Recent advances in the total syntheses of oxazole-containing natural products

Tetrahedron

Volumn 60, Issue 52, 2004, Pages 11995-12042

  Yeh, Vince S C ^a  

^a ABBOTT LABORATORIES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBIOTIC AGENT; BENGAZOLE A; BISTRATAMIDE D; CALYCULIN A; CALYCULIN B; CALYCULIN C; CYCLOPEPTIDE; DALFOPRISTIN; DENDROAMIDE A; DIAZONAMIDE A; DISORAZOLE C; GRISEOVIRIDIN; HENNOXAZOLE A; LEUCAMIDE A; LEUCASCANDROLIDE A; MADUMYCIN; MUSCORIDE A; MYCALOLIDE A; NATURAL PRODUCT; NOSTOCYCLAMIDE; OXAZOLE DERIVATIVE; PEPTIDE DERIVATIVE; PHORBOXAZOLE A; PHORBOXAZOLE B; PROMOTHIOCIN A; THIANGAZOLE; ULAPUALIDE A; UNCLASSIFIED DRUG; VIRGINIAMYCIN;

ARTICLE; DIASTEREOISOMER; DRUG STRUCTURE; DRUG SYNTHESIS; PRIORITY JOURNAL;

EID: 9644264170     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.10.001     Document Type: Review

References (406)

1. Z. Jin, Z. Li, and R. Huang Nat. Prod. Rep. 19 2002 454
2. J.R. Lewis Nat. Prod. Rep. 19 2002 223 and earlier reviews by the same author
3. R.S. Roy, A.M. Gehring, J.C. Milne, P.J. Belshaw, and C.T. Walsh Nat. Prod. Rep. 16 1999 249
4. D.C. Palmer Oxazoles: Synthesis, Reactions, and Spectroscopy Vol. 1 2003 Wiley New Jersey
5. M. Adamczeski, E. Quinoa, and P. Crews J. Am. Chem. Soc. 110 1988 1598
6. P.A. Searle, R.K. Richter, and T.F. Molinski J. Org. Chem. 61 1996 4073
7. J. Rodriguez, R.M. Nieto, and P. Crews J. Nat. Prod. 56 1993 2034
8. A. Rudi, Y. Kashman, Y. Benayahu, and M. Schleyer J. Nat. Prod. 57 1994 829
9. J. Antonio, and T.F. Molinski J. Nat. Prod. 56 1993 54
10. Molinski, T. F. Unpublished results.
11. R.J. Mulder, C.M. Shafer, and T.F. Molinski J. Org. Chem. 64 1999 4995
12. C.M. Shafer, and T.F. Molinski Carbohydr. Res. 310 1998 223
13. C.M. Shafer, and T.F. Molinski Tetrahedron Lett. 39 1998 2903
14. P. Chittari, Y. Hamada, and T. Shioiri Heterocycles 59 2003 465
15. J.C. Hodges, W.C. Patt, and C.J. Connolly J. Org. Chem. 56 1991 449
16. E. Vedejs, and S.D. Manahan J. Org. Chem. 61 1996 5192
17. Y. Kato, N. Fusetani, S. Matsunaga, K. Hashimoto, S. Fujita, and T. Furuya J. Am. Chem. Soc. 108 1986 2780
18. S. Matsunaga, and N. Fusetani Tetrahedron Lett. 32 1991 5605
19. Y. Hamada, Y. Tanada, F. Yokokawa, and T. Shioiri Tetrahedron Lett. 32 1991 5983
20. Y. Kato, N. Fusetani, S. Matsunaga, K. Hashimoto, and K. Koseki J. Org. Chem. 53 1988 3930
21. S. Matsunaga, T. Wakimoto, N. Fusetani, and M. Suganuma Tetrahedron Lett. 38 1997 3763
22. S. Matsunaga, T. Wakimoto, and N. Fusetani J. Org. Chem. 62 1997 2640
23. E.J. Dumdei, J.W. Blunt, M.H.G. Munro, and L.K. Pannell J. Org. Chem. 62 1997 2636
24. S. Matsunaga, T. Wakimoto, and N. Fusetani J. Org. Chem. 26 1997 9388
25. H. Ishihara, B.L. Martin, D.L. Brautigan, H. Karaki, H. Ozaki, Y. Kato, N. Fusetani, S. Watabe, K. Hashimoto, D. Uemura, and D.J. Hartshorne Biochem. Biophys. Res. Commun. 159 1989 871
26. J.E. Scheppeck II, C.-M. Gauss, and A.R. Chamberlin Bioorg. Med. Chem. 5 1997 1739 and references therein
27. P. Cohen, C.F.B. Holmes, and Y. Tsukitani Trends Biochem. Sci. 15 1990 98
28. D.A. Evans, and J.R. Gage Tetrahedron Lett. 31 1990 6129
29. O. Hara, K. Nakao, Y. Tanada, A. Nishio, J. Matsubara, F. Yokokawa, Y. Hamada, and T. Shioiri Tennen Yuki Kagobutsu Toronkai Koen Yoshishu 32 1990 617
30. O. Hara, Y. Hamada, and T. Shioiri Synlett 1991 283
31. O. Hara, Y. Hamada, and T. Shioiri Synlett 1991 285
32. A.B. Smith III, J.J.-W. Duan, K.G. Hull, and B.A. Salvatore Tetrahedron Lett. 32 1991 4855
33. A.B. Smith III, B.A. Salvatore, K.G. Hull, and J.J.-W. Duan Tetrahedron Lett. 32 1991 4859
34. R.W. Armstrong, and J.A. Demattei Tetrahedron Lett. 32 1991 5749
35. Y. Hamada, Y. Tanada, F. Yokokawa, and T. Shioiri Tetrahedron Lett. 32 1991 5983
36. A.M.P. Koskinen, and J. Chen Tetrahedron Lett. 32 1991 6977
37. D.A. Evans, J.R. Gage, J.L. Leighton, and A.S. Kim J. Org. Chem. 57 1992 1961
38. D.A. Evans, J.R. Gage, and J.L. Leighton J. Org. Chem. 57 1992 1964
39. D.A. Evans, and J.R. Gage J. Org. Chem. 57 1992 1958
40. F. Yokokawa, Y. Hamada, and T. Shioiri Synlett 1992 149
41. F. Yokokawa, Y. Hamada, and T. Shioiri Synlett 1992 151
42. H.A. Vaccaro, D.E. Levy, A. Sawabe, T. Jaetsch, and S. Masamune Tetrahedron Lett. 33 1992 1937
