Fischer Indolization of N. ALPHA.-Alkyl-2-allylphenylhydrazones.

片山肇, 高津徳行, 竹内庸子, 山際道代

Index: Chemical and Pharmaceutical Bulletin, , vol. 41, # 5 p. 816 - 821

Full Text: HTML

Citation Number: 0

Abstract

... The chemical shift of 2-H for 1b also supports E configuration of 1b as assigned from the IR spectrum, vide supra. ... 1d Ph H 1e Me H 1f COOH H 3: R1=CHZCH=CH2 F12=COOEt 5: H1=R2=H Chart 1 © 1993 Pharmaceutical Society of ... The reaction mixture was evaporated Vol. ...

Related Articles:

Development of high-affinity 5-HT3 receptor antagonists. Structure-affinity relationships of novel 1, 7-annulated indole derivatives. 1

[Van Wijngaarden; Hamminga; Van Hes; Standaar; Tipker; Tulp; Mol; Olivier; De Jonge Journal of Medicinal Chemistry, 1993 , vol. 36, # 23 p. 3693 - 3699]

An efficient one pot transfer hydrogenation and N-alkylation of quinolines with alcohols mediated by Pd/C/Zn

[Organic and Biomolecular Chemistry, , vol. 10, # 9 p. 1826 - 1833]

Development of high-affinity 5-HT3 receptor antagonists. Structure-affinity relationships of novel 1, 7-annulated indole derivatives. 1

[Journal of Medicinal Chemistry, , vol. 36, # 23 p. 3693 - 3699]

An efficient one pot transfer hydrogenation and N-alkylation of quinolines with alcohols mediated by Pd/C/Zn

[Abarca, Belen; Adam, Rosa; Ballesteros, Rafael Organic and Biomolecular Chemistry, 2012 , vol. 10, # 9 p. 1826 - 1833]

Development of high-affinity 5-HT3 receptor antagonists. Structure-affinity relationships of novel 1, 7-annulated indole derivatives. 1

[Journal of Medicinal Chemistry, , vol. 36, # 23 p. 3693 - 3699]

More Articles...