@article{oai:kitami-it.repo.nii.ac.jp:00007610,
 author = {Hoshi, Masayuki and Yamazaki, Hirokazu and Okimoto, Mitsuhiro},
 issue = {16},
 journal = {Synlett},
 month = {Oct},
 note = {(Trimethylsilyl)ethynyl bromide can be easily transformed into conjugated (E)-enynones, whose skeleton consists of consecutive carbonyl, ethynyl, and (E)-ethenyl units, via a one-pot multicomponent Suzuki-type reaction-Sonogashira reaction sequence. Thus, a three-component coupling of (trimethylsilyl)ethynyl bromide, (E)-alk-1-enyldisiamylborane and acid chloride is achieved in a two-step, one-pot procedure, in which (E)-alk-1-enyl group is installed as nucleophile in the sp-carbon atom attached to bromine atom and acyl group is installed as electrophile in the other sp-carbon atom., (trimethylsilyl)ethynyl bromide},
 pages = {2461--2464},
 title = {One-Pot Synthesis of Conjugated (E)-Enynones via Two Types of Cross-Coupling Reaction},
 year = {2010}
}