43. J. Matsubara, K. Nakao, Y. Hamada, and T. Shioiri Tetrahedron Lett. 33 1992 4187
44. F. Yokokawa, Y. Hamada, and T. Shioiri Synlett 1992 703
45. A. Sawabe, S.A. Filla, and S. Masamune Tetrahedron Lett. 33 1992 7685
46. F. Yokokawa, Y. Hamada, and T. Shioiri Tetrahedron Lett. 34 1993 6559
47. J.J.-W. Duan, and A.B. Smith III J. Org. Chem. 58 1993 3703
48. F. Yokokawa, Y. Hamada, and T. Shioiri Tenne Yuki Kagobutsu Toronkai Koen Yoshishu 35 1993 127
49. B.A. Salvadore, and A.B. Smith III Tetrahedron Lett. 35 1994 1329
50. K. Takebuchi, Y. Hamada, and T. Shioiri Tetrahedron Lett. 35 1994 5239
51. B.M. Trost, and J.A. Flygare Tetrahedron Lett. 35 1994 4059
52. A.M.P. Koskinen, and P.M. Pihko Tetrahrdron Lett. 35 1994 7417
53. A.B. Smith III, and M. Iwashima Tetrahedron Lett. 35 1994 6051
54. M. Iwashima, T. Kinsho, and A.B. Smith III Tetrahedron Lett. 36 1995 2199
55. K. Shinozaki, K. Mizuno, H. Wakamatsu, and Y. Masaki Chem. Pharm. Bull. 44 1996 1823
56. A.K. Ogawa, J.A. Demattei, G.R. Scarlato, J.E. Tellew, L.S. Chong, and R.W. Armstrong J. Org. Chem. 61 1996 6153
57. G.R. Scarlato, J.A. Demattei, L.S. Chong, A.K. Ogawa, M.R. Lin, and R.W. Armstrong J. Org. Chem. 61 1996 6139
58. K. Shinozaki, K. Mizuno, and Y. Masaki Heterocycles 43 1996 11
59. Y. Hamada, F. Yokokawa, M. Kabeya, K. Hatano, Y. Kurono, and T. Shioiri Tetrahedron 52 1996 8297
60. Y. Hamada Ikagaku Oyo Kenkyu Zaidan Kenyu Hokoku 15 1997 293
61. M. Kabeya, Y. Hamada, and T. Shioiri Tetrahedron 53 1997 13969
62. M. Kabeya, Y. Hamada, and T. Shioiri Tetrahedron 53 1997 9769
63. M. Kabeya, Y. Hamada, and T. Shioiri Tetrahedron 53 1997 9777
64. P.M. Pihko, and A.M.P. Koshinen J. Org. Chem. 63 1998 92
65. M.F. Jacobs, and W. Kitching Curr. Org. Chem. 2 1998 395
66. P.M. Pihko, and A.M.P. Koshinen Synlett 1999 1966
67. P.M. Pihko, A.M.P. Koshinen, M.J. Nissinen, and K. Rissanen J. Org. Chem. 64 1999 652
68. D.A. Evans, J.R. Gage, and J.L. Leighton J. Am. Chem. Soc. 114 1992 9434
69. N. Tanimono, S.W. Gerritz, A. Sawabe, T. Noda, S.A. Filla, and S. Masamune Angew. Chem., Int. Ed. Engl. 33 1994 673
70. A.K. Ogawa, and R.W. Armstrong J. Am. Chem. Soc. 120 1998 12435
71. A.B. Smith III, G.K. Friestad, J. Barbosa, E. Bertounesque, K.G. Hull, M. Iwashima, Y. Qui, B.A. Salvatore, P.G. Spoors, and J.J.-W. Duan J. Am. Chem. Soc. 121 1999 10468
72. A.B. Smith III, G.K. Friestad, J. Barbosa, E. Bertounesque, J.J.-W. Duan, K.G. Hull, M. Iwashima, Y. Qui, P.G. Spoors, and B.A. Salvatore J. Am. Chem. Soc. 121 1999 10478
73. F. Yokokawa, Y. Hamada, and T. Shioiri J. Chem. Soc., Chem. Commun. 1996 871
74. O.P. Anderson, A.G.M. Barrett, J.J. Edmunds, S.-I. Hachiya, J.A. Hendrix, K. Horita, J.W. Malecha, C.J. Parkinson, and A. VanSickle Can. J. Chem. 79 2001 1562 and references therein
75. Selected papers on Evans chiral oxazolidinone: (a) J.R. Gage, and D.A. Evans Org. Synth. 68 1989 77
76. D.A. Evans, M.M. Morrissey, and R.L. Dorow J. Am. Chem. Soc. 107 1985 4346
77. D.A. Evans, J.S. Clark, R. Metternich, V.J. Novack, and G.S. Sheppard J. Am. Chem. Soc. 112 1990 866
78. D.A. Evans, H.P. Ng, J.S. Clark, and D.L. Rieger Tetrahedron 48 1992 2127
79. D.A. Evans, F. Urpi, T.C. Somers, J.S. Clark, and M.T. Bilodeau J. Am. Chem. Soc. 112 1990 8215
80. D.A. Evans, M.T. Bilodeau, T.C. Somers, J. Clardy, D. Cherry, and Y. Kato J. Org. Chem. 56 1991 5750
81. D.L. Evans, D.K. Minster, U. Jordis, S.M. Hecht, A.L. Mazzu, and A.I. Meyers J. Org. Chem. 44 1979 497
82. G. Theilig Chem. Ber. 86 1953 96
83. G.Y. Kondrateva, and K. Chzhi-Khen J. Gen. Chem. USSR 32 1962 2315
84. H.C. Brown, and K.S. Bhat J. Am. Chem. Soc. 108 1986 5919 and references cited therein
85. A.I. Meyers, M. Harre, and R. Garland J. Am. Chem. Soc. 106 1984 1146
86. A.I. Meyers, B.A. Lefker, K.T. Wanner, and R.A. Aitken J. Org. Chem. 51 1986 1936
87. J.K. Thottathil, J.L. Moniot, R.H. Mueller, M.K.Y. Wong, and T.P. Kissich J. Org. Chem. 51 1986 3140
88. E.M. Burgess, H.R. Penton Jr., E.A. Taylor, and W.M. Williams Organic Syntheses Vol. V1 1988 Wiley New York p 788
89. E.M. Burgess, H.R. Penton Jr., and E.A. Taylor J. Org. Chem. 38 1973 26
90. P. Wipf, and C.P. Miller Tetrahedron Lett. 33 1992 907
