1173280-41-5Relevant academic research and scientific papers
Highly E-Selective, Stereoconvergent Nickel-Catalyzed Suzuki-Miyaura Cross-Coupling of Alkenyl Ethers
Ho, Guo-Ming,Sommer, Heiko,Marek, Ilan
supporting information, p. 2913 - 2917 (2019/04/25)
An improved method for the nickel-catalyzed Suzuki-Miyaura cross-coupling of alkenyl ethers is reported. This stereoconvergent protocol allows for the utilization of a wide range of alkenyl ethers and aryl boronic esters for the synthesis of variously sub
Nickel-catalyzed cross-coupling reaction of alkenyl methyl ethers with aryl boronic esters
Shimasaki, Toshiaki,Konno, Yuko,Tobisu, Mamoru,Chatani, Naoto
supporting information; experimental part, p. 4890 - 4892 (2010/01/06)
The Ni(0)-catalyzed cross-coupling of alkenyl methyl ethers with boronic esters is described. Several types of alkenyl methyl ethers can be coupled with a wide range of boronic esters to give the stilbene derivatives.
Studies toward the photochemical synthesis of functionalized [5]- and [6] carbohelicenes
Pearson, Morwenna S. M.,Carbery, David R.
supporting information; experimental part, p. 5320 - 5325 (2009/11/30)
(Chemical Equation Presented) An efficient route to nonsymmetrical helical menthyl esters by means of an oxidative photocyclization reaction of dissymmetric bis-stilbenes is reported. The developed route allows the introduction of functionality on rings A, E, or F, and the influence of the substituent pattern on the photochemical reaction has been examined. Diastereoselectivity is observed when a double chiral induction strategy with dimenthyl helicene esters synthesized in a 70:30 ratio of isomers is used.
