464200-92-8Relevant academic research and scientific papers
Diastereoselective Synthesis of trans-2,3-Diaryl(heteroaryl)-3,6-dihydropyrans by an Allylboration/Ring-Closing-Metathesis Sequence
Nocquet, Pierre-Antoine,Corbu, Andrei,Meerpoel, Lieven,Stansfield, Ian,Berthelot, Didier,Angibaud, Patrick,Cossy, Janine
, p. 3343 - 3354 (2017)
trans-2,3-Diaryl(heteroaryl)-dihydropyrans were synthesized by an allylboration/ring-closing-metathesis sequence, using allylboranes formed in situ from the corresponding allylic alcohols. Aryl(heteroaryl) substituents were thus installed diastereoselectively onto dihydropyran rings in a trans fashion. These disubstituted dihydropyrans were further transformed into monosaccharide-like tetrahydropyrans.
Synthesis and serotonin receptor affinities of a series of trans-2- (indol-3-yl)cyclopropylamine derivatives
Vangveravong, Suwanna,Kanthasamy, Arthi,Lucaites, Virginia L.,Nelson, David L.,Nichols, David E.
, p. 4995 - 5001 (2007/10/03)
A series of four racemic ring-substituted trans-2-(indol-3- yl)cyclopropylamine derivatives was synthesized and tested for affinity at the 5-HT(1A) receptor, by competition with [3H]-8-OH-DPAT in rat hippocampal homogenates, and for affinity at