91. P. Wipf, and C.P. Miller J. Am. Chem. Soc. 114 1992 10975
92. P. Wipf, and C.P. Miller J. Org. Chem. 58 1993 1575
93. J.C. Barrish, J. Singh, S.H. Spergel, W.-C. Han, T.P. Kissick, D.R. Kronenthal, and R.H. Mueller J. Org. Chem. 58 1993 4494
94. L.A. Silks III, R.B. Dunlap, and J.D. Odom J. Am. Chem. Soc. 112 1990 4979
95. L.A. Silks III, J. Peng, J.D. Odom, and R.B. Dunlap J. Org. Chem. 56 1991 6733
96. N. Lindquist, W. Fenical, G.D. Van Duyne, and J. Clardy J. Am. Chem. Soc. 113 1991 2303
97. For highlights of previous synthetic studies towards the diazonamides, see: (a) V. Wittmann Nachr. Chem. 50 2002 477
98. T. Ritter, and E.M. Carreira Angew. Chem., Int. Ed. 41 2002 2489
99. For additional synthetic studies, see: (a) K.S. Feldman, K.J. Eastman, and G. Lessene Org. Lett. 4 2002 3525
100. S. Schley, A. Radspieler, G. Christoph, and J. Liebscher Eur. J. Org. Chem. 2002 369
101. A. Radspieler, and J. Liebscher Synthesis 2001 745
102. H.C. Hang, E. Drotleff, G.I. Elliott, T.A. Ritsema, and J.P. Konopelski Synthesis 1999 398
103. J.P. Konopelski, J.M. Hottenroth, H.M. Oltra, E.A. Veliz, and Z.C. Yang Synlett 1996 609
104. A. Boto, M. Ling, G. Meek, and G. Pattenden Tetrahedron Lett. 39 1998 8167
105. J.D. Kreisberg, P. Magnus, and E.G. McIver Tetrahedron Lett. 42 2001 627
106. P. Magnus, and E.G. McIver Tetrahedron Lett. 41 2000 831
107. F. Chan, P. Magnus, and E.G. McIver Tetrahedron Lett. 41 2000 835
108. P. Magnus, and J.D. Kreisberg Tetrahedron Lett. 40 1999 451
109. F. Lach, and C.J. Moody Tetrahedron Lett. 41 2000 6893
110. M.C. Bagley, S.L. Hind, and C.J. Moody Tetrahedron Lett. 41 2000 6897
111. M.C. Bagley, C.J. Moody, and A.G. Pepper Tetrahedron Lett. 41 2000 6901
112. C.J. Moody, K.J. Doyle, M.C. Elliott, and T.J. Mowlem J. Chem. Soc., Perkin Trans. 1 1997 2413
113. C.J. Moody, K.J. Doyle, M.C. Elliott, and T.J. Mowlem Pure Appl. Chem. 66 1994 2107
114. E. Vedejs, and M.A. Zajac Org. Lett. 3 2001 2451
115. E. Vedejs, and J. Wang Org. Lett. 2 2000 1031
116. E. Vedejs, and D.A. Barba Org. Lett. 2 2000 1033
117. P. Wipf, and J.-L. Methot Org. Lett. 3 2001 1261
118. P. Wipf, and F. Yokokawa Tetrahedron Lett. 39 1998 2223
119. T. Sawada, D.E. Fuerst, and J.L. Wood Tetrahedron Lett. 44 2003 4919
120. D.E. Fuerst, B.M. Stoltz, and J.L. Wood Org. Lett. 2 2000 3521
121. J. Li, S. Jeong, L. Esser, and P.G. Harran Angew. Chem., Int. Ed. 40 2001 4765
122. J. Li, A.W.G. Burgett, L. Esser, C. Amezcua, and P.G. Harran Angew., Chem. Int. Ed. 40 2001 4770
123. J. Li, X. Chen, A.W.G. Burgett, and P.G. Harran Angew. Chem., Int. Ed. 40 2001 2682
124. X. Chen, L. Esser, and P.G. Harran Angew. Chem., Int. Ed. 39 2000 937
125. S. Jeong, X. Chen, and P.G. Harran J. Org. Chem. 63 1998 8640
126. A.W.G. Burgett, Q. Li, Q. Wei, and P.G. Harran Angew. Chem., Int. Ed. 42 2003 4961
127. K.C. Nicolaou, P.B. Rao, J. Hao, M.V. Reddy, G. Rassias, X. Huang, D.Y.-K. Chen, and S.A. Snyder Angew. Chem., Int. Ed. 42 2003 1753
128. K.C. Nicolaou, M. Bella, D.Y.-K. Chen, X. Huang, T. Ling, and S.A. Snyder Angew. Chem., Int. Ed. 41 2002 3495
129. K.C. Nicolaou, X. Huang, N. Giuseppone, P. Bheema Rao, M. Bella, M.V. Reddy, and S.A. Snyder Angew. Chem., Int. Ed. 40 2001 4705
130. K.C. Nicolaou, S.A. Snyder, K.B. Simonsen, and A.E. Koumbis Angew. Chem., Int. Ed. 39 2000 3473
131. M.P. Dolye, B. Siegfried, and J.F. Dellaria Jr. J. Org. Chem. 42 1977 2426
132. F. Freeman, T. Chen, and J.B. van der Linden Synthesis 1997 861
133. S. Hanessian, P. Meffre, S. Girard, S. Beaudoin, J.-Y. Sanceau, and Y. Bennani J. Org. Chem. 58 1993 1991
134. O. Yonemitsu, P. Cerutti, and B. Witkop J. Am. Chem. Soc. 88 1966 3941
135. H.G. Theuns, H.B.M. Lenting, C.A. Salemink, H. Tanaka, M.S. Shibata, K. Ito, and R.J.J.C. Kousberg Heterocycles 22 1984 2007
136. R.L. Dow J. Org. Chem. 55 1990 386
137. P. Wipf, and C.P. Miller J. Org. Chem. 58 1993 3604
138. A. Padwa, D. Dehm, T. Oine, and G.A. Lee J. Am. Chem. Soc. 97 1975 1837
139. R. Jansen, H. Irschik, H. Reichenbach, V. Wray, and G. Hofle Liebigs Ann. Chem. 1994 759
140. H. Irschik, R. Jansen, K. Gerth, G. Hofle, and H. Reichenbach J. Antibiot. 48 1995 31
141. M.C. Hillier, A.T. Price, and A.I. Meyers J. Org. Chem. 66 2001 6037
