Synthesis and olfactory properties of spirocyclic Georgywood® analogues

Synthesis

Volumn , Issue 13, 2006, Pages 2215-2223

  Kraft, Philip ^a   Frech, David ^a   Müller, Urs ^a   Fráter, Georg ^a  

^a GIVAUDAN SCHWEIZ AG   (Switzerland)

Author keywords

Cyclizations; Diels Alder reactions; Georgywood; Odorants; Spiro compounds

Indexed keywords

ALKYLATION; CATALYSTS; IODINE COMPOUNDS; ODORS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

CYCLIZATIONS; DIELS-ALDER REACTIONS; GEORGYWOOD; ODORANTS; SPIRO COMPOUNDS;

AROMATIC COMPOUNDS;

1 METHYL 3,4,5,6,7,8,9,10 OCTAHYDRO 1H SPIRO(BENZO[8]ANNULENE 2,1' CYCLOHEXAN) 2' ONE; 1 METHYL 3,4,5,6,7,8,9,10 OCTAHYDRO 1H SPIRO(BENZO[8]ANNULENE 2,1' CYCLOPENTAN) 2' ONE; 1',8',8' TRIMETHYL 3',4',5',6',7',8' HEXAHYDRO 1'H SPIRO(CYCLOPENTANE 1,2' NAPHTHALEN) 2 ONE; 1',8',8' TRIMETHYL 3',4',5',6',7',8' HEXAHYDRO 1'H SPIRO(CYCLOPENTANE 1,2' NAPHTHALEN) 2 ONE OXIME; 1,3' DIMETHYL 3,4,5,6,7,8,9,10 OCTAHYDRO 1'H SPIRO(BENZO[8]ANNULENE 2,1' CYCLOHEXAN) 2' ONE; 1,3' DIMETHYL 3,4,5,6,7,8,9,10 OCTAHYDRO 1H SPIRO(BENZO[8]ANNULENE 2,1' CYCLOHEXAN) 2' ONE; 10 ACETYL 9,10 DIMETHYLBICYCLO[6.4.0]DODEC 1 (8) ENE; 2 (DIMETHYLAMINOMETHYL)CYCLOPENTANONE; 3,1',8',8' TETRAMETHYL 3',4',5',6',7',8 HEXAHYDRO 1'H SPIRO(CYCLOPENTANE 1,2' NAPHTHALEN) 2 ONE; 3,1',8',8' TETRAMETHYL 3',4',5',6',7',8' HEXAHYDRO 1'H SPIRO(CYCLOPENTANE 1,2' NAPHTHALEN) 2 ONE; 3,3,1',8',8' PENTAMETHYL 3',4',5',6',7',8 HEXAHYDRO 1'H SPIRO(CYCLOPENTANE 1,2' NAPHTHALEN) 2 ONE; 4 METHYLENESPIRO[2.7]DECANE; 6 METHYL 8 (4' METHYLPENT 3' ENYL)SPIRO[4.5]DEC 7 EN 1 ONE; 8A HOMOMYRCENE; ALKANONE; ALLYL 1 (ACETOXYMETHYL) 2 OXOCYCLOALKANECARBOXYLATE DERIVATIVE; CYCLOPROPANE; GEORGYWOOD; ISO E SUPER; METHYL IODIDE; MYRCENE; SPIRO COMPOUND; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; CYCLOADDITION; DIELS ALDER REACTION; DRUG BINDING; DRUG STRUCTURE; DRUG SYNTHESIS; ODOR; PROTON NUCLEAR MAGNETIC RESONANCE; SMELLING; STEREOCHEMISTRY;

EID: 33746040826     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-942418     Document Type: Article

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