The conjugate addition of enantiomerically pure lithium amides as chiral ammonia equivalents part II: 2005-2011

Tetrahedron Asymmetry

Volumn 23, Issue 15-16, 2012, Pages 1111-1153

  Davies, Stephen G ^a   Fletcher, Ai M ^a   Roberts, Paul M ^a   Thomson, James E ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

2 PIPERIDONE DERIVATIVE; ALPHA DEUTERIO BETA AMINO ACID DERIVATIVE; ALPHA FLUORO BETA AMINO ACID DERIVATIVE; ALPHA HYDROXY BETA AMINO ACID DERIVATIVE; ALPHA THIO BETA AMINO ACID DERIVATIVE; AMINO ACID DERIVATIVE; AMINOSUGAR; AMMONIA; BETA AMINO ACID; BETA AMINO ESTER DERIVATIVE; ESTER DERIVATIVE; GAMMA LACTAM DERIVATIVE; HETEROCYCLIC COMPOUND; IODINE; LACTAM DERIVATIVE; LITHIUM AMIDE DERIVATIVE; LITHIUM DERIVATIVE; PIPERIDINE DERIVATIVE; PYRROLIDINE DERIVATIVE; PYRROLIZIDINE DERIVATIVE; UNCLASSIFIED DRUG; ZETA HALO BETA AMINO ESTER;

ADDITION REACTION; ASYMMETRIC SYNTHESIS; CHEMICAL MODIFICATION; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHIRALITY; CONJUGATION; CYCLIZATION; DEPROTECTION REACTION; ENANTIOMER; KINETICS; ONE POT SYNTHESIS; PRIORITY JOURNAL; RACEMIZATION; REDUCTION; REVIEW; RING CLOSING IODOAMINATION; RING CLOSING METATHESIS; STEREOCHEMISTRY; SYNTHESIS;

EID: 84866973898     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2012.08.009     Document Type: Review

References (153)

