STEREOSELECTIVE 1,3-DIPOLAR CYCLOADDITION OF UNSATURATED NITRILES TO ISOQUINOLINIUM YLIDS. MOLECULAR AND CRYSTAL STRUCTURE OF 1,2-trans-3,3-DICYANO-1-CARBAMOYL-2-(3-PYRIDYL)-1,2,3,4-TETRAHYDROBENZOINDOLIZINE

DOI: 10.1007/BF00484367

Source and publish data:

Chemistry of Heterocyclic Compounds p. 1006 - 1011 (1991)

Update date:2022-09-26

Topics: Stereoselective 1,3-Dipolar Cycloaddition

Authors:

Shestopalov, A. M.

Sharanin, Yu. A.

Nesterov, V. N.

Rodinovskaya, L. A.

Shklover, V. E.

et al. et al.

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Article abstract of DOI:10.1007/BF00484367

The reactions of isoquinolinium ylids with arylmethylenemalononitriles proceed highly stereoselectively via a pathway involving synchronous 1,3-dipolar cycloaddition to give 1,2-trans-2-aryl-3,3-dicyano-1-carbamoyl(benzoyl)-1,2,3,4-tetrahydrobenzoindol

Full text of DOI:10.1007/BF00484367

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