A convenient synthesis of dibenzo[a,c]cyclooctene based on thioenol ether reduction

DOI: 10.1016/S0040-4039(00)61640-4

Source and publish data:

Tetrahedron Letters p. 639 - 642 (1992)

Update date:2022-09-26

Topics:

Authors:

Lottaz, Pierre Andre

Edwards, Timothy R. G.

Mentha, Yves G.

Burger, Ulrich

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Article abstract of DOI:10.1016/S0040-4039(00)61640-4

9,10,11,12-Tetrahydrodibenzo[a,b]cyclooctane-9,12-diol (6) is found to be reluctant to double bond forming elimination. It gives a bridge ether (7) instead. The corresponding diketone (5) reacts with benzyl mercaptan to provide the bis-thioenol ether (8-a

Full text of DOI:10.1016/S0040-4039(00)61640-4

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