Stereoselective synthesis of 7E,9E- and 7E,9Z-β-ionylidene-acetaldehydes by use of tricarbonyl iron complex

DOI: 10.1248/cpb.42.757

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 757 - 759 (1994)

Update date:2022-08-16

Topics:

Authors:

Wada Wada

Hiraishi

Ito Ito

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

Article abstract of DOI:10.1248/cpb.42.757

Stereoselective synthesis of 7E,9E- and 7E,9Z-β-ionylideneacetaldehydes was accomplished from the β-ionone tricarbonyl iron complex, and the latter was converted to 9Z-retinoic acid.

Full text of DOI:10.1248/cpb.42.757

NII-Electronic Library Service

Products guided by the article

Product name:7-cis-retinoic acid

Cas No:124510-04-9

R&D Labs maybe for 124510-04-9

Clearsynth Labs Limited

Contact:+91 - 22 - 26355700

Address:17, Lotus Business Park, Andheri West
XI'AN CHUKANG BIOTECHNOLOGY CO.,LTD

Contact:29-63685658 63685359

Address:Room 3-1202,Building 1,Oriental oasis,East of Xianning Road,Xi'an,Shaanxi 710043 P.R.China
BOC Sciences

website:https://www.bocsci.com/

Contact:1-631-485-4226

Address:Ramsey Road
Shanghai Sunway Pharmaceutical Technology Co.,Ltd.

Contact:+86-21-5161 3915

Address:Shanghai YangPu
Jiangxi Province Bethel Pharmaceutical Co., Ltd.

Contact:+86-795-259 3456 ，+86-15957688008 13566650571

Address:Huangjindui Chemical Park， Shanggao County ，Yichun city，Jiangxi Province

Relevant to this article

Synthesis, structures, characterizations and catalytic behaviors for hydrogen evolution of copper(II) and copper(I) complexes supported by diiminodiphosphines

Doi:10.1016/j.inoche.2021.108719
(2021)
Doi:10.1016/S0040-4039(00)72460-9
(1973)
(S)-6-(1-HYDROXYPROPYL)LUMAZINE DERIVATIVES FROM THE MARINE POLYCHAETE, ODONTOSYLLIS UNDECIMDONTA

Doi:10.3987/COM-94-6690
(1994)
Doi:10.1002/mpr.103
(1917)
Cobalt-catalyzed cycloaddition of alkynes and nitriles to pyridines: A new route to pyridoxine (vitamin B₆)

Doi:10.1002/hlca.19840670513
(1984)
The reactivity of new (1,5-cyclooctadiene)rhodium acylpyrazolonates towards N- and P-donor ligands: X-ray structures of [Rh(1,5-COD)Q^s], [Rh(1,5-COD)(phen)]Q^s·0.5H₂O (HQ^s=1-phenyl-3-methyl-4-(2-thenoyl)-pyrazol-5-one) and [Rh(1,5-COD)Br]₂

Doi:10.1016/S0022-328X(02)01122-1
(2002)

Article Doi