1. S.G. Davies, A.D. Smith, and P.D. Price Tetrahedron: Asymmetry 16 2005 2833
2. S.G. Davies, and O. Ichihara Tetrahedron: Asymmetry 2 1991 183
3. J.F. Costello, S.G. Davies, and O. Ichihara Tetrahedron: Asymmetry 5 1994 1999
4. For selected examples, see: S.G. Davies, K. Iwamoto, C.A.P. Smethurst, A.D. Smith, and H. Rodríguez-Solla Synlett 2002 1146
5. S.G. Davies, R.J. Kelly, and A.J. Price Mortimer Chem. Commun. 2003 2132
6. A.J. Burke, S.G. Davies, A.C. Garner, T.D. McCarthy, P.M. Roberts, A.D. Smith, H. Rodríguez-Solla, and R.J. Vickers Org. Biomol. Chem. 2 2004 1387
7. S.G. Davies, J.R. Haggitt, O. Ichihara, R.J. Kelly, M.A. Leech, A.J. Price Mortimer, P.M. Roberts, and A.D. Smith Org. Biomol. Chem. 2 2004 2630
8. D. Ma, and H. Sun J. Org. Chem. 65 2000 6009
9. A.M. Chippindale, S.G. Davies, K. Iwamoto, R.M. Parkin, C.A.P. Smethurst, A.D. Smith, and H. Rodríguez-Solla Tetrahedron 59 2003 3253
10. M.E. Bunnage, A.J. Burke, S.G. Davies, and C.J. Goodwin Tetrahedron: Asymmetry 6 1995 165
11. S.G. Davies, and D.R. Fenwick Chem. Commun. 1997 565
12. S.G. Davies, G.D. Smyth, and A.M. Chippindale J. Chem. Soc., Perkin Trans. 1 1999 3089
13. S.G. Davies, and G.D. Smyth Tetrahedron: Asymmetry 7 1996 1273
14. S.G. Davies, C.J.R. Hedgecock, and J.M. McKenna Tetrahedron: Asymmetry 6 1995 2507
15. S.G. Davies, and D.J. Dixon J. Chem. Soc., Perkin Trans. 1 1998 2635
16. S.G. Davies, and D.J. Dixon Chem. Commun. 1996 1797
17. S.G. Davies, O. Ichihara, I. Lenoir, and I.A.S. Walters J. Chem. Soc., Perkin Trans. 1 1994 1411
18. S.G. Davies, and G. Bhalay Tetrahedron: Asymmetry 7 1996 1595
19. S.G. Davies, D.G. Hughes, R.L. Nicholson, A.D. Smith, and A.J. Wright Org. Biomol. Chem. 2 2004 1549
20. M.E. Bunnage, S.G. Davies, C.J. Goodwin, and O. Ichihara Tetrahedron 50 1994 3975
21. C.B. de Konig, J.P. Michael, and D.L. Riley Heterocycles 79 2009 935
22. P.R. Krishna, A. Sreeshailam, and R. Srinivas Tetrahedron 65 2009 9657
23. S.G. Davies, A.M. Fletcher, and P.M. Roberts Org. Synth. 87 2010 143
24. T.D.W. Claridge, S.G. Davies, J.A. Lee, R.L. Nicholson, P.M. Roberts, A.J. Russell, A.D. Smith, and S.M. Toms Org. Lett. 10 2008 5437
25. T.D.W. Claridge, S.G. Davies, M.E.C. Polywka, P.M. Roberts, A.J. Russell, E.D. Savory, and A.D. Smith Org. Lett. 10 2008 5433
26. S.A. Bentley, S.G. Davies, J.A. Lee, P.M. Roberts, A.J. Russell, J.E. Thomson, and S.M. Toms Tetrahedron 66 2010 4604
27. S.A. Bentley, S.G. Davies, J.A. Lee, P.M. Roberts, and J.E. Thomson Org. Lett. 13 2011 2544
28. S. Fustero, S. Monteagudo, M. Sánchez-Roselló, S. Flores, P. Barrio, and C. del Pozo Chem. Eur. J. 16 2010 9835
29. M. Koutsaplis, P.C. Andrews, S.D. Bull, P.J. Duggan, B.H. Fraser, and P. Jensen Chem. Commun. 2007 3580
30. M. Node, D. Hashimoto, T. Katoh, S. Ochi, M. Ozeki, T. Watanabe, and T. Kajimoto Org. Lett. 10 2008 2653
