-
1
-
-
0348233454
-
Chemistry perfumes your daily life
-
Fortineau, D. Chemistry perfumes your daily life. J. Chem. Educ., 2004, 81, 45-50.
-
(2004)
J. Chem. Educ
, vol.81
, pp. 45-50
-
-
Fortineau, D.1
-
2
-
-
52649118166
-
Marine fragrance chemistry
-
Hügel, H.M.; Drevermann, B.; Lingham, A.R.; Marriott, P.J. Marine fragrance chemistry. Chem. Biodiv., 2008, 5, 1034-1044.
-
(2008)
Chem. Biodiv
, vol.5
, pp. 1034-1044
-
-
Hügel, H.M.1
Drevermann, B.2
Lingham, A.R.3
Marriott, P.J.4
-
3
-
-
0032770704
-
Scandium triflate in organic synthesis
-
doi:10.1002(SIC)1099-0690(199901)
-
Kobayashi, S. Scandium triflate in organic synthesis. Eur. J. Org. Chem., 1999, 15-27; doi:10.1002(SIC)1099-0690(199901)
-
(1999)
Eur. J. Org. Chem
, pp. 15-27
-
-
Kobayashi, S.1
-
4
-
-
9644295973
-
Enhancing electrophilic alkene activation by increasing the positive net charge in transitionmetal complexes and application in homogeneous catalysis
-
Hahn, C. Enhancing electrophilic alkene activation by increasing the positive net charge in transitionmetal complexes and application in homogeneous catalysis. Chem. Eur. J., 2004, 10, 5888-5899.
-
(2004)
Chem. Eur. J
, vol.10
, pp. 5888-5899
-
-
Hahn, C.1
-
5
-
-
18844451530
-
Catalytic formation of C-O bonds by alkene activation: Lewis acid-cycloisomerisation of olefinic alcohols
-
Coulombel, L.; Favier, I.; Duñach, E. Catalytic formation of C-O bonds by alkene activation: Lewis acid-cycloisomerisation of olefinic alcohols. Chem. Commun., 2005, 17, 2286-2288.
-
(2005)
Chem. Commun
, vol.17
, pp. 2286-2288
-
-
Coulombel, L.1
Favier, I.2
Duñach, E.3
-
6
-
-
33748287037
-
Aluminium(iii) trifluoromethanesulfonate as an efficient catalyst for the intramolecular hydroalkoxylation of unactivated olefins: Experimental and theoretical approaches
-
Coulombel, L.; Rajzmann, M.; Pons, J.M.; Olivero, S.; Duñach, E. Aluminium(iii) trifluoromethanesulfonate as an efficient catalyst for the intramolecular hydroalkoxylation of unactivated olefins: Experimental and theoretical approaches. Chem. Eur. J., 2006, 12, 6356-6365.
-
(2006)
Chem. Eur. J
, vol.12
, pp. 6356-6365
-
-
Coulombel, L.1
Rajzmann, M.2
Pons, J.M.3
Olivero, S.4
Duñach, E.5
-
7
-
-
13944251987
-
Cycloisomerization of olefinic carboxylic acids catalysed by trifluoromethanesulfonic acid
-
Coulombel, L.; Duñach, E. Cycloisomerization of olefinic carboxylic acids catalysed by trifluoromethanesulfonic acid. Synth. Commun., 2005, 35, 153-160.
-
(2005)
Synth. Commun
, vol.35
, pp. 153-160
-
-
Coulombel, L.1
Duñach, E.2
-
8
-
-
52649092925
-
Lewis super-acid catalysed cyclisations: A new route to fragrance compounds
-
Coulombel, L.; Grau, F.; Weïwer, M.; Favier, I.; Chaminade, X.; Heumann, A.; Bayón, J.; Aguirre, P.A.; Duñach, E. Lewis super-acid catalysed cyclisations: a new route to fragrance compounds. Chem. Biodiv., 2008, 5, 1070-1082.
-
(2008)
Chem. Biodiv
, vol.5
, pp. 1070-1082
-
-
Coulombel, L.1
Grau, F.2
Weïwer, M.3
Favier, I.4
Chaminade, X.5
Heumann, A.6
Bayón, J.7
Aguirre, P.A.8
Duñach, E.9
-
9
-
-
33645458624
-
Regioselective indium(III) trifluoromethanesulfonate-catalysed hydrothiolation of non-activated olefins
-
Weïwer, M.; Coulombel, L.; Duñach, E. Regioselective indium(III) trifluoromethanesulfonate-catalysed hydrothiolation of non-activated olefins. Chem. Commun., 2006, 3, 3332-3334.
-
(2006)
Chem. Commun
, vol.3
, pp. 3332-3334
-
-
Weïwer, M.1
Coulombel, L.2
Duñach, E.3
-
10
-
-
28844492474
-
Indium(III)-catalysed highly regioselective addition of thiolacetic acid to non-activated olefins
-
Weïwer, M.; Duñach, E. Indium(III)-catalysed highly regioselective addition of thiolacetic acid to non-activated olefins. Tetrahedron Lett., 2006, 47, 287-289.
