有機合成化学協会誌
Online ISSN : 1883-6526
Print ISSN : 0037-9980
ISSN-L : 0037-9980
総説および総合論文
アラインのσ結合挿入反応
吉田 拡人大下 浄治
著者情報
ジャーナル 認証あり

2011 年 69 巻 8 号 p. 877-888

詳細
抄録

Arynes were found to be utilizable as unsaturated hydrocarbons in the insertion reactions into σ-bonds. Nitrogen-silicon (aminosilane), halogen-carbon (acid halide) and carbon-phosphorus bonds (phosphorylacetonitrile), as well as strain-free carbon-carbon bonds of active methylene compounds and fluorene derivatives were easily cleaved and added across arynes via electrophilic coupling of arynes with in situ-generated carbanions. Furthermore, total synthesis of cytosporone B and phomopsin C was accomplished by using the C-C bond cleavage reaction. In the presence of transition metal catalysts, arynes could also be inserted into tin-tin (distannane), boron-boron (diboron), carbon-bromine (alkynyl bromide) and carbon-hydrogen bonds (terminal alkyne).

著者関連情報
© 2011 社団法人 有機合成化学協会
前の記事 次の記事
feedback
Top