Mechanistic Study of the Transformation from 3-Decyn-2-one to (Z)-4-Iodo-4-decen-2-one
- 10 July 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 63 (16), 5656-5657
- https://doi.org/10.1021/jo980154l
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Stereoselective Synthesis of (Z)-a-Alkylidene-g-butyrolactone from 2-Alkyn-1-oneHETEROCYCLES, 1996
- Novel chlorotrimethylsilane catalyzed stereoselective deconjugation of β-bromo (or iodo) substituted α,β-unsaturated acyclic ketoneTetrahedron Letters, 1994
- A novel stereoselective synthesis of (Z)-3-iodo-3-alken-1-one from 2-alkyn-1-oneTetrahedron Letters, 1994
- The Asymmetric Synthesis of 2-Bromohomoallylic Alcohols Using the Tartrate Ester of (2-Bromoallyl)boronic Acid Prepared by Bromoboration Reaction of AlleneSynlett, 1994
- Cyclic stereocontrol via organobismetallic reagents. Part V. Diastereoselective synthesis of substituted cyclopropyl zinc reagents by the metalla-claisen reactionTetrahedron Letters, 1993
- A practical and efficient method for enantioselective allylation of aldehydesJournal of the American Chemical Society, 1989