28272-96-0Relevant articles and documents
Construction of 4-Isochromanones through Cu(OTf)2-Catalysed Sequential C=O and C–O Bond Formation
Xing, Siyang,Gu, Nan,Qin, Jiajing,Cui, Hong,Li, Yan,Wang, Kui,Tian, Dawei,Chen, Bo,Yu, Guo
, p. 926 - 931 (2018)
A new strategy for the facile and efficient synthesis of 4-isochromanones has been developed. The reaction involves a Cu(OTf)2-catalysed sequential reaction of epoxides carrying electron-deficient alkenes using the solvent DMSO as the oxidant.
Diastereoselective Synthesis of the ABCD Ring System of Rubriflordilactone B
Roth, Hudson G.,Nicewicz, David A.
supporting information, p. 48 - 51 (2021/11/09)
A novel nine-step diastereoselective route to the ABCD ring system of the natural product rubriflordilactone B is reported. Use of an α-substituted butenolide derived from maleic anhydride facilitated a 1,4-conjugate addition to provide a diene. The order in which a ringclosing metathesis and enolate oxidation were performed on this compound dictated the relative stereochemistry of the target. The final product exhibited anisotropic effects during roomerature NMR studies, requiring elevatederature experiments to confirm its identity.
Enantioselective synthesis of 1-aminoindene derivativesviaasymmetric Br?nsted acid catalysis
Ding, Du,Jiang, Hua-Jie,Wang, Tao,Wu, Xiang,Zhang, Ying,Zhao, Li-Ping
supporting information, p. 9680 - 9683 (2021/09/30)
We describe a catalytic asymmetric iminium ion cyclization reaction of simple 2-alkenylbenzaldimines using a BINOL-derived chiralN-triflyl phosphoramide. The corresponding 1-aminoindenes and tetracyclic 1-aminoindanes are formed in good yields and high enantioselectivities. Further, the chemical utility of the obtained enantiopure 1-aminoindene is demonstrated for the asymmetric synthesis of (S)-rasagiline.