A practical synthesis of (R)-(+)-cyclohex-3-enecarboxylic acid via an asymmetric Diels-Alder reaction

DOI: 10.1055/s-1993-25885

Source and publish data:

Synthesis p. 475 - 477 (1993)

Update date:2022-08-02

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Authors:

Thom Thom

Kocienski

Jarowicki

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Article abstract of DOI:10.1055/s-1993-25885

The polymerisation which complicates the ethylaluminum dichloride-catalysed asymmetric Diels-Alder reaction between N-propenoylbornane-10,2-sultam[10,10-dimethyl-3-thia-4-azatricyclo[5.2 .1.0^1,5]decane 3,3-dioxide] and butadiene can be suppress

Full text of DOI:10.1055/s-1993-25885

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Product name:(S)-Cyclohex-3-enyl-((1R,5S,7S)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-methanone

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