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Construction of sulfur-containing moieties in the total synthesis of natural products.
- Source :
-
Natural product reports [Nat Prod Rep] 2020 Feb 01; Vol. 37 (2), pp. 246-275. Date of Electronic Publication: 2019 Jun 17. - Publication Year :
- 2020
-
Abstract
- Covering: January 2013 to September 2018Sulfur-containing natural products are a large class of significant functional molecules. Many of these compounds exhibit potent biological activities and pharmacological properties; in fact, some of them have been developed into important drugs. The total synthesis of sulfur-containing natural products is a subject that has long attracted significant attention from synthetic organic chemists; to achieve this goal, various methods have been developed over the past years. This review surveys total syntheses of sulfur-containing natural products that introduce sulfur atoms using different sulfurization agents to construct related sulfur-containing moieties.
- Subjects :
- Alkaloids chemical synthesis
Alkaloids chemistry
Biological Products chemistry
Carbolines chemical synthesis
Carbolines chemistry
Disaccharides chemical synthesis
Disaccharides chemistry
Disulfides chemistry
Enediynes chemical synthesis
Enediynes chemistry
Ferrichrome analogs & derivatives
Ferrichrome chemical synthesis
Ferrichrome chemistry
Indole Alkaloids chemical synthesis
Indole Alkaloids chemistry
Indoles chemical synthesis
Indoles chemistry
Isothiocyanates chemical synthesis
Isothiocyanates chemistry
Molecular Structure
Peptides, Cyclic chemical synthesis
Peptides, Cyclic chemistry
Piperazines chemistry
Sulfates chemistry
Sulfoxides chemical synthesis
Sulfoxides chemistry
Thiazoles chemical synthesis
Thiazoles chemistry
Biological Products chemical synthesis
Sulfur chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1460-4752
- Volume :
- 37
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Natural product reports
- Publication Type :
- Academic Journal
- Accession number :
- 31204423
- Full Text :
- https://doi.org/10.1039/c8np00093j