107328-74-5Relevant articles and documents
Atom-efficient vinylic arylations with triarylbismuths as substoichiometric multicoupling reagents under palladium catalysis
Rao, Maddali L.N.,Jadhav, Deepak N.,Venkatesh, Varadhachari
experimental part, p. 4300 - 4306 (2011/02/24)
The first atom-efficient arylation of vinylic iodides was achieved by using triarylbismuths as substoichiometric multicoupling reagents under palladium catalysis. Vinylic iodides were efficiently coupled with electronically divergent triarylbismuths to furnish the corresponding arylated products in short reaction times.
Process for the enantiospecific synthesis of intermediates for hexahydro-benzo[d]-naphtho[2,1-b]azepines
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, (2008/06/13)
Biologically active, enantiomerically substantially pure intermediates of trans-hexahydro-benzo[d]naphtho[2,1-b]azepines are prepared. The present invention involves a process for preparing compounds of the general formula 3: STR1 wherein: R* is STR2 Each