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 287-289
-
-
Weïwer, M.1
Duñach, E.2
-
11
-
-
34250658996
-
Indium triflatecatalysed addition of thio compounds to camphene: A Novel Route to 2,3,3-Trimethyl-2-thiobicyclo[2.2.1]heptane derivatives
-
doi:10.1002/ejoc.200601112
-
Weïwer, M.; Chaminade, X.; Bayon, J.C.; Duñach, E. Indium triflatecatalysed addition of thio compounds to camphene: A Novel Route to 2,3,3-Trimethyl-2-thiobicyclo[2.2.1]heptane derivatives. Eur. J. Org. Chem., 2007, 2464-2469. doi:10.1002/ejoc.200601112.
-
(2007)
Eur. J. Org. Chem
, pp. 2464-2469
-
-
Weïwer, M.1
Chaminade, X.2
Bayon, J.C.3
Duñach, E.4
-
12
-
-
33750989379
-
Cycloisomerization of 1, 6-dienes mediated by lewis super acids without additives: Easy access to polysubstituted six-membered carbocycle
-
Grau, F.; Heumann, A.; Duñach, E. Cycloisomerization of 1, 6-dienes mediated by lewis super acids without additives: Easy access to polysubstituted six-membered carbocycle. Angew. Chem. Int. Ed., 2006, 45, 7285-7289.
-
(2006)
Angew. Chem. Int. Ed
, vol.45
, pp. 7285-7289
-
-
Grau, F.1
Heumann, A.2
Duñach, E.3
-
13
-
-
53849127506
-
New aldehydes by catalytic diene cycloisomerisations
-
Grau, F.; Bayón, J.C.; Aguirre, P.A.; Parella, T.; Duñach, E. New aldehydes by catalytic diene cycloisomerisations. Eur. J. Org. Chem., 2008, 1214-1223.
-
(2008)
Eur. J. Org. Chem
, pp. 1214-1223
-
-
Grau, F.1
Bayón, J.C.2
Aguirre, P.A.3
Parella, T.4
Duñach, E.5
-
14
-
-
30144439471
-
Revisited after 50 years: The stereochemical interpretation of the biogenetic isoprene rule for the triterpenes
-
Eschenmoser, A.; Arigoni, D. Revisited after 50 years: The stereochemical interpretation of the biogenetic isoprene rule for the triterpenes. Helv. Chim. Acta, 2005, 88, 3011-3354.
-
(2005)
Helv. Chim. Acta
, vol.88
, pp. 3011-3354
-
-
Eschenmoser, A.1
Arigoni, D.2
-
16
-
-
33750173220
-
Sequential transformations in organic chemistry: A synthetic strategy with a future
-
Tietze, L.F.; Beifuss, U. Sequential transformations in organic chemistry: A synthetic strategy with a future. Angew. Chem. Int. Ed. Engl., 1993, 32, 131-163
-
(1993)
Angew. Chem. Int. Ed. Engl
, vol.32
, pp. 131-163
-
-
Tietze, L.F.1
Beifuss, U.2
-
17
-
-
0345862320
-
Comments on recent achievements in biomimetic organic synthesis
-
De la Torre, M.C.; Sierra, M.A. Comments on recent achievements in biomimetic organic synthesis. Angew. Chem. Int. Ed., 2004, 43, 160-181
-
(2004)
Angew. Chem. Int. Ed
, vol.43
, pp. 160-181
-
-
de la Torre, M.C.1
Sierra, M.A.2
-
18
-
-
30744447448
-
A case study in biomimetic total synthesis: Polyolefin carbocyclisations to terpenes and steroids
-
Yoder, R.A.; Johnston, J.N. A case study in biomimetic total synthesis: polyolefin carbocyclisations to terpenes and steroids. Chem. Rev., 2005, 105, 4730-4756.
-
(2005)
Chem. Rev
, vol.105
, pp. 4730-4756
-
-
Yoder, R.A.1
Johnston, J.N.2
-
21
-
-
33846976722
-
Cyclisation of 1,5-Dienes: An Efficient Synthesis of β-Georgywood
-
Fráter G.; Schröder, F. Cyclisation of 1,5-Dienes: An Efficient Synthesis of β-Georgywood. J. Org. Chem., 2007, 72, 1112-1120.
-
(2007)
J. Org. Chem
, vol.72
, pp. 1112-1120
-
-
Fráter, G.1
Schröder, F.2
-
22
-
-
85196432610
-
-
EP 0743297, to Givaudan
-
Bajgrowicz, J.; Bringhen, A.; Fráter, G.; Müller, U. Novel Perfume, EP 0743297 1995, to Givaudan.
-
(1995)
Novel Perfume
-
-
Bajgrowicz, J.1
Bringhen, A.2
Fráter, G.3
Müller, U.4
-
23
-
-
0000096497
-
Internal nucleophilic termination in biomimetic acid mediated polyene cyclisations: Stereochemical and mechanistic implications. Synthesis of (±)-Ambrox and its diastereoisomers
-
Snowden, R.L.; Eichenberger, J.-C.; Linder, S.M.; Sonnay, P.; Vial, C.; Schulte-Elte, K.-H. Internal nucleophilic termination in biomimetic acid mediated polyene cyclisations: stereochemical and mechanistic implications. Synthesis of (±)-Ambrox and its diastereoisomers. J. Org. Chem., 1992, 57, 955-960
-
(1992)
J. Org. Chem
, vol.57
, pp. 955-960
-
-
Snowden, R.L.1
Eichenberger, J.-C.2
Linder, S.M.3
Sonnay, P.4
Vial, C.5
Schulte-Elte, K.-H.6
-
24
-
-
52649177846
-
® and Analogues: Synthesis via acidmediated polyene cyclisations
-
® and Analogues: Synthesis via acidmediated polyene cyclisations. Chem. Biodiv., 2008, 5, 958-969.
