1393364-40-3Relevant academic research and scientific papers
Modular synthesis of polyene side chain analogues of the potent macrolide antibiotic etnangien by a flexible coupling strategy based on hetero-bis-metallated alkenes
Altendorfer, Mario,Raja, Aruna,Sasse, Florenz,Irschik, Herbert,Menche, Dirk
, p. 2116 - 2139 (2013/04/23)
An efficient procedure for the concise synthesis of hetero-bis-metallated alkenes as useful building blocks for the modular access to highly elaborate polyenes and stabilized analogues is reported. By applying these bifunctional olefins in convergent Stille/Suzuki-Miyaura couplings, novel, carefully selected side chain analogues of the potent RNA polymerase inhibitor etnangien were synthesized by a modular late stage coupling strategy and evaluated for antibacterial and antiproliferative activities. The Royal Society of Chemistry 2013.
Efficient synthesis of diverse hetero-bis-metallated alkenes as modular reagents towards highly conjugated and isolated olefinic systems
Altendorfer, Mario,Menche, Dirk
, p. 8267 - 8269 (2012/09/21)
An efficient synthesis of diverse hetero-bis-metallated alkenes with conjugated and isolated olefin subunits is reported. Relying on those useful tin/boron reagents a convergent, palladium-catalyzed fragment coupling strategy has been developed as an eleg
Design, synthesis and biological evaluation of simplified side chains of the macrolide antibiotic etnangien
Altendorfer, Mario,Irschik, Herbert,Menche, Dirk
, p. 5731 - 5734 (2012/10/07)
Novel simplified side chains of the potent RNA polymerase inhibitor etnangien were designed, synthesized and evaluated for antibacterial activity against Gram-positive bacteria and one Gram-negative bacterium.
