Silane-mediated direct condensation of nitroarenes with cinnamyl-type sulfones. The way to 2-aryl-4-X-quinolines and their hetero analogs

DOI: 10.1016/S0040-4020(98)00023-4

Source and publish data:

Tetrahedron p. 2607 - 2618 (1998)

Update date:2022-08-05

Topics:: Authors:

Wrobel, Zbigniew

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Article abstract of DOI:10.1016/S0040-4020(98)00023-4

DBU/silane mediated double condensation of nitroarenes with cinnamyl-type sulfones proceeds smoothly to yield 2-arl-4-arylsulfonyl quinolines and their hetero analogs. Arylsulfonyl group can be easily replaced by different nucleophiles.

Full text of DOI:10.1016/S0040-4020(98)00023-4

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Article Doi

Silane-mediated direct condensation of nitroarenes with cinnamyl-type sulfones. The way to 2-aryl-4-X-quinolines and their hetero analogs

DOI: 10.1016/S0040-4020(98)00023-4

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4020(98)00023-4

Full text of DOI:10.1016/S0040-4020(98)00023-4

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