-
(2008)
Chem. Biodiv
, vol.5
, pp. 958-969
-
-
Snowden, R.L.1
-
25
-
-
0004805428
-
® and its diastereoisomers
-
® and its diastereoisomers. Helv. Chim. Acta, 1993, 76, 1608-1618.
-
(1993)
Helv. Chim. Acta
, vol.76
, pp. 1608-1618
-
-
Snowden, R.L.1
Eichenberger, J.-C.2
Giersch, W.3
Thommen, W.4
Schulte-Elte, K.-H.5
-
29
-
-
33750437237
-
Stereoselective synthesis of superambrox: Stereoselective type iii intramolecular ene reaction and oh-assisted ru-catalysed isomerization
-
Fehr, C.; Farris, I. Stereoselective synthesis of superambrox: stereoselective type iii intramolecular ene reaction and oh-assisted ru-catalysed isomerization. Angew. Chem., Int. Ed., 2006, 45, 6904-6907.
-
(2006)
Angew. Chem., Int. Ed
, vol.45
, pp. 6904-6907
-
-
Fehr, C.1
Farris, I.2
-
30
-
-
39349096556
-
A new, Fe based, heterogeneous Lewis acid: Selective isomerization of α-pinene oxide
-
Ravasio, N.; Zaccheria, F.; Gervasini, A.; Messi, C. A new, Fe based, heterogeneous Lewis acid: Selective isomerization of α-pinene oxide. Catal. Commun., 2008, 9, 1125-1127
-
(2008)
Catal. Commun
, vol.9
, pp. 1125-1127
-
-
Ravasio, N.1
Zaccheria, F.2
Gervasini, A.3
Messi, C.4
-
31
-
-
0000930765
-
The use of zeolites in the synthesis of fine and intermediate chemicals
-
Hölderich, W.F.; Röseler, J.; Heitmann, G.; Liebens, A.T. The use of zeolites in the synthesis of fine and intermediate chemicals. Catal. Today, 1997, 37, 353-366
-
(1997)
Catal. Today
, vol.37
, pp. 353-366
-
-
Hölderich, W.F.1
Röseler, J.2
Heitmann, G.3
Liebens, A.T.4
-
32
-
-
33749251287
-
Probing the lewis acidity and catalytic activity of the metal-organic framework [Cu3(btc)2] (BTC=Benzene-1,3,5-tricarboxylate)
-
Alaerts, L.; Séguin, E.; Poelman, H.; Thibault-Starzyk, F.; Jacobs, P.A.; De Vos, D.E. Probing the lewis acidity and catalytic activity of the metal-organic framework [Cu3(btc)2] (BTC=Benzene-1,3,5-tricarboxylate). Chem. Eur. J., 2006, 12, 7353-7363.
-
(2006)
Chem. Eur. J
, vol.12
, pp. 7353-7363
-
-
Alaerts, L.1
Séguin, E.2
Poelman, H.3
Thibault-Starzyk, F.4
Jacobs, P.A.5
de Vos, D.E.6
-
33
-
-
24644490728
-
Isomerisation of α-pinene oxide over silica supported heteropoly acid H3PW12O40
-
da Silva Rocha, K.A.; Kozhevnikov, I.V.; Gusevskaya, E.V. Isomerisation of α-pinene oxide over silica supported heteropoly acid H3PW12O40. Appl. Catal. A, 2005, 294, 106-110.
-
(2005)
Appl. Catal. A
, vol.294
, pp. 106-110
-
-
da Silva, R.K.A.1
Kozhevnikov, I.V.2
Gusevskaya, E.V.3
-
34
-
-
4243355207
-
Catalysis by heteropoly acids and multicomponent polyoxometalates in liquid-phase reactions
-
Kozhevnikov, I.V. Catalysis by heteropoly acids and multicomponent polyoxometalates in liquid-phase reactions. Chem. Rev., 1998, 98, 171-198
-
(1998)
Chem. Rev
, vol.98
, pp. 171-198
-
-
Kozhevnikov, I.V.1
-
35
-
-
0346266386
-
Acid catalysis by heteropoly acids
-
Timofeeva, M.N. Acid catalysis by heteropoly acids. Appl. Catal. A, 2003, 256, 19-35.
-
(2003)
Appl. Catal. A
, vol.256
, pp. 19-35
-
-
Timofeeva, M.N.1
-
36
-
-
53849148229
-
Phosphotungstic Acid as a versatile catalyst for the synthesis of fragrance compounds by - pinene oxide isomerization: Solvent-induced chemoselectivity
-
Da Silva Rocha, K.A.; Hoehne, J.L.; Gusevskaya, E.V. Phosphotungstic Acid as a versatile catalyst for the synthesis of fragrance compounds by - pinene oxide isomerization: solvent-induced chemoselectivity. Chem. Eur. J., 2008, 14, 6166-6172.
