Synlett

Thieme Chemistry Journal Awardees-Where are They Now? A General One-Step Synthesis of Alkynes from Enolisable Carbonyl Compounds

IM Lyapkalo, MAK Vogel, EV Boltukhina, J Vavřík

Index: Lyapkalo, Ilya M.; Vogel, Michael A. K.; Boltukhina, Ekaterina V.; Vavrik, Jiri Synlett, 2009 , # 4 p. 558 - 561

Full Text: HTML

Citation Number: 6

Abstract

Abstract Terminal and internal acetylenes were obtained in good to excellent isolated yields from carbonyl compounds by converting the carbonyl functionality into the enol nonaflate intermediate followed by elimination to give the CC triple bond. The one-pot transformations were uniformly induced by phosphazene bases combined with mildly electrophilic nonafluorobutane-1-sulfonyl fluoride. The method is the most general among those ...

Related Articles:

Photooxidation of strained olefins. 4. Cyclopropenes

[Journal of Organic Chemistry, , vol. 45, # 12 p. 2334 - 2340]

The behaviors of metal acetylides with dinitrogen tetroxide

[Helvetica Chimica Acta, , vol. 88, # 2 p. 354 - 369]

Selective synthesis of alkynes by catalytic dehydrogenation of alkenes over polymer-supported palladium acetate in the liquid phase

[Journal of the Chemical Society, Chemical Communications, , # 22 p. 1571 - 1573]

Some reactions and properties of molecular diatomic carbon C2. An experimental and theoretical treatment

[Journal of the American Chemical Society, , vol. 111, # 12 p. 4422 - 4429]

More Articles...