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A NEW STRATEGY FOR THE ENANTIOSELECTIVE SYNTHESIS OF ASPIDOSPERMA ALKALOIDS: I - CONSTRUCTION OF THE -TYPE TRICYCLIC INTERMEDIATES

DOI: 10.1016/S0040-4039(00)94653-7

Source and publish data:

Tetrahedron Letters p. 879 - 882 (1990)

Update date:2022-08-05

Topics:

Authors:

d'Angelo, Jeand'Angelo, Jean

Desmaele, DidierDesmaele, Didier

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Article abstract of DOI:10.1016/S0040-4039(00)94653-7

Carbazole 19 has been prepared in eight steps from cyclohexanone 11 (36percent overall yield).

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Full text of DOI:10.1016/S0040-4039(00)94653-7

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Product name:3-((R)-1-Methyl-2-trimethylsilanyloxy-cyclohex-2-enyl)-propionic acid methyl ester

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