Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kenta Rakumitsu"'
Autor:
Nanako Nakashima, Jukiya Sakamoto, Kenta Rakumitsu, Mariko Kitajima, Lia Dewi Juliawaty, Hayato Ishikawa
Publikováno v:
Chemical and Pharmaceutical Bulletin. 70:187-191
A new pentacyclic monoterpenoid indole alkaloid glycoside named secorubenine (1) was isolated from the heartwood of Adina rubescens, collected in Indonesia. The structure was elucidated by spectroscopic analysis and chemical modification of isolated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::416b11294bd207340b6159f6a24fd5c1
https://doi.org/10.1248/cpb.c21-00931
https://doi.org/10.1248/cpb.c21-00931
Publikováno v:
RSC advances. 12(40)
The palladium-mediated intramolecular biarylation of the cyclic triamide of 2-bromo-4-(isobutylamino)benzoic acid proceeded effectively by the introduction of three methyl groups and the use of tri-tert-butylphosphine as the ligand.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::555e4947fe2661ba3c3d5bd23dd5eb14
https://pubmed.ncbi.nlm.nih.gov/36275098
https://pubmed.ncbi.nlm.nih.gov/36275098
Publikováno v:
Angewandte Chemie. 132:13516-13524
A collective synthesis of glycosylated monoterpenoid indole alkaloids is reported. A highly diastereoselective Pictet-Spengler reaction with α-cyanotryptamine and secologanin tetraacetate as substrates, followed by a reductive decyanation reaction,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b171f6d2eb02701ec1b91d3c96aa0897
https://doi.org/10.1002/ange.202005748
https://doi.org/10.1002/ange.202005748
Publikováno v:
Chemistry – A European Journal. 25:8996-9000
The first enantioselective total syntheses of (-)-secologanin (1), (-)-5-carboxystrictosidine (2), and (-)-rubenine (3) were accomplished in 10, 9, and 14 steps, respectively. The key transformation in the synthesis of 1 was a sequential anti-selecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f8857e0c6caa235b85971b02251516e
https://doi.org/10.1002/chem.201902073
https://doi.org/10.1002/chem.201902073
