![]() |
Volumn , Issue 6, 2002, Pages 771-783
|
An improved and stereoselective route to all-cis-2,6-disubstituted 4-hydroxypiperidines from accessible 4-substituted 4-N-benzylaminobut-1-enes
|
Author keywords
1 aza 7 oxabicyclo 2.2.1 heptanes; 4 hydroxy 2 spiropiperidines; 4 hydroxypiperidines; Homoallylamines; Nitrones; Stereoselective intramolecular 1,3 dipolar cycloadditions
|
Indexed keywords
KETONES;
STEREOCHEMISTRY;
SUBSTITUTION REACTIONS;
SYNTHESIS (CHEMICAL);
STEREOSELECTIVE ROUTES;
BUTENES;
1 AZA 7 OXABICYCLO[2.2.1]HEPTANE;
4 HYDROXY 6 PHENYL 2 NONYLPIPERIDINE;
4 N BENZYLAMINOBUT 1 ENE;
ALLYLAMINE DERIVATIVE;
BROMIDE;
HEPTANE;
MAGNESIUM;
NITRONE DERIVATIVE;
PIPERIDINE DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
CHEMICAL STRUCTURE;
CYCLOADDITION;
OXIDATION;
PROTON NUCLEAR MAGNETIC RESONANCE;
REACTION ANALYSIS;
STEREOCHEMISTRY;
SYNTHESIS;
|
EID: 0036257511
PISSN: 00397881
EISSN: None
Source Type: Journal
DOI: 10.1055/s-2002-25770 Document Type: Article |
Times cited : (19)
|
References (41)
|