-
5
-
-
0043236240
-
-
For a racemic total synthesis of 1: (a) Inoue, M.; Sato, T.; Hirama, M. J. Am. Chem. Soc. 2003, 125, 10772. For asymmetric total synthesis of (-)- and (+)-1:
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 10772
-
-
Inoue, M.1
Sato, T.2
Hirama, M.3
-
6
-
-
33746787198
-
-
(b) Inoue, M.; Sato, T.; Hirama, M. Angew. Chem. Int. Ed. Engl. 2006, 45, 4843;
-
(2006)
Angew. Chem. Int. Ed. Engl.
, vol.45
, pp. 4843
-
-
Inoue, M.1
Sato, T.2
Hirama, M.3
-
7
-
-
34247183754
-
-
(c) Inoue, M.; Lee, N.; Kasuya, S.; Sato, T.; Hirama, M.; Moriyama, M.; Fukuyama, Y. J. Org. Chem. 2007, 72, 3065.
-
(2007)
J. Org. Chem.
, vol.72
, pp. 3065
-
-
Inoue, M.1
Lee, N.2
Kasuya, S.3
Sato, T.4
Hirama, M.5
Moriyama, M.6
Fukuyama, Y.7
-
8
-
-
68949122370
-
-
S. Ogawa, D. Urabe, Y. Yokokura, H. Arai, M. Arita, and M. Inoue Org. Lett. 11 2009 3602
-
(2009)
Org. Lett.
, vol.11
, pp. 3602
-
-
Ogawa, S.1
Urabe, D.2
Yokokura, Y.3
Arai, H.4
Arita, M.5
Inoue, M.6
-
9
-
-
58149514666
-
-
2- symmetric intermediates, see: Hagiwara, K.; Himuro, M.; Hirama, M.; Inoue, M. Tetrahedron Lett. 2009, 50, 1035.
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 1035
-
-
Hagiwara, K.1
Himuro, M.2
Hirama, M.3
Inoue, M.4
-
10
-
-
0027972153
-
-
For a review on neurotrophic activity, see: (a) Hefti, F. J. Neurobiol. 1994, 25, 1418;
-
(1994)
J. Neurobiol.
, vol.25
, pp. 1418
-
-
Hefti, F.1
-
12
-
-
0034941330
-
-
(c) Sofroniew, M. V.; Howe, C. L.; Mobley, W. C. Annu. Rev. Neurosci. 2001, 24, 1217.
-
(2001)
Annu. Rev. Neurosci.
, vol.24
, pp. 1217
-
-
Sofroniew, M.V.1
Howe, C.L.2
Mobley, W.C.3
-
14
-
-
0024470413
-
-
For examples, see: Eudesobovatol A: Fukuyama, Y.; Otoshi, Y.; Kodama, M.; Hasegawa, T.; Okazaki, H.; Nagasawa, M. Tetrahedron Lett. 1989, 30, 5907. Caryolanemagnolol: Fukuyama, Y.; Otoshi, Y.; Miyoshi, K.; Nakamura, K.; Kodama, M.; Nagasawa, M.; Hasegawa, T.; Okazaki, M.; Sugawara, M. Tetrahedron 1992, 48, 377. Clovanemagnolol: Fukuyama, Y.; Otoshi, Y.; Kodama, M.; Hasegawa, T.; Okazaki, H. Tetrahedron Lett. 1990, 31, 4477. Mastigophorene: Fukuyama, Y.; Asakawa, Y. J. Chem. Soc., Perkin Trans. 1 1991, 2737. Isodunnianin: Fukuyama, Y.; Shida, N.; Kodama, M.; Planta Med. 1993, 59, 181. Tricycloillicinone: Fukuyama, Y.; Shida, N.; Kodama, M.; Chaki, H.; Yugami, T. Chem. Pharm. Bull. 1995, 43, 2270. Bicycloillicinone asarone acetal: Fukuyama, Y.; Hata, Y.; Kodama, M. Planta Med. 1997, 63, 275. Garsubellin A: Fukuyama, Y.; Kuwayama, A.; Minami, H. Chem. Pharm. Bull. 1997, 45, 947. Jiadifenin: Yokoyama, R.; Huang, J.-M.; Yang, C.-S.; Fukuyama, Y. J. Nat. Prod. 2002, 65, 527. 11-O-Debenzoyltashironin: Huang, J.-M.; Yokoyama, R.; Yang, C.-S.; Fukuyama, Y. J. Nat. Prod. 2001, 64, 428.
