Journal of the Chemical Society. Perkin transactions I p. 2677 - 2679 (1981)
Update date:2022-08-05
Topics:
Bruce, J. Malcolm
Roshan-Ali, Yusuf
Electron-releasing substituents at the 3-position of allyl phenyl ethers favour Claisen rearangement of the allyl group to the 6-position, whereas electron-acceptors favour migration to the 2-position. 2-Acylhydroquinone 4-allyl ethers yield, predominantly, the 3-allyl isomers, probably because internal hydrogen bonding confers naphthalenoid character on the aryl residue.
View MoreZhejiang Kente Chemical Co.,Ltd.
Contact:86-0576-87651912
Address:No.7, Fengxi West Road, Modern Industrial Zone
Contact:86-551-63540590
Address:No 1388 Furong Rd., Hefei, Anhui, China
website:https://www.yurisolar.com/en
Contact:86--18092602675
Address:No. 560, East Hangtian Road, Xi'an, China
FUJIAN SHANSHUI CHEMICAL CORP.LTD.
Contact:+86-151-59920036
Address:Jinqiao Gareden, jo@fj-xinyi.com
Huaihua Baohua Biotechnology Co.,Ltd
website:http://www.baochengchem.com
Contact:86-519-82698291
Address:HouYang chemical development zone,Jintan,Jiangsu,China (213200)
Doi:10.1039/b409870f
(2004)Doi:10.1039/b102192n
(2001)Doi:10.1021/ja00389a038
(1982)Doi:10.1021/jo00342a055
(1982)Doi:10.1007/BF00963428
(1981)Doi:10.1039/P19810002415
(1981)
