G Evano, B Michelet, C Zhang - Comptes Rendus Chimie, 2017 - Elsevier
Ynamides have recently evolved as remarkably reactive and versatile building blocks for chemical synthesis. The development of efficient and robust methods for their preparation …
H Baguia, C Deldaele, E Romero, B Michelet… - Synthesis, 2018 - thieme-connect.com
A general and efficient procedure for the copper-catalyzed photoinduced radical domino cyclization of ynamides and cyanamides providing an efficient access to complex tri-, tetra …
Ynamides are accessed via copper-catalyzed coupling of Grignard or organozinc nucleophiles with chloroynamides, formed in situ from 1, 2-dichloroenamides. The reaction …
S Vercruysse, K Jouvin, O Riant, G Evano - Synthesis, 2016 - thieme-connect.com
A highly efficient catalytic silylcupration of activated alkynes is reported. Upon reaction with silylboronates and methanol in THF at room temperature in the presence of copper (I) …
X Ye, P Bao, Y Pan, H Xiao, Q Li, G He - Organic & Biomolecular …, 2024 - pubs.rsc.org
A K2CO3-promoted tandem ring-opening/ring-closing of N-alkynyl-2-oxazolidinones has been described, affording 2-oxazolines in 42–99% yields without column chromatography …
C Theunissen, P Thilmany, M Lahboubi, N Blanchard… - Org. Synth, 2019 - orgsyn.org
Org. Synth. 2019, 96, 195-213 X DOI: 10.15227/orgsyn. 096.0195 196 character of the nitrogen atom strongly polarizes the carbon–carbon triple bond, which can furnish …
A Saadane, G Evano - The Chemistry of Ynamides, 2024 - taylorfrancis.com
Ynamides have recently emerged as versatile and powerful building blocks in modern synthetic chemistry over the past decades. Unlike ynamines, which are extremely reactive …
M Lahboubi, G Evano - The Chemistry of Ynamides, 2024 - taylorfrancis.com
Over the past 20 years, ynamides have clearly emerged as versatile building blocks in organic synthesis allowing the construction of various nitrogen-containing molecules with …
C Theunissen, P Thilmany, M Lahboubi… - Organic …, 2003 - Wiley Online Library
Ynamides provide unique opportunities not only for the introduction of nitrogen‐containing motifs into organic molecules but also for the generation of otherwise hardly accessible …