Total Syntheses of Lycopodium and Monoterpenoid Indole Alkaloids Based on Biosynthesis-Inspired Strategies.


Journal

Chemical & pharmaceutical bulletin
ISSN: 1347-5223
Titre abrégé: Chem Pharm Bull (Tokyo)
Pays: Japan
ID NLM: 0377775

Informations de publication

Date de publication:
2020
Historique:
entrez: 4 2 2020
pubmed: 6 2 2020
medline: 7 3 2020
Statut: ppublish

Résumé

The merits of biogenetic considerations in the chemical syntheses of natural products have been emphasized by describing the total syntheses of Lycopodium alkaloids; lycodine, flabellidine, lycopodine, and flabelliformine, as well as monoterpenoid indole alkaloids; C-mavacurine, kopsiyunnanine K, koumine, and 11-methoxy-19R-hydroxygelselegine.

Identifiants

pubmed: 32009077
doi: 10.1248/cpb.c19-00872
doi:

Substances chimiques

Alkaloids 0
Biological Products 0
Secologanin Tryptamine Alkaloids 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

103-116

Auteurs

Hiromitsu Takayama (H)

Graduate School of Pharmaceutical Sciences, Chiba University.

Articles similaires

Humans Osteoporosis Wnt Signaling Pathway Animals Osteoblasts
Humans Drug Monitoring Inflammatory Bowel Diseases Psoriasis Adult

Mitoepigenetics pathways and natural compounds: a dual approach to combatting hepatocellular carcinoma.

Abdulrahman Hatawsh, Roya Hadi Al-Haddad, Ukamaka Gladys Okafor et al.
1.00
Humans Carcinoma, Hepatocellular Liver Neoplasms Epigenesis, Genetic Biological Products

Natural compounds targeting miRNAs: a novel approach in oral cancer therapy.

Youssef A Doghish, Ahmed S Doghish, Sherif S Abdel Mageed et al.
1.00
Humans MicroRNAs Mouth Neoplasms Biological Products Gene Expression Regulation, Neoplastic

Classifications MeSH