887761-84-4Relevant articles and documents
Facile approach to alkaloid-like 6/6/5/5-tetracyclic spiroheterocycles via 1,3-dipolar cycloaddition reaction of fused 1H-pyrrole-2,3-diones with nitrones
Stepanova, Ekaterina E.,Dmitriev, Maksim V.,Maslivets, Andrey N.
supporting information, (2020/01/22)
A facile synthetic approach towards 6/6/5/5-tetracyclic spiroheterocycles has been developed from the highly diastereoselective 1,3-dipolar cycloaddition reaction of [e]-fused 1H-pyrrole-2,3-diones with nitrones. The described novel heterocyclic systems are heteroanalogs of cytotoxic alkaloids, kibalaurifoline and gitingensine. The developed reaction represents the first example of involvement of 1H-pyrrole-2,3-diones fused at [e]-side in a 1,3-dipolar cycloaddition reaction.
Five-membered 2,3-dioxo heterocycles: LXXVII. [4 + 2]-cycloaddition of alkyl vinyl ethers to 3-aroylpyrrolo[2,1-c][1,4]benzoxazine-1,2,4(4H)-triones
Stepanova,Babenysheva,Maslivets
experimental part, p. 937 - 940 (2011/10/09)
[4 + 2]-Cycloaddition of 3-aroylpyrrolo[2,1-c][1,4]benzoxazine-1,2,4(4H)- triones to alkyl vinyl ethers gave substituted stereoisomeric (1R,16R)- and (1S,16R*)-16-alkoxy-14-aryl-3,15-dioxa-10-azatetracyclo[ 8.7.0.0 1,13.04,9]heptadec