6533b857fe1ef96bd12b4cca
RESEARCH PRODUCT
A Decade of Advance in the Asymmetric Vinylogous Mannich Reaction
Santos FusteroCarlos Del PozoMaria Sanchez Rosellosubject
Natural productSilylation010405 organic chemistryOrganic ChemistrySynthonEnantioselective synthesisKeteneVinylogy010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundchemistryElectrophileOrganic chemistryMannich reactiondescription
When the principle of vinylogy is applied to imines as electrophiles, the so-called vinylogous Mannich reaction (VMR), γ-aminocarbonyl (such as butenolides) and β-aminocarbonyl compounds are generated in a very efficient manner. The asymmetric version of this vinylogous Mannich reaction gives access to highly functionalized chiral synthons, which are suitable for further transformations. The versatility of this methodology is exemplified with the synthesis of several alkaloids and natural products. 1 Introduction 2 Asymmetric Vinylogous Mannich Reactions (VMR) with 2-Silyloxyfurans and 2-Silyloxypyrroles 3 Asymmetric VMR with Acyclic Silyl Dienolates and Silyl Dienol Ketene Acetals 4 Asymmetric VMR with γ-Butenolides and γ-Butyrolactams 5 Asymmetric VMR with α,α-Dicyanoolefins 6 Miscellaneous Donors in Asymmetric VMR 7 Application of the VMR to Natural Product Synthesis 8 Conclusions
| year | journal | country | edition | language |
|---|---|---|---|---|
| 2016-06-21 | Synthesis |