Tetrahedron Letters p. 2729 - 2732 (1995)
Update date:2022-08-11
Topics:
Zhang, Wei
Collins, Michael R.
Mahmood, Khalid
Dowd, Paul
Free radical expansion of fused-cyclobutanones gives bicyclic ketones expanded by three and four carbons, with the carbonyl group β to the ring junction.Four-carbon ring expansion shows stereoselectivity favoring the trans-fused product 6-trans.The radical precursor cyclobutanones are readily prepared by intramolecular <2+2> cycloaddition of ketenes or keteniminium salts to olefins.
View More
Contact:86-371-63655023
Address:No.85,jinshui road,zhengzhou,China
Wuhan Better Organic Technology Inc.
Contact:13307163183
Address:Wuhan Economic&Technology Development Zone, Hubei
Shenyang Xingzhenghe Chemical Co., Ltd.
Contact:024-23509232
Address:No. 33, Naner Road, Heping Dist.
Shanghai Rainbow Chemistry Co., Ltd.
Contact:+86-21-64968086-5815/5812
Address:3rd floor, Building 7, 251 Faladi Road, Zhangjiang Hi-Tech Park, Pudong District, Shanghai, P.R. China
Contact:86-516-66656369
Address:The west road of Huaihai, Xuzhou, China
Doi:10.1016/j.molstruc.2020.128894
(2020)Doi:10.1007/s11173-005-0067-5
(2005)Doi:10.1016/j.tetlet.2008.11.116
(2009)Doi:10.1039/jr9510002225
(1951)Doi:10.1016/j.dyepig.2016.10.020
(2017)Doi:10.1016/S0040-4020(01)92689-4
(1962)
