-
1
-
-
0003878417
-
-
Academic Press: New York, NY, USA
-
Brunke, E.J.; Klein, E. Fragrance Chemistry, The Science of the Sense of Smell; Academic Press: New York, NY, USA, 1982; p. 397.
-
(1982)
Fragrance Chemistry, The Science of the Sense of Smell
, pp. 397
-
-
Brunke, E.J.1
Klein E2
-
2
-
-
0003755861
-
Perfumes. art, science and technology
-
London, UK
-
Ohloff, G.; Winter, B.; Fehr, C. Perfumes. Art, Science and Technology; Elsevier Applied Science: London, UK, 1991; p. 287.
-
(1991)
Elsevier Applied Science
, pp. 287
-
-
Ohloff, G.1
Winter, B.2
Fehr, C.3
-
3
-
-
0032474807
-
Fragrance chemistry
-
Fráter, G.; Bajgrowicz, J.A.; Kraft, P. Fragrance chemistry. Tetrahedron 1998, 54, 7633-7703.
-
(1998)
Tetrahedron
, vol.54
, pp. 7633-7703
-
-
Fráter, G.1
Bajgrowicz, J.A.2
Kraft, P.3
-
4
-
-
1542287089
-
Cyclopentene derivatives and their use as odorants
-
US4696766 (Priority 19 March 1986, to Givaudan & CIE)
-
Naipawer, R.E. Cyclopentene derivatives and their use as odorants. US4696766 (Priority 19 March 1986, to Givaudan & CIE); [Chem. Abstr. 1987, 106, 175828].
-
(1987)
Chem. Abstr.
, vol.106
, pp. 175828
-
-
Naipawer, R.E.1
-
5
-
-
24544451207
-
Use of optically active isomers of (E)-3,3-dimethyl-5-(2,2,3-trimethyl-3- cyclopenten-1-yl-)-4-penten-2-ol in perfumery
-
US5512543 (Priority 17 Aug. 1993, to Firmenich S.A.)
-
Chapuis, C.; Gautier, A.; Blanc, P.A. Use of optically active isomers of (E)-3,3-dimethyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl-)-4-penten-2-ol in perfumery. US5512543 (Priority 17 Aug. 1993, to Firmenich S.A.); [Chem. Abstr. 1995, 123, 17516].
-
(1995)
Chem. Abstr.
, vol.123
, pp. 17516
-
-
Chapuis, C.1
Gautier, A.2
Blanc, P.A.3
-
6
-
-
0032100161
-
Synthesis and olfactoric activity of keto-β-santalol and methoxy-β-santalol
-
Buchbauer, G.; Spreitzer, H.; Zechmeister-Machhart, F.; Klinsky, A.; Weiss-Greiler, P.; Wolschann, P. Synthesis and olfactoric activity of keto-b-santalol and methoxy-b-santalol. Eur. J. Med. Chem. 1998, 33, 463-470.
-
(1998)
Eur. J. Med. Chem.
, vol.33
, pp. 463-470
-
-
Buchbauer, G.1
Spreitzer, H.2
Zechmeister-Machhart, F.3
Klinsky, A.4
Weiss-Greiler, P.5
Wolschann, P.6
-
7
-
-
9644268879
-
Structure-activity relationships of sandalwood odorants: Synthesis and odor of tricyclo β-santalol
-
Buchbauer, G.; Stappen, I.; Pretterklieber, C.; Wolschann, P. Structure-activity relationships of sandalwood odorants: synthesis and odor of tricyclo b-santalol. Eur. J. Med. Chem. 2004, 39, 1039-1046.
-
(2004)
Eur. J. Med. Chem.
