122950-98-5Relevant articles and documents
Synthesis of Functionalized Alkylidene Indanes and Indanones through Tandem Phosphine-Palladium Catalysis
Fan, Yi Chiao,Kwon, Ohyun
supporting information, p. 2058 - 2061 (2015/05/20)
Densely functionalized alkylidene indanes and indanones can be prepared efficiently in one pot, in high yields with good stereoselectivities (in some cases exclusively the Z-isomer), through a route involving phosphine-catalyzed Michael addition followed
Novel cyclization cascades to functionalized indanes and tetrahydronaphthalenes
Khan, Zulfiqar A.,Iwaoka, Michio,Wirth, Thomas
experimental part, p. 6639 - 6646 (2010/10/19)
Cyclization cascades involving C-C bond formations followed by lactonization reactions provide fast access to structurally complex tricyclic indane and tetrahydronaphthalene derivatives. Crown Copyright
Highly regio- And stereoselective synthesis of indene derivatives via electrophilic cyclization
Bi, Hai-Peng,Guo, Li-Na,Duan, Xin-Hua,Gou, Fa-Rong,Huang, Shu-Hao,Liu, Xue-Yuan,Liang, Yong-Min
, p. 397 - 400 (2008/02/12)
Indene or naphthalene derivatives are readily prepared in moderate to excellent yields with high regio- and stereoselectivity under very mild reaction conditions by the reaction of acetylenic malonates and ketones with I 2, ICI, or NIS. The res