl ethers/benzyl compounds was developed to synthesize a series of N9 alkylated purine derivatives using n-Bu4NI as a catalyst and t-BuOOH as an oxidant. This protocol uses commercially available,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::719495e4d6dd61ee596060d5a9fb0257
https://pubmed.ncbi.nlm.nih.gov/29509015
https://pubmed.ncbi.nlm.nih.gov/29509015