Convenient synthesis of pyrano[3,2-c]quinolines and indeno[2,1- c]quinolines by imino Diels-Alder reactions

DOI: 10.1016/S0040-4039(98)00397-9

Source and publish data:

Tetrahedron Letters p. 3225 - 3228 (1998)

Update date:2022-08-16

Topics:

Authors:

Babu, Govindarajulu

Perumal, Paramasivan T.

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Article abstract of DOI:10.1016/S0040-4039(98)00397-9

Anhydrous indium trichloride (InCl₃) is found to catalyze the imino Diels-Alder reaction of 3,4-dihydro-2H-pyran and indene with Schiff's bases to afford pyrano[3,2-c]quinolines and indeno[2,1-c]quinolines. Imino Diels- Alder reactions of N-ben

Full text of DOI:10.1016/S0040-4039(98)00397-9

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Product name:trans-5-phenyl-3,4,4a,5,6,10b-hexahydro-2H-pyrano[3,2-c]-quinoline

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