-
1
-
-
84890587838
-
Odor and (bio)diversity: Single enantiomers of chiral fragrant substances
-
Kraft P, Swift KAD, editors. Zurich: VHCA-Wiley-VCH
-
Abate A, Brenna E, Fuganti C, Gatti FG. Serra S. Odor and (bio)diversity: single enantiomers of chiral fragrant substances. In: Kraft P, Swift KAD, editors. Perspectives in flavor and fragrance research. Zurich: VHCA-Wiley-VCH; 2005. p 55-65.
-
(2005)
Perspectives in Flavor and Fragrance Research
, pp. 55-65
-
-
Abate, A.1
Brenna, E.2
Fuganti, C.3
Gatti, F.G.4
Serra, S.5
-
2
-
-
84890673841
-
Scent through the looking glass
-
Kraft P, Swift KAD, editors. Zurich: VHCA-Wiley-VCH
-
Sell CS. Scent through the looking glass. In: Kraft P, Swift KAD, editors. Perspectives in flavor and fragrance research. Zurich: VHCA-Wiley-VCH; 2005. p 67-88.
-
(2005)
Perspectives in Flavor and Fragrance Research
, pp. 67-88
-
-
Sell, C.S.1
-
3
-
-
0026091950
-
Chiral 2-alkylbranched acids, esters and alcohols. Preparation and stereospecific flavour evaluation
-
Rettinger K, Burschka C, Scheeben P, Fuchs H, Mosandl A. Chiral 2-alkylbranched acids, esters and alcohols. Preparation and stereospecific flavour evaluation. Tetrahedron: Asymmetry 1991;2:965-968.
-
(1991)
Tetrahedron: Asymmetry
, vol.2
, pp. 965-968
-
-
Rettinger, K.1
Burschka, C.2
Scheeben, P.3
Fuchs, H.4
Mosandl, A.5
-
7
-
-
0037240975
-
Efficient asymmetric synthesis of β-amino acid BAY 10-8888/PLD-118, a novel antifungal for the treatment of yeast infections
-
Mittendorf J, Benet-Bucholz J, Fey P, Mohrs K-H. Efficient asymmetric synthesis of β-amino acid BAY 10-8888/PLD-118, a novel antifungal for the treatment of yeast infections. Synthesis 2003;136-140. (Pubitemid 36110778)
-
(2003)
Synthesis
, Issue.1
, pp. 136-140
-
-
Mittendorf, J.1
Benet-Buchholz, J.2
Fey, P.3
Mohrs, K.-H.4
-
8
-
-
0001678831
-
Highly enantioselective ring opening of cyclic meso-anhydrides to isopropyl hemiesters with Ti-TADDOLates: An alternative to hydrolytic enzymes?
-
Jaeschke G, Seebach D. Highly enantioselective ring opening of cyclic meso-anhydrides to isopropyl hemiesters with Ti-TADDOLates: an alternative to hydrolytic enzymes? J Org Chem 1998;63:1190-1197.
-
(1998)
J Org Chem
, vol.63
, pp. 1190-1197
-
-
Jaeschke, G.1
Seebach, D.2
-
9
-
-
0000598105
-
Stereoselective pig liver esterase-catalyzed hydrolysis of rigid bicyclic meso-diesters: Preparation of optically pure 4,7-epoxytetra- and hexa-hydrophtalides
-
Bloch R, Guibe-Jampel E, Girard C. Stereoselective pig liver esterase-catalyzed hydrolysis of rigid bicyclic meso-diesters: preparation of optically pure 4,7-epoxytetra- and hexa-hydrophtalides. Tetrahedron Lett 1985;26:4087-4090.