, vol.39
, pp. 1039-1046
-
-
Buchbauer, G.1
Stappen, I.2
Pretterklieber, C.3
Wolschann, P.4
-
8
-
-
4043147734
-
Enantioselectivity in odor perception synthesis and olfactory properties of the new tricyclic sandalwood odorant Fleursandol
-
Hölscher, B.; Braun, N.A.; Weber, B.; Kappey, C.H.; Meier, M.; Pickenhagen, W. Enantioselectivity in odor perception synthesis and olfactory properties of the new tricyclic sandalwood odorant Fleursandol. Helv. Chim. Acta 2004, 87, 1666-1680.
-
(2004)
Helv. Chim. Acta
, vol.87
, pp. 1666-1680
-
-
Hölscher, B.1
Braun, N.A.2
Weber, B.3
Kappey, C.H.4
Meier, M.5
Pickenhagen, W.6
-
9
-
-
25844523169
-
Scents and sensibility: A molecular logic of olfactory perception (Nobel lecture)
-
Axel, R. Scents and sensibility: A molecular logic of olfactory perception (Nobel Lecture). Angew. Chem. Int. Ed. 2005, 44, 6111-6127.
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 6111-6127
-
-
Axel, R.1
-
10
-
-
25844436982
-
Unraveling the sense of smell (Nobel lecture)
-
Buck, L. Unraveling the sense of smell (Nobel Lecture). Angew. Chem. Int. Ed. 2005, 44, 6128-6140.
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 6128-6140
-
-
Buck, L.1
-
11
-
-
0000416894
-
Conformational parameters of the sandalwood-odor activity: Conformational calculations on sandalwood odor. Part X
-
Buchbauer, G.; Hillisch, A.; Mraz, K.; Wolschann, P. Conformational parameters of the sandalwood-odor activity: conformational calculations on sandalwood odor. Part X. Helv. Chim. Acta 1994, 77, 2286-2296.
-
(1994)
Helv. Chim. Acta
, vol.77
, pp. 2286-2296
-
-
Buchbauer, G.1
Hillisch, A.2
Mraz, K.3
Wolschann, P.4
-
12
-
-
0000819682
-
Synthesis and structure elucidation of a new potent sandalwood-oil substitute
-
Bajgrowicz, J.A.; Frank, I.; Fráter, G. Synthesis and structure elucidation of a new potent sandalwood-oil substitute. Helv. Chim. Acta 1998, 81, 1349-1358.
-
(1998)
Helv. Chim. Acta
, vol.81
, pp. 1349-1358
-
-
Bajgrowicz, J.A.1
Frank, I.2
Fráter, G.3
-
13
-
-
69549131953
-
Preparation of formylpinanes for fragrances
-
WO9311094 (Priority 5 December 1991, to Givaudan-Roure)
-
Auger, B.; Bajgrowicz, J.A.; Giraudi, E. Preparation of formylpinanes for fragrances. WO9311094 (Priority 5 December 1991, to Givaudan-Roure); [Chem. Abstr. 1993, 119, 146389].
-
(1993)
Chem. Abstr.
, vol.119
, pp. 146389
-
-
Auger, B.1
Bajgrowicz, J.A.2
Giraudi, E.3
-
14
-
-
24544481758
-
Preparation of 3,3-dimethyl-5-(2,2,3-trimethyl-3-cyclohexenyl)-4-penten- 2-ol enantiomers and analogs as perfume fragrances
-
EP572797 (Priority 2 June 1992, to Firmenich)
-
Chapuis, C. Preparation of 3,3-dimethyl-5-(2,2,3-trimethyl-3- cyclohexenyl)-4-penten-2-ol enantiomers and analogs as perfume fragrances. EP572797 (Priority 2 June 1992, to Firmenich); [Chem. Abstr. 1994, 121, 83680].
-
(1994)
Chem. Abstr.
, vol.121
, pp. 83680
-
-
Chapuis, C.1
-
15
-
-
0000462492
-
Investigation of the relationship between sandalwood odor and chemical structure: Electrontopological approach
-
Dimoglo, A.S.; Beda, A.A.; Shvets, N.M.; Gorvachov, M.Y.; Kheifits, L.A.; Aulchenko, I.S. Investigation of the relationship between sandalwood odor and chemical structure: Electrontopological approach. New J. Chem. 1995, 19, 149-154.