-
(1989)
Tetrahedron Lett.
, vol.30
, pp. 5907
-
-
Eudesobovatol, A.1
Fukuyama, Y.2
Otoshi, Y.3
Kodama, M.4
Hasegawa, T.5
Okazaki, H.6
Nagasawa, M.7
-
17
-
-
0037182748
-
-
Synthetic studies on merrilactone A. (a) Hong, B.-C.; Shr, Y.-J.; Wu, J.-L.; Gupta, A. K.; Lin, K.-J. Org. Lett. 2002, 4, 2249;
-
(2002)
Org. Lett.
, vol.4
, pp. 2249
-
-
Hong, B.-C.1
Shr, Y.-J.2
Wu, J.-L.3
Gupta, A.K.4
Lin, K.-J.5
-
19
-
-
24944486849
-
-
(c) Iriondo-Alberdi, J.; Perea-Buceta, J. E.; Greaney, M. F. Org. Lett. 2005, 7, 3969;
-
(2005)
Org. Lett.
, vol.7
, pp. 3969
-
-
Iriondo-Alberdi, J.1
Perea-Buceta, J.E.2
Greaney, M.F.3
-
20
-
-
25444500997
-
-
(d) Harada, K.; Kato, H.; Fukuyama, Y. Tetrahedron Lett. 2005, 46, 7407;
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 7407
-
-
Harada, K.1
Kato, H.2
Fukuyama, Y.3
-
21
-
-
34547486972
-
-
(e) Harada, K.; Ito, H.; Hioki, H.; Fukuyama, Y. Tetrahedron Lett. 2007, 48, 6105.
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 6105
-
-
Harada, K.1
Ito, H.2
Hioki, H.3
Fukuyama, Y.4
-
28
-
-
84861881557
-
-
J. Chen, P. Gao, F. Yu, Y. Yang, S. Zhu, and H. Zhai Angew. Chem. Int. Ed. Engl. 51 2012 5897
-
(2012)
Angew. Chem. Int. Ed. Engl.
, vol.51
, pp. 5897
-
-
Chen, J.1
Gao, P.2
Yu, F.3
Yang, Y.4
Zhu, S.5
Zhai, H.6
-
33
-
-
0026721571
-
-
For reviews on the construction of eight-membered rings, see: (a) Petasis, N. A.; Patane, M. A. Tetrahedron 1992, 48, 5757;
-
(1992)
Tetrahedron
, vol.48
, pp. 5757
-
-
Petasis, N.A.1
Patane, M.A.2
-
36
-
-
0034246704
-
-
(d) Yet, L. Chem. Rev. 2000, 100, 2963.
-
(2000)
Chem. Rev.
, vol.100
, pp. 2963
-
-
Yet, L.1
-
37
-
-
0001004614
-
-
For selected examples of the synthesis of bicyclo[3.3.0]octane systems from eight-membered rings, see: (a) Negri, J. T.; Morwick, T.; Doyon, J.; Wilson, P. D.; Hickey, E. R.; Paquette, L. A. J. Am. Chem. Soc. 1993, 115, 12189;
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 12189
-
-
Negri, J.T.1
Morwick, T.2
Doyon, J.3
Wilson, P.D.4
Hickey, E.R.5
Paquette, L.A.6
-
39
-
-
0001947119
-
-
For a review of extensive studies in this field by Paquette, see: (c) Paquette, L. A. Eur. J. Org. Chem. 1998, 1709;
-
(1998)
Eur. J. Org. Chem.
, pp. 1709
-
-
Paquette, L.A.1
-
41
-
-
0037181346
-
-
(e) Wender, P. A.; Gamber, G. G.; Hubbard, R. D.; Zhang, L. J. Am. Chem. Soc. 2002, 124, 2876;
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 2876
-
-
Wender, P.A.1
Gamber, G.G.2
Hubbard, R.D.3
Zhang, L.4
-
42
-
-
0034596443
-
-
(f) Zora, M.; Koyuncu, I.; Yucel, B. Tetrahedron Lett. 2000, 41, 7111;
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 7111
-
-
Zora, M.1
Koyuncu, I.2
Yucel, B.3
-
43
-
-
0034670586
-
-
(g) Verma, S. K.; Fleischer, E. B.; Moore, H. W. J. Org. Chem. 2000, 65, 8564;
-
(2000)
J. Org. Chem.
, vol.65
, pp. 8564
-
-
Verma, S.K.1
Fleischer, E.B.2
Moore, H.W.3
-
46
-
-
0036012051
-
-
(j) Hamura, T.; Tsuji, S.; Matsumoto, T.; Suzuki, K. Chem. Lett. 2002, 31, 280.