142. M.C. Hillier, D.H. Park, A.T. Price, R. Ng, and A.I. Meyers Tetrahedron Lett. 41 2000 2821
143. I.G. Hartung, B. Niess, L.O. Haustedt, and H.M.R. Hoffmann Org. Lett. 4 2002 3239
144. A. Vakalopoulos, R. Smits, and H.M.R. Hoffmann Eur. J. Org. Chem. 2002 1538
145. W.J. Middleton J. Org. Chem. 40 1975 574
146. P. Lafargue, P. Geunot, and J.-P. Lellouch Heterocycles 41 1995 947
147. A.J. Phillips, Y. Uto, P. Wipf, M.J. Reno, and D.R. Williams Org. Lett. 2 2000 1165
148. D.R. Williams, P.D. Lowder, Y.-G. Gu, and D.A. Brooks Tetrahedron Lett. 38 1997 331
149. S. Kiyooka, Y. Kaneko, M. Komura, H. Matsuo, and M. Nakano J. Org. Chem. 56 1991 2276
150. K. Saitoh, I. Shiina, and T. Mukaiyama Chem. Lett. 1998 679
151. M. Hikota, T. Hitoshi, K. Horita, and O. Yonemitsu Tetrahedron 46 1990 4613
152. D.A. Evans, H.P. Ng, and D.L. Rieger J. Am. Chem. Soc. 115 1993 11446
153. M. Berger, and J. Mulzer J. Am. Chem. Soc. 121 1999 8393
154. T. Ichiba, W.Y. Yoshida, P.J. Scheuer, T. Higa, and D.G. Gravalos J. Am. Chem. Soc. 113 1991 3173
155. T. Higa, J. Tanaka, A. Kitamura, T. Koyama, M. Takahashi, and T. Uchida Pure Appl. Chem. 66 1994 2227
156. For synthetic studies of 131, see: (a) T.E. Smith, and E.P. Balskus Heterocycles 57 2002 1219
157. A.G.M. Barrett, and J.T. Kohrt Synlett 1995 415
158. A. Vakalopoulos, and H.M.R. Hoffman Org. Lett. 3 2001 177
159. P. Wipf, and S. Lim J. Am. Chem. Soc. 117 1995 558
160. P. Wipf, and S. Lim Chimia 50 1996 157
161. D.R. Williams, D.A. Brooks, and M.A. Berliner J. Am. Chem. Soc. 121 1999 4924
162. F. Yokokawa, T. Asano, and T. Shioiri Tetrahedron 57 2001 6311
163. N. Minami, S.S. Ko, and Y. Kishi J. Am. Chem. Soc. 104 1982 1109
164. W.R. Roush, and M.A. Adam J. Org. Chem. 50 1985 3752
165. E. Negishi, and Z. Owczarczyk Tetrahedron Lett. 32 1991 6683
166. J. Coste, E. Frerot, and P. Jouin J. Org. Chem. 59 1994 2437
167. E.J. Corey, C.-M. Yu, and S.S. Kim J. Am. Chem. Soc. 111 1989 5495
168. D.R. Williams, D.A. Brooks, K.G. Meyer, and M.P. Clark Tetrahedron Lett. 39 1998 7251
169. P.R. Blakemore, W.J. Cole, P.J. Kocienski, and A. Morley Synlett 1998 26
170. M.D'. Ambrosio, A. Guerriero, C. Debitus, and F. Pietra Helv. Chim. Acta 79 1996 51
171. M.D'. Ambrosio, M. Tato, C. Pocsfalvi, C. Debitus, and F. Pietra Helv. Chim. Acta 82 1999 347
172. For the synthesis of fragments of leucascandrolide A, see: (a) M.T. Crimmins, C.A. Carroll, and B.W. King Org. Lett. 2 2000 597
173. A. Vakalopoulos, and H.M.R. Hoffmann Org. Lett. 3 2001 177
174. T.J. Hunter, and G.A. Doherty Org. Lett. 3 2001 1049
175. L.A. Dakin, N.F. Langille, and J.S. Panek J. Org. Chem. 67 2002 6812
176. K.R. Hornberger, C.L. Hamblett, and J.L. Leighton J. Am. Chem. Soc. 122 2000 12894
177. D.J. Kopecky, and S.D. Rychnovsky J. Am. Chem. Soc. 123 2001 8420
178. P. Wipf, and J.T. Reeves J. Chem. Soc., Chem. Commun. 2002 2066
179. P. Wipf, and T.H. Graham J. Org. Chem. 66 2001 3242
180. A. Fettes, and E.M. Carreira Angew. Chem., Int. Ed. 41 2002 4098
181. Y. Wang, J. Janjic, and S.A. Kozmin J. Am. Chem. Soc. 124 2002 13670
182. S.A. Kozmin Org. Lett. 3 2001 755
183. I. Paterson, and M. Tudge Angew. Chem., Int. Ed. 42 2003 343
184. W.C. Still, and C. Gennari Tetrahedron Lett. 24 1983 4405
185. K. Sonogashira F. Diederich P.J. Stang Metal-Catalyzed Cross-Coupling Reactions Vol. 9 1997 Wiley Weinheim 9203
186. (b) For a related Pd(0) mediated oxazole coupling study, see: J.V. Schaus, and J.S. Panek Org. Lett. 2 2000 469
187. R.D. Connell, F. Scavo, P. Helquist, and B. Akermark Tetrahedron Lett. 27 1986 5559
188. R.D. Connell, M. Tebbe, A.R. Gangloff, and P. Helquist Tetrahedron 49 1993 5445
189. C. Cocito Microbiol. Rev. 43 1979 145
190. D. Vazquez The Streptogramin Family of Antibiotics J.W. Corcoran F.H. Hahn Antibiotics III 1975 Springer New York
191. M.G. Brazhnikova, M.K. Kudinova, N.P. Potapova, T.M. Fillipova, E. Borowski, Y. Zelinski, and J. Golik Bioorg. Khim. 2 1976 149
192. J.W. Chamberlin, and S. Chen J. Antibiot. 30 1977 197
193. G.R. Delpierre, F.W. Eastwood, G.E. Gream, D.G.I. Kingston, A.R. Lord Todd, and D.H. Williams J. Chem. Soc. C 1966 1653
194. R.C. Mollering, P.K. Linden, J. Reinhardt, E. Blumberg, G. Bompart, and G.H. Talbot J. Antimicrob. Chemother. 44 1999 251
