-
1
-
-
0027995010
-
Potato micro-tuber inducing substances from Lasiodiplodia teobromae
-
Nakamori, K.; Matsuura, H.; Yoshihara, T.; Ichihara, A.; Koda, Y. Potato micro-tuber inducing substances from Lasiodiplodia teobromae. Phytochemistry 1994, 35, 835-839.
-
(1994)
Phytochemistry
, vol.35
, pp. 835-839
-
-
Nakamori, K.1
Matsuura, H.2
Yoshihara, T.3
Ichihara, A.4
Koda, Y.5
-
2
-
-
0034438186
-
Induction of plant tubers and flower buds under noninducing photoperiod conditions by a natural product, theobroxide
-
Yoshihara, T.; Ohmori, F.; Nakamori, K.; Amanuma, M.; Tsutsumi, T.; Ichihara, A.; Matsuura, H. Induction of plant tubers and flower buds under noninducing photoperiod conditions by a natural product, theobroxide. J. Plant Growth Regul. 2000, 19, 457-461.
-
(2000)
J. Plant Growth Regul.
, vol.19
, pp. 457-461
-
-
Yoshihara, T.1
Ohmori, F.2
Nakamori, K.3
Amanuma, M.4
Tsutsumi, T.5
Ichihara, A.6
Matsuura, H.7
-
3
-
-
0028912641
-
The enantiodivergent total synthesis of natural and unnatural enantiomers of theobroxide
-
Kamikubo, T.; Ogasawara, K. The enantiodivergent total synthesis of natural and unnatural enantiomers of theobroxide. Tetrahedron Lett. 1995, 36, 1685-1688.
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 1685-1688
-
-
Kamikubo, T.1
Ogasawara, K.2
-
4
-
-
85046528671
-
The first synthesis of (-)-asperpentyn and efficient syntheses of (+)-harveynone, (+)-epiepoformin and (-)-theobroxide
-
Barros, M. T.; Maycock, C. D.; Ventura, M. R. The first synthesis of (-)-asperpentyn and efficient syntheses of (+)-harveynone, (+)-epiepoformin and (-)-theobroxide. Chem. Eur. J. 2000, 6, 3991-3996.
-
(2000)
Chem. Eur. J.
, vol.6
, pp. 3991-3996
-
-
Barros, M.T.1
Maycock, C.D.2
Ventura, M.R.3
-
5
-
-
0035802999
-
Synthesis of (+)-epiepoformin using the base-catalyzed Diels - Alder reaction of 3-hydroxy-2-pyrone
-
Shimizu, H.; Okamura, H.; Yamashita, N.; Iwagawa, T.; Nakatani, M. Synthesis of (+)-epiepoformin using the base-catalyzed Diels - Alder reaction of 3-hydroxy-2-pyrone. Tetrahedron Lett. 2001, 42, 8649-8651.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 8649-8651
-
-
Shimizu, H.1
Okamura, H.2
Yamashita, N.3
Iwagawa, T.4
Nakatani, M.5
-
6
-
-
0037416957
-
Total synthesis of (+)-epiepoformin, (+)-epiepoxydon and (+)-bromoxone employing a useful chiral building block, ethyl (1R,2S)-5,5-ethylenedioxy-2-hydroxycyclohexanecarboxylate
-
Tachihara, T.; Kitahara, T. Total synthesis of (+)-epiepoformin, (+)-epiepoxydon and (+)-bromoxone employing a useful chiral building block, ethyl (1R,2S)-5,5-ethylenedioxy-2-hydroxycyclohexanecarboxylate. Tetrahedron 2003, 59, 1773-1780.
-
(2003)
Tetrahedron
, vol.59
, pp. 1773-1780
-
-
Tachihara, T.1
Kitahara, T.2
-
7
-
-
0033954172
-
New stereoselective route to the epoxyquinol core of manumycin-type natural products, synthesis of enantiopure (+)-bromoxone, (-)-LL-C10037 alpha, and (+)-KT 8110
-
Block, O.; Klein, G.; Altenbach, H. J.; Brauer, D. J. New stereoselective route to the epoxyquinol core of manumycin-type natural products, synthesis of enantiopure (+)-bromoxone, (-)-LL-C10037 alpha, and (+)-KT 8110. J. Org. Chem. 2000, 65, 716-721.
-
(2000)
J. Org. Chem.
, vol.65
, pp. 716-721
-
-
Block, O.1
Klein, G.2
Altenbach, H.J.3
Brauer, D.J.4
-
8
-
-
0028823790
-
2 symmetrical diol derived from p-benzoquinone-Synthesis of (+)-bromoxone and (-)-bromoxone
-
2 symmetrical diol derived from p-benzoquinone-Synthesis of (+)-bromoxone and (-)-bromoxone. J. Org. Chem. 1995, 60, 6674-6675.
-
(1995)
J. Org. Chem.
, vol.60
, pp. 6674-6675
-
-
Johnson, C.R.1
Miller, M.W.2
-
10
-
-
0017318075
-
Sym-Oxepin oxide
-
Rastetter, W. H. sym-Oxepin oxide. J. Am. Chem. Soc. 1976, 98, 6350-6353.