-
(2002)
Chem. Lett.
, vol.31
, pp. 280
-
-
Hamura, T.1
Tsuji, S.2
Matsumoto, T.3
Suzuki, K.4
-
51
-
-
0037847519
-
-
For recent reviews on cyclobutane derivatives, see: (a) Lee-Ruff, E.; Mladenova, G. Chem. Rev. 2003, 103, 1449;
-
(2003)
Chem. Rev.
, vol.103
, pp. 1449
-
-
Lee-Ruff, E.1
Mladenova, G.2
-
54
-
-
78249281266
-
-
(a) Fu, G. C.; Nguyen, S. T.; Grubbs, R. H. J. Am. Chem. Soc. 1993, 115, 9856;
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 9856
-
-
Fu, G.C.1
Nguyen, S.T.2
Grubbs, R.H.3
-
55
-
-
0001855961
-
-
(b) Schwab, P.; Grubbs, R. H.; Ziller, J. W. J. Am. Chem. Soc. 1996, 118, 100.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 100
-
-
Schwab, P.1
Grubbs, R.H.2
Ziller, J.W.3
-
58
-
-
22744448499
-
-
(e) Nicolaou, K. C.; Bulger, P. G.; Sarlah, D. Angew. Chem. Int. Ed. Engl. 2005, 44, 4490.
-
(2005)
Angew. Chem. Int. Ed. Engl.
, vol.44
, pp. 4490
-
-
Nicolaou, K.C.1
Bulger, P.G.2
Sarlah, D.3
-
60
-
-
33947295730
-
-
A trans-fused 5-5 ring system was not obtained in the aldol reaction, probably due to its highly strained nature: (a) Chang, S.; McNally, D.; Shary-Tehrany, S.; Hickey, S. M. J.; Boyd, R. H. J. Am. Chem. Soc. 1970, 92, 3109;
-
(1970)
J. Am. Chem. Soc.
, vol.92
, pp. 3109
-
-
Chang, S.1
McNally, D.2
Shary-Tehrany, S.3
Hickey, S.M.J.4
Boyd, R.H.5
-
61
-
-
0000543018
-
-
(b) Allinger, N. L.; Tribble, M. T.; Miller, M. A.; Wertz, D. H. J. Am. Chem. Soc. 1971, 93, 1637;
-
(1971)
J. Am. Chem. Soc.
, vol.93
, pp. 1637
-
-
Allinger, N.L.1
Tribble, M.T.2
Miller, M.A.3
Wertz, D.H.4
-
69
-
-
85047698822
-
-
(d) Plaquevent, J.-C.; Perrard, T.; Cahard, D. Chem. Eur. J. 2002, 8, 3300.
-
(2002)
Chem. Eur. J.
, vol.8
, pp. 3300
-
-
Plaquevent, J.-C.1
Perrard, T.2
Cahard, D.3
-
70
-
-
33751385836
-
-
Simpkins and Majewski independently reported that the presence of lithium chloride improved the enantioselectivity of asymmetric deprotonation: (a) Bunn, B. J.; Simpkins, N. S. J. Org. Chem. 1993, 58, 533;
-
(1993)
J. Org. Chem.
, vol.58
, pp. 533
-
-
Bunn, B.J.1
Simpkins, N.S.2
-
71
-
-
37049071721
-
-
(b) Bunn, B. J.; Simpkins, N. S.; Spavold, Z.; Crimmin, M. J. J. Chem. Soc., Perkin Trans. 1 1993, 3113;
-
(1993)
J. Chem. Soc., Perkin Trans.
, vol.1
, pp. 3113
-
-
Bunn, B.J.1
Simpkins, N.S.2
Spavold, Z.3
Crimmin, M.J.4
-
73
-
-
0000129485
-
-
(d) Majewski, M.; Gleave, D. M.; Nowak, P. Can. J. Chem. 1995, 73, 1616;
-
(1995)
Can. J. Chem.
