Catalysis and regioselectivity in the Michael addition of azoles. Kinetic vs. thermodynamic control

DOI: 10.1016/0040-4039(96)00845-3

Source and publish data:

Tetrahedron Letters p. 4423 - 4426 (1996)

Update date:2022-07-30

Topics:: Authors:

Horvath, Andras

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Article abstract of DOI:10.1016/0040-4039(96)00845-3

Bicyclic guanidine bases, TBD and MTBD were found to be high]y efficient catalysts in the Michael addition of azoles with α,β-unsaturated nitriles and esters. The factors influencing regioselectivity have been elucidated, and some new azole-Michael adduct

Full text of DOI:10.1016/0040-4039(96)00845-3

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Article Doi

Catalysis and regioselectivity in the Michael addition of azoles. Kinetic vs. thermodynamic control

DOI: 10.1016/0040-4039(96)00845-3

Source and publish data:

Authors:

Article abstract of DOI:10.1016/0040-4039(96)00845-3

Full text of DOI:10.1016/0040-4039(96)00845-3

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