1402591-97-2Relevant academic research and scientific papers
Asymmetric Intermolecular Heck Reaction of Propargylic Acetates and Cycloalkenes to Access Fused Cyclobutenes
Jiao, Zhiwei,Shi, Qi,Zhou, Jianrong Steve
, p. 14567 - 14571 (2017)
An asymmetric Heck annulation of propargylic acetates with several types of cyclic olefins affords highly strained cyclobutenes in high enantioselectivity.
C-C bond formation with carbon dioxide promoted by a silver catalyst
Kikuchi, Satoshi,Sekine, Kohei,Ishida, Tomonobu,Yamada, Tohru
supporting information; scheme or table, p. 6989 - 6992 (2012/09/25)
A catalytic amount of silver benzoate with 7-methyl-1,5,7-triazabicyclo[4. 4.0]dec-5-ene (MTBD) was an effective catalytic system for the reaction of carbon dioxide with various ketones containing an alkyne group at an appropriate position (see scheme). These reactions afforded the corresponding γ-lactone derivatives in good to high yields under mild conditions. Copyright
