A practical synthesis of enantiomerically pure (-)-geosmin via highly diastereoselective reduction of (4aS,8S)-4,4a,5,6,7,8-hexahydro-4a,8-dimethyl$MI N@2(3H)- naphthalenone

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Tetrahedron Asymmetry | / 10卷 / 2923期

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[1] A practical synthesis of enantiomerically pure (-)-geosmin via highly diastereoselective reduction of (4aS,8S)-4,4a,5,6,7,8-hexahydro-4a,8-dimethyl-2(3H)-naphthalenone
Saito, A
Tanaka, A
Oritani, T
TETRAHEDRON-ASYMMETRY, 1996, 7 (10) : 2923 - 2928
[2] First stereoselective synthesis of (4aS,5R)-4,4a,5,6,7,8-hexahydro-4a,5-dimethyl-2(3H)-naphthalenone
Cuesta, X
González, A
Bonjoch, J
TETRAHEDRON-ASYMMETRY, 1999, 10 (17) : 3365 - 3370
[3] A practical and efficient preparation of (-)-(4aS,5R)-4,4a,5,6,7,8-hexahydro-4a,5-dimethyl-2(3H)-naphthalenone:: a key intermediate in the synthesis of (-)-dehydrofukinone
Schenato, RA
dos Santos, EM
Tenius, BSM
Costa, PRR
Caracelli, I
Zukerman-Schpector, J
TETRAHEDRON-ASYMMETRY, 2001, 12 (04) : 579 - 584
[4] IMPROVED PREPARATION OF ENANTIOMERICALLY PURE (+)-(4AS,5S)-5-TERT-BUTOXY-4A-METHYL-4,4A,5,6,7,8-HEXAHYDRO-2(3H)-NAPHTHALENONE
TIETZE, LF
UTECHT, J
SYNTHESIS-STUTTGART, 1993, (10): : 957 - 958
[5] Access to enantiomerically pure intermediates for (-)-geosmin synthesis starting from (4aS,5S)-4,4a,5,6,7,8-hexahydro-5-hydroxy-4a-methyl-naphthalen-2(3H)-one
Fuhshuku, K
Sugai, T
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2002, 66 (10) : 2267 - 2272
[6] Lipase-catalyzed asymmetric synthesis of enantiomerically pure (2S,4aS,8S)-4a,8-dimethyl-2,3,4,4a,5,6,7,8-octahydro-2-naphthalenol
Tanaka, A
Tokuyama, T
Saito, A
Oritani, T
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1998, 62 (12) : 2435 - 2437
[7] A convenient chemoenzymatic synthesis of (4aS,5S)-(+)-4,4a,5,6,7,8-hexahydro-5-hydroxy-4a-methylnaphthalen-2(3H)-one
Lo, LC
Shie, JJ
Chou, TC
JOURNAL OF ORGANIC CHEMISTRY, 2002, 67 (01): : 282 - 285
[8] ACID-CATALYSED REARRANGEMENT OF 4,4A,5,6,7,8-HEXAHYDRO-5-HYDROXY-4A-METHYL-2(3H)-NAPHTHALENONE
LOS, M
MIGHELL, AD
TETRAHEDRON, 1965, 21 (09) : 2297 - &
[9] SYNTHESIS OF OPTICALLY PURE (R)-4A-METHYL-4,4A,5,6,7,8-HEXAHYDRO-2(3H)-NAPHTHALENONE AND ITS TRANSFORMATION INTO (+)-7-HYDROXYCOSTAL
TANAKA, A
KAMATA, H
YAMASHITA, K
AGRICULTURAL AND BIOLOGICAL CHEMISTRY, 1988, 52 (08): : 2043 - 2048
[10] Regio- and stereoselective aspects in the oxidation of (R) and (S) 4a-methyl-(4,4a,5,6,7,8)-hexahydro-2(3H)naphthalenones in living rats
Verite, P
Menager, S
Cave, C
Andre, D
dAngelo, J
Revial, G
Farnoux, CC
Lafont, O
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1997, 7 (05) : 587 - 592

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