ditryptophenaline and tryptamine

ditryptophenaline has been researched along with tryptamine* in 1 studies

Other Studies

1 other study(ies) available for ditryptophenaline and tryptamine

Article	Year
Copper-mediated dimerization to access 3a,3a'-bispyrrolidinoindoline: diastereoselective synthesis of (+)-WIN 64821 and (-)-ditryptophenaline. Organic letters, 2015, Jan-16, Volume: 17, Issue:2 A copper-mediated cyclization and dimerization of tryptamine or tryptophan was developed to generate a C2-symmetry C3(sp(3))-C3(sp(3)) bridge with two contiguous stereogenic quaternary carbons in one step. Impressively, the ratio between exo and endo cyclization products varies when different protecting groups of Nb are utilized. This dimerization reaction could be conducted in gram scale. With this dimerization method, both endocyclotryptophan (+)-WIN 64821 and exocyclotryptophan (-)-ditryptophenaline were synthesized in 5 steps. Topics: Copper; Cyclization; Dimerization; Indoles; Molecular Structure; Piperazines; Pyrroles; Stereoisomerism; Tryptamines; Tryptophan	2015

Article

Year

Copper-mediated dimerization to access 3a,3a'-bispyrrolidinoindoline: diastereoselective synthesis of (+)-WIN 64821 and (-)-ditryptophenaline.

Organic letters, 2015, Jan-16, Volume: 17, Issue:2

A copper-mediated cyclization and dimerization of tryptamine or tryptophan was developed to generate a C2-symmetry C3(sp(3))-C3(sp(3)) bridge with two contiguous stereogenic quaternary carbons in one step. Impressively, the ratio between exo and endo cyclization products varies when different protecting groups of Nb are utilized. This dimerization reaction could be conducted in gram scale. With this dimerization method, both endocyclotryptophan (+)-WIN 64821 and exocyclotryptophan (-)-ditryptophenaline were synthesized in 5 steps.

Topics: Copper; Cyclization; Dimerization; Indoles; Molecular Structure; Piperazines; Pyrroles; Stereoisomerism; Tryptamines; Tryptophan

2015