CONDENSATION OF AZAFLUORENES WITH AROMATIC ALDEHYDES UNDER PHASE-TRANSFER-CATALYSIS CONDITIONS

DOI: 10.1007/BF00516217

Source and publish data:

Chemistry of Heterocyclic Compounds p. 432 - 435 (1983)

Update date:2022-08-04

Topics:

Authors:

Prostakov, N. S.

Beshenko, M. A.

Soldatova, S. A.

Fomichev, A. A.

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1007/BF00516217

Aryl-substituted (in the oxirane ring) spiro were obtained, and their configuration was established.The substances that are formed under phase-transfer catalysis conditions in the condensation of 1-azafluorene with benzaldehyde

Full text of DOI:10.1007/BF00516217

Products guided by the article

Product name:E-3'-(p-nitrophenyl)spiro<4-azafluorene-9,2'-oxirane>

Cas No:86445-17-2

R&D Labs maybe for 86445-17-2

Shanghai Hope Chem Co., Ltd

website:http://www.hope-chem.com

Contact:86-21-58090396-805

Address:Floor 4, Building 5, No.588 Tianxiong Road, Zhoupu International Medical Zone, ShangHai, China
Anhui Redstar Pharmaceutical Corp., Ltd

Contact:+86-563-5120837

Address:Jingxian Industrial Development Zone, Anhui , China
Quzhou Aokai Chemical Co., Ltd.

Contact:86-570-3032832

Address:NO.16 , Laodong Road,Quzhou City, Zhejiang Province,China
Hangzhou Eastbiopharm Co.,Ltd.

Contact:+86-571-88931780

Address:Hangzhou,China
Beijing Top Science biological technology co., LTD

Contact:+86-13439059536

Address:15-1705 jre three mile, Beijing 100000,CHINA

Relevant to this article

REACTION OF PYRIDINIUM PHENACYLIDES AND RELATED YLIDES WITH CYCLOPENTADIENONE DERIVATIVES

Doi:10.1246/cl.1983.489
(1983)
Antineoplastic agents. 515. Synthesis of human cancer cell growth inhibitors derived from 3,4-methylenedioxy-5,4′-dimethoxy-3′-amino- Z-stilbene

Doi:10.1021/np058033l
(2005)
Doi:10.1021/ja01868a014
(1940)
Structurally simple farnesyltransferase inhibitors arrest the growth of malaria parasites

Doi:10.1002/anie.200500674
(2005)
Doi:10.1021/ja01642a071
(1954)
Highly regioselective lipase-catalyzed acetylation and hydrolysis of acyclic α,α′-alkenediols and their diacetates

Doi:10.1016/j.tetlet.2005.07.039
(2005)

Article Doi