Synthesis of Dodecahydro-3a,6,6,69a-tetramethyl naphthofuran via Alkoxy Radical Fragmentation.

DOI: 10.1016/S0040-4020(01)90335-7

Source and publish data:

Tetrahedron p. 1925 - 1932 (1988)

Update date:2022-08-17

Topics:: Authors:

Christenson, Philip A.

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Article abstract of DOI:10.1016/S0040-4020(01)90335-7

Alkoxy radicals of several sclareol derivatives undergo β-fragmentation reactions to provide decahydro-1-(2-haloethyl)-2,5,5,8a-tetramethyl-2-naphthalenol acetates (9b,c) which are converted to dodecahydro-naphthofuran 5 and ambreinolide 6.

Full text of DOI:10.1016/S0040-4020(01)90335-7

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Synthesis of Dodecahydro-3a,6,6,69a-tetramethyl naphthofuran via Alkoxy Radical Fragmentation.

DOI: 10.1016/S0040-4020(01)90335-7

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4020(01)90335-7

Full text of DOI:10.1016/S0040-4020(01)90335-7

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