195. J.-C. Barriere, E. Bacque, G. Puchault, Y. Quenet, C. Molherat, J. Cassayre, and J.-M. Paris Tetrahedron 54 1998 12859
196. D.R. Allington, and M.P. Rivey Clin. Ther. 23 2001 24
197. G. Delgado, M.M. Neuhauser, D. Bearden, and L.H. Danzinger Pharmacotherapy 20 2000 1469
198. F. Tavares, J.P. Lawson, and A.I. Meyers J. Am. Chem. Soc. 118 1996 3303
199. R.H. Schlessinger, and Y.-J. Li J. Am. Chem. Soc. 118 1996 3301
200. P. Breuilles, and D. Uguen Tetrahedron Lett. 39 1998 3149
201. M. Bergdhal, R. Hett, T.L. Friebe, A.R. Gangloff, J. Iqbal, Y. Wu, and P. Helquist Tetrahedron Lett. 34 1993 7371
202. Y.-M. Lin, P. Helquist, and M.J. Miller Synthesis 1999 1510
203. C.J. Brenna, and J.M. Campagne Tetrahedron Lett. 42 2001 5195
204. D.A. Entwistle, S.I. Jordan, J. Montgomery, and G. Pattenden Synthesis 1998 603
205. A.K. Ghosh, and W. Liu J. Org. Chem. 62 1997 7908
206. C.A. Dvorak, W.D. Schmitz, D.J. Poon, D.C. Pryde, J.P. Lawson, R.A. Amos, and A.I. Meyers Angew. Chem., Int. Ed. 39 2000 1664
207. A.I. Meyers, and R.A. Amos J. Am. Chem. Soc. 102 1980 870
208. J. Butera, J. Rini, and P. Helquist J. Org. Chem. 50 1985 3676
209. L. Liu, R.S. Tanke, and M.J. Miller J. Org. Chem. 51 1986 5332
210. E. Marcantoni, M. Massaccesi, M. Petrini, G. Bartoli, M.C. Bellucci, M. Bosco, and L. Sambri J. Org. Chem. 65 2000 4553
211. C. Kuligowski, S. Bezzenine-Lafollee, G. Chaume, J. Mahuteau, J.-C. Marriere, E. Baque, A. Pancrazi, and J. Ardisson J. Org. Chem. 67 2002 4565
212. A.K. Ghosh, and H. Lei Synthesis 2002 371
213. A.I. Meyers, and F.X. Tavares J. Org. Chem. 61 1996 8207
214. J. Tsuji, and T. Mandai Tetrahedron Lett. 21 1978 1817
215. R.H. Grubbs, and S. Chang Tetrahedron 54 1998 4413 and references therein
216. A. Nagatsu, H. Kajitani, and J. Sakakibara Tetrahedron Lett. 36 1995 4097
217. P. Wipf, and S. Venkatraman J. Org. Chem. 61 1996 6517
218. J.C. Muir, G. Pattenden, and R.M. Thomas Synthesis 1998 613
219. P.-Y. Conqueron, C. Didier, and M.A. Ciufolini Angew. Chem., Int. Ed. 42 2003 1411
220. D.B. Dess, and J.C. Martin J. Am. Chem. Soc. 113 1991 7277
221. B.M. Nilsson, and U. Hacksell J. Heterocycl. Chem. 26 1989 269
222. F. Elroy, and A. Deryckere Chim. Ther. 1973 437
223. Y. Yura Chem. Pharm. Bull. Jpn 10 1962 1087
224. P. Wipf, L.T. Rahman, and S.R. Rector J. Org. Chem. 63 1998 7132
225. A. Arcadi, S. Cacchi, L. Cascia, G. Fabrizi, and F. Marinelli Org. Lett. 3 2001 2501
226. N. Fusetani, K. Yasumuro, S. Matsunaga, and K. Hashimoto Tetrahedron Lett. 30 1989 2809
227. J.A. Roesener, and P.J. Scheuer J. Am. Chem. Soc. 108 1986 846
228. S. Matsunaga, N. Fusetani, and K. Hashimoto J. Am. Chem. Soc. 108 1986 847
229. S. Matsunaga, N. Fusetani, K. Hashimoto, K. Koseki, M. Noma, H. Noguchi, and U. Sankawa J. Org. Chem. 54 1989 1360
230. M.R. Kernan, T.F. Molinski, and J.D. Faulkner J. Org. Chem. 53 1988 5014
231. J. Kobayashi, O. Murata, and H. Shigemori J. Nat. Prod. 56 1993 787
232. M. Hori, S. Saito, Y. Shin, H. Ozaki, N. Fusetani, and H. Karaki FEBS Lett. 322 1993 151
233. S. Saito, S. Watabe, H. Ozaki, N. Fusetani, and H. Karaki J. Biol. Chem. 269 1994 29710
234. S. Matsunaga, P. Liu, C.A. Celatka, J.S. Panek, and N. Fusetani J. Am. Chem. Soc. 121 1999 5605
235. For earlier synthetic studies on related trisoxazoles, see (a) D.W. Knight, G. Pattenden, and D.E. Rippon Synlett 1990 36
236. M.J. Kiefel, J. Maddock, and G. Pattenden Tetrahedron Lett. 33 1992 3227
237. G. Pattenden J. Heterocycl. Chem. 29 1992 607
238. S.-K. Yoo Tetrahedron Lett. 33 1992 2159
239. S.K. Chattopadhyay, and G. Pattenden Tetrahedron Lett. 36 1995 5271
240. J.S. Panek, R.T. Beresis, and C.A. Celatka J. Org. Chem. 61 1996 6494
241. J.S. Panek, and R.T. Beresis J. Org. Chem. 61 1996 6496
242. P. Liu, C.A. Celatka, and J.S. Panek Tetrahedron Lett. 38 1997 5445
243. C.A. Celatka, P. Liu, and J.S. Panek Tetrahedron Lett. 38 1997 5449
244. S.K. Chattopadhyay, and G. Pattenden Synlett 1997 1342
245. S.K. Chattopadhyay, and G. Pattenden Synlett 1997 1345
246. P. Liu, and J.S. Panek Tetrahedron Lett. 39 1998 6143
247. P. Liu, and J.S. Panek Tetrahedron Lett. 39 1998 6147
248. J. Kempson, and G. Pattenden Synlett 1999 533
249. J.S. Panek, and P. Liu J. Am. Chem. Soc. 122 2000 11090
