Facile Enantioselective Synthesis of Propargylic Alcohols by Direct Addition of Terminal Alkynes to Aldehydes
Top Cited Papers
- 9 February 2000
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 122 (8), 1806-1807
- https://doi.org/10.1021/ja993838z
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Catalytic in Situ Generation of Zn(II)-Alkynilides under Mild Conditions: A Novel CN Addition Process Utilizing Terminal AcetylenesJournal of the American Chemical Society, 1999
- A Novel, Highly Enantioselective Ketone Alkynylation Reaction Mediated by Chiral Zinc AminoalkoxidesAngewandte Chemie International Edition, 1999
- Direct Catalytic Enantioselective Reduction of Achiral α,β-Ynones. Strong Remote Steric Effects Across the C−C Triple BondJournal of the American Chemical Society, 1996
- Catalytic, Enantioselective Acetone Aldol Additions with 2-MethoxypropeneJournal of the American Chemical Society, 1995
- Highly Enantioselective Alkynylation of Aldehydes Promoted by Chiral OxazaborolidinesJournal of the American Chemical Society, 1994
- Synthesis of enantioenriched homopropargylic alcohols through diastereoselective SE' additions of chiral allenylstannanes to aldehydesThe Journal of Organic Chemistry, 1992
- Systematic synthesis design. 6. Yield analysis and convergencyJournal of the American Chemical Society, 1977
- Preparation of optically active benzyl-.alpha.-d alcohol via reduction by B-3.alpha.-pinanyl-9-borabicyclo[3.3.1]nonane. A new highly effective chiral reducing agentJournal of the American Chemical Society, 1977