Construction of dihydropyrimidine skeleton using 1,2,4-trisubstituted-1,3-diaza-1,3-butadienes
β Scribed by Hidetsura Cho; Yoshio Nishimura; Yoshizumi Yasui; Masahiko Yamaguchi
- Book ID
- 113930457
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- French
- Weight
- 442 KB
- Volume
- 53
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The title compound, C 20 H 16 N 6 , consists of electron-delocalized trans-planar molecules possessing a crystallographically imposed centre of symmetry. In the crystal packing, the molecules are stacked along the c axis by van der Waals forces.
cycloaddition reactions of I-aryl-4-dimethylamino-1,3diaza-1,3-butadienes (~),l-aryl-4-dimethylamino-2-methylthio-l,3-diaza-l,3butadienes 12). l-aryl-4-methylthio-2-phenyl-4-sec.amino-l,3-diaza-l,3butadienes ( 2) and 4, 4-bis~sec.amino~-l,2-diphenyl-l,3-diaza-l,3-bu~adienes 112) with monophenylketen
The title Schiff base compound, C 18 H 22 N 4 , is derived from the condensation reaction of hydrazine and 4-(dimethylamino)benzaldehyde. There is a crystallographic centre of symmetry at the mid-point of the N-N bond.