, vol.73
, pp. 1616
-
-
Majewski, M.1
Gleave, D.M.2
Nowak, P.3
-
74
-
-
85047673542
-
-
(e) Majewski, M.; Lazny, R.; Nowak, P. Tetrahedron Lett. 1995, 36, 5465.
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 5465
-
-
Majewski, M.1
Lazny, R.2
Nowak, P.3
-
79
-
-
0029929870
-
-
Although 18g and ent-18g are commercially available, these bases have not been applied to enantioselective deprotonation reaction to the best of our knowledge. For their preparation, see: Kowalczyk, B. A.; Rohloff, J. C.; Dvorak, C. A.; Gardner, J. O. Syn. Commun. 1996, 26, 2009.
-
(1996)
Syn. Commun.
, vol.26
, pp. 2009
-
-
Kowalczyk, B.A.1
Rohloff, J.C.2
Dvorak, C.A.3
Gardner, J.O.4
-
81
-
-
0035921040
-
-
For recent reviews on radical reactions, see: (a) Zhang, W. Tetrahedron 2001, 57, 7237;
-
(2001)
Tetrahedron
, vol.57
, pp. 7237
-
-
Zhang, W.1
-
84
-
-
2742528871
-
-
Y. Ueno, K. Chino, M. Watanabe, O. Moriya, and M. Okawara J. Am. Chem. Soc. 104 1982 5564
-
(1982)
J. Am. Chem. Soc.
, vol.104
, pp. 5564
-
-
Ueno, Y.1
Chino, K.2
Watanabe, M.3
Moriya, O.4
Okawara, M.5
-
88
-
-
33845281717
-
-
(a) Nozaki, K.; Oshima, K.; Utimoto, K. J. Am. Chem. Soc. 1987, 109, 2547.
-
(1987)
J. Am. Chem. Soc.
, vol.109
, pp. 2547
-
-
Nozaki, K.1
Oshima, K.2
Utimoto, K.3
-
99
-
-
84986437005
-
-
The three-dimensional structure of 30 was generated by the molecular modeling calculation (Macro Model Ver 6.0). Mohamadi, F.; Richards, N. G. J.; Guida, W. C.; Liskamp, R.; Lipton, M.; Caufield, C.; Chang, G.; Hendrickson, T.; Still, W. C. J. Comput. Chem. 1990, 11, 440.
-
(1990)
J. Comput. Chem.
, vol.11
, pp. 440
-
-
Mohamadi, F.1
Richards, N.G.J.2
Guida, W.C.3
Liskamp, R.4
Lipton, M.5
Caufield, C.6
Chang, G.7
Hendrickson, T.8
Still, W.C.9
-
102
-
-
42649089790
-
-
For reviews, see: (a) Serhan, C. N.; Chiang, N.; Van Dyke, T. E. Nat. Rev. Immunol. 2008, 8, 349;
-
(2008)
Nat. Rev. Immunol.
, vol.8
, pp. 349
-
-
Serhan, C.N.1
Chiang, N.2
Van Dyke, T.E.3
-
105
-
-
12344321136
-
-
M. Arita, F. Bianchini, J. Aliberti, A. Sher, N. Chiang, S. Hong, R. Yang, N.A. Petasis, and C.N. Serhan J. Exp. Med. 201 2005 713
-
(2005)
J. Exp. Med.
, vol.201
, pp. 713
-
-
Arita, M.1
Bianchini, F.2
Aliberti, J.3
Sher, A.4
Chiang, N.5
Hong, S.6
Yang, R.7
Petasis, N.A.8
Serhan, C.N.9
-
107
-
-
33751020561
-
-
E. Tjonahan, S.F. Oh, J. Siegelman, S. Elangovan, K.B. Percarpio, S. Hong, M. Arita, and C.N. Serhan Chem. Biol. 13 2006 1193
-
(2006)
Chem. Biol.
