Lewis acid mediated Michael addition of non-aromatic multiple C C bonds to α,β-unsaturated dicarbonyl compounds

Lewis acid mediated Michael addition of non-aromatic multiple C C bonds to α,β-unsaturated dicarbonyl compounds Full article

Journal

Tetrahedron Letters
ISSN: 0040-4039 , E-ISSN: 1873-3581

Output data

Year: 2021, Volume: 80, Article number : 153272, Pages count : DOI: 10.1016/j.tetlet.2021.153272

Authors

Denisov Dmitry A. ¹ , Novikov Roman A. ¹ , Tomilov Yury V. ¹

Affiliations

1	N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991,Moscow, Russian Federation

Michael addition is widely used in organic synthesis, being one of the key methods for the formation of C–C and C–X bonds. This mini-review is focused on the addition reactions of non-activated and non-aromatic multiple C–C bonds to α,β-unsaturated dicarbonyl compounds and donor–acceptor cyclopropanes under activation of various Lewis acids.

Denisov D.A. , Novikov R.A. , Tomilov Y.V.
Lewis acid mediated Michael addition of non-aromatic multiple C C bonds to α,β-unsaturated dicarbonyl compounds
Tetrahedron Letters. 2021. V.80. 153272 . DOI: 10.1016/j.tetlet.2021.153272 WOS Scopus OpenAlex

≡ Web of science:	WOS:000701789400013
≡ Scopus:	2-s2.0-85113760421
≡ OpenAlex:	W3184120425