6057-87-0Relevant articles and documents
Carbonylative cycloaddition between two different alkenes enabled by reactive directing groups: Expedited construction of bridged polycyclic skeletons
Gao, Bingjian,Zou, Suchen,Yang, Guoqing,Ding, Yongzheng,Huang, Hanmin
supporting information, p. 12198 - 12201 (2020/10/26)
A novel palladium-catalyzed highly selective hydrocarbonylative cycloaddition reaction with two different alkenes in the presence of CO enabled by a reactive directing-group is developed, which offers efficient and convenient access to lactone-containing bridged polycyclic compounds in high yield with high chemo- and stereoselectivities.
Gold(I)-catalyzed double migration cascades toward (1E,3E)-dienes and naphthalenes
Dudnik, Alexander S.,Schwier, Todd,Gevorgyan, Vladimir
experimental part, p. 1859 - 1870 (2009/07/04)
A novel gold(I)-catalyzed cascade cycloisomerization of a variety of propargylic esters leading to unsymmetrically substituted naphthalenes has been developed. This domino process involves an unprecedented tandem sequence of 1,3- and 1,2-migrations of two
Synthesis of 1,2-disubstituted naphthalenes and tetrahydronaphthalenes from dihydronaphthalenes obtained by conjugate addition of organolithium reagents to 2,6-bis(tert-butyl)-4-methoxyphenyl naphthalenecarboxylates
Shindo, Mitsuru,Koga, Kenji,Tomioka, Kiyoshi
, p. 1318 - 1321 (2007/10/03)
A method of the conversion of 2,6-bis(tert-butyl)-4-methoxyphenyl dihydronaphthalenecarboxylates into substituted naphthalenes and tetrahydronaphthalenes was developed. Aromatization of substituted dihydronaphthalenecarboxylates with 2,3-dichloro-5,6-dicy