-
(2008)
Chem. Eur. J
, vol.14
, pp. 6166-6172
-
-
da Silva, R.K.A.1
Hoehne, J.L.2
Gusevskaya, E.V.3
-
37
-
-
33845536463
-
The Heck-Mizoroki cross-coupling reaction: A mechanistic perspective
-
Knowles, J.P.; Whiting, A. The Heck-Mizoroki cross-coupling reaction: a mechanistic perspective. Org. Biomol. Chem., 2007, 5, 31-44
-
(2007)
Org. Biomol. Chem
, vol.5
, pp. 31-44
-
-
Knowles, J.P.1
Whiting, A.2
-
38
-
-
33645865241
-
On the nature of the active species in palladium catalysed mizoroki-heck and suzuki-miyaura couplings-homogeneous or heterogeneous catalysis. A critical review
-
Phan, N.T.S.; Van Der Sluys, M.; Jones, C.W. On the nature of the active species in palladium catalysed mizoroki-heck and suzuki-miyaura couplings-homogeneous or heterogeneous catalysis. A critical review. Adv. Synth. Catal. 2006, 348, 609-679
-
(2006)
Adv. Synth. Catal
, vol.348
, pp. 609-679
-
-
Phan, N.T.S.1
van der Sluys, M.2
Jones, C.W.3
-
39
-
-
15044345663
-
Neighbouring-group effects in heck reactions
-
Oestreich, M. Neighbouring-group effects in heck reactions. Eur. J. Org. Chem., 2005, 783-792
-
(2005)
Eur. J. Org. Chem
, pp. 783-792
-
-
Oestreich, M.1
-
40
-
-
0037112673
-
Palladium-catalysed coupling reactions of aryl chlorides
-
Littke, A.F.; Fu, G. Palladium-catalysed coupling reactions of aryl chlorides. Angew. Chem., Int. Ed., 2002, 41, 4176-4211
-
(2002)
Angew. Chem., Int. Ed
, vol.41
, pp. 4176-4211
-
-
Littke, A.F.1
Fu, G.2
-
41
-
-
33747071481
-
Selected patented cross-coupling reaction technologies
-
Corbet, J.-P.; Mignani, G. Selected patented cross-coupling reaction technologies. Chem. Rev., 2006, 106, 2651-2710.
-
(2006)
Chem. Rev
, vol.106
, pp. 2651-2710
-
-
Corbet, J.-P.1
Mignani, G.2
-
42
-
-
36549029331
-
Arylation of β- methallyl alcohol catalysed by Pd(OAc)2 in combination with P(t-Bu)3: Application to fragrance synthesis
-
Scrivanti, A.; Bertoldini, M.; Beghetto, V.; Matteoli, U. Arylation of β- methallyl alcohol catalysed by Pd(OAc)2 in combination with P(t-Bu)3: application to fragrance synthesis. Tetrahedron, 2008, 64, 543-548.
-
(2008)
Tetrahedron
, vol.64
, pp. 543-548
-
-
Scrivanti, A.1
Bertoldini, M.2
Beghetto, V.3
Matteoli, U.4
-
43
-
-
14844333561
-
®; 3-(4-t-butylphenyl)-2-methylpropanal]
-
®; 3-(4-t-butylphenyl)-2-methylpropanal]. J. Mol. Cat. A: Chemical, 2005, 231, 61-66.
-
(2005)
J. Mol. Cat. A: Chemical
, vol.231
, pp. 61-66
-
-
Forsyth, S.A.1
Gunaratne, H.Q.N.2
Hardacre, C.3
McKeown, A.4
Rooney, D.W.5
Seddon, K.R.6
-
44
-
-
85196433637
-
Method of flavoring food by addition of benzoxepin-3-ones and benzodioxepin-3-ones
-
US 3647479, to Pfizer
-
Beereboom, J.J.; Cameron, D.P.; Stephens, C.R. Method of flavoring food by addition of benzoxepin-3-ones and benzodioxepin-3-ones. US 3647479 1972, to Pfizer.
-
(1972)
-
-
Beereboom, J.J.1
Cameron, D.P.2
Stephens, C.R.3
-
45
-
-
0141960459
-
Conception, characterization and correlation of new marine odorants
-
Kraft, P.; Eichenberger, W. Conception, characterization and correlation of new marine odorants. Eur. J. Org. Chem., 2003, 3753-3743.
-
(2003)
Eur. J. Org. Chem
, pp. 3753-3743
-
-
Kraft, P.1
Eichenberger, W.2
-
46
-
-
34547585786
-
Structure-activity relationship in the domain of odorants having marine notes
-
Gaudin, J.-M.; Nikolaenko, O.; de Saint Laumer, J.-Y.; Winter, B.; Blanc, P. A. Structure-activity relationship in the domain of odorants having marine notes. Helv. Chim. Acta, 2007, 90, 1245-1265.
-
(2007)
Helv. Chim. Acta
, vol.90
, pp. 1245-1265
-
-
Gaudin, J.-M.1
Nikolaenko, O.2
de Saint, L.J.-Y.3
Winter, B.4
Blanc, P.A.5
-
47
-
-
34250703803
-
Synthesis and qualitative olfactory evaluation of benzodioxepine analogues
-
Drevermann, B.; Lingham, A.; Hügel, H.; Marriott, P. Synthesis and qualitative olfactory evaluation of benzodioxepine analogues. Helv. Chim. Acta, 2007, 90, 854-863.
