Journal of Organic Chemistry p. 2834 - 2838 (1989)
Update date:2022-08-02
Topics: Regioselectivity Column chromatography Yield NMR spectroscopy Catalyst Nucleophile Electrophile Mass spectrometry (MS) Diels-Alder Reaction Solvent Effects Stereoselectivity Cycloaddition Staudinger Reaction 1,3-Dipolar Cycloaddition Ketenes Pericyclic reaction Transition state HOMO-LUMO interaction
Brady, William T.
Gu, Yi Qi
(Arylalkylamino)ketenes were prepared from the corresponding glycine derivatives and underwent in situ cycloadditions with cyclopentadiene, cycloheptene, and cyclooctene to yield only the endo-bicyclocyclobutanones.The cycloheptene and cyclooctene cycload
View MoreChengdu D-Innovation Pharmaceutical Co., Ltd
Contact:86-28-85105536
Address:1001, B6, No.88 Keyuan South Road, Chengdu Hi-Tech Zone
Contact:+86-25-52346955
Address:199,JIANYE ROAD,NANJING,CHINA
Shandong Wanda Organosilicon New Material Co., Ltd
Contact:+86-21-54177116;54302881
Address:R1318 Greenland No. 3 Lane 58 Xinjian East Rd., Minhang
Shanghai Bosman Industrial Co., Ltd
Contact:86-21-63065878-8006
Address:Rm907, No.1611, North Sichuan Road, Hongkou District, Shanghai, 200080 China
Contact:+86-021-58123769
Address:No.780 of Cailun Road,Zhangjiang Hi-tech Park,Pudong,Shanghai
Doi:10.1039/a806823b
(1998)Doi:10.1055/s-0035-1560480
(2015)Doi:10.1039/c3ra44363a
(2014)Doi:10.1016/S0040-4039(03)01519-3
(2003)Doi:10.1055/s-1998-1944
(1998)Doi:10.1021/ja00995a007
(1967)
