Chemistry of odorants: Stereoselective synthesis of octahydronaphthalene- based perfumery Georgywood, (+,-)-1-[(1R*,2S*)-1,2,3,4,5,6,7,8- octahydro-1,2,8,8-tetramethylnaphthalen-2-yl]ethan-1-one

Tetrahedron

Volumn 60, Issue 22, 2004, Pages 4821-4827

  Bella, Marco ^a   Cianflone, Marcello ^a   Montemurro, Gabriele ^a   Passacantilli, Pietro ^a   Piancatelli, Giovanni ^a  

^a SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

Diels Alder reactions; Georgywood; Lewis acid mediated conjugate addition; Octahydronaphthalene skeleton; Odorants

Indexed keywords

1 (1,2,3,4,5,6,7,8 OCTAHYDRO 1,2,8,8 TETRAMETHYLNAPHTHALEN 2 YL)ETHAN 1 ONE; KETONE DERIVATIVE; LEWIS ACID; METHYL IODIDE; MYRCENE; NAPHTHALENE DERIVATIVE; PERFUME; SODIUM DERIVATIVE; TETRAHYDROFURAN; TIN CHLORIDE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CYCLIZATION; CYCLOADDITION; HALOGENATION; MICHAEL ADDITION; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; STEREOCHEMISTRY;

BETULACEAE;

EID: 2342651975     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.04.007     Document Type: Article

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