ChemInform Abstract: STEREOSELECTIVE CONVERSION OF (+)‐CIS‐2‐OXABICYCLO(3,3,0)OCT‐6‐EN‐3‐ONE INTO METHYL R‐(+)‐7‐(3‐HYDROXY‐5‐OXO‐CYCLOPENTENYL)‐5‐CIS‐HEPTENOATE

Gruber, L.; TOEMOESKOEZI, I.; Major, E.; Kovács, Gábor

doi:10.1002/chin.197502223

Chemischer Informationsdienst

1975

DOI: 10.1002/chin.197502223

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ChemInform Abstract: STEREOSELECTIVE CONVERSION OF (+)‐CIS‐2‐OXABICYCLO(3,3,0)OCT‐6‐EN‐3‐ONE INTO METHYL R‐(+)‐7‐(3‐HYDROXY‐5‐OXO‐CYCLOPENTENYL)‐5‐CIS‐HEPTENOATE

L. Gruber¹,

I. TOEMOESKOEZI²,

E. Major³

et al.

Abstract: Das bicyclische Lacton (I) wird zum Diol (II) hydroxyliert und nach Überführung in die Isopropylidenverbindung zu (III) reduziert.

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ChemInform Abstract: STEREOSELECTIVE CONVERSION OF (+)‐CIS‐2‐OXABICYCLO(3,3,0)OCT‐6‐EN‐3‐ONE INTO METHYL R‐(+)‐7‐(3‐HYDROXY‐5‐OXO‐CYCLOPENTENYL)‐5‐CIS‐HEPTENOATE

Abstract: Das bicyclische Lacton (I) wird zum Diol (II) hydroxyliert und nach Überführung in die Isopropylidenverbindung zu (III) reduziert.

Cited by 0 publications

References 1 publication

No citations

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