Back to Search
Start Over
Highly Diastereo- and Enantioselective Synthesis of α-Spiro-δ-lactams by an Organocascade Reaction
- Source :
- European Journal of Organic Chemistry. 2017:1749-1756
- Publication Year :
- 2017
- Publisher :
- Wiley, 2017.
-
Abstract
- An asymmetric synthesis of α-spiro-δ-lactam via organocascade reaction from easily accessible starting materials is reported. The catalytic sequence undergoes enantioselective Michael addition of β-ketoamide to α,β-unsaturated aldehyde catalysed by a secondary amine catalyst, followed by hemiaminal annulation. Optically enantiopure compounds with two contiguous stereogenic centres are obtained in good yields and excellent selectivities (up to >20:1 dr and up to >99% ee).
- Subjects :
- chemistry.chemical_classification
Annulation
010405 organic chemistry
Stereochemistry
Organic Chemistry
Enantioselective synthesis
010402 general chemistry
01 natural sciences
Aldehyde
0104 chemical sciences
Stereocenter
chemistry.chemical_compound
Enantiopure drug
chemistry
Organocatalysis
Hemiaminal
Michael reaction
Physical and Theoretical Chemistry
Subjects
Details
- ISSN :
- 1434193X
- Volume :
- 2017
- Database :
- OpenAIRE
- Journal :
- European Journal of Organic Chemistry
- Accession number :
- edsair.doi...........2c5b77f7db29d9e7160d61b56009fd50