18442-29-0Relevant articles and documents
Copper-Catalyzed Chemoselective Silylative Cyclization of 2,2′-Diethynylbiaryl Derivatives
Zhao, Meng,Wang, Ying,Wang, Zi-Lu,Xu, Jian-Lin,Dai, Kai-Yang,Xu, Yun-He
supporting information, p. 3859 - 3863 (2021/05/26)
In this protocol, copper-catalyzed diverse silylative carbocyclization reactions of 2,2′-diethynylbiaryl derivatives with silaboronate were reported. Three new and novel types of domino reactions for the copper-catalyzed transformation of silaboronate were discovered. The corresponding cyclobuta[l]phenanthrene, bis((silyl)methyl)phenanthrene, and silyl-substituted exocyclic diene products were chemoselectively formed with high efficiency.
Ruthenium-Catalyzed Cycloisomerization of 2,2′-Diethynyl- biphenyls Involving Cleavage of a Carbon-Carbon Triple Bond
Matsuda, Takanori,Kato, Kotaro,Goya, Tsuyoshi,Shimada, Shingo,Murakami, Masahiro
supporting information, p. 1941 - 1943 (2016/02/14)
A ruthenium complex catalyzes a new cycloisomerization reaction of 2,2′-diethynylbiphenyls to form 9-ethynylphenanthrenes, thereby cleaving the carbon-carbon triple bond of the original ethynyl group. A metal-vinylidene complex is generated from one of th
Synthesis of a 2D lander
Basu, Chaitali,Barthes, Cecile,Sadhukhan, Subir K.,Girdhar, Navdeep K.,Gourdon, Andre
, p. 136 - 140 (2007/10/03)
A method for the preparation of an asymmetric superbenzene is presented. The synthesis proceeds through the 12-fold cyclodehydrogenation of a polyaromatic precursor obtained by successive Diels-Alder additions of cyclopentadienones and alkynes. Wiley-VCH