347376-17-4Relevant articles and documents
Tandem Michael/Michael reactions mediated by phosphines or aryl thiolates
Brown, Paul M.,K?ppel, Nina,Murphy, Patrick J.,Coles, Simon J.,Hursthouse, Michael B.
, p. 1100 - 1106 (2007)
Tri-n-butyl phosphine was found to effect tandem Michael/Michael cyclisations leading to the formation of cyclopentenes and cyclohexenes in good yields, whilst p-TolSH in conjunction with a catalytic amount of p-TolSNa effected cyclisation to the correspo
A highly nucleophilic multifunctional chiral phosphane-catalyzed asymmetric intramolecular rauhut-currier reaction
Zhang, Xiao-Nan,Shi, Min
supporting information, p. 6271 - 6279 (2013/01/15)
An asymmetric variant of the intramolecular Rauhut-Currier (RC) reaction can be achieved using a highly nucleophilic multifunctional chiral phosphane; the corresponding cyclopentene and cyclohexene derivatives are produced in moderate to good yields and w
Diastereoselective cycloreductions and cycloadditions catalyzed by Co(dpm)2-silane (dpm = 2,2,6,6-tetramethylheptane-3,5-dionate): Mechanism and partitioning of hydrometallative versus anion radical pathways
Wang, Long-Cheng,Jang, Hye-Young,Roh, Yeonsuk,Lynch, Vincent,Schultz, Arthur J.,Wang, Xiaoping,Krische, Michael J.
, p. 9448 - 9453 (2007/10/03)
In the presence of phenylsilane and 5 mol % cobalt(II) bis(2,2,6,6-tetramethylheptane-3,5-dionate), aryl-substituted monoenone monoaldehydes and bis(enones) undergo reductive cyclization to afford synaldol and anti-Michael products, respectively. For both