-
(2007)
Helv. Chim. Acta
, vol.90
, pp. 854-863
-
-
Drevermann, B.1
Lingham, A.2
Hügel, H.3
Marriott, P.4
-
48
-
-
34250704316
-
Synthesis of enzodioxepinone analogues via a novel synthetic route with qualitative olfactory evaluation
-
Drevermann, B.; Lingham, A.; Hügel, H.; Marriott, P. Synthesis of enzodioxepinone analogues via a novel synthetic route with qualitative olfactory evaluation. Helv. Chim. Acta, 2007, 90, 1006-1027.
-
(2007)
Helv. Chim. Acta
, vol.90
, pp. 1006-1027
-
-
Drevermann, B.1
Lingham, A.2
Hügel, H.3
Marriott, P.4
-
51
-
-
0034496026
-
Constituents of haitian vetiver oil
-
Weyerstahl, P.; Marshall, H.; Splittgerber, U.; Wolf, D.; Surburg, H. Constituents of haitian vetiver oil. Flavour fragrance J., 2000, 15, 395-412.
-
(2000)
Flavour Fragrance J
, vol.15
, pp. 395-412
-
-
Weyerstahl, P.1
Marshall, H.2
Splittgerber, U.3
Wolf, D.4
Surburg, H.5
-
52
-
-
0000429707
-
Structure of beta-vetivone and related vetivane sesquiterpenes
-
Marshall, J.A.; Johnson, P.C. Structure of beta-vetivone and related vetivane sesquiterpenes. J. Am. Chem. Soc., 1967, 89, 2750-2751
-
(1967)
J. Am. Chem. Soc
, vol.89
, pp. 2750-2751
-
-
Marshall, J.A.1
Johnson, P.C.2
-
53
-
-
0001208691
-
Structure and synthesis of beta-vetivone
-
Marshall, J.A.; Johnson, P.C. Structure and synthesis of beta-vetivone. J. Org. Chem., 1970, 35, 192-196.
-
(1970)
J. Org. Chem
, vol.35
, pp. 192-196
-
-
Marshall, J.A.1
Johnson, P.C.2
-
54
-
-
0001071839
-
Spirovetivanes from fulvenes
-
Büchi, G.; Berthet, D.; Decorzant, R.; Gieder, A.; Hauser, A. Spirovetivanes from fulvenes. J. Org. Chem., 1976, 41, 3208-3209.
-
(1976)
J. Org. Chem
, vol.41
, pp. 3208-3209
-
-
Büchi, G.1
Berthet, D.2
Decorzant, R.3
Gieder, A.4
Hauser, A.5
-
55
-
-
0036413382
-
Design, Synthesis and structure-odor correlation of novel spiro[4.5]-decan-2-ones
-
Kraft, P.; Cadalbert, R. Design, Synthesis and structure-odor correlation of novel spiro[4.5]-decan-2-ones. Synthesis, 2002, 15, 2243-2253.
-
(2002)
Synthesis
, vol.15
, pp. 2243-2253
-
-
Kraft, P.1
Cadalbert, R.2
-
56
-
-
23044496339
-
From Vetiver to Patchouli: Discovery of a newhigh-impact spirocyclic patchouli odorant
-
Kraft, P.; Eichenberger, W.; Frech, D. From Vetiver to Patchouli: Discovery of a newhigh-impact spirocyclic patchouli odorant. Eur. J. Org. Chem. 2005, 3233-3245.
-
(2005)
Eur. J. Org. Chem
, pp. 3233-3245
-
-
Kraft, P.1
Eichenberger, W.2
Frech, D.3
-
57
-
-
0343695055
-
Total synthesis of (±)-patchouli alcohol and (±)-seychellene via a common homoisotwistane intermediate
-
Yamada, K.; Kyotani, Y.; Manabe, S.; Suzuki, M. Total synthesis of (±)-patchouli alcohol and (±)-seychellene via a common homoisotwistane intermediate. Tetrahedron, 1979, 35, 293-298.
-
(1979)
Tetrahedron
, vol.35
, pp. 293-298
-
-
Yamada, K.1
Kyotani, Y.2
Manabe, S.3
Suzuki, M.4
-
58
-
-
33645059935
-
Total synthesis and olfactory evaluation of (1R*,3S*,6S*,7S*,8S*)-3-Hydroxy-6,8-dimethyltricyclo[5.3.1.03,8]undecan-2-one: A new synthetic route to the patchoulol skeleton
-
Kraft, P.; Weymuth, C.; Nussbaumer, C. Total synthesis and olfactory evaluation of (1R*,3S*,6S*,7S*,8S*)-3-Hydroxy-6,8-dimethyltricyclo[5.3.1.03,8]undecan-2-one: A new synthetic route to the patchoulol skeleton. Eur. J. Org. Chem., 2006, 1403-1412.
-
(2006)
Eur. J. Org. Chem
, pp. 1403-1412
-
-
Kraft, P.1
Weymuth, C.2
Nussbaumer, C.3
-
59
-
-
34250635144
-
Ring reversal of a spirocyclic patchouli odorant: Molecular modeling, synthesis, and odor of 6-Hydroxy-1,1,6-trimethylspiro[4.5]decan-7-one
-
Kraft, P.; Bruneau, A. Ring reversal of a spirocyclic patchouli odorant: molecular modeling, synthesis, and odor of 6-Hydroxy-1,1,6-trimethylspiro[4.5]decan-7-one. Eur. J. Org. Chem., 2007, 2257-2267.
