Bulletin of the Chemical Society of Japan p. 3721 - 3730 (1987)
Update date:2022-08-04
Topics:
Takekuma, Shin-ichi
Matsubara, Yoshiharu
Yamamoto, Hiroshi
Nozoe, Tetsuo
Autoxidation of the title azulenes at 100 deg C in HMPA of DMF afforded a wide variety of products: Namely, the oxidation products of the side-chains, 1-substituted azulenes, 1H-inden-1-ols, naphthoquinones, benzenoids, and dimeric and trimeric compounds, with or without rearrangements. 1H NMR (200-MHz) parameters of various azulene derivatives are given for comparative study.Possible reaction pathways for the formation of these products are discussed in comparison with the results of the previous studies on guaiazulene and 4,6,8-trimethylazulene.
View MoreNanjing Samwon International Limited
Contact:+86-25-84873444
Address:1108, BLDG B, New Century Plaza, No 1, South Taiping Rd.,
Contact:021-36356756
Address:Room601,Building No.14,280 Yangcheng Road,Shanghai
Contact:+86 021-51698675
Address:1701, Jielong Plaza, No.618 Pingliang Rd, ShangHai,China
Suzhou HeChuang Chemical Co.,Ltd.
Contact:+86-512-88800520
Address:No.9 Guanchao Rd,Changshu Advanced Materials Industy Park
Contact:86-575-86132822，86-575-86085355
Address:No.418 Dadao West Road,Qixing Street,Xinchang, Zhejiang Province, China.
Doi:10.1039/c39840001487
(1984)Doi:10.1002/ejoc.201600429
(2016)Doi:10.1016/j.ejmech.2007.05.006
(2008)Doi:10.1016/S0040-4039(01)91255-9
(1984)Doi:10.1021/ic700838s
(2007)Doi:10.1016/j.bmcl.2007.08.019
(2007)
