Model Reactions for the Stereo‐Controlled Synthesis of Aminopolyols; Reduction of Isoxazolines with Free or Protected Hydroxy Groups in Position 4 or in Side Chains | Zendy

Jäger Volker | Zendy; Schwab Wilfried | Zendy; Buss Volker | Zendy

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Model Reactions for the Stereo‐Controlled Synthesis of Aminopolyols; Reduction of Isoxazolines with Free or Protected Hydroxy Groups in Position 4 or in Side Chains

Author(s) -

Jäger Volker,

Schwab Wilfried,

Buss Volker

Publication year - 1981

Publication title -

angewandte chemie international edition in english

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 5.831

H-Index - 550

eISSN - 1521-3773

pISSN - 0570-0833

DOI - 10.1002/anie.198106011

Subject(s) - chemistry , side chain , hydride , asymmetric induction , reduction (mathematics) , sphingolipid , amino acid , stereochemistry , position (finance) , combinatorial chemistry , organic chemistry , catalysis , biochemistry , enantioselective synthesis , mathematics , hydrogen , polymer , geometry , finance , economics

The effects of substituents on asymmetric induction in hydride additions have been investigated on isoxazoline derivatives; the results, which are of importance for the synthesis of hydroxylated amino acids, sphingolipid bases or amino sugars, can be rationalized with the models (1) and (2) .

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