31. S.G. Davies, N.M. Garrido, D. Kruchinin, O. Ichihara, L.J. Kotchie, P.D. Price, A.J. Price Mortimer, A.J. Russell, and A.D. Smith Tetrahedron: Asymmetry 17 2006 1793
32. A. Bariau, J.-L. Canet, P. Chalard, and Y. Troin Tetrahedron: Asymmetry 16 2005 3650
33. M. Sivaprokasham, F. Couty, G. Evano, B. Srinivas, R. Sridhar, and K.R. Rao ARKIVOC x 2007 71
34. C. Miniejew, F. Outurquin, and X. Pannecoucke Tetrahedron 62 2006 2657
35. P.J. Duggan, M. Johnston, and T.L. March J. Org. Chem. 75 2010 7365
36. S.G. Davies, A.W. Mulvaney, A.J. Russell, and A.D. Smith Tetrahedron: Asymmetry 18 2007 1554
37. M. Ahari, A. Perez, C. Menant, J.-L. Vasse, and J. Szymoniak Org. Lett. 10 2008 2473
38. A. Chernega, S.G. Davies, D.L. Elend, A.P. Smethurst, P.M. Roberts, A.D. Smith, and G.D. Smyth Tetrahedron 63 2007 7036
39. S. Yu, W. Zhu, and D. Ma J. Org. Chem. 70 2005 7364
40. E. Kiss, I.E. Markó, and M. Guillaume Tetrahedron 67 2011 9173
41. S.G. Davies, A.M. Fletcher, P.M. Roberts, and A.D. Smith Tetrahedron 65 2009 10192
42. S.K. Bagal, S.G. Davies, A.M. Fletcher, A.J. Lee, P.M. Roberts, P.M. Scott, and J.E. Thomson Tetrahedron Lett. 52 2011 2216
43. K. Csatayová, S.G. Davies, J.A. Lee, P.M. Roberts, A.J. Russell, J.E. Thomson, and D.L. Wilson Org. Lett. 13 2011 2606
44. Y. Yamamoto, and H. Hayashi Tetrahedron 63 2007 10149
45. N.M. Garrido, D. Díez, S.H. Domínguez, M.R. Sánchez, M. García, and J.G. Urones Molecules 11 2006 435
46. H. Henon, and Y. Troin Synlett 2007 1446
47. N.M. Garrido, M. Blanco, I.F. Cascón, D. Díez, V.M. Vincente, F. Sanz, and J.G. Urones Tetrahedron: Asymmetry 19 2008 2895
48. E. Abraham, C.W. Bailey, T.D.W. Claridge, S.G. Davies, K.B. Ling, B. Odell, T.L. Rees, P.M. Roberts, A.J. Russell, A.D. Smith, L.J. Smith, H.R. Storr, M.J. Sweet, A.L. Thompson, J.E. Thomson, G.E. Tranter, and D.J. Watkin Tetrahedron: Asymmetry 21 2010 1797
49. S.G. Daives, D.G. Hughes, P.D. Price, P.M. Roberts, A.J. Russell, A.D. Smith, J.E. Thomson, and O.M.H. Williams Synlett 2010 567
50. S.G. Davies, A.M. Fletcher, D.G. Hughes, J.A. Lee, P.D. Price, P.M. Roberts, A.J. Russell, A.D. Smith, J.E. Thomson, and O.M.H. Williams Tetrahedron 67 2011 9975
51. N.M. Garrido, A.G. Rubia, C. Nieto, and D. Díez Synlett 2010 587
52. F. Liu, W. Yu, W. Ou, X. Wang, L. Ruan, Y. Li, X. Peng, X. Tao, and X. Pan J. Chem. Res. 34 2010 230
53. E. Abraham, J.W.B. Cooke, S.G. Davies, A. Naylor, R.L. Nicholson, P.D. Price, and A.D. Smith Tetrahedron 63 2007 5855
54. R. Bischoff, D.J. Hamilton, N.K. Jobson, and A. Sutherland J. Labelled Compd. Radiopharm. 50 2007 323
55. R. Bischoff, N. McDonald, and A. Sutherland Tetrahedron Lett. 46 2005 7147
56. S.G. Davies, A.C. Garner, E.C. Goddard, D. Kruchinin, P.M. Roberts, H. Rodríguez-Solla, and A.D. Smith Chem. Commun. 2006 2664
57. S.G. Davies, A.C. Garner, E.C. Goddard, D. Kruchinin, P.M. Roberts, A.D. Smith, H. Rodríguez-Solla, J.E. Thomson, and S.M. Toms Org. Biomol. Chem. 5 2007 1961
