133381-98-3Relevant academic research and scientific papers
Applications of the β-azidonation reaction to organic synthesis. α,β- Enones, conjugate addition, and γ-lactam annulation
Magnus, Philip
, p. 12486 - 12499 (2007/10/03)
The β-azido functionalization reaction provides a mechanistically different enone synthesis that involves treatment of 2 with fluoride anion to effect desilylation and concomitant β-elimination to give 3. Table 1 lists a number of examples of the direct conversion of a TIPS enol ether into the corresponding α,β-enone via a β-azido TIPS enol ether. The β-azido group can be ionized with Me3Al or Me2AlCl and the intermediate enonium ion trapped by a variety of nucleophiles such as an allylstannane, electron-rich aromatics, TMS enol ethers, Et2AlCN, Me2AlCCR, Me4AlLi, and vinylaluminum reagents to give the products listed in Table 2. The diastereoselectivity of the reaction of a 4-substituted enonium ion with indole shows an unusual increase of selectivity with increasing temperature. Reduction of the azide 2 provides access to β-amino TIPS enol ethers 5, which, for example, can be converted into a cinnamide derivative and cyclized via a putative 'ene' process into a γ-lactam.
Trialkylsilyl triflate promoted conjugate addition of alkynylzinc compounds to α,β-enones
Kim,Lee
, p. 7627 - 7630 (2007/10/02)
Trialkylsilyl triflate promotes conjugate addition of alkynylzinc compounds to α,β-enones to afford γ,δ-acetylenic silyl enol ethers.