250. P. Liu, and J.S. Panek J. Am. Chem. Soc. 122 2000 1235
251. S.K. Chattopadhyay, and G. Pattenden Tetrahedron Lett. 39 1998 6095
252. (b) Ulapualide: S.K. Chattopadhyay, and G. Pattenden J. Chem. Soc., Perkin Trans. 1 15 2000 2429
253. (c) Trisoxazole: S.K. Chattopadhyay, J. Kempson, A. McNeil, G. Pattenden, M. Reader, D.E. Rippon, and D. Waite J. Chem. Soc., Perkin Trans. 1 15 2000 2415
254. J.S. Allingham, J. Tanaka, G. Marriott, and I. Rayment Org. Lett 6 2004 597
255. (a) For a review, see: C.E. Masse, and J.S. Panek Chem. Rev. 95 1995 1293
256. For literature precedent of anti crotylation, see: (b) P. Liu, and J.S. Panek Tetrahedron Lett. 39 1998 6143
257. C.E. Masse, and J.S. Panek Angew. Chem., Int. Ed. 38 1999 1093
258. H. Jin, J. Uenishi, W.J. Christ, and Y. Kishi J. Am. Chem. Soc. 108 1986 5644
259. K. Takai, M. Tagashira, T. Kuroda, K. Oshima, K. Utimoto, and H. Nozaki J. Am. Chem. Soc. 108 1986 6048
260. E. Aguilar, and A.I. Meyers Tetrahedron Lett. 35 1994 2473
261. R.H. Wiley, D.C. England, and C.C. Behr Org. Reac. 6 1951 367
262. J. Maddock, G. Pattenden, and P.G. Wight J. Comput. Aided Mol. Des. 7 1993 573
263. A.I. Meyers, and F. Tavares Tetrahedron Lett. 35 1994 2481
264. P.A. Searle, and T.F. Molinski J. Am. Chem. Soc. 117 1995 8126
265. P.A. Searle, T.F. Molinski, L.J. Brzezinski, and J.W. Leahy J. Am. Chem. Soc. 118 1996 9422
266. T.F. Molinski Tetrahedron Lett. 37 1996 7879
267. T.F. Molinski, L.J. Brzezinski, and J.W. Leahy Tetrahedron: Asymmetry 13 2002 1013
268. C.S. Lee, and C.J. Forsyth Tetrahedron Lett. 37 1996 6449
269. R.D. Cink, and C.J. Forsyth J. Org. Chem. 62 1997 5672
270. F. Ahmed, and C.J. Forsyth Tetrahedron Lett. 39 1998 183
271. T. Ye, and G. Pattenden Tetrahedron Lett. 39 1998 319
272. G. Pattenden, A.T. Plowright, J.A. Tornos, and T. Ye Tetrahedron Lett. 39 1998 6099
273. I. Paterson, and E.A. Arnott Tetrahedron Lett. 39 1998 7185
274. P. Wolbers, and H.M.R. Hoffmann Tetrahedron 55 1999 1905
275. A.M. Misske, and H.M.R. Hoffmann Tetrahedron 55 1999 4315
276. D.R. Williams, M.P. Clark, and M.A. Berliner Tetrahedron Lett. 40 1999 2287
277. D.R. Williams, and M.P. Clark Tetrahedron Lett. 40 1999 2291
278. P. Wolbers, and H.M.R. Hoffmann Synthesis 1999 797
279. D.A. Evans, V.J. Cee, T.E. Smith, and K.J. Santiago Org. Lett. 1 1999 87
280. P. Wolbers, A.M. Misske, and H.M.R. Hoffmann Tetrahedron Lett. 40 1999 4527
281. P. Wolbers, H.M.R. Hoffmann, and F. Sasse Synlett 11 1999 1808
282. G. Pattenden, and A.T. Plowright Tetrahedron Lett. 41 2000 983
283. J.V. Schaus, and J.S. Panek Org. Lett. 2 2000 469
284. S.D. Rychnovsky, and C.R. Thomas Org. Lett. 2 2000 1217
285. D.R. Williams, M.P. Clark, U. Emde, and M.A. Berliner Org. Lett. 2 2000 3023
286. P.B. Greer, and W.A. Donaldson Tetrahedron Lett. 41 2000 3801
287. D.A. Evans, V.J. Cee, T.E. Smith, D.M. Fitch, and P.S. Cho Angew. Chem., Int. Ed. 39 2000 2533
288. H. Huang, and J.S. Panek Org. Lett. 3 2001 1693
289. J.D. White, C.L. Kranemann, and P. Kuntiyong Org. Lett. 3 2001 4003
290. P.B. Greer, and W.A. Donaldson Tetrahedron 58 2002 6009
291. I. Paterson, and C.A. Luckhurst Tetrahedron Lett. 44 2003 3749
292. A.B. Smith III, P.R. Verhoest, K.P. Minbiole, and J.J. Lim Org. Lett. 1 1999 909
293. A.B. Smith III, K.P. Minbiole, P.R. Verhoest, and T.J. Beauchamp Org. Lett. 1 1999 913
294. C.J. Forsyth, F. Ahmed, R.D. Cink, and C.S. Lee J. Am. Chem. Soc. 120 1998 5597
295. D.A. Evans, D.M. Fitch, T.E. Smith, and V.J. Cee J. Am. Chem. Soc. 122 2000 10033
296. A.B. Smith III, K.P. Minbiole, P.R. Verhoest, and M. Schelhaas J. Am. Chem. Soc. 123 2001 10942
297. M.A. Gonzalez, and G. Pattenden Angew. Chem., Int. Ed. 42 2003 1255
298. D.R. Williams, A.A. Kiryanov, U. Emde, M.P. Clark, M.A. Berliner, and J.T. Reeves Angew. Chem., Int. Ed. 42 2003 1258
299. D.A. Evans, M.C. Kozlowski, J.A. Murry, C.S. Burgey, K.R. Campos, B.T. Connell, and R.J. Staples J. Am. Chem. Soc. 121 1999 669
300. D.A. Evans, C.S. Burgey, M.C. Kozlowski, and S.W. Tregay J. Am. Chem. Soc. 121 1999 686
301. D.A. Evans, D.W.C. MacMillan, and K.R. Campos J. Am. Chem. Soc. 119 1997 10859
302. (d) For a review on catalytic asymmetric aldol reaction, see: S.G. Nelson Tetrahedron: Asymmetry 9 1998 357
