Diels-Alder reactions of 1-sulfinyldienes with an endocyclic double bond: The unexpected evolution of the N-methylmaleimide adducts

DOI: 10.1016/0957-4166(94)80106-1

Source and publish data:

Tetrahedron Asymmetry p. 1439 - 1442 (1994)

Update date:2022-07-31

Topics:

Authors:

Carreno Carreno

Cid Cid

Colobert

Garcia Ruano

Solladie

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Article abstract of DOI:10.1016/0957-4166(94)80106-1

(R)-(1E,3E)-2-Cyclohexenyl-1-vinyl-p-tolylsulfoxide 1a and (R)-(1E,3E)-N-methyl-3-[2-(p-tolylsulfinyl) vinyl]-1H-indole 1b reacted with N-methylmaleimide to give Diels-Alder adducts whose in situ evolution through a tandem sulfoxide-sulfenate rearrangemen

Full text of DOI:10.1016/0957-4166(94)80106-1

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