-
(1985)
Tetrahedron Lett
, vol.26
, pp. 4087-4090
-
-
Bloch, R.1
Guibe-Jampel, E.2
Girard, C.3
-
10
-
-
1842524255
-
Detection thresholds for phenyl ethyl alcohol using serial dilutions in different solvents
-
DOI 10.1093/chemse/28.1.25
-
Tsukatani T, Miwa T, Furukawa M, Costanzo RM. Detection thresholds for phenyl ethyl alcohol using serial dilutions in different solvents. Chem Senses 2003;28:25-32. (Pubitemid 41288791)
-
(2003)
Chemical Senses
, vol.28
, Issue.1
, pp. 25-32
-
-
Tsukatani, T.1
Miwa, T.2
Furukawa, M.3
Costanzo, R.M.4
-
11
-
-
0034160976
-
Lipase-catalyzed transesterification of primary alcohols: Resolution of 2-ethylhexan-1-ol and 2-ethylhex-5-en-1-ol
-
Baczko K, Larpent C. Lipase-catalyzed transesterification of primary alcohols: resolution of 2-ethylhexan-1-ol and 2-ethylhex-5-en-1-ol. J Chem Soc Perkin Trans 2 2000;2:521-526. (Pubitemid 35165974)
-
(2000)
Journal of the Chemical Society. Perkin Transactions 2
, Issue.3
, pp. 521-526
-
-
Baczko, K.1
Larpent, C.2
-
12
-
-
0033442105
-
Combined Biocatalytic Preparation of (R)-2-Ethylhexanol and 2-Ethylhexyl Laurate
-
Ćiško-Anić B, Majerić-Elenkov M, Hameršak Z, Šunjić V. Combined biocatalytic preparation of (R)-2-ethylhexanol and 2-ethylhexyl laurate. Food Technol Biotechnol 1999;37:65-70. (Pubitemid 129622508)
-
(1999)
Food Technology and Biotechnology
, vol.37
, Issue.1
, pp. 65-70
-
-
Cisko-Anic, B.1
Majeric-Elenkov, M.2
Hamersak, Z.3
Sunjic, V.4
-
13
-
-
0242626789
-
An alkaloid-mediated desymmetrization of meso-anhydrides via a nucleophilic ring opening with benzyl alcohol and its application in the synthesis of highly enantiomerically enriched β-amino acids
-
DOI 10.1016/S0957-4166(03)00579-2
-
Bolm C, Schifers I, Atodiresei I, Hackenberger PR. An alkaloid-mediated desymmetrization of meso-anhydrides via a nucleophilic ring opening with benzyl alcohol and its application in the synthesis of highly enantiomerically enriched β-amino acids. Tetrahedron: Asymmetry 2003;14:3455-3467. (Pubitemid 37412468)
-
(2003)
Tetrahedron Asymmetry
, vol.14
, Issue.22
, pp. 3455-3467
-
-
Bolm, C.1
Schiffers, I.2
Atodiresei, I.3
Hackenberger, C.P.R.4
-
14
-
-
85026884880
-
ASYMMETRIC ALCOHOLYSIS of MESO-ANHYDRIDES MEDIATED by ALKALOIDS
-
Bolm C, Atodiresei I, Schiffers I. Asymmetric alcoholysis of meso-anhydrides mediated by alkaloids. Org Synth 2005;82:120-125. (Pubitemid 41823437)
-
(2005)
ORGANIC SYNTHESES
, vol.82
, pp. 120-125
-
-
Bolm, C.1
Atodiresei, I.2
Schiffers, I.3
-
15
-
-
0041378031
-
Asymmetric alcoholysis of cyclic anhydrides
-
Chen Y, McDaid P, Deng L. Asymmetric alcoholysis of cyclic anhydrides. Chem Rev 2003;103:2965-2983.
-
(2003)
Chem Rev
, vol.103
, pp. 2965-2983
-
-
Chen, Y.1
McDaid, P.2
Deng, L.3
-
16
-
-
38349102187
-
Stereoselective anhydride openings
-
Atodiresei I, Schifers I, Bolm C. Stereoselective anhydride openings. Chem Rev 2007;107:5683-5712.
