Acid-Mediated Cyclisations: Efficient Access to Functionalised trans-Decalins

DOI: 10.1016/S0040-4039(00)74089-5

Source and publish data:

Tetrahedron Letters p. 4789 - 4792 (1993)

Update date:2022-07-31

Topics:

Authors:

Linder, Simon M.

Reichlin, Daniel

Simmons, Dana P.

Snowden, Roger L.

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Article abstract of DOI:10.1016/S0040-4039(00)74089-5

Acid-mediated cyclisation of monocyclic, (E)- and (Z)-β-phosphoroxyenoate 5d using 98percent aq.H2SO4 in toluene at 2 deg C affords, after decarbomethoxylation, trans-2-decalone 1 in 79percent and 68percent yield, respectively.Key Words: cyclisation; deca

Full text of DOI:10.1016/S0040-4039(00)74089-5

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