Mechanistic Study of the Transformation from 3-Decyn-2-one to (Z)-4-Iodo-4-decen-2-one
Author:
Affiliation:
1. Institute of Chemistry, Academia Sinica, Nankang, Taipei, Taiwan, Republic of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo980154l
Reference7 articles.
1. A novel stereoselective synthesis of (Z)-3-iodo-3-alken-1-one from 2-alkyn-1-one
2. Novel chlorotrimethylsilane catalyzed stereoselective deconjugation of β-bromo (or iodo) substituted α,β-unsaturated acyclic ketone
3. A practical and efficient method for enantioselective allylation of aldehydes
4. The Asymmetric Synthesis of 2-Bromohomoallylic Alcohols Using the Tartrate Ester of (2-Bromoallyl)boronic Acid Prepared by Bromoboration Reaction of Allene
5. Cyclic stereocontrol via organobismetallic reagents. Part V. Diastereoselective synthesis of substituted cyclopropyl zinc reagents by the metalla-claisen reaction
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2. Transformation of Amides into Esters by the Use of Chlorotrimethylsilane;Journal of the Chinese Chemical Society;2004-04
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5. Efficient Synthesis of Alkyl End-Capped Oligoheterocycles via the Use of Palladacycle Catalyst;Journal of the Chinese Chemical Society;2000-02
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