-
(1995)
New J. Chem.
, vol.19
, pp. 149-154
-
-
Dimoglo, A.S.1
Beda, A.A.2
Shvets, N.M.3
Gorvachov, M.Y.4
Kheifits, L.A.5
Aulchenko, I.S.6
-
16
-
-
0033551749
-
Synthesis of syn-and antiepoxides of α-campholenic and fencholenic derivatives
-
Wahren, U.; Sprung, I.; Schulze, K.; Findensen, M.; Buchbauer, G. Synthesis of syn- and antiepoxides of a-campholenic and fencholenic derivatives. Tetrahedron Lett. 1999, 40, 5991-5992.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 5991-5992
-
-
Wahren, U.1
Sprung, I.2
Schulze, K.3
Findensen, M.4
Buchbauer, G.5
-
17
-
-
69549121237
-
3-(3,3,5-Trimethylcyclohexyloxy)-1-propanols and perfume compositions containing them
-
JP 7165655 (Priority 8 December 1993, to Kao)
-
Ono, S.; Etsuno, J.; Fukuda, K.; Toi, S.; Fujikura, Y. 3-(3,3,5-Trimethylcyclohexyloxy)-1- propanols and perfume compositions containing them. JP 7165655 (Priority 8 December 1993, to Kao); [Chem. Abstr. 1995, 123, 208525].
-
(1995)
Chem. Abstr.
, vol.123
, pp. 208525
-
-
Ono, S.1
Etsuno, J.2
Fukuda, K.3
Toi, S.4
Fujikura, Y.5
-
18
-
-
0000636575
-
Aroma chemical syntheses with fencholenic aldehyde
-
Schulze, K.; Uhlig, H. Aroma chemical syntheses with fencholenic aldehyde. Monatsh. Chem. 1989, 120, 547-559.
-
(1989)
Monatsh. Chem.
, vol.120
, pp. 547-559
-
-
Schulze, K.1
Uhlig, H.2
-
19
-
-
33746159920
-
Synthesis and odor evaluation of stereoisomers of octahydrobenzopyran derivatives
-
Linares-Palomino, P.J.; Salido, S.; Altarejos, J.; Nogueras, M.; Sánchez, A. Synthesis and odor evaluation of stereoisomers of octahydrobenzopyran derivatives. Flavour Fragr. J. 2006, 21, 659-666.
-
(2006)
Flavour Fragr. J.
, vol.21
, pp. 659-666
-
-
Linares-Palomino, P.J.1
Salido, S.2
Altarejos, J.3
Nogueras, M.4
Sánchez, A.5
-
20
-
-
0042671133
-
Chlorosulfonic acid as a convenient electrophilic olefin cyclization agent
-
Linares-Palomino, P.J.; Salido, S.; Altarejos, J.; Sánchez, A. Chlorosulfonic acid as a convenient electrophilic olefin cyclization agent. Tetrahedron Lett. 2003, 44, 6651-6655.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 6651-6655
-
-
Linares-Palomino, P.J.1
Salido, S.2
Altarejos, J.3
Sánchez, A.4
-
21
-
-
0037100285
-
Synthesis of Ambrox from labdanolic acid
-
Castro, J.M.; Salido, S.; Altarejos, J.; Nogueras, M.; Sánchez, A. Synthesis of Ambrox from labdanolic acid. Tetrahedron 2002, 58, 5941-5949.
-
(2002)
Tetrahedron
, vol.58
, pp. 5941-5949
-
-
Castro, J.M.1
Salido, S.2
Altarejos, J.3
Nogueras, M.4
Sánchez, A.5
-
22
-
-
1542332375
-
Synthesis of Polysantol and related sandalwood-type odorants using magnesium a-bromoketone enolates
-
Castro, J.M.; Linares-Palomino, P.J.; Salido, S.; Altarejos, J.; Nogueras, M.; Sánchez, A. Synthesis of Polysantol and related sandalwood-type odorants using magnesium a-bromoketone enolates. Tetrahedron Lett. 2004, 45, 2619-2622.