303. D.A. Evans, P.J. Coleman, and B. Cote J. Org. Chem. 62 1997 788
304. I. Paterson, K.R. Gibson, and R.M. Oballa Tetrahedron Lett. 37 1996 8585
305. D.A. Evans, M.D. Ennis, T. Le, N. Mandel, and G. Mandel J. Am. Chem. Soc. 106 1984 1154
306. D.A. Evans, H.P. Ng, J.S. Clark, and D.L. Rieger Tetrahedron 48 1992 2127
307. N.A. Petasis, and S.-P. Lu Tetrahedron Lett. 37 1996 141
308. R.J. Ferrier, and S. Middleton Chem. Rev. 93 1993 2779
309. Y. Nagao, S. Yamada, T. Kumagai, M. Ochiai, and E. Fujita J. Chem. Soc., Chem. Commun. 1985 1418
310. N.A. Petasis, and E.I. Bzowej J. Am. Chem. Soc. 112 1990 6392
311. J.C. Sheehan, and P.T. Izzo J. Am. Chem. Soc. 71 1949 4059
312. J. Lee, R. Velarde-Ortiz, A. Guijarro, J.R. Wurst, and R.D. Rieke J. Org. Chem. 65 2000 5428
313. T. Delacroix, L. Berillon, G. Cahiez, and P. Knochel J. Org. Chem. 65 2000 8108
314. B.-S. Yun, T. Hidaka, K. Furihata, and H. Seto J. Antibiot. 47 1994 510
315. B. Anderson, D. Crowfoot-Hodgkin, and M.A. Viswamitra Nature 225 1970 233
316. C. Pascard, A. Ducroix, J. Lunel, and T. Prange J. Am. Chem. Soc. 99 1977 6418
317. J. Walker, A. Olesker, L. Valente, R. Rabanal, and G. Lukacs J. Chem. Soc., Chem. Commun. 1977 706
318. B.W. Bycroft, and M.S. Gowland J. Chem. Soc., Chem. Commun. 1978 256
319. K. Shimanaka, Y. Takahashi, H. Iinuma, H. Naganawa, and T. Takeuchi J. Antibiot. 47 1994 1145
320. K. Shimanaka, Y. Takahashi, H. Iinuma, H. Naganawa, and T. Takeuchi J. Antibiot. 47 1994 1153
321. K. Shimanaka, H. Iinuma, M. Hamada, S. Ikeno, K.S. Tsuchiya, M. Arita, and M. Hori J. Antibiot. 48 1995 182
322. Y.Y. Xing, and D.E. Draper Biochemistry 35 1996 1581
323. S.E. Heffron, and F. Jurnak Biochemistry 39 2000 37
324. D.E. Draper D.E. Draper Protein-RNA Recognition in a Highly Conserved Ribosomal Domain Targeted by Thiazole Antibiotics 1998 Academic San Diego 113
325. M.C. Bagley, K.E. Bashford, C.L. Hesketh, and C.J. Moody J. Am. Chem. Soc. 122 2000 3301
326. C.-G. Shin, K. Okumura, M. Shigekuni, and Y. Nakamura Chem. Lett. 1998 139
327. K. Okumura, Y. Nakamura, and C. Shin Bull. Chem. Soc. Jpn 72 1999 1561
328. K. Okumura, A. Ito, D. Yoshioka, and C.-G. Shin Heterocycles 48 1998 1319
329. K. Okumura, T. Suzuki, Y. Nakamura, and C.-G. Shin Bull. Chem. Soc. Jpn 72 1999 2483
330. (e) A recent synthesis of the reported structure of micrococcin P1 indicates that the structure of the natural product is not secure: M.A. Ciufolini, and Y.-C. Shen Org. Lett. 1 1999 1843
331. K. Koerber-Ple', and G. Massiot Synlett 1994 759
332. C. Shin, Y. Nakamura, Y. Yamada, Y. Yonezawa, K. Umemura, and J. Yoshimura Bull. Chem. Soc. Jpn 68 1995 3151
333. K. Koerber-Ple', and G. Massiot J. Heterocycl. Chem. 32 1995 1309
334. K. Umemura, T. Tate, M. Yamaura, J. Yoshimura, Y. Yonezawa, and C. Shin Synthesis 1995 1423
335. C. Shin, Y. Yamada, K. Hayashi, Y. Yonezawa, K. Umemura, T. Tanji, and J. Yoshimura Heterocycles 43 1996 891
336. K. Umemura, H. Noda, J. Yoshimura, A. Konn, Y. Yonezawa, and C.G. Shin Tetrahedron Lett. 38 1997 3539
337. K. Umemura, H. Noda, J. Yoshimura, A. Konn, Y. Yonezawa, and C.G. Shin Bull. Chem. Soc. Jpn 71 1998 1391
338. T.R. Kelly, A. Echavarren, N.S. Chandrakumar, and Y. Köksal Tetrahedron Lett. 25 1984 2127
339. T.R. Kelly, C.T. Jagoe, and Z. Gu Tetrahedron Lett. 32 1991 4263
340. K. Okumura, M. Shigekuni, Y. Nakamura, and C.G. Shin Chem. Lett. 1996 1025
341. T.R. Kelly, and F. Lang Tetrahedron Lett. 36 1995 5319
342. T.R. Kelly, and F. Lang J. Org. Chem. 61 1996 4623
343. K. Umemura, S. Ikeda, J. Yoshimura, K. Okumura, H. Saito, and C.G. Shin Chem. Lett. 1997 1203
344. K. Okumura, H. Saito, C. Shin, K. Umemura, and J. Yoshimura Bull. Chem. Soc. Jpn 71 1998 1863
345. M.C. Bagley, R.T. Buck, S.L. Hind, and C.J. Moody J. Chem. Soc., Perkin Trans. 1 1998 591
346. G. Bram, and M. Vilkas Bull. Soc. Chim. Fr. 1964 945
347. F. Bohlmann, and D. Rahtz Chem. Ber. 90 1957 2265
348. U. Schmidt, R. Meyer, V. Leitenberger, A. Lieberknecht, and H. Griesser J. Chem. Soc., Chem. Commun. 1991 275
349. U. Schmidt, and F. Stäbler J. Chem. Soc., Chem. Commun. 1992 1353
350. U. Schmidt, R. Meyer, V. Leitenberger, H. Griesser, and A. Lieberknecht Synthesis 1992 1025 1030
