Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jeongwoo, Sim"'
Publikováno v:
Organic Letters. 24:4264-4269
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1da14d8d3ecf1b4bfc899510b6d52dc
https://doi.org/10.1021/acs.orglett.2c01528
https://doi.org/10.1021/acs.orglett.2c01528
Publikováno v:
Organic letters. 24(23)
We describe the electrochemical α-amidoalkylation of γ-lactams based on transition-metal-free cross-coupling via hydrogen atom transfer. The highly selective hydrogen atom transfer process allows for a broad substrate scope including both inter- an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2b932b720b697196ea2cc4150bd36017
https://pubmed.ncbi.nlm.nih.gov/35675591
https://pubmed.ncbi.nlm.nih.gov/35675591
Publikováno v:
Angewandte Chemie International Edition. 59:11886-11891
Oxidative [3+3] cycloadditions offer an efficient route for six-membered-ring formation. This approach has been realized based on an electrochemical oxidative coupling of indoles/enamines with active methylene compounds followed by tandem 6π-electro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::842f15bf7d6076687f4a5d959ec34aba
https://doi.org/10.1002/anie.202003364
https://doi.org/10.1002/anie.202003364
Publikováno v:
Organic letters. 22(14)
The synthesis of versatile scaffold indolopyrans based on C-C radical-radical cross-coupling under metal-free conditions is described. The reaction involving single electron transfer between coupling partners followed by cage collapse allows highly s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31831ded37d4a50a1d6df24e78170763
https://pubmed.ncbi.nlm.nih.gov/32628496
https://pubmed.ncbi.nlm.nih.gov/32628496