The bromination reaction of p-benzoquinone-fused norbornadiene was studied at various temperatures (− 78,− 50, 0, 25, and 77° C). At room temperature, the double bonds of the p …
R Çalışkan, MF Ali, E Şahin, WH Watson… - The Journal of Organic …, 2007 - ACS Publications
Benzonorbornadiene and heterobenzonorbornadiene were reacted with dimedone/ acetylacetone and Mn (OAc) 3 in the presence and absence of Cu (OAc) 2. The reaction of …
The low and high temperature bromination of 7-bromobicyclo [2.2. 1] hept-2-ene and 2, 7- dibromobicyclo [2.2. 1] hept-2-ene were studied and the possible role of a neighboring …
The reaction of alcohol 13a with SOCl2 gave 13b, 14a and 15a, and the reaction of chloride 13b with AgNO3 (in MeO−/MeOH) gave 13c, 14b and 15b. In these reactions, 14a, 14b, 15a …
The electrophilic addition of bromine to homobenzonorbornadiene (3) at 10° C led in quantitative yield to the formation of di-anti-bromo adduct 4. However, high-temperature …
C Kazaz, A Daştan, M Balcı - Magnetic Resonance in …, 2005 - Wiley Online Library
The electrophilic addition of bromine to dibromohomobenzonorbornadiene derivatives at− 45±5° C led to the formation of the rearranged and non‐rearranged tetrabromides in a ratio …
Bromination of 2-bromo-1, 4-dihydro-1, 4-ethenonaphthalene (7) at-0 0C has been found to give five rearranged tribromides 8, 9, 10, 11, and 12 via Wagner-Meerwein rearrangement …
The bromination reaction of a benzobicyclic system with 1, 2-dibromotetracholoroethane (DBTCE) was studied. For tricyclo [6.2. 2.02, 7] dodeca-2, 4, 6, 9, 11-pentaene, rearranged …
Homobenzonorbornadiene and benzobarrelene were reacted with dimedone/acetylacetone and Mn (OAc) 3 in the presence of Cu (OAc) 2 in acetic acid. Mainly rearranged products …