Internal nucleophilic termination in acid-mediated polyene cyclizations part 3. Synthetic access to didehydro and methyl didehydro analogues of (±)-ambrox®

Helvetica Chimica Acta

Volumn 87, Issue 7, 2004, Pages 1711-1723

  Snowden, Roger L ^a   Eichenberger, Jean Claude ^a   Linder, Simon ^a   Sonnay, Philippe ^a  

^a Analysis and Perception Department   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOLS; ETHERS; MATHEMATICAL TRANSFORMATIONS; MIXTURES; STEREOCHEMISTRY;

ALLENIC ALCOHOLS; NUCLEOPHILIC TERMINATION; TRICYCLIC ETHERS;

UNSATURATED COMPOUNDS;

2,3A,4,5,5A,6,7,8,9,9A DECAHYDRO 3A,6,6,7,9A PENTAMETHYLNAPHTHO[2,1 B]FURAN; 2,3A,4,5,5A,6,7,8,9,9A DECAHYDRO 3A,6,6,9A TETRAMETHYLNAPHTHO[2,1 B]FURAN; 4 METHYL 6 (2,5,6,6 TETRAMETHYLCYCLOHEX 1 EN 1 YL)HEXA 2,3 DIEN 1 OL; 4 METHYL 6 (2,6,6 TRIMETHYLCYCLOHEX 1 EN 1 YL)HEXA 2,3 DIEN 1 OL; ALKENE; ALLENE DERIVATIVE; AMBROX; DODECAHYDRO 3A,6,6,9A TETRAMETHYLNAPHTHO[2,1 B]FURAN; FURAN DERIVATIVE; POLYENE; UNCLASSIFIED DRUG;

ARTICLE; CONFORMATION; CYCLIZATION; DIASTEREOISOMER; PRIORITY JOURNAL; RACEMIC MIXTURE; STEREOCHEMISTRY; STEREOSPECIFICITY;

EID: 4043110478     PISSN: 0018019X     EISSN: None     Source Type: Journal    
DOI: 10.1002/hlca.200490155     Document Type: Article

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