Stereoselective syntheses of trans-fused 6,6- and 6,7-membered ether ring systems having an angular methyl group based on SmI2-induced reductive intramolecular cyclization

DOI: 10.1016/S0040-4039(99)01861-4

Source and publish data:

Tetrahedron Letters p. 8859 - 8862 (1999)

Update date:2022-08-05

Topics:

Authors:

Matsuo, Goh

Hori, Nobuyuki

Nakata, Tadashi

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Article abstract of DOI:10.1016/S0040-4039(99)01861-4

Highly stereoselective syntheses of trans-fused 6,6- and 6,7-membered ether ring systems having an angular methyl group were achieved based on SmI₂-induced reductive intramolecular cyclizations of an aldehyde or a methyl ketone and a β-alkoxy a

Full text of DOI:10.1016/S0040-4039(99)01861-4

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