A new route to vitamin E Key-intermediates by olefin cross-metathesis

Helvetica Chimica Acta

Volumn 89, Issue 4, 2006, Pages 797-812

  Malaisé, Grégory ^a   Bonrath, Werner ^a   Breuninger, Manfred ^a   Netscher, Thomas ^a  

^a Research and Development   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL BONDS; CHEMICAL REACTIONS; DERIVATIVES; MIXTURES; OLEFINS; RUTHENIUM; SUBSTRATES;

CROSS-METATHESIS (CM); GRUBBS CATALYST; HOVEYDA-GRUBBS CATALYST; PHYTYL DERIVATIVES;

VITAMINS;

2,3,5 TRIMETHYL 6 (3 METHYLBUT 2 EN 1 YL)BENZENE 1,4 DIYL DIACETATE; 2,3,5 TRIMETHYL 6 (3,7,11,15 TETRAMETHYLHEXADEC 2 EN 1 YL)BENZENE 1,4 DIYL DIACETATE; 2,3,6 TRIMETHYL 4 [(3 PHENYLPROP 2 EN 1 YL)OXY]PHENYL ACETATE; 2,3,6 TRIMETHYL 4 [(3,7,11,15 TETRAMETHYLHEXADEC 2 EN 1 YL)OXY]PHENYL ACETATE; 2,3,6 TRIMETHYL 5 (3 METHYLBUT 2 EN 1 YL) 4 [(TRIBUTYLSILYL)OXY]PHENYL ACETATE; 2,3,6 TRIMETHYL 5 (3,7,11,15 TETRAMETHYLHEXADEC 2 EN 1 YL) 4 [(TRIBUTYLSILYL)OXY]PHENYL ACETATE; 3 (PROP 2 ENYL) 2,5,6 TRIMETHYLHYDROQUINONE 1,4 DIACETATE; 3,3,6 TRIMETHYL 4 [(3 METHYLBUT 2 EN 1 YL)OXY]PHENYL ACETATE; 4 (BUT 2 EN 1 YLOXY) 2,3,6 TRIMETHYLPHENYL ACETATE; 4 [[(1,1 DIMETHYLETHYL)(DIMETHYL)SILYL]OXY] 2,3,6 TRIMETHYL 5 (3 METHYLBUT 2 EN 1 YL)PHENYL ACETATE; 4 [[(1,1 DIMETHYLETHYL)(DIMETHYL)SILYL]OXY] 2,3,6 TRIMETHYL 5 (3,7,11,15 TETRAMETHYLHEXADEC 2 EN 1 YL)PHENYL ACETATE; 4 HYDROXY 2,3,6 TRIMETHYL 5 (3 METHYLBUT 2 EN 1 YL)PHENYL ACETATE; 4 HYDROXY 2,3,6 TRIMETHYL 5 (3,7,11,15 TETRAMETHYLHEXADEC 2 EN 1 YL)PHENYL ACETATE; ALKENE DERIVATIVE; ALPHA TOCOPHEROL; BUT 2 ENE 1,4 DIYLBIS(3,5,6 TRIMETHYLBENZENE 2,1,4 TRIYL)TETRAACETATE; BUT 2 ENE 1,4 DIYLBIS(4 HYDROXY 2,5,6 TRIMETHYLBENZENE 3,1 DIYL)DIACETATE; HYDROQUINONE DERIVATIVE; PHENYLACETIC ACID DERIVATIVE; PHYTYL ACETATE; PHYTYL BENZOATE; PHYTYL FORMIATE; RUTHENIUM DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CATALYST; COVALENT BOND; DRUG STRUCTURE; DRUG SYNTHESIS; GAS LIQUID CHROMATOGRAPHY; PRIORITY JOURNAL; RING CLOSING METATHESIS;

EID: 33646237115     PISSN: 0018019X     EISSN: None     Source Type: Journal    
DOI: 10.1002/hlca.200690072     Document Type: Article

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