-
(2007)
Eur. J. Org. Chem
, pp. 2257-2267
-
-
Kraft, P.1
Bruneau, A.2
-
61
-
-
0032942725
-
Design and synthesis of violet odorants with Bicyclo[6.4.0]dodecene and Bicyclo[5.4.0]undecene Skeletons
-
Kraft, P. Design and synthesis of violet odorants with Bicyclo[6.4.0]dodecene and Bicyclo[5.4.0]undecene Skeletons. Synthesis, 1999, 695-703
-
(1999)
Synthesis
, pp. 695-703
-
-
Kraft, P.1
-
62
-
-
1442359955
-
(-)-(9R,10S)-10-Acetyl-9,10-dimethylbicyclo-[6.4.0]dodec-1(8)-ene: Optical resolution, catalyst systems, derivatives and olfactory properties
-
Kraft, P.; Gallo, S. (-)-(9R,10S)-10-Acetyl-9,10-dimethylbicyclo-[6.4.0]dodec-1(8)-ene: Optical resolution, catalyst systems, derivatives and olfactory properties. Synthesis, 2004, 381-388.
-
(2004)
Synthesis
, pp. 381-388
-
-
Kraft, P.1
Gallo, S.2
-
64
-
-
0037421315
-
Enantioselective perception of chiral odorants
-
Brenna, E.; Fuganti, C.; Serra, S. Enantioselective perception of chiral odorants. Tetrahedron: Asymmetry, 2003, 14, 1-42.
-
(2003)
Tetrahedron: Asymmetry
, vol.14
, pp. 1-42
-
-
Brenna, E.1
Fuganti, C.2
Serra, S.3
-
65
-
-
0001366795
-
Catalytic opportunities in the flavor and fragrance industry
-
Mimoun, H. Catalytic opportunities in the flavor and fragrance industry. Chimia, 1996, 50, 620-625
-
(1996)
Chimia
, vol.50
, pp. 620-625
-
-
Mimoun, H.1
-
66
-
-
0035560640
-
Catalysis in the preparation of fragrances and flavours
-
Chapuis, C.; Jacoby, D. Catalysis in the preparation of fragrances and flavours. Appl. Catal. A: Gen., 2001, 221, 93-117.
-
(2001)
Appl. Catal. A: Gen
, vol.221
, pp. 93-117
-
-
Chapuis, C.1
Jacoby, D.2
-
67
-
-
38049087010
-
Hydrogenation processes in the synthesis of perfumery ingredients
-
Saudan, L. A. Hydrogenation processes in the synthesis of perfumery ingredients. Acc. Chem. Res., 2007, 40, 1309-1319
-
(2007)
Acc. Chem. Res
, vol.40
, pp. 1309-1319
-
-
Saudan, L.A.1
-
68
-
-
52649132403
-
Homogeneous asymmetric catalysis in fragrance chemistry
-
Ciappa, A.; Bovo, S.; Bertoldini, M.; Scrivanti, A.; Matteoli, U. Homogeneous asymmetric catalysis in fragrance chemistry. Chem. Biodiv., 2008, 5, 1058-1069.
-
(2008)
Chem. Biodiv
, vol.5
, pp. 1058-1069
-
-
Ciappa, A.1
Bovo, S.2
Bertoldini, M.3
Scrivanti, A.4
Matteoli, U.5
-
70
-
-
34247158967
-
®
-
®. Tetrahedron Asymmetry, 2007, 18, 797-802.
-
(2007)
Tetrahedron Asymmetry
, vol.18
, pp. 797-802
-
-
Matteoli, U.1
Ciappa, A.2
Bovo, S.3
Bertoldini, M.4
Scrivanti, A.5
-
72
-
-
33751146774
-
Enantioselective protonation of enolates and enols
-
Fehr, C. Enantioselective protonation of enolates and enols. Angew. Chem., Int. Ed., 1996, 35, 2566-2587
-
(1996)
Angew. Chem., Int. Ed
, vol.35
, pp. 2566-2587
-
-
Fehr, C.1
-
73
-
-
0035808857
-
Recent advances into the enantioselective protonation of prostereogenic enol derivatives
-
Eames, J.; Weerasooriya, N. Recent advances into the enantioselective protonation of prostereogenic enol derivatives. Tetrahedron: Asymmetry, 2001, 12, 1-24
-
(2001)
Tetrahedron: Asymmetry
, vol.12
, pp. 1-24
-
-
Eames, J.1
Weerasooriya, N.2
-
74
-
-
9644291545
-
Enantioselective protonations: Fundamental insights and new concepts
-
Duhamel, L.; Duhamel, P.; Plaquevent, J.-C. Enantioselective protonations: fundamental insights and new concepts. Tetrahedron Asymmetry, 2004, 15, 3653-3651
-
(2004)
Tetrahedron Asymmetry
, vol.15
, pp. 3653-3651
-
-
Duhamel, L.1
Duhamel, P.2
Plaquevent, J.-C.3
-
75
-
-
33748361789
-
Catalytic Enantioselective Decarboxylative Protonation
-
Mohr, J.T.; Nishimata, T.; Behenna, D.C.; Stoltz, B.M. Catalytic Enantioselective Decarboxylative Protonation. J. Am. Chem. Soc., 2006, 128, 11348-11349
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 11348-11349
-
-
Mohr, J.T.1
Nishimata, T.2
Behenna, D.C.3
Stoltz, B.M.4
-
76
-
-
22744444589
-
Catalytic asymmetric couplings of ketenes with aldehydes to generate enol esters
-
Schaefer, C.; Fu, G. Catalytic asymmetric couplings of ketenes with aldehydes to generate enol esters. Angew. Chem. Int. Ed., 2005, 44, 4606-4608.
