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Studies towards the total synthesis of batzelladine A
- Source :
- Organicbiomolecular chemistry. 2(14)
- Publication Year :
- 2004
-
Abstract
- Application of a diastereoselective three-component coupling to the bicyclic core of the batzelladine alkaloids is described. The synthesis features the elaboration of glutamic acid by use of Eschenmoser sulfide contraction. An earlier approach is also included, which shows some limitations of dithiane chemistry when applied to the particular compounds required for this target.
- Subjects :
- Models, Molecular
Bicyclic molecule
Molecular Structure
Chemistry
Stereochemistry
Organic Chemistry
Total synthesis
Stereoisomerism
General Medicine
Biochemistry
Guanidines
chemistry.chemical_compound
Alkaloids
Pyrimidines
Organic chemistry
Animals
Physical and Theoretical Chemistry
Eschenmoser sulfide contraction
Dithiane
Guanidine
Subjects
Details
- ISSN :
- 14770520
- Volume :
- 2
- Issue :
- 14
- Database :
- OpenAIRE
- Journal :
- Organicbiomolecular chemistry
- Accession number :
- edsair.doi.dedup.....11bb15f0b95c7147b71bb601ba9f27db