ChemInform Abstract: ASYMMETRIC SYNTHESIS OF AMINO ACIDS BY CATALYTIC REDUCTION OF AZLACTONES OF SUBSTITUTED ACYLAMINOACRYLIC ACIDS. PART 11. REDUCTIVE AMINOLYSIS OF 4‐SEC‐BUTYLIDENE‐5‐OXAZOLONES

Khatskevich, I. E.; Kalnin, I. K.; Karpeiskaya, E. I.; Клабуновский, Е. И.

doi:10.1002/chin.198332324

Chemischer Informationsdienst

1983

DOI: 10.1002/chin.198332324

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ChemInform Abstract: ASYMMETRIC SYNTHESIS OF AMINO ACIDS BY CATALYTIC REDUCTION OF AZLACTONES OF SUBSTITUTED ACYLAMINOACRYLIC ACIDS. PART 11. REDUCTIVE AMINOLYSIS OF 4‐SEC‐BUTYLIDENE‐5‐OXAZOLONES

I. E. Khatskevich¹,

I. K. Kalnin²,

E. I. Karpeiskaya³

et al.

Abstract: Die Z‐ und E‐Isomeren von 4‐sek.‐Butyliden‐5‐oxazolen (I) werden in Gegenwart von S‐ J‐a‐Phenyl‐ethylamin (III) hydriert, wobei die Diastereomeren (IV) entstehen.

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ChemInform Abstract: ASYMMETRIC SYNTHESIS OF AMINO ACIDS BY CATALYTIC REDUCTION OF AZLACTONES OF SUBSTITUTED ACYLAMINOACRYLIC ACIDS. PART 11. REDUCTIVE AMINOLYSIS OF 4‐SEC‐BUTYLIDENE‐5‐OXAZOLONES

Abstract: Die Z‐ und E‐Isomeren von 4‐sek.‐Butyliden‐5‐oxazolen (I) werden in Gegenwart von S‐ J‐a‐Phenyl‐ethylamin (III) hydriert, wobei die Diastereomeren (IV) entstehen.

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See others like this or search for similar articles

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