Synthesis and molluscicidal activity of 5-oxo-5,6,7,8-tetrahydro-4H-chromene derivatives

被引：103

作者：

Abdelrazek, FM

Metz, P

Farrag, EK

机构：

[1] Tech Univ Dresden, Inst Organ Chem, D-8027 Dresden, Germany

[2] Natl Res Ctr, Dept Med Chem, Giza, Egypt

来源：

ARCHIV DER PHARMAZIE | 2004年 / 337卷 / 09期

关键词：

furfurylidenemalononitriles; thienylidenemalononitriles; 1,3-cyclo-hexanediones; 2-Amino-4-hetaryl-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carbonitriles;

D O I：

10.1002/ardp.200400881

中图分类号：

R914 [药物化学];

学科分类号：

100701 [药物化学];

摘要：

Furfurylidenemalononitriles and thienylidenemalononitriles were treated with 1, 3-cyclohexanediones to afford 2-amino-4-hetaryl-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carbonitrile derivatives. The molluscicidal activity of these compounds was investigated.

引用

页码：482 / 485

页数：4

共 23 条

[1]

Abdel-Latif F. F., 1995, J CHEM RES MINIPRINT, P1220

[2]

ABDELRAZEK FM, 1991, EGYPT J CHEM, V34, P559

[3]

Ammonium acetate-basic alumina catalyzed Knoevenagel condensation under microwave irradiation under solvent-free condition [J].

Balalaie, S ;

Nemati, N .

SYNTHETIC COMMUNICATIONS, 2000, 30 (05) :869-875

[4]

DYER JR, 1965, APPLICATIONS ABSORPT, P11

[5]

GOENNERT R, 1961, B WORLD HEALTH ORGAN, V25, P483

[6]

GONNERT R., 1962, Comparative investigations of some mollusci-cides. Ciba Foundation Symposium on Bilhar-ziasis, Cairo, March 18-22, 1962., P326

[7]

Held C, 2002, ADV SYNTH CATAL, V344, P720, DOI 10.1002/1615-4169(200208)344:6/7<720::AID-ADSC720>3.0.CO

[8]

2-#

[9]

Held C, 2001, ANGEW CHEM INT EDIT, V40, P1058, DOI 10.1002/1521-3773(20010316)40:6<1058::AID-ANIE10580>3.0.CO

[10]

2-3

← 1 2 3 →