A NEW SYNTHESIS OF CYCLOPENTANONES BY THE RING EXPANSION OF 1-ACYL-1-CYCLOBUTANES

DOI: 10.1016/S0040-4039(00)81332-5

Source and publish data:

Tetrahedron Letters p. 79 - 82 (1983)

Update date:2022-08-05

Topics:

Authors:

Yamashita, Mitsuo

Onozuka, Junko

Tsuchihashi, Gen-ichi

Ogura, Katsuyuki

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

Article abstract of DOI:10.1016/S0040-4039(00)81332-5

A new ring expansion of 1-acyl-1-cyclobutanes to give 2-cyclopentanones and its application to the synthesis of 2-, 2,4-, or 2,5-substituted cyclopentanones were studied.

Full text of DOI:10.1016/S0040-4039(00)81332-5

Products guided by the article

Product name:1-cyano-1-(p-tolylthio)cyclobutane

Cas No:85901-31-1

R&D Labs maybe for 85901-31-1

QUZHOU ZIO I/E CO.;LTD

Contact:13357117572

Address:No.149 Shiji dadao Road.
Tianjin SPHINX SCIENTIFIC LAB.

Contact:+86-022-66211289

Address:Tianda high-tech Park. No.80,the 4th Avenue
Hangzhou Ledun Technology Co.,Ltd.

Contact:86-571-18767088918

Address:No.6 street,XiaSha,Hangzhou,China.
QINGDAO HONG JIN CHEMICAL CO.,LTD.

website:http://www.hongjinchem.com

Contact:+86-532-83657313

Address:2ND Building, 8 Shangqing Road, Qingdao, Shandong Province, China.
Nanjing Zelang Medical Technology Co. Ltd

Contact:86-25-83063290/13770714480

Address:Ganjiabian 108# 01 Unit,701-702 room,Yao Hua Street,Qixia District,Nanjing,Jiangsu,China

Relevant to this article

Synthesis and structure investigation of the antibiotic amoxicillin complexes of d-block elements

Doi:10.1016/j.saa.2004.08.022
(2005)
Adducts of Mn and Re vinylidenes with P–OR nucleophiles: Hydrolysis rather than the intramolecular Michaelis–Arbuzov rearrangement

Doi:10.1016/j.jorganchem.2017.10.008
(2018)
Sequentially Labile Water-Soluble Prodrugs of Alprazolam

Doi:10.1021/jm00158a004
(1986)
Cobalt-Catalyzed Reductive Cross-Coupling Between Benzyl Chlorides and Aryl Halides

Doi:10.1002/adsc.201600378
(2016)
Doi:10.1039/jr9350000667
(1935)
(+)-Sorangicin A synthetic studies. Construction of the C(1-15) and C(16-29) subtargets

Doi:10.1021/ol051119l
(2005)

Article Doi