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 2619-2622
-
-
Castro, J.M.1
Linares-Palomino, P.J.2
Salido, S.3
Altarejos, J.4
Nogueras, M.5
Sánchez, A.6
-
23
-
-
27144527334
-
Enantiospecific synthesis, separation and olfactory evaluation of all diastereomers of a homologue of the sandalwood odorant Polysantol
-
Castro, J.M.; Linares-Palomino, P.J.; Salido, S.; Altarejos, J.; Nogueras, M.; Sánchez, A. Enantiospecific synthesis, separation and olfactory evaluation of all diastereomers of a homologue of the sandalwood odorant Polysantol. Tetrahedron 2005, 61, 11192-11203.
-
(2005)
Tetrahedron
, vol.61
, pp. 11192-11203
-
-
Castro, J.M.1
Linares-Palomino, P.J.2
Salido, S.3
Altarejos, J.4
Nogueras, M.5
Sánchez, A.6
-
24
-
-
69549121236
-
Preparation of a novel odorant with sandalwood fragrance
-
WO 2008092981 (Priority 31 January 2007, to University of Jaén)
-
Chapado, L.; Linares-Palomino, P.J.; Salido, S.; Nogueras, M.; Sánchez, A; Altarejos, J. Preparation of a novel odorant with sandalwood fragrance. WO 2008092981 (Priority 31 January 2007, to University of Jaén); [Chem. Abstr. 2008, 149, 246672].
-
(2008)
Chem. Abstr.
, vol.149
, pp. 246672
-
-
Chapado, L.1
Linares-Palomino, P.J.2
Salido, S.3
Nogueras, M.4
Sánchez A5
Altarejos, J.6
-
25
-
-
33746795550
-
Syntheses and odor of "bulky group"-modified sandalwood odorants: Isophorono-β-santalol analogues
-
and references cited therein
-
Höfinghoff, J.; Buchbauer, G.; Holzer, W.; Wolschann, P. Syntheses and odor of "bulky group"- modified sandalwood odorants: isophorono-β-santalol analogues. Eur. J. Med. Chem. 2006, 41, 905-913, and references cited therein.
-
(2006)
Eur. J. Med. Chem.
, vol.41
, pp. 905-913
-
-
Höfinghoff, J.1
Buchbauer, G.2
Holzer, W.3
Wolschann, P.4
-
26
-
-
69549130195
-
-
(1R)-(-)-Nopol is a commercially available compound, but it can be prepared by reaction of b- pinene with formaldehyde [28]
-
(1R)-(-)-Nopol is a commercially available compound, but it can be prepared by reaction of b- pinene with formaldehyde [28].
-
-
-
-
27
-
-
69549130194
-
Preparation of cis-dihydronopol
-
EP406742 (Priority 7 July 1989, to Kali-Chemie Pharma GmbH)
-
Heitmann, W.; Mätzel, U. Preparation of cis-dihydronopol. EP406742 (Priority 7 July 1989, to Kali-Chemie Pharma GmbH); [Chem. Abstr. 1991, 114, 164560].
-
(1991)
Chem. Abstr.
, vol.114
, pp. 164560
-
-
Heitmann, W.1
Mätzel, U.2
-
28
-
-
33947468237
-
Stereospecific hydrogenation of a-pinene derivatives
-
Eigenmann, G.W.; Arnold, R.T. Stereospecific hydrogenation of a-pinene derivatives. J. Am. Chem. Soc. 1959, 81, 3440-3442.
