Divinylbenzene derivatives represent an important class of molecular building blocks in organic chemistry and materials science. Reported herein is the palladium-catalyzed synthesis of divinylbenzenes by meta-C-H olefination of sulfone-based arenes. Successful sequential olefinations in a position-selective manner provided a novel route for the synthesis of hetero-dialkenylated products, which are difficult to access using conventional methods. Additionally, 1,3,5-trialkenylated compounds can be generated upon successful removal of the directing group
2014-11-11Hydroalkenylation cross-coupling reactions between various substituted vinyl arenes and cy...
This thesis describes transition metal (Pd, Rh, Cu) catalyzed olefin functionalization for the creat...
Site selective C-H bond activation/C-C bond formation is an ideal target for organic chemists owing ...
Development of meta-C-H functionalization reactions at room temperature continues to be a tough chal...
Owing to the synthetic importance of branched olefinated products, we report palladium catalyzed for...
Chapter 1 is a brief literature review of the most recent progress in the area of C-H functionalizat...
A nitrile-based template attached with a phenylacetic acid framework promoted meta-selective CH bond...
A nitrile-based template attached with a phenylacetic acid framework promoted meta-selective C–H bon...
Palladium-catalyzed coupling between aryl halides and alkenes (Mizoroki-Heck reaction) is one of the...
The palladium-catalyzed meta-olefination of arene-tethered diols attached to a well-designed pyrimid...
A novel palladium-catalyzed sulfination of aryl and heteroaryl halides is described. This reaction o...
The elaboration of simple arenes in order to access more complex substitution patterns is a crucial ...
Chapter 1 is a brief review on some of the recents developments in palladium-catalysed C-H functiona...
Palladium-catalyzed coupling is a very convenient and useful method for the synthesis of heterocycle...
We have described two important classes of palladium-catalyzed reactions for the synthesis of hetero...
2014-11-11Hydroalkenylation cross-coupling reactions between various substituted vinyl arenes and cy...
This thesis describes transition metal (Pd, Rh, Cu) catalyzed olefin functionalization for the creat...
Site selective C-H bond activation/C-C bond formation is an ideal target for organic chemists owing ...
Development of meta-C-H functionalization reactions at room temperature continues to be a tough chal...
Owing to the synthetic importance of branched olefinated products, we report palladium catalyzed for...
Chapter 1 is a brief literature review of the most recent progress in the area of C-H functionalizat...
A nitrile-based template attached with a phenylacetic acid framework promoted meta-selective CH bond...
A nitrile-based template attached with a phenylacetic acid framework promoted meta-selective C–H bon...
Palladium-catalyzed coupling between aryl halides and alkenes (Mizoroki-Heck reaction) is one of the...
The palladium-catalyzed meta-olefination of arene-tethered diols attached to a well-designed pyrimid...
A novel palladium-catalyzed sulfination of aryl and heteroaryl halides is described. This reaction o...
The elaboration of simple arenes in order to access more complex substitution patterns is a crucial ...
Chapter 1 is a brief review on some of the recents developments in palladium-catalysed C-H functiona...
Palladium-catalyzed coupling is a very convenient and useful method for the synthesis of heterocycle...
We have described two important classes of palladium-catalyzed reactions for the synthesis of hetero...
2014-11-11Hydroalkenylation cross-coupling reactions between various substituted vinyl arenes and cy...
This thesis describes transition metal (Pd, Rh, Cu) catalyzed olefin functionalization for the creat...
Site selective C-H bond activation/C-C bond formation is an ideal target for organic chemists owing ...