BINOL−Salen-Catalyzed Highly Enantioselective Alkyne Additions to Aromatic Aldehydes
作者:Zi-Bo Li、Lin Pu
DOI:10.1021/ol0498139
日期:2004.3.1
BINOL-Salen compound (-)-1 can catalyze the addition of both aryl- and alkylalkynes to aromatic aldehydes at room temperature with high enantioselectivity (86-97% ee). The conditions for this catalytic process are both mild and simple. Unlike most other BINOL-based catalysts, using ligand (-)-1 not only avoids heating or cooling but also does not require the addition of Ti(O(i)Pr)(4).
Chiral Macrocycle-Catalyzed Highly Enantioselective Phenylacetylene Addition to Aliphatic and Vinyl Aldehydes
作者:Zi-Bo Li、Tian-Dong Liu、Lin Pu
DOI:10.1021/jo070091j
日期:2007.6.1
The 1,1‘-binaphthyl macrocycle (S)-2 is found to be an excellent catalyst for the alkyne addition to aldehydes. In the presence of (S)-2 (20 mol %) and Me2Zn (2 equiv) in THF at room temperature, the addition of phenylacetylene to linear or branched aliphatic aldehydes and vinylaldehydes gave various propargylic alcohols with 89−96% ee.