-
(1959)
J. Am. Chem. Soc.
, vol.81
, pp. 3440-3442
-
-
Eigenmann, G.W.1
Arnold, R.T.2
-
29
-
-
2042524507
-
Useful procedures for the oxidation of alcohols involving pyridinium dichromate in aprotic media
-
Corey, E.J.; Schmidt, G. Useful procedures for the oxidation of alcohols involving pyridinium dichromate in aprotic media. Tetrahedron Lett. 1979, 20, 399-402.
-
(1979)
Tetrahedron Lett.
, vol.20
, pp. 399-402
-
-
Corey, E.J.1
Schmidt, G.2
-
30
-
-
69549097122
-
-
We also obtained cis-dihydronopol (17) by hydrogenation of nopol (1 g) in absolute MeOH (50 mL) over Raney-Ni (1.5 g) under pressure of H2 gas on a hydrogenation apparatus for 48 h. The GC analysis indicated a conversion of ca. 82% [24]
-
We also obtained cis-dihydronopol (17) by hydrogenation of nopol (1 g) in absolute MeOH (50 mL) over Raney-Ni (1.5 g) under pressure of H2 gas on a hydrogenation apparatus for 48 h. The GC analysis indicated a conversion of ca. 82% [24].
-
-
-
-
31
-
-
0031510479
-
13C NMR spectra of trans- and cismyrtanol
-
Kim, K.Y.; Lee, S.G. Complete assignment of 1H and 13C NMR spectra of trans- and cismyrtanol. Magn. Reson. Chem. 1997, 35, 451-454.
-
(1997)
Magn. Reson. Chem.
, vol.35
, pp. 451-454
-
-
Kim, K.Y.1
Lee, S.G.2
-
32
-
-
84989093822
-
Structural studies in the bicyclo[3.1.1]heptane series by proton and carbon-13 NMR
-
Badjah-Hadj-Ahmed, A.Y.; Meklati, B.Y.; Waton, H.; Pham, Q.T. Structural studies in the bicyclo[3.1.1]heptane series by proton and carbon-13 NMR. Magn. Reson. Chem. 1992, 30, 807-816.
-
(1992)
Magn. Reson. Chem.
, vol.30
, pp. 807-816
-
-
Badjah-Hadj-Ahmed, A.Y.1
Meklati, B.Y.2
Waton, H.3
Pham, Q.T.4
-
33
-
-
0030574609
-
Catalytic hydroformylation of (1S,5S)-(-)- and (1R,5R)-(+)-β-pinene: stereoselective synthesis and spectroscopic characterization of (1S,2R,5S)-, (1S,2S,5S)-, (1R,2R,5R)- and (1R,2S,5R)-10-formylpinane
-
Azzaroni, F.; Biscarini, P.; Bordoni, S.; Longoni, G.; Venturini, E. Catalytic hydroformylation of (1S,5S)-(-)- and (1R,5R)-(+)-b-pinene: stereoselective synthesis and spectroscopic characterization of (1S,2R,5S)-, (1S,2S,5S)-, (1R,2R,5R)- and (1R,2S,5R)-10-formylpinane. J. Organomet. Chem. 1996, 508, 59-67.
-
(1996)
J. Organomet. Chem.
, vol.508
, pp. 59-67
-
-
Azzaroni, F.1
Biscarini, P.2
Bordoni, S.3
Longoni, G.4
Venturini, E.5
-
34
-
-
69549125615
-
Oxides of some of a,b-unsaturated ketones with branched chains
-
Tishchenko, I.G.; Bubel, O.N.; Kovaleva, A.F. Oxides of some of a,b-unsaturated ketones with branched chains. Zhur. Org. Khim. 1965, 1, 869-873;
-
(1965)
Zhur. Org. Khim.
, vol.1
, pp. 869-873
-
-
Tishchenko, I.G.1
Bubel, O.N.2
Kovaleva, A.F.3
-
35
-
-
69549128935
-
-
[Chem. Abstr. 1965, 63, 38927].
