The systhesis of a 5,7-membered fused-ring compound by a tandem pummerer rearrangement and intramolecular [4+3] cycloaddition

DOI: 10.1016/S0040-4039(98)02404-6

Source and publish data:

Tetrahedron Letters p. 545 - 548 (1999)

Update date:2022-08-02

Topics:

Authors:

Hu, Youhong

Ou, Ligong

Bai, Donglu

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Article abstract of DOI:10.1016/S0040-4039(98)02404-6

A 5, 7-membered fused-ring compound with a functionalized angular substituent, 8-methoxy-8aα-methoxymethyl-7-phenylthio-1, 2, 3, 6-tetrahydro- 3aα, 6β-epoxyazulene, was synthesized via a tandem. Pummerer rearrangement and intramolecular [4+3] cycloaddition.

Full text of DOI:10.1016/S0040-4039(98)02404-6

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