ChemInform Abstract: ERGAENZUNG VON (4+2)‐CYCLOADDITIONEN DURCH (2,3)‐SIGMATROPE UMLAGERUNGEN IN SYNTH., NEUE SYNTH. VON FUNKTIONALISIERTEN HASUBANAN‐DERIVATEN

Evans, David A.; Bryan, C. A.; Sims, Charles L.

doi:10.1002/chin.197227216

Chemischer Informationsdienst

1972

DOI: 10.1002/chin.197227216

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ChemInform Abstract: ERGAENZUNG VON (4+2)‐CYCLOADDITIONEN DURCH (2,3)‐SIGMATROPE UMLAGERUNGEN IN SYNTH., NEUE SYNTH. VON FUNKTIONALISIERTEN HASUBANAN‐DERIVATEN

David A. Evans¹,

C. A. Bryan²,

Charles L. Sims³

Abstract: Die Cycloaddition des Diens (I) an das Tetrahydrobenzindol (II) bei 70°C in Acetonitril ergibt ein Gemisch der diastereomeren Sulfoxide (III) und das Sulfenat (IVa).

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ChemInform Abstract: ERGAENZUNG VON (4+2)‐CYCLOADDITIONEN DURCH (2,3)‐SIGMATROPE UMLAGERUNGEN IN SYNTH., NEUE SYNTH. VON FUNKTIONALISIERTEN HASUBANAN‐DERIVATEN

Abstract: Die Cycloaddition des Diens (I) an das Tetrahydrobenzindol (II) bei 70°C in Acetonitril ergibt ein Gemisch der diastereomeren Sulfoxide (III) und das Sulfenat (IVa).

Cited by 0 publications

References 1 publication

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