A stereoselective access to dihydroxylated pyrrolidines by reductive ring contraction of 1,2-oxazines

Synthesis

Volumn , Issue 17, 2007, Pages 2681-2689

  Reissig, Hans Ulrich ^a   Homann, Kai ^b   Hiller, Florian ^c   Zimmer, Reinhold ^a  

^a FREIE UNIVERSITÄT BERLIN   (Germany)

^b DARMSTADT UNIVERSITY OF TECHNOLOGY   (Germany)

^c DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

Author keywords

1,2 oxazines; Cycloaddition; Hydrogenation; Pyrrolidines; Ring contraction

Indexed keywords

ENANTIOMERIC HYDROXYLATED PYRROLIDINE DERIVATIVES; PYRROLIDINES; RING CONTRACTION;

CYCLOADDITION; DERIVATIVES; ENANTIOMERS; HYDROGENATION; STEREOSELECTIVITY;

AMINES;

2 ISOPROPYL 5 METHYLCYCLOHEXYLOXY 4,5 ISOPROPYLIDENE 3 PHENYL 3,4,5,6 TETRAHYDRO 2H 1,2 OXAZINE; 3,4,5,6 TETRAHYDRO 4,5 O ISOPROPYLIDENE 3 PHENYL 2H 1,2 OXAZINE; 4,5 HIDROXYLATED 1,2 OXAZINE DERIVATIVE; 5,6 DIHYDRO 4H 1,4 OXAZINE DERIVATIVE; OXAZINE DERIVATIVE; PYRROLIDINE DERIVATIVE; TETRAHYDRO 2H 1,2 OXAZINE DERIVATIVE; UNCLASSIFIED DRUG;

ADDITION REACTION; ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHROMATOGRAPHY; DIELS ALDER REACTION; DIHYDROXYLATION; ENANTIOMER; HYDROGENATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; RACEMIZATION; REDUCTION; STEREOCHEMISTRY; X RAY ANALYSIS;

EID: 34548691624     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-983802     Document Type: Article

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