-
(1965)
Chem. Abstr.
, vol.63
, pp. 38927
-
-
-
36
-
-
27144500205
-
3-Methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pentan-2-ol compound and perfume compositions
-
US4052341 (Priority 29 April 1976, to Givaudan Corp.)
-
Naipawer, R.E.; Easter, W.M. 3-Methyl-5-(2,2,3-trimethylcyclopent-3-en-1- yl)pentan-2-ol compound and perfume compositions. US4052341 (Priority 29 April 1976, to Givaudan Corp.); [Chem. Abstr. 1978, 88, 22229].
-
(1978)
Chem. Abstr.
, vol.88
, pp. 22229
-
-
Naipawer, R.E.1
Easter, W.M.2
-
37
-
-
0037907301
-
Stereoselective synthesis of (Z)-α,β-unsaturated ketones via hydromagnesiation of alkynylsilanes
-
Zhao, H.; Cai, M.Z. Stereoselective synthesis of (Z)-a,b-unsaturated ketones via hydromagnesiation of alkynylsilanes. Synth. Commun. 2003, 33, 1643-1650.
-
(2003)
Synth. Commun.
, vol.33
, pp. 1643-1650
-
-
Zhao, H.1
Cai, M.Z.2
-
38
-
-
84986984366
-
Synthesis of α,β-unsaturated carbonyl compounds by titanium tetraalkoxide-induced aldol condensation under neutral conditions
-
Mahrwald, R.; Schick, H. Synthesis of a,b-unsaturated carbonyl compounds by titanium tetraalkoxide-induced aldol condensation under neutral conditions. Synthesis 1990, 7, 592-595.
-
(1990)
Synthesis
, vol.7
, pp. 592-595
-
-
Mahrwald, R.1
Schick, H.2
-
39
-
-
69549125288
-
-
Together with compound 20, the a,β-unsaturated aldehyde, (Z)-2-pentylnon-2-enal (21) was obtained (24% yield) [37]. Despite the molar excess of butanone over heptanal (4:1), the reaction between two molecules of the aldehyde 13 was also feasible. This type of by-product (aldol self condensation), also observed in the case of phenylacetaldehyde (15), is largely due to the wellknown acid-base equilibrium established between heptanal (13) and the enolate ion of butanone
-
Together with compound 20, the a,β-unsaturated aldehyde, (Z)-2-pentylnon-2-enal (21) was obtained (24% yield) [37]. Despite the molar excess of butanone over heptanal (4:1), the reaction between two molecules of the aldehyde 13 was also feasible. This type of by-product (aldol self condensation), also observed in the case of phenylacetaldehyde (15), is largely due to the wellknown acid-base equilibrium established between heptanal (13) and the enolate ion of butanone.
-
-
-
-
40
-
-
2542458777
-
Synthesis and sensorial properties of 2-alkylalk-2-enals and 3-(acetylthio)-2-alkyl alkanals
-
Robert, F.; Héritier, J.; Quiquerez, J.; Simian, H.; Blank, I. Synthesis and sensorial properties of 2-alkylalk-2-enals and 3-(acetylthio)-2-alkyl alkanals. J. Agric. Food Chem. 2004, 52, 3525-3529.
-
(2004)
J. Agric. Food Chem.
, vol.52
, pp. 3525-3529
-
-
Robert, F.1
Héritier, J.2
Quiquerez, J.3
Simian, H.4
Blank, I.5
-
41
-
-
0013602013
-
A modified Wittig synthesis of 6,10-dimethyl-3,9-undecadien-2-one, ethyl 5,9-dimethyl-2,8-decadienonate, and their α-alkyl homologs: stereochemistry of the reaction and conformation of the products
-
Sasaki, K. A modified Wittig synthesis of 6,10-dimethyl-3,9-undecadien-2- one, ethyl 5,9-dimethyl-2,8-decadienonate, and their a-alkyl homologs: stereochemistry of the reaction and conformation of the products. Bull. Chem. Soc. Jpn. 1968, 41, 1252-1254.