-
(2005)
Angew. Chem. Int. Ed
, vol.44
, pp. 4606-4608
-
-
Schaefer, C.1
Fu, G.2
-
77
-
-
4043131581
-
Efficient Synthesis of (-)-(R)-Muscone by Enantioselective Protonation
-
Fehr, C.; Galindo, J.; Farris, I.; Cuenca, A. Efficient Synthesis of (-)-(R)-Muscone by Enantioselective Protonation. Helv. Chim. Acta, 2004, 87, 1737-1747.
-
(2004)
Helv. Chim. Acta
, vol.87
, pp. 1737-1747
-
-
Fehr, C.1
Galindo, J.2
Farris, I.3
Cuenca, A.4
-
78
-
-
0037083801
-
Synthesis of (-)-Vulcanolide by enantioselective protonation
-
Fehr, C.; Chaptal-Gradoz, N.; Galindo, J. Synthesis of (-)-Vulcanolide by enantioselective protonation. Chem.-Eur. J., 2002, 8, 853-858.
-
(2002)
Chem.-Eur. J
, vol.8
, pp. 853-858
-
-
Fehr, C.1
Chaptal-Gradoz, N.2
Galindo, J.3
-
79
-
-
0000221693
-
Synthesis of (R)-(+)- and (S)-(-)-alpha-damascone by tandem Grignard reaction-enantioselective protonation: Evidence for the intermediacy of a chiral complex
-
Fehr, C.; Galindo, J. Synthesis of (R)-(+)- and (S)-(-)-alpha-damascone by tandem Grignard reaction-enantioselective protonation: evidence for the intermediacy of a chiral complex. J. Am. Chem. Soc., 1988, 110, 6909-6911
-
(1988)
J. Am. Chem. Soc
, vol.110
, pp. 6909-6911
-
-
Fehr, C.1
Galindo, J.2
-
80
-
-
84987587748
-
Efficient Synthesis of Enantiomerically Pure α-Ionone from (R)- and (S) - Damascone
-
Fehr, C.; Guntern, O. Efficient Synthesis of Enantiomerically Pure α-Ionone from (R)- and (S) - Damascone. Helv. Chim. Acta, 1992, 75, 1023-1028.
-
(1992)
Helv. Chim. Acta
, vol.75
, pp. 1023-1028
-
-
Fehr, C.1
Guntern, O.2
-
81
-
-
52649149877
-
Synthetic applications of enantioselective protonation and case study for (S)-α-Damascone
-
Fehr C.; Randall, H. Synthetic applications of enantioselective protonation and case study for (S)-α-Damascone. Chem. Biodiv., 2008, 5, 942-957.
-
(2008)
Chem. Biodiv
, vol.5
, pp. 942-957
-
-
Fehr, C.1
Randall, H.2
-
82
-
-
31944433641
-
Enantioselective Syntheses of georgyone, arborone, and structural relatives. relevance to the molecular-level understanding of olfaction
-
Hong S.; Corey, E.J. Enantioselective Syntheses of georgyone, arborone, and structural relatives. relevance to the molecular-level understanding of olfaction. J. Am. Chem. Soc., 2006, 128, 1346-1352.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 1346-1352
-
-
Hong, S.1
Corey, E.J.2
-
83
-
-
9944265713
-
Synthesis and olfactory properties of (-)-(1R,2S)-Georgywood
-
Fráter, G.; Müller U.; Schröder, F. Synthesis and olfactory properties of (-)-(1R,2S)-Georgywood. Tetrahedron Asymmetry, 2004, 15, 3967-3972.
-
(2004)
Tetrahedron Asymmetry
, vol.15
, pp. 3967-3972
-
-
Fráter, G.1
Müller, U.2
Schröder, F.3
-
84
-
-
58149171608
-
Stereoselective synthesis of woody fragrances related to georgyone and arborone
-
Hicken E.J.; Corey, E.J. Stereoselective synthesis of woody fragrances related to georgyone and arborone. Org. Lett., 2008, 10, 1135-1138.
