3 research outputs found
Palladium(0)-Catalyzed Dearomative [3 + 2] Cycloaddition of 3‑Nitroindoles with Vinylcyclopropanes: An Entry to Stereodefined 2,3-Fused Cyclopentannulated Indoline Derivatives
The palladium(0)-catalyzed
diastereoselective dearomative cyclopentannulation
of 3-nitroindoles with vinylcyclopropanes is described. This straightforward
and highly atom-economical method leads to a wide range of functionalized
indolines in good yields and diastereoselectivities and represents
an unprecedented entry toward the valuable 2,3-fused cyclopentannulated
indoline scaffold
Palladium(0)-Catalyzed Dearomative [3 + 2] Cycloaddition of 3‑Nitroindoles with Vinylcyclopropanes: An Entry to Stereodefined 2,3-Fused Cyclopentannulated Indoline Derivatives
The palladium(0)-catalyzed
diastereoselective dearomative cyclopentannulation
of 3-nitroindoles with vinylcyclopropanes is described. This straightforward
and highly atom-economical method leads to a wide range of functionalized
indolines in good yields and diastereoselectivities and represents
an unprecedented entry toward the valuable 2,3-fused cyclopentannulated
indoline scaffold
Palladium(0)-Catalyzed Dearomative [3 + 2] Cycloaddition of 3‑Nitroindoles with Vinylcyclopropanes: An Entry to Stereodefined 2,3-Fused Cyclopentannulated Indoline Derivatives
The palladium(0)-catalyzed
diastereoselective dearomative cyclopentannulation
of 3-nitroindoles with vinylcyclopropanes is described. This straightforward
and highly atom-economical method leads to a wide range of functionalized
indolines in good yields and diastereoselectivities and represents
an unprecedented entry toward the valuable 2,3-fused cyclopentannulated
indoline scaffold