, vol.13
, pp. 1193
-
-
Tjonahan, E.1
Oh, S.F.2
Siegelman, J.3
Elangovan, S.4
Percarpio, K.B.5
Hong, S.6
Arita, M.7
Serhan, C.N.8
-
108
-
-
84858705961
-
-
Y. Isobe, M. Arita, S. Matsueda, R. Iwamoto, T. Fujihara, H. Nakanishi, R. Taguchi, K. Masuda, K. Sasaki, D. Urabe, M. Inoue, and H. Arai J. Biol. Chem. 287 2012 10525
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 10525
-
-
Isobe, Y.1
Arita, M.2
Matsueda, S.3
Iwamoto, R.4
Fujihara, T.5
Nakanishi, H.6
Taguchi, R.7
Masuda, K.8
Sasaki, K.9
Urabe, D.10
Inoue, M.11
Arai, H.12
-
109
-
-
84858706517
-
-
Total syntheses of lipid mediators from our group. Resolvin E3: (a) Urabe, D.; Todoroki, H.; Masuda, K.; Inoue, M. Tetrahedron 2012, 68, 3210.
-
(2012)
Tetrahedron
, vol.68
, pp. 3210
-
-
Urabe, D.1
Todoroki, H.2
Masuda, K.3
Inoue, M.4
-
110
-
-
79251484672
-
-
See also ref. 3.
-
Maresin: (b) Sasaki, K.; Urabe, D.; Arai, H.; Arita, M.; Inoue, M. Chem. Asian J. 2011, 6, 534. See also ref. 3.
-
(2011)
Chem. Asian J.
, vol.6
, pp. 534
-
-
Sasaki, K.1
Urabe, D.2
Arai, H.3
Arita, M.4
Inoue, M.5
-
112
-
-
79955468795
-
-
(b) Allard, M.; Barnes, K.; Chen, X.; Cheung, Y.-Y.; Duffy, B.; Heap, C.; Inthavongsay, J.; Johnson, M.; Krishnamoorthy, R.; Manley, C.; Steffke, S.; Varughese, D.; Wang, R.; Wang, Y.; Schwartz, C. E. Tetrahedron Lett. 2011, 52, 2623.
-
(2011)
Tetrahedron Lett.
, vol.52
, pp. 2623
-
-
Allard, M.1
Barnes, K.2
Chen, X.3
Cheung, Y.-Y.4
Duffy, B.5
Heap, C.6
Inthavongsay, J.7
Johnson, M.8
Krishnamoorthy, R.9
Manley, C.10
Steffke, S.11
Varughese, D.12
Wang, R.13
Wang, Y.14
Schwartz, C.E.15
-
113
-
-
77549087702
-
-
See also ref. 53a. Resolvin E2: (c) Kosaki, Y.; Ogawa, N.; Kobayashi, Y. Tetrahedron Lett. 2010, 51, 1856;
-
(2010)
Tetrahedron Lett.
, vol.51
, pp. 1856
-
-
Kosaki, Y.1
Ogawa, N.2
Kobayashi, Y.3
-
118
-
-
0025914829
-
-
For a review of syntheses of eicosanoids, see: (h) Nicolaou, K. C.; Ramphal, J. Y.; Petasis, N. A.; Serhan, C. N. Angew. Chem. Int. Ed. Engl. 1991, 30, 1100.
-
(1991)
Angew. Chem. Int. Ed. Engl.
, vol.30
, pp. 1100
-
-
Nicolaou, K.C.1
Ramphal, J.Y.2
Petasis, N.A.3
Serhan, C.N.4
-
119
-
-
0001414464
-
-
For rationalization of torquoselectivity, see: (a) Rudolf, K.; Spellmeyer, D. C.; Houk, K. N. J. Org. Chem. 1987, 52, 3708;
-
(1987)
J. Org. Chem.
, vol.52
, pp. 3708
-
-
Rudolf, K.1
Spellmeyer, D.C.2
Houk, K.N.3
-
120
-
-
0000203981
-
-
(b) Niwayama, S.; Kallel, E. A.; Spellmeyer, D. C.; Sheu, C.; Houk, K. N. J. Org. Chem. 1996, 61, 2813;
-
(1996)
J. Org. Chem.
, vol.61
, pp. 2813
-
-
Niwayama, S.1
Kallel, E.A.2
Spellmeyer, D.C.3
Sheu, C.4
Houk, K.N.5
-
121
-
-
0001261240
-
-
(c) Dolbier, W. R. Jr.; Koroniak, H.; Houk, K. N.; Sheu, C. Acc. Chem. Res. 1996, 29, 471.
