Palladium-catalyzed cross-coupling reactions have reshaped modern synthetic chemistry, giving chemists reliable ways to forge carbon-carbon bonds that were once notoriously difficult to construct.
Increasing our understanding of cellular processes requires information about the types of biomolecules involved, their locations, and their interactions. This requires the molecules to be labeled ...
Recently, Prof. Shou-Fei Zhu’s research group at Nankai University reported in CCS Chemistry a highly efficient and selective hydro-silylation reaction of asymmetric internal alkynes with ...
A collaborative academic-industry research team in the U.K. has devised a method to convert the terminal triple bond of an alkyne into a diester with the two ester groups at opposite ends of the ...
Researchers have discovered a biosynthetic pathway that makes amino acids containing terminal alkynes. Because such functional groups are rare in natural products, they provide a handle for chemistry ...
Increasing our understanding of cellular processes requires information about the types of biomolecules involved, their locations, and their interactions. This requires the molecules to be labeled ...
Click chemistry is a strategy for building molecules by snapping together two complementary chemical handles in a single, dependable step. Rather than relying on long multi-step syntheses, it uses a ...
Increasing our understanding of cellular processes requires information about the types of biomolecules involved, their locations, and their interactions. This requires the molecules to be labeled ...
A transition-metal-free click polymerisation of aldehyde-activated internal diynes and diphenols has produced a new family of ...
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