942599-73-7Relevant articles and documents
Stereoselective synthesis of a potent human NK1 receptor antagonist via acyl-Claisen rearrangement
Raubo, Piotr,Giuliano, Claudio,Hill, Alastair W.,Huscroft, Ian T.,London, Clare,Reeve, Austin,Seward, Eileen M.,Swain, Christopher G.,Kulagowski, Janusz J.
, p. 600 - 604 (2007/10/03)
Stereoselective synthesis of the tetrahydropyran derivative 1 is reported. Diastereoselective acyl-Claisen rearrangement was employed for formation of C3 and C4 chiral centres on the tetrahydropyran ring. Georg Thieme Verlag Stuttgart.