-
(1968)
Bull. Chem. Soc. Jpn.
, vol.41
, pp. 1252-1254
-
-
Sasaki, K.1
-
42
-
-
69549128936
-
Cyclization of 6,10-dimethyl-3,9-undecadien-2-one and its homologs by concentrated phosphoric acid
-
Sasaki, K. Cyclization of 6,10-dimethyl-3,9-undecadien-2-one and its homologs by concentrated phosphoric acid. Nippon Kagaku Zasshi 1968, 89, 1140-1141;
-
(1968)
Nippon Kagaku Zasshi
, vol.89
, pp. 1140-1141
-
-
Sasaki, K.1
-
43
-
-
69549109476
-
-
[Chem. Abstr. 1969, 70, 87446].
-
(1969)
Chem. Abstr.
, vol.70
, pp. 87446
-
-
-
44
-
-
17044419509
-
Dehydration of a,b-ethylenic 1,2-diols. IV. Role of the stereomutation of α-hydroxyl allylic carbocations on the orientation of observed reactions
-
Dana, G.; Gharbi-Benarous, J.; Thuan, S.L.T. Dehydration of a,b-ethylenic 1,2-diols. IV. Role of the stereomutation of a-hydroxyl allylic carbocations on the orientation of observed reactions. Can. J. Chem. 1980, 58, 1451-1462.
-
(1980)
Can. J. Chem.
, vol.58
, pp. 1451-1462
-
-
Dana, G.1
Gharbi-Benarous, J.2
Thuan, S.L.T.3
-
45
-
-
33845279922
-
Trisubstituted stannyllithium as a double electron equivalent. Reaction with α,β-enones
-
Sato, T.; Watanabe, M.; Watanabe, T.; Onoda, Y.; Murayama, E. Trisubstituted stannyllithium as a double electron equivalent. Reaction with a,b-enones. J. Org. Chem. 1988, 53, 1894-1899.
-
(1988)
J. Org. Chem.
, vol.53
, pp. 1894-1899
-
-
Sato, T.1
Watanabe, M.2
Watanabe, T.3
Onoda, Y.4
Murayama, E.5
-
46
-
-
0000882747
-
A Tandem epoxide isomerization-aldol condensation process catalyzed by palladium acetate-tributylphosphine
-
and references cited therein
-
Kim, J.H.; Kulawiec, R.J. A Tandem epoxide isomerization-aldol condensation process catalyzed by palladium acetate-tributylphosphine. J. Org. Chem. 1996, 61, 7656-7657, and references cited therein.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 7656-7657
-
-
Kim, J.H.1
Kulawiec, R.J.2
-
47
-
-
69549143351
-
-
The presence of the β,?-unsaturated ketone 25, along with the desired 24 (24:25; 4:1) was not necessarily a drawback, since it was also a suitable reactant for the subsequent deconjugative a- methylation step. For that reason no chromatographic separation was undertaken. Furthermore, the NMR data of both isomers 24 and 25 agree with those already reported [46]
-
The presence of the β,?-unsaturated ketone 25, along with the desired 24 (24:25; 4:1) was not necessarily a drawback, since it was also a suitable reactant for the subsequent deconjugative a- methylation step. For that reason no chromatographic separation was undertaken. Furthermore, the NMR data of both isomers 24 and 25 agree with those already reported [46].
