Dihydroisobenzofurans and isoindolines by intramolecular inverse Diels-Alder reactions of pyridines

DOI: 10.1016/S0040-4020(01)85441-7

Source and publish data:

Tetrahedron p. 607 - 614 (1990)

Update date:2022-07-29

Topics:

Authors:

Biedrzycki, Marek

De Bie, Dick A.

Van Der Plas, Henk C.

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Article abstract of DOI:10.1016/S0040-4020(01)85441-7

Pyridines being substituted at position 2 or 3 with a silylated propynyloxymethyl side-chain undergo a thermolytic intramolecular Diels-Alder reaction with formation of dihydroisobenzofurans. The 3-substituted pyridines are found to be more reactive than

Full text of DOI:10.1016/S0040-4020(01)85441-7

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