Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Jiye Jeon"'
Autor:
Cheol-Hong Cheon, JIYE JEON
Publikováno v:
Organic letters. 24(39)
Herein, we report the first asymmetric total synthesis of iheyamine B from 2,2'-bisindoloazepinone using the stereoselective construction of theitrans/i-vicinal 2-oxopropyl moiety in the azepine scaffold. The asymmetric decarboxylative allylic alkyla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c78145c83e353e4d3e937e7c545490bf
https://pubmed.ncbi.nlm.nih.gov/36169573
https://pubmed.ncbi.nlm.nih.gov/36169573
Publikováno v:
The Journal of Organic Chemistry. 85:8149-8156
The total synthesis of iheyamine A from readily available ethyl 2-aminocinnamate and 5-methoxyindole-2-carboxaldehyde is described. The cyanide-catalyzed imino-Stetter reaction of an aldimine derived from ethyl 2-aminocinnamate and 5-methoxyindole-2-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1131c05e9b076de3f239de3b297dc3cf
https://doi.org/10.1021/acs.joc.0c01051
https://doi.org/10.1021/acs.joc.0c01051
Publikováno v:
Advanced Synthesis & Catalysis. 361:2360-2364
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fbdfab3f37ba273984944caed2baa66
https://doi.org/10.1002/adsc.201900029
https://doi.org/10.1002/adsc.201900029
Publikováno v:
Organic letters. 23(6)
The total synthesis of (±)-hinckdentine A is described herein. A cyanide-catalyzed imino-Stetter reaction of the aldimine derived from ethyl 2-amino-3,5-dibromocinnamate and 5-bromo-2-nitrobenzaldehyde followed by oxidative rearrangement afforded a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::610480d9193854e513134f5a81ba7e1e
https://pubmed.ncbi.nlm.nih.gov/33630599
https://pubmed.ncbi.nlm.nih.gov/33630599
Autor:
Jiye Jeon, Cheol Hong Cheon
Publikováno v:
Organic Chemistry Frontiers. 6:456-467
A new protocol to access benzo[a]carbazole derivatives was developed, via the cyanide-catalyzed imino-Stetter reaction/Friedel–Crafts reaction sequence. The cyanide-catalyzed imino-Stetter reaction of aldimines derived from 2-aminochalcones and aro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3f88fc40d11904442baa7e1cc20689d
https://doi.org/10.1039/c8qo01209a
https://doi.org/10.1039/c8qo01209a
Publikováno v:
The Journal of Organic Chemistry. 83:12486-12495
A new asymmetric protocol for the synthesis of chiral tetrahydroquinolines from 2-aminochalcones via a two-step one-pot consecutive process (cyclization/asymmetric reduction) has been developed using chiral phosphoric acid as the sole catalyst. 2-Ami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f067b43d756cb2336a08facfd15869fd
https://doi.org/10.1021/acs.joc.8b01709
https://doi.org/10.1021/acs.joc.8b01709
Publikováno v:
The Journal of Organic Chemistry. 83:5177-5186
A new protocol for the synthesis of 2-substituted quinolines from 2-aminostyryl ketones has been developed using iodide as a nucleophilic catalyst. Conjugate addition of iodide to 2-aminostyryl ketones yielded the corresponding β-iodoketones, which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05061f57cae29ed5267c84354878066b
https://doi.org/10.1021/acs.joc.8b00552
https://doi.org/10.1021/acs.joc.8b00552
Publikováno v:
Chemical record (New York, N.Y.). 18(10)
The chemistry of hydrogen cyanide adducts of imines is well-developed, but that of cyanide adducts remains unexplored. This is presumably because these cyanide adducts are not stable and thus not readily available in their isolated forms. In this per
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dce240a5239b00cce04b2fa7add11cd4
https://pubmed.ncbi.nlm.nih.gov/29665280
https://pubmed.ncbi.nlm.nih.gov/29665280
Publikováno v:
Journal of Organic Chemistry; 5/4/2018, Vol. 83 Issue 9, p5177-5186, 10p