-
(1996)
Acc. Chem. Res.
, vol.29
, pp. 471
-
-
Dolbier Jr., W.R.1
Koroniak, H.2
Houk, K.N.3
Sheu, C.4
-
122
-
-
0026565383
-
-
Wallace demonstrated selective ring opening of cyclobutene aldehydes and substrate-controlled stereoselective introductions of various carbon nucleophiles to disubstituted cyclobutenes: (a) Binns, F.; Hayes, R.; Ingham, S.; Saengchantara, S. T.; Turner, R. W.; Wallace, T. W. Tetrahedron 1992, 48, 515;
-
(1992)
Tetrahedron
, vol.48
, pp. 515
-
-
Binns, F.1
Hayes, R.2
Ingham, S.3
Saengchantara, S.T.4
Turner, R.W.5
Wallace, T.W.6
-
123
-
-
0028303651
-
-
(b) Hodgetts, K. J.; Wallis, C. J.; Wallace, T. W. Tetrahedron Lett. 1994, 35, 4645;
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 4645
-
-
Hodgetts, K.J.1
Wallis, C.J.2
Wallace, T.W.3
-
125
-
-
0030069041
-
-
(d) Binns, F.; Hayes, R.; Hodgetts, K. J.; Saengchantara, S. T.; Wallace, T. W.; Wallis, C. J. Tetrahedron 1996, 52, 3631.
-
(1996)
Tetrahedron
, vol.52
, pp. 3631
-
-
Binns, F.1
Hayes, R.2
Hodgetts, K.J.3
Saengchantara, S.T.4
Wallace, T.W.5
Wallis, C.J.6
-
126
-
-
0033548151
-
-
Enantioselective syntheses of (+)- and (-)-41 by enzymatic resolution were reported: Gourdel-Martin, M.-E.; Comoy, C.; Huet, F. Tetrahedron: Asymm. 1999, 10, 403, see also ref 59b and 59c.
-
(1999)
Tetrahedron: Asymm.
, vol.10
, pp. 403
-
-
Gourdel-Martin, M.-E.1
Comoy, C.2
Huet, F.3
-
130
-
-
54749152753
-
-
S.H. Oh, H.S. Rho, J.W. Lee, J.E. Lee, S.H. Youk, J. Chin, and C.E. Song Angew. Chem. Int. Ed. Engl. 47 2008 7872
-
(2008)
Angew. Chem. Int. Ed. Engl.
, vol.47
, pp. 7872
-
-
Oh, S.H.1
Rho, H.S.2
Lee, J.W.3
Lee, J.E.4
Youk, S.H.5
Chin, J.6
Song, C.E.7
-
131
-
-
0041378031
-
-
For a review of asymmetric alcoholysis of cyclic anhydrides, see: Chen, Y.; McDaid, P.; Deng, L. Chem. Rev. 2003, 103, 2965.
-
(2003)
Chem. Rev.
, vol.103
, pp. 2965
-
-
Chen, Y.1
McDaid, P.2
Deng, L.3
-
134
-
-
33845378873
-
-
D. Wenkert, S.B. Ferguson, B. Porter, A. Qvarnstrom, and A.T. McPhail J. Org. Chem. 50 1985 4114
-
(1985)
J. Org. Chem.
, vol.50
, pp. 4114
-
-
Wenkert, D.1
Ferguson, S.B.2
Porter, B.3
Qvarnstrom, A.4
McPhail, A.T.5
-
135
-
-
33845375225
-
-
Y. Leblanc, B.J. Fitzsimmons, J. Adams, F. Perez, and J. Rokach J. Org. Chem. 51 1986 789
-
(1986)
J. Org. Chem.
, vol.51
, pp. 789
-
-
Leblanc, Y.1
Fitzsimmons, B.J.2
Adams, J.3
Perez, F.4
Rokach, J.5
-
141
-
-
33646554176
-
-
H. Fujioka, T. Okitsu, Y. Sawama, N. Murata, R. Li, and Y. Kita J. Am. Chem. Soc. 128 2006 5930.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 5930
-
-
Fujioka, H.1
Okitsu, T.2
Sawama, Y.3
Murata, N.4
Li, R.5
Kita, Y.6
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