192514-54-8Relevant articles and documents
Enantioselective Alkyne Conjugate Addition Enabled by Readily Tuned Atropisomeric P,N-Ligands
Mishra, Sourabh,Liu, Ji,Aponick, Aaron
, p. 3352 - 3355 (2017/03/15)
By the nature of its structure, the 5-membered chiral biaryl heterocyclic scaffold represents a departure from 6-membered P,N-ligands that facilitates tuning and enables ligand evolution to address issues of selectivity and reactivity. In this vein, the C
Characterization of orally active nonpeptide vasopressin V2 receptor agonist. Synthesis and biological evaluation of both the (5R)- and (5S)-enantioisomers of 2-[1-(2-chloro-4-pyrrolidin-1-yl-benzoyl)- 2,3,4,5-tetrahydro-1H-1-benzazepin-5-yl]-N
Kondo, Kazumi,Kan, Keizo,Tanada, Yoshihisa,Bando, Masahiko,Shinohara, Tomoichi,Kurimura, Muneaki,Ogawa, Hidenori,Nakamura, Shigeki,Hirano, Takahiro,Yamamura, Yoshitaka,Kido, Masaru,Mori, Toyoki,Tominaga, Michiaki
, p. 3805 - 3808 (2007/10/03)
The synthesis and evaluation of both the (R)- and (S)-enantioisomers about the 5-position on a tetrahydro-1H-1-benzazepine derivative were described. The absolute configuration of the (R,R)-isomer (10) was determined by x-ray crystallographic analysis. Af
Benzazepine derivatives with vasopressin agonistic activity
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, (2008/06/13)
PCT No. PCT/JP96/03652 Sec. 371 Date Jun. 12, 1998 Sec. 102(e) Date Jun. 12, 1998 PCT Filed Dec. 13, 1996 PCT Pub. No. WO97/22591 PCT Pub. Date Jun. 26, 1997Novel benzazepine derivative of the formula [1]: wherein R1 is H or halogen, A is lower alkylene,