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Stereospecificity in Intramolecular Photoredox Reactions of Naphthoquinones: Enantioselective Total Synthesis of (−)-Spiroxin C
- Source :
- Angewandte Chemie. 129:11618-11623
- Publication Year :
- 2017
- Publisher :
- Wiley, 2017.
-
Abstract
- Intramolecular photoredox reactions of naphthoquinone derivatives were found to proceed in a stereospecific manner. This method was used as a basis for the enantioselective total synthesis of (-)-spiroxin C.
- Subjects :
- Spiroxin C
Chemistry
Stereochemistry
010405 organic chemistry
Enantioselective synthesis
Total synthesis
General Chemistry
General Medicine
010402 general chemistry
Redox
01 natural sciences
Catalysis
Naphthoquinone
0104 chemical sciences
chemistry.chemical_compound
Stereospecificity
Intramolecular force
Subjects
Details
- ISSN :
- 00448249
- Volume :
- 129
- Database :
- OpenAIRE
- Journal :
- Angewandte Chemie
- Accession number :
- edsair.doi.dedup.....235b91f4fffda62bc53120c72dd62d15
- Full Text :
- https://doi.org/10.1002/ange.201705562