67175-80-8Relevant articles and documents
Synthesis of cationic 1-substituted-dicarbonyl(η5-4- methoxycyclohexadienyl)-(triphenylphosphine)iron complexes
Guillou, Catherine,Millot, Nicolas,Reboul, Vincent,Thal, Claude
, p. 4515 - 4518 (1996)
Cationic 1-substituted-dicarbonyl(π5-4-methoxycyclohexadienyl)- (triphenylphosphine)iron complexes 10 form a new class of highly functionalised iron complexes which have never been described. They were obtained from neutral 1-substituted (πsup
Reductive cyclization strategy for construction of the highly oxygenated CD ring system of aconitine
Matsuzawa, Akinobu,Kasamatsu, Akihiko,Sugita, Kazuyuki
, p. 4585 - 4587 (2016)
The synthesis of a CD ring analogue of aconitine is described. The SmI2-mediated reductive cyclization of an α,β-epoxyketone with a pendant formyl group allowed for stereocontrolled construction of the bicyclo[3.2.1]octane framework. Further ox
From meiogynin A to the synthesis of dual inhibitors of Bcl-xL and Mcl-1 anti-apoptotic proteins
Desrat,Remeur,Gény,Rivière,Colas,Dumontet,Birlirakis,Iorga,Roussi
supporting information, p. 8593 - 8596 (2014/07/22)
The synthesis of one of the most potent dual inhibitors of the anti-apoptotic proteins Bcl-xL and Mcl-1 is reported. This analogue of a natural sesquiterpenoid dimer meiogynin A was elaborated by a convergent asymmetric synthesis with 36% yield in ten steps. the Partner Organisations 2014.