351. U. Schmidt, V. Leitenberger, H. Griesser, J. Schmidt, and R. Meyer Synthesis 1992 1248 1254
352. U. Schmidt, and S. Weinbrenner J. Chem. Soc., Chem. Commun. 1994 1003
353. R. Jansen, B. Kunze, H. Reichenbach, E. Jurkiewicz, G. Hunsmann, and G. Hofle Liebigs Ann. Chem. 1992 357
354. S. Carmelli, R.E. Moore, G.M. Patterson, T.H. Corbett, and F.A. Valeriote J. Am. Chem. Soc. 112 1990 8195
355. S. Carmelli, R.E. Moore, and G.M. Patterson Tetrahedron Lett. 32 1991 2593
356. E. Jurkiewicz, R. Jansen, B. Kunze, W. Trowitzsch-Kienast, E. Forche, H. Reichenbach, G. Hofle, and G. Hunsmann Antiviral Chem. Chemother. 3 1992 189
357. For previous synthetic work on the tantazoles, see: (a) T. Fukuyama, and L. Xu J. Am. Chem. Soc. 115 1993 8449
358. S. Carmelli, S. Paik, R.E. Moore, G.M.L. Patterson, and W.Y. Yoshida Tetrahedron Lett. 34 1993 6681
359. R.L. Parson Jr., and C.H. Heathcock Synlett 1996 1168
360. For previous synthetic work in the mirabazoles, see: (d) G. Pattenden, and S.M. Thom Synlett 1992 533
361. M.A. Walker, and C.H. Heathcock J. Org. Chem. 57 1992 5566
362. G. Pattenden, and S.M. Thom J. Chem. Soc., Perkin Trans. 1 1993 1629
363. R.L. Parsons Jr., and C.H. Heathcock Tetrahedron Lett. 35 1994 1376
364. R.J. Boyce, G. Pattenden, and S.M. Thom Synlett 1994 587
365. R.J. Boyce, G. Pattenden, and S.M. Thom Tetrahedron 51 1995 7313
366. R.L. Parson Jr., and C.H. Heathcock J. Org. Chem. 59 1994 4733
367. J. Ehrler, and S. Farooq Synlett 9 1994 702
368. R.J. Boyce, G.C. Mulqueen, and G. Pattenden Tetrahedron 51 1995 7321
369. P. Wipf, and S. Venkatraman J. Org. Chem. 60 1995 7224
370. K. Akaji, and Y. Kiso Tetrahedron 55 1999 10685
371. M.A. Walker, and C.H. Heathcock J. Org. Chem. 57 1993 5566
372. D.J. Faulkner Nat. Prod. Rep. 19 2002 1 and previous reviews in the series
373. P. Wipf S.W. Pelletier Alkaloids: Chemical and Biological Perspectives 1998 Pergamon New York 187 228
374. G.R. Pettit Pure Appl. Chem. 66 1994 2271
375. M.J. Garson Chem. Rev. 93 1993 1699
376. B.S. Davidson Chem. Rev. 93 1993 1771
377. N. Fesetani, and S. Matsunoga Chem. Rev. 93 1993 1793
378. J. Ogino, R.E. Moore, G.M.L. Patterson, and C.D. Smith J. Nat. Prod. 59 1996 581
379. J.P. Michael, and G. Pattenden Angew. Chem., Int. Ed. Engl. 32 1993 1
380. P. Wipf Chem. Rev. 95 1995 2115
381. S.V. Downing, E. Aguilar, and A.I. Meyers J. Org. Chem. 64 1999 826
382. E. Aguilar, and A.I. Meyers Tetrahedron Lett. 35 1994 2477
383. F. Yokokawa, H. Sameshima, Y. In, K. Minoura, T. Ishida, and T. Shioiri Tetrahedron 58 2002 8127
384. S. Deng, and J. Taunton J. Am. Chem. Soc. 124 2002 916
385. A. Arrault, A. Witczak-Legrand, P. Gonzalez, N. Bontemps-Subielos, and B. Banaigs Tetrahedron Lett. 43 2002 4041
386. C.D.J. Boden, M. Norley, and G. Pattenden J. Chem. Soc., Perkin Trans. 1 6 2000 883
387. A. Bertram, and G. Pattenden Heterocycles 58 2002 521
388. Z. Xia, and C.D. Smith J. Org. Chem. 66 2001 3459
389. H. Kigoshi, and S. Yamada Tetrahedron 55 1999 12301
390. W. Wang, and F. Nan J. Org. Chem. 68 2003 1636
391. C.D.J. Boden, and G. Pattenden J. Chem. Soc., Perkin Trans. 1 6 2000 875
392. P. Wipf, and P.C. Fritch J. Am. Chem. Soc. 118 1996 12358
393. A. Bertram, and G. Pattenden Synlett 12 2001 1873
394. C.J. Moody, and M.C. Bagley J. Chem. Soc, Perkin Trans. 1 1998 601
395. P. Wipf, and Y. Uto J. Org. Chem. 65 2000 1037
396. M.P. Foster, G.P. Conception, G.B. Caraan, and C.M. Ireland J. Org. Chem. 57 1992 6671
397. F. Tavares, and A.I. Meyers Tetrahedron Lett. 35 1994 6803
398. P. Wipf, and C.P. Miller J. Am. Chem. Soc. 114 1992 10975
399. M.W. Bredenkamp, C.W. Holzapfel, and W.J. van Zyl Synth. Commun. 20 1990 2235
400. R.E. Moore, J. Ogino, G.M.I. Patterson, and C.D. Smith J. Nat. Prod. 59 1996 581
401. V. Admi, U. Afek, and S. Carmeli J. Nat. Prod. 59 1996 396
402. A. Bertram, J.S. Hannam, K.A. Jolliffe, and G. Pattenden Synlett 1999 1723
403. A.J. Blake, J.S. Hannam, K.A. Jollife, and G. Pattenden Synlett 2000 1515
404. L. Somogyi, G. Haberhauer, and J. Rebek Jr. Tetrahedron 57 2001 1699
405. S. Kehraus, G.M. Konig, and A.D. Wright J. Org. Chem. 67 2002 4989
406. T.L. Tan, R.T. Williamson, W.H. Gerwick, K.S. Watt, K. McGough, and R. Jacobs J. Org. Chem. 65 2000 419