-
(2007)
Chem Rev
, vol.107
, pp. 5683-5712
-
-
Atodiresei, I.1
Schifers, I.2
Bolm, C.3
-
17
-
-
33947713571
-
Quinine-mediated parallel kinetic resolution of racemic cyclic anhydride: Stereoselective synthesis, relative and absolute configuration of novel alicyclic β-amino acids
-
DOI 10.1016/j.tetasy.2007.02.019, PII S095741660700153X
-
Hameršak Z, Roje M, Avdagić A, Šunjić V. Quinine-mediated parallel kinetic resolution of racemic cyclic anhydride: stereoselective synthesis, relative and absolute configuration of novel alicyclic β-amino acids. Tetrahedron: Asymmetry 2007;18:635-644. (Pubitemid 46507755)
-
(2007)
Tetrahedron Asymmetry
, vol.18
, Issue.5
, pp. 635-644
-
-
Hamersak, Z.1
Roje, M.2
Avdagic, A.3
Sunjic, V.4
-
18
-
-
34447521909
-
An efficient synthesis of (S)-3-aminomethyl-5-methylhexanoic acid (Pregabalin) via quinine-mediated desymmetrization of cyclic anhydride
-
DOI 10.1016/j.tetasy.2007.06.014, PII S0957416607004569
-
Hameršak Z, Stipetić I, Avdagić A. An efficient synthesis of (S)-3-aminomethyl-5-methylhexanoic acid (Pregabalin) via quinine-mediated desymmetrization of cyclic anhydride. Tetrahedron: Asymmetry 2007;18:1481-1485. (Pubitemid 47069927)
-
(2007)
Tetrahedron Asymmetry
, vol.18
, Issue.12
, pp. 1481-1485
-
-
Hamersak, Z.1
Stipetic, I.2
Avdagic, A.3
-
19
-
-
0030957931
-
Proton-decoupled carbon-13 NMR spectroscopy in a lyotropic chiral nematic solvent as an analytical tool for the measurement of the enantiomeric excess
-
DOI 10.1021/ja964002o
-
Meddour A, Berdague P, Hedli A, Courtieu J, Lesot P. Proton-decoupled carbon-13 nmr spectroscopy in a lyotropic chiral nematic solvent as an analytical tool for the measurement of the enantiomeric excess. J Am Chem Soc 1997;119:4502-4508. (Pubitemid 27244911)
-
(1997)
Journal of the American Chemical Society
, vol.119
, Issue.19
, pp. 4502-4508
-
-
Meddour, A.1
Berdague, P.2
Hedli, A.3
Courtieu, J.4
Lesot, P.5
-
20
-
-
0033551874
-
Double diastereoselection in asymmetric [2+3] cycloaddition of chiral oxazoline N-oxides: Application to the kinetic resolution of a racemic α,β-unsaturated γ-lactone
-
DOI 10.1016/S0957-4166(99)00317-1, PII S0957416699003171
-
Dirat O, Kouklovsky C, Langlois Y, Lesot ,P, Courtieu J. Double diastereoselection in asymmetric [2+3] cycloaddition of chiral oxazoline N-oxides: application to the kinetic resolution of a racemic α,β-unsaturated γ-lactone. Tetrahedron: Asymmetry 1999;10:3197-3207. (Pubitemid 29481236)
-
(1999)
Tetrahedron Asymmetry
, vol.10
, Issue.16
, pp. 3197-3207
-
-
Dirat, O.1
Kouklovsky, C.2
Langlois, Y.3
Lesot, P.4
Courtieu, J.5
-
21
-
-
37049072812
-
Enantiotopic-group differentiation. catalitic asymmetric ring-opening of prochiral cyclic acid anhydrides with methanol, using cinchona alkaloids
-
Hiratake J, Inagaki M, Yamamoto Y, Oda J. Enantiotopic-group differentiation. catalitic asymmetric ring-opening of prochiral cyclic acid anhydrides with methanol, using cinchona alkaloids. J Chem Soc Perkin Trans I 1987;1053-1058.
-
(1987)
J Chem Soc Perkin Trans I
, pp. 1053-1058
-
-
Hiratake, J.1
Inagaki, M.2
Yamamoto, Y.3
Oda, J.4
-
22
-
-
0034693091
-
Practical and highly enantioselective ring opening of cyclic meso-anhydrides mediated by cinchona alkaloids
-
DOI 10.1021/jo000638t
-
Bolm C, Schifers I, Gerlach A. Practical and highly enantioselective ring opening of cyclic meso-anhydrides mediated by cinchona alkaloids. J Org Chem 2000;65:6984-6991. (Pubitemid 30796477)
-
(2000)
Journal of Organic Chemistry
, vol.65
, Issue.21
, pp. 6984-6991
-
-
Bolm, C.1
Schiffers, I.2
Dinter, C.L.3
Gerlach, A.4
|