The intermolecular carbon–carbon bond formation between two alkenes also known as 1, 2‐
hydrovinylation reaction can be realised with different transition metal catalysts. The …

Attempts to introduce the highly versatile vinyl group into other organic molecules in a
chemo-, regio-, and stereoselective fashion via catalytic activation of ethylene provided …

The selective, intermolecular [1, 4]-hydrovinylation of conjugated dienes with unactivated α-
olefins catalyzed by α-diimine iron complexes is described. Value-added “skipped” diene …

Monosubstituted acyclic (E)-1, 3-dienes undergo efficient hydrovinylation giving (Z)-3-
alkylhexa-1, 4-dienes upon treatment with catalytic amounts of bidentate phosphine-CoCl2 …

Catalytic cross-dimerization is one of the powerful synthetic methods to produce linear
molecules with high atom and step economy. Because this process involves a carbon …

The hydrovinylation reaction is a codimerization of a 1, 3-diene or vinyl arene and ethene
with great potential for fine chemicals and pharmaceuticals. For the first time …

1-Vinylcycloalkenes undergo highly regio-and enantioselective (> 98% ee) 1, 4-
hydrovinylation (HV) when treated with ethylene (1 atm) at room temperature in the …

Cyclic and acyclic 1, 3-dienes undergo efficient (substrate/catalyst= 72) heterodimerization
with ethylene in the presence of a Ni catalyst prepared from [o-(PhCH2O)] C6H4PPh2,[(allyl) …

In the presence of bidentate 1, n-bis-diphenylphosphinoalkane-CoCl2 complexes {Cl2Co
[P∼ P]} and Me3Al or methylaluminoxane, acyclic (E)-1, 3-dienes react with ethylene (1 …

Through a systematic examination of ligand and counterion effects, new protocols for a
nearly quantitative and highly selective codimerization of ethylene and various …