-
(1976)
J. Am. Chem. Soc.
, vol.98
, pp. 6350-6353
-
-
Rastetter, W.H.1
-
11
-
-
0000267821
-
Chemistry of singlet oxygen. IV. Oxygenations with hypochlorite-hydrogen peroxide
-
Foote, C. S.; Wexler, S.; Ando, W.; Higgins, R. Chemistry of singlet oxygen. IV. Oxygenations with hypochlorite-hydrogen peroxide. J. Am. Chem. Soc. 1968, 90, 975-981.
-
(1968)
J. Am. Chem. Soc.
, vol.90
, pp. 975-981
-
-
Foote, C.S.1
Wexler, S.2
Ando, W.3
Higgins, R.4
-
12
-
-
0036967985
-
Trapping of benzene oxide-oxepin and methyl-substituted derivatives with 4-phenyl- And 4-pentafluorophenyl-1,2,4-triazoline-3,5-dione
-
It was shown that dienophiles approach the diene portion of arene oxide and to the epoxide moiety. See: Henderson, A. P.; Mutlu, E.; Leclercq, A.; Bleasdale, C.; Clegg, W.; Henderson, R. A.; Golding, B. T. Trapping of benzene oxide-oxepin and methyl-substituted derivatives with 4-phenyl- and 4-pentafluorophenyl-1,2,4-triazoline-3,5-dione. Chem. Commun. 2002, 1956-1957.
-
(2002)
Chem. Commun.
, pp. 1956-1957
-
-
Henderson, A.P.1
Mutlu, E.2
Leclercq, A.3
Bleasdale, C.4
Clegg, W.5
Henderson, R.A.6
Golding, B.T.7
-
13
-
-
33847086328
-
Trapping of benzene oxide-oxepin and methyl-substituted derivatives with 4-phenyl- And 4-pentafluorophenyl-1,2,4-triazoline-3,5-dione
-
Hayes, D. M.; Nelson, S. D.; Garland, W. A.; Kollman, P. A. Trapping of benzene oxide-oxepin and methyl-substituted derivatives with 4-phenyl- and 4-pentafluorophenyl-1,2,4-triazoline-3,5-dione. J. Am. Chem. Soc. 1980, 102, 1255-1362.
-
(1980)
J. Am. Chem. Soc.
, vol.102
, pp. 1255-1362
-
-
Hayes, D.M.1
Nelson, S.D.2
Garland, W.A.3
Kollman, P.A.4
-
14
-
-
0013195385
-
Examination of the valence tautomers benzene oxide and oxepin and two derivative systems by ab initio methods
-
Pye, C. C.; Xidos, J. D.; Poirier, R. A.; Burnell, D. J. Examination of the valence tautomers benzene oxide and oxepin and two derivative systems by ab initio methods. J. Phys. Chem. A 1997, 101, 3371-3376.
-
(1997)
J. Phys. Chem. A
, vol.101
, pp. 3371-3376
-
-
Pye, C.C.1
Xidos, J.D.2
Poirier, R.A.3
Burnell, D.J.4
-
15
-
-
0001496354
-
Addition of singlet oxygen to arene oxides
-
Foster, C. H.; Berchtold, G. A. Addition of singlet oxygen to arene oxides. J. Org. Chem. 1975, 40, 3743-3746.
-
(1975)
J. Org. Chem.
, vol.40
, pp. 3743-3746
-
-
Foster, C.H.1
Berchtold, G.A.2
-
16
-
-
0000151805
-
Oxidations of thioureas with photochemically generated singlet oxygen
-
In the presence of thiourea, the reaction mixture became cloudy, such that efficient irradiation was rendered difficult. Presumably, urea was formed from thiourea by the reaction with singlet oxygen. Crank, G.; Mursyidi, A. Oxidations of thioureas with photochemically generated singlet oxygen. J. Photochem. Photobiol. A 1992, 64, 263-271.
-
(1992)
J. Photochem. Photobiol. A
, vol.64
, pp. 263-271
-
-
Crank, G.1
Mursyidi, A.2
-
17
-
-
21644454904
-
-
Personal communication
-
Yoshihara, T. Personal communication.
-
-
-
Yoshihara, T.1
-
18
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21644470722
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note
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These diastereomers (ratio 1.2:1) could be separated from each other by silica gel column chromatography (hexane/EtOAc, 15: 1). The major isomer was further purified by recrystalization from hexane/EtOAc (15:1), and the minor isomer was recrystalized from hexane.
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19
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21644485215
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note
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+) 188.9915, found 188.9904.
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20
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85047540488
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Arene oxides-oxepins
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Hassner, A., Ed.; Interscience: New York
-
Boyd, D. R.; Jerina, D. M. Arene oxides-oxepins. In Small Rings Heterocycles, Part 3; Hassner, A., Ed.; Interscience: New York, 1985; Vol. 45, pp 197-282.
-
(1985)
Small Rings Heterocycles, Part 3
, vol.45
, pp. 197-282
-
-
Boyd, D.R.1
Jerina, D.M.2
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