Reaction of 1,3-disubstituted acetone derivatives with pseudohalides: A simple approach to spiro[4.4]nonane-Type bis-oxazolidines and -imidazolidines (bicyclic carbamates, thiocarbamates, ureas, and thioureas)

European Journal of Organic Chemistry

Volumn , Issue 1, 2000, Pages 205-209

  Saul, Robert ^a   Kern, Thorsten ^a   Kopf, Jürgen ^b   Pintér, István ^c,d   Köll, Peter ^a  

^a UNIVERSITY OF OLDENBURG   (Germany)

^b UNIVERSITY OF HAMBURG   (Germany)

^c INSTITUTE OF EXPERIMENTAL MEDICINE   (Hungary)

^d Prochem Ltd   (Hungary)

Author keywords

Carbohydrates; Heterocycles; Imidazolidines; Oxazolidines; Spiro 4.4 nonanes

Indexed keywords

ACETONE; BRUCINE; CARBAMIC ACID DERIVATIVE; CARBOHYDRATE; HETEROCYCLIC COMPOUND; IMIDAZOLINE DERIVATIVE; OXAZOLIDINE DERIVATIVE; REAGENT; SPIRO COMPOUND; THIOCARBAMIC ACID DERIVATIVE; THIOUREA DERIVATIVE; UREA DERIVATIVE;

ACETYLATION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; CHEMICAL STRUCTURE; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

EID: 0033986036     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1099-0690(200001)2000:1<205::aid-ejoc205>3.0.co;2-j     Document Type: Article

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