-
-
-
-
48
-
-
0000436592
-
Carbon-carbon bond forming reactions of h3-allyl iron tricarbonyl anions with carbon electrophiles
-
Chang, S.; Yoon, J.; Brookhart, M. Carbon-carbon bond forming reactions of h3-allyl iron tricarbonyl anions with carbon electrophiles. J. Am. Chem. Soc. 1994, 116, 1869-1879.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 1869-1879
-
-
Chang, S.1
Yoon, J.2
Brookhart, M.3
-
49
-
-
69549131952
-
Use of methylsubstituted pinyl oxopentenes, for augmenting, enhancing or modifying the aroma or taste of smoking tobacco and smoking tobacco articles
-
US4428387 (Priority 26 March 1982, to IFF)
-
Mookherjee, B.D.; Trenkle, R.W.; Wolff, R.K.; Boden, R.M.; Yoshida, T. Use of methylsubstituted pinyl oxopentenes, for augmenting, enhancing or modifying the aroma or taste of smoking tobacco and smoking tobacco articles. US4428387 (Priority 26 March 1982, to IFF); [Chem. Abstr. 1984, 101, 20773].
-
(1984)
Chem. Abstr.
, vol.101
, pp. 20773
-
-
Mookherjee, B.D.1
Trenkle, R.W.2
Wolff, R.K.3
Boden, R.M.4
Yoshida, T.5
-
50
-
-
1542287089
-
Cyclopentene derivatives and their use as odorants
-
EP0203528 (Priority 31 May 1985, to Givaudan & CIE)
-
Naipawer, R.E. Cyclopentene derivatives and their use as odorants. EP0203528 (Priority 31 May 1985, to Givaudan & CIE); [Chem. Abstr. 1986, 106, 175828].
-
(1986)
Chem. Abstr.
, vol.106
, pp. 175828
-
-
Naipawer, R.E.1
-
51
-
-
0003473238
-
Preparation of optically pure isomers of campholenic aldehyde derivatives for use as detergent fragrances
-
EP0841318 (Priority 6 November 1996, to Givaudan-Roure)
-
Bajgrowicz, J.A.; Fráter, G. Preparation of optically pure isomers of campholenic aldehyde derivatives for use as detergent fragrances. EP0841318 (Priority 6 November 1996, to Givaudan-Roure); [Chem. Abstr. 1998, 129, 28103].
-
(1998)
Chem. Abstr.
, vol.129
, pp. 28103
-
-
Bajgrowicz, J.A.1
Fráter, G.2
-
52
-
-
28744451534
-
Novel Oxa-di-p-methane and Norrish type I reactions in the S2 (π,π*) excited state of a series of β,γ-unsaturated ketones
-
Armesto, D.; Ortiz, M.J.; Agarrabeitia, A.R.; Martín-Fontecha, M. Novel Oxa-di-p -methane and Norrish type I reactions in the S2 (p,p*) excited state of a series of b,g-unsaturated ketones. Org. Lett. 2005, 7, 2687-2690.
-
(2005)
Org. Lett.
, vol.7
, pp. 2687-2690
-
-
Armesto, D.1
Ortiz, M.J.2
Agarrabeitia, A.R.3
Martín-Fontecha, M.4
-
53
-
-
0027943932
-
Meerwein-Ponndorf-Verley reductions and Oppenauer oxidations: An integrated approach
-
de Graauw, C.F.; Peters, J.A.; van Bekkum, H.; Huskeus, J. Meerwein-Ponndorf-Verley reductions and Oppenauer oxidations: an integrated approach. Synthesis 1994, 10, 1007-1017.
-
(1994)
Synthesis
, vol.10
, pp. 1007-1017
-
-
De Graauw, C.F.1
Peters, J.A.2
Van Bekkum, H.3
Huskeus, J.4
-
54
-
-
0035991222
-
The creation of a database of odorous compounds focused on molecular rigidity and analysis of the molecular features of the compounds in the database
-
Yoshii, F.; Yamada, Y.; Hoshy, T.; Hagiwara, H. The creation of a database of odorous compounds focused on molecular rigidity and analysis of the molecular features of the compounds in the database. Chem. Senses 2002, 27, 399-405.
-
(2002)
Chem. Senses
, vol.27
, pp. 399-405
-
-
Yoshii, F.1
Yamada, Y.2
Hoshy, T.3
Hagiwara, H.4
|