Synthesis of 1,2- and 1,4-amino alcohols from 1,3-dienes via oxazines. Rearrangements of 1,4-amino alcohol derivatives to oxazolines

Tetrahedron

Volumn 66, Issue 21, 2010, Pages 3761-3769

  Werner, Lukas ^a   Hudlicky, Jason Reed ^a   Wernerova, Martina ^a   Hudlicky, Tomas ^a  

^a BROCK UNIVERSITY   (Canada)

Author keywords

1,2 Amino alcohols; 1,4 Amino alcohols; Hetero Diels Alder reaction; Oxazines; Oxazolines

Indexed keywords

1 HYDROXY 2 ACETYLAMINOCYCLOHEX 5 ENE; 1 HYDROXY 2 ACETYLAMINOCYCLOPENT 4 ENE; 1 HYDROXY 2 ACETYLAMINOCYCLOPENT 6 ENE; 2,2,7 TRIMETHYL 4 CYCLOHEXYL 3A,5A,8A,8B TETRAHYDRO[1,3]DIOXOLO[4,5 E][1,3]BENZOXAZOLE; 2,3A DIMETHYL 4 5 O ISOPROPYLIDEN 3A,4,5,7A TETRAHYDROBENZO[D]OXAZOLE 4,5 DIOL; 2,6 DIMETHYL 4 5 O ISOPROPYLIDEN 3A,4,5,7A TETRAHYDROBENZO[D]OXAZOLE 4,5 DIOL; 4 ACETAMIDO 7 CYCLOHEXYL N,N,N, TRIETHYL 2,2 DIMETHYL 3A,4,5,7A TETRAHYDROBENZO[D][1,3]DIOXOL 5 AMMONIUM METHANESULFONATE; 6 ACETYLAMINO 1,2 O ISOPROPYLIDENE 3 METHYL CYCLOHEX 3 ENE; 6 ACETYLAMINO 1,2 O ISOPROPYLIDENE 5 CHLORO 3 CYCLOHEXYLCYCLOHEX 3 ENE 1,2 DIOL; ALCOHOL DERIVATIVE; ALKADIENE; ETHYL 4 HYDROXY 4 ACETYLAMINO HEX 2 ENOATE; ETHYL 7 (ACETYLAMINO) 6 HYDROXY 2,2, DIMETHYL 3A,6,7,7A TETRA HYDRO 1,3 BENZODIOXOLE 4 CARBOXYLATE; MESYLIC ACID; N (7 CYCLOHEXYL 5 HYDROXY 2,2 DIMETHYL 3A,4,5,7A TETRAHYDROBENZO[D][1,3]DIOXOL 4 YL)ACETAMIDE; OXAZINE DERIVATIVE; OXAZOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CYCLOADDITION; DIELS ALDER REACTION; HYDROLYSIS; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; SYNTHESIS; THIN LAYER CHROMATOGRAPHY;

ALNUS;

EID: 77951127839     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.03.059     Document Type: Article

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