497093-06-8Relevant academic research and scientific papers
Tandem Wittig Reaction-Ring Contraction of Cyclobutanes: A Route to Functionalized Cyclopropanecarbaldehydes
Aitken, David J.,Caboni, Pierluigi,Cuccu, Federico,Frongia, Angelo,Luridiana, Alberto,Secci, Francesco,Serusi, Lorenzo
supporting information, (2019/10/08)
An original tandem reaction consisting of a Wittig reaction-ring contraction process between α-hydroxycyclobutanone and phosphonium ylides has been developed. Highly functionalized cyclopropanecarbaldehydes are obtained in good to high yield.
Highly efficient route to functionalized tetrahydrocarbazoles using a tandem cross-metathesis/intramolecular-hydroarylation sequence
An, Xiao-Lei,Chen, Jia-Rong,Li, Chang-Feng,Zhang, Fu-Gen,Zou, You-Quan,Guo, Ying-Cen,Xiao, Wen-Jing
supporting information; experimental part, p. 2258 - 2265 (2011/06/11)
The scope of the novel ruthenium-catalyzed tandem cross-metathesis/ intramolecular-hydroarylation sequence is described. This methodology offers a practical and efficient synthesis of structurally diverse and complex tetrahydrocarbazoles in good to excellent yields (up to 98%). Moreover, preliminary efforts towards the development of an enantioselective version of the current process by sequential catalysis with ruthenium complex and chiral amine are presented, with high yields and enantioselectivities (up to 88% yield and 91% ee).
Elongated phosphoranes by C-C coupling of haloaroylmethylidene-triphenylphosphoranes: Synthesis and applications
Thiemann, Thies,Umeno, Kuniharu,Wang, Jian,Tabuchi, Yumiko,Arima, Kazuya,Watanabe, Masataka,Tanaka, Yasuko,Gorohmaru, Hideki,Mataka, Shuntaro
, p. 2090 - 2110 (2007/10/03)
Haloaroylmethylidenephosphoranes 3 can be subjected to Pd(o) mediated C-C coupling reactions to yield diaryl-, arylhetaryl-, dihetaryl, arylethenylaryl/hetaryl- and arylethynylaryl/hetaryl-carbonylmethylidenephosphoranes 4-9. Suzuki-Kumada reactions can a
