The Reduction of Crown Lactones to Crown Ethers

DOI: 10.1039/c39820000248

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 248 - 249 (1982)

Update date:2022-08-23

Topics:

Authors:

Ager, David J.

Sutherland, O.

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

Article abstract of DOI:10.1039/c39820000248

Crown lactones may be reduced to crown ethers using lithium aluminium hydride.

Full text of DOI:10.1039/c39820000248

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:18-Crown-6

Cas No:17455-13-9

R&D Labs maybe for 17455-13-9

KINHENG CHEMICAL(SHANGHAI)CO., LTD.

Contact:+8621-60490170

Address:Room401, No.28,Lane 189, Yangshupu Rd. Shanghai, China.
NINGBO YINZHOU PRECISE COLOR CO.,LTD.

Contact:86-574-88139809 86-574-83033159

Address:Qiming Road,Yinzhou,Ningbo,China
ChengduChroma-BiotechCo.,Ltd.

Contact:86-28-61993785

Address:No.70-13-21, North Section, Erhuan
Zhejiang Sucon Silicone Co.,Ltd

Contact:+86-575-88046692

Address:Qisheng Rd., Paojiang Industrial Zone, Shaoxing, Zhejiang, China.
Shenzhen JYMed Technology Co.,Ltd.

website:http://www.jymedtech.com

Contact:+86-755-26612112

Address:1#8,9/F, Biomedicine innovation Industrial Park, No.14, Jinhui Road, Pingshan Sistrict, Shenzhen, China

Relevant to this article

Azo-containing pyridine amide ligand. A six-coordinate nickel(II) complex and its one-electron oxidized species: Structure and properties

Doi:10.1016/j.ica.2010.03.056
(2010)
Enhance the fluorescence and singlet oxygen generation ability of BODIPY: Modification on the meso-phenyl unit with electron withdrawing groups

Doi:10.1016/j.jphotochem.2017.09.040
(2017)
Doi:10.1103/PhysRevB.37.10619
()
Catalytic oxidation of aromatic hydrocarbons by mono-oxido- alkoxidovanadium(V) complexes of ONNO donor ethylenediaminebis(phenolate) ligands

Doi:10.1016/j.poly.2013.07.013
(2013)
Oxygen-ion and electron conductivity in Sr₂(Fe_1-xGa_x)₂ O₅

Doi:10.1016/j.jssc.2006.05.028
(2006)
Novel anticancer oridonin derivatives possessing a diazen-1-ium-1,2-diolate nitric oxide donor moiety: Design, synthesis, biological evaluation and nitric oxide release studies

Doi:10.1016/j.bmcl.2016.04.068
(2016)

Article Doi