-
(2008)
Org. Lett
, vol.10
, pp. 1135-1138
-
-
Hicken, E.J.1
Corey, E.J.2
-
85
-
-
0036208861
-
Optically active ionones and derivatives: Preparation and olfactory properties
-
Reviews
-
Reviews: Brenna, E.; Fuganti, C.; Serra, S.; Kraft, P. Optically active ionones and derivatives: preparation and olfactory properties. Eur. J. Org. Chem. 2002, 967-978
-
(2002)
Eur. J. Org. Chem
, pp. 967-978
-
-
Brenna, E.1
Fuganti, C.2
Serra, S.3
Kraft, P.4
-
86
-
-
0042694527
-
Enzyme-mediated syntheses of chiral communication substances: Fragrances for perfumery applications
-
Brenna, E. Enzyme-mediated syntheses of chiral communication substances: Fragrances for perfumery applications. Curr. Org. Chem., 2003, 7, 1347-1367
-
(2003)
Curr. Org. Chem
, vol.7
, pp. 1347-1367
-
-
Brenna, E.1
-
87
-
-
9644303305
-
Lipase-catalysed preparation of enantiomerically enriched odorants
-
Abate, A.; Brenna, E.; Fuganti, C.; Gatti, F.G.; Serra, S. Lipase-catalysed preparation of enantiomerically enriched odorants. J. Mol. Cat. B: Enzym., 2004, 32, 33-51
-
(2004)
J. Mol. Cat. B: Enzym
, vol.32
, pp. 33-51
-
-
Abate, A.1
Brenna, E.2
Fuganti, C.3
Gatti, F.G.4
Serra, S.5
-
88
-
-
39049188162
-
Odor and (Bio)diversity: Single Enantiomers of Chiral Fragrant Substances
-
Abate, A.; Brenna, E.; Fuganti, C.; Gatti, F.G.; Serra, S. Odor and (Bio)diversity: Single Enantiomers of Chiral Fragrant Substances. Chem. Biodiv., 2004, 1, 1888-1898
-
(2004)
Chem. Biodiv
, vol.1
, pp. 1888-1898
-
-
Abate, A.1
Brenna, E.2
Fuganti, C.3
Gatti, F.G.4
Serra, S.5
-
89
-
-
54449084497
-
Applications of biocatalysis in fragrance chemistry: The enantiomers of α-, β-, and γ-irones
-
Brenna, E.; Fuganti C.; Serra, S. Applications of biocatalysis in fragrance chemistry: the enantiomers of α-, β-, and γ-irones. Chem. Soc. Rev., 2009, 37, 2443 -2451.
-
(2009)
Chem. Soc. Rev
, vol.37
, pp. 2443-2451
-
-
Brenna, E.1
Fuganti, C.2
Serra, S.3
-
90
-
-
43049106811
-
Synthesis and olfactory evaluation of all stereoisomers of the fragrance Nectaryl
-
Specific examples
-
Specific examples:Brenna, E.; Fuganti, C.; Gatti, F.G.; Malpezzi, L.; Serra, S. Synthesis and olfactory evaluation of all stereoisomers of the fragrance Nectaryl. Tetrahedron: Asymmetry, 2008, 19, 800-807
-
(2008)
Tetrahedron: Asymmetry
, vol.19
, pp. 800-807
-
-
Brenna, E.1
Fuganti, C.2
Gatti, F.G.3
Malpezzi, L.4
Serra, S.5
-
91
-
-
34249982911
-
The enantiomers of Iralia: Preparation and odour evaluation
-
Abate, A.; Brenna, E.; Fuganti, C.; Malpezzi, L.; Serra, S. The enantiomers of Iralia: Preparation and odour evaluation. Tetrahedron: Asymmetry 2007, 18, 1145-1153
-
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 1145-1153
-
-
Abate, A.1
Brenna, E.2
Fuganti, C.3
Malpezzi, L.4
Serra, S.5
-
92
-
-
33644696397
-
Enzymatic approach to and odor description of the twelve enantiomerically pure isomers of Pelargene
-
Abate, A.; Allievi, M.; Brenna, E.; Fuganti, C.; Gatti, F.G.; Serra, S. Enzymatic approach to and odor description of the twelve enantiomerically pure isomers of Pelargene. Helv. Chim. Acta, 2006, 89, 177-189.
-
(2006)
Helv. Chim. Acta
, vol.89
, pp. 177-189
-
-
Abate, A.1
Allievi, M.2
Brenna, E.3
Fuganti, C.4
Gatti, F.G.5
Serra, S.6
-
93
-
-
13844313024
-
Chirality and Fragrance Chemistry: Stereoisomers of the commercial chiral odorants muguesia and pamplefleur
-
Abate, A.; Brenna, E.; Fuganti, C.; Gatti, F.G.; Giovenzana, T.; Malpezzi, L.; Serra, S. Chirality and Fragrance Chemistry: Stereoisomers of the commercial chiral odorants muguesia and pamplefleur. J. Org. Chem., 2005, 70, 1281-290.
-
(2005)
J. Org. Chem
, vol.70
, pp. 1281-1290
-
-
Abate, A.1
Brenna, E.2
Fuganti, C.3
Gatti, F.G.4
Giovenzana, T.5
Malpezzi, L.6
Serra, S.7
-
94
-
-
61849106493
-
Chemoenzymatic synthesis of optically active Mugetanol isomers: Use of lipases and oxoreductases in fragrance chemistry
-
Vieira, G.A.B.; Lemos, T.L.G.; de Mattos, M.C.; de Oliveira, M.F.; Melo, V.M.M.; de Gonzalo, G.; Gotor-Fernandez, V.; Gotor, V. Chemoenzymatic synthesis of optically active Mugetanol isomers: use of lipases and oxoreductases in fragrance chemistry. Tetrahedron Asymmetry, 2009, 20, 214-219.
-
(2009)
Tetrahedron Asymmetry
, vol.20
, pp. 214-219
-
-
Vieira, G.A.B.1
Lemos, T.L.G.2
de Mattos, M.C.3
de Oliveira, M.F.4
Melo, V.M.M.5
de Gonzalo, G.6
Gotor-Fernandez, V.7
Gotor, V.8
-
95
-
-
84889336887
-
Common fragrances and flavor materials: Preparation, properties, and uses
-
Wiley - VCH: Weinheim
-
Surburg, H.; Panten, J. Common fragrances and flavor materials: preparation, properties, and uses.Wiley - VCH: Weinheim, 2006.
-
(2006)
-
-
Surburg, H.1
Panten, J.2
|