Oxidative Cyclization at

anti-mycobacterial agent demethyl(oxy)aaptamine hypervalent iodine reagent oxidative cyclization total synthesis

Journal

Marine drugs
ISSN: 1660-3397
Titre abrégé: Mar Drugs
Pays: Switzerland
ID NLM: 101213729

Informations de publication

Date de publication:
19 May 2023
Historique:
received: 28 04 2023
revised: 13 05 2023
accepted: 17 05 2023
medline: 29 5 2023
pubmed: 26 5 2023
entrez: 26 5 2023
Statut: epublish

Résumé

A shorter synthesis of the demethyl(oxy)aaptamine skeleton was developed via oxidative intramolecular cyclization of 1-(2-azidoethyl)-6-methoxyisoquinolin-7-ol followed by dehydrogenation with a hypervalent iodine reagent. This is the first example of oxidative cyclization at the

Identifiants

pubmed: 37233505
pii: md21050311
doi: 10.3390/md21050311
pmc: PMC10221624
pii:
doi:

Substances chimiques

3-(phenethylamino)demethyl(oxy)aaptamine 0
aaptamine FGW9D01COE
Phenol 339NCG44TV
Phenols 0
Naphthyridines 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Japan Society for the Promotion of Science
ID : 18K05363
Organisme : Japan Society for the Promotion of Science
ID : 22K05339
Organisme : Research Promotion Program for Acquiring KAKENHI from Ritsumeikan University
ID : B21-0051

Références

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pubmed: 32577043
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pubmed: 35200628
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pubmed: 34226909
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pubmed: 17915931
J Nat Med. 2014 Apr;68(2):372-6
pubmed: 24414399

Auteurs

Yuki Nakatani (Y)

College of Pharmaceutical Sciences, Ritsumeikan University, 1-1-1 Noji-higashi, Kusatsu 525-8577, Shiga, Japan.

Risa Kimura (R)

College of Pharmaceutical Sciences, Ritsumeikan University, 1-1-1 Noji-higashi, Kusatsu 525-8577, Shiga, Japan.

Tomoyo Kimata (T)

College of Pharmaceutical Sciences, Ritsumeikan University, 1-1-1 Noji-higashi, Kusatsu 525-8577, Shiga, Japan.

Naoyuki Kotoku (N)

College of Pharmaceutical Sciences, Ritsumeikan University, 1-1-1 Noji-higashi, Kusatsu 525-8577, Shiga, Japan.

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Classifications MeSH