On starting from N-allyl-substituted 2-indolecarbaldehydes and exploiting the intramolecular nitrone cycloaddition methodology, we synthesized a number of the title fused-ring indole derivatives in racemic as well as enantiopure form.
Access to pyrrolo- and pyrido[1,2-a]indole derivatives by intramolecular nitrone cycloadditions. Effect of steric factors on the regioselective product formation / E. Beccalli, G. Broggini, C. La Rosa, D. Passarella, T. Pilati, A. Terraneo, G. Zecchi. - In: JOURNAL OF ORGANIC CHEMISTRY. - ISSN 0022-3263. - 65:26(2000), pp. 8924-8932.
Access to pyrrolo- and pyrido[1,2-a]indole derivatives by intramolecular nitrone cycloadditions. Effect of steric factors on the regioselective product formation
E. BeccalliPrimo
;C. La Rosa;D. Passarella;
2000
Abstract
On starting from N-allyl-substituted 2-indolecarbaldehydes and exploiting the intramolecular nitrone cycloaddition methodology, we synthesized a number of the title fused-ring indole derivatives in racemic as well as enantiopure form.
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