58. M. Breuning, and D. Hein Tetrahedron: Asymmetry 18 2007 1410
59. S.G. Davies, E.M. Foster, C.R. McIntosh, P.M. Roberts, T.E. Rosser, A.D. Smith, and J.E. Thomson Tetrahedron: Asymmetry 22 2011 1035
60. L.-J. Ma, Z.-W. Mei, K. Toyohara, H. Kawafuchi, J. Nokami, and T. Inokuchi Bull. Chem. Soc. Jpn. 83 2010 1545
61. R. Tannert, L.-G. Milroy, B. Ellinger, T.-S. Hu, H.-D. Arndt, and H. Waldmann J. Am. Chem. Soc. 132 2010 3063
62. H. Waldmann, T.-S. Hu, S. Renner, S. Menninger, R. Tannert, T. Oda, and H.-D. Arndt Angew. Chem., Int. Ed. 47 2008 6473
63. X. Fan, H.-S. Zhang, L. Chen, and Y.-Q. Long Eur. J. Med. Chem. 45 2010 2827
64. Y. Zhu, X. Zhu, G. Wu, Y. Ma, Y. Li, X. Zhao, Y. Yuan, J. Yang, S. Yu, F. Shao, R. Li, Y. Ke, A. Lu, Z. Liu, and L. Zhang J. Med. Chem. 53 2010 1990
65. S.G. Davies, M.J. Durbin, E.C. Goddard, P.M. Kelly, W. Kurosawa, J.A. Lee, R.L. Nicholson, P.D. Price, P.M. Roberts, A.J. Russell, P.M. Scott, and A.D. Smith Org. Biomol. Chem. 7 2009 761
66. S.G. Davies, J.A. Lee, P.M. Roberts, J.E. Thomson, and J. Yin Tetrahedron 67 2011 6382
67. J. Magano, D. Bowles, B. Conway, T.N. Nanninga, and D.D. Winkle Tetrahedron Lett. 50 2009 6325
68. S.G. Davies, A.M. Fletcher, G.J. Hermann, G. Poce, P.M. Roberts, A.D. Smith, M.J. Sweet, and J.E. Thomson Tetrahedron: Asymmetry 21 2010 1635
69. S.G. Davies, O. Ichihara, P.M. Roberts, and J.E. Thomson Tetrahedron 67 2011 216
70. E. Abraham, T.D.W. Claridge, S.G. Davies, B. Odell, P.M. Roberts, A.J. Russell, A.D. Smith, L.J. Smith, H.R. Storr, M.J. Sweet, A.L. Thompson, J.E. Thomson, G.E. Tranter, and D.J. Watkin Tetrahedron: Asymmetry 22 2011 69
71. Y. Aye, S.G. Davies, A.C. Garner, P.M. Roberts, A.D. Smith, and J.E. Thomson Org. Biomol. Chem. 6 2008 2195
72. E. Abraham, S.G. Davies, A.J. Docherty, K.B. Ling, P.M. Roberts, A.J. Russell, J.E. Thomson, and S.M. Toms Tetrahedron: Asymmetry 19 2008 1356
73. Z. Szakonyi, and F. Fülöp Amino Acids 41 2011 597
74. S.G. Davies, A.J. Russell, R.L. Sheppard, A.D. Smith, and J.E. Thomson Org. Biomol. Chem. 5 2007 3190
75. S.G. Davies, M.J. Durbin, S.J.S. Hartman, A. Matsuno, P.M. Roberts, A.J. Russell, A.D. Smith, J.E. Thomson, and S.M. Toms Tetrahedron: Asymmetry 19 2008 2870
76. S. Terracciano, I. Bruno, E. D'Amico, G. Bifulco, A. Zampella, V. Sepe, C.D. Smith, and R. Riccio Bioorg. Med. Chem. 16 2008 6580
77. J.I. Candela-Lena, S.G. Davies, P.M. Roberts, B. Roux, A.J. Russell, E.M. Sánchez-Fernández, and A.D. Smith Tetrahedron: Asymmetry 17 2006 1135
78. S.D. Bull, S.G. Davies, G. Fenton, A.W. Mulvany, R.S. Prasad, and A.D. Smith J. Chem. Soc., Perkin Trans. 1 1 2000 3765
79. S.D. Bull, S.G. Davies, G. Fenton, A.W. Mulvaney, R.S. Prasad, and A.D. Smith Chem. Commun. 2000 337
80. E. Abraham, S.G. Davies, P.M. Roberts, A.L. Thompson, and J.E. Thomson J. Chem. Crystallogr. 41 2011 1722
81. E. Abraham, S.G. Davies, N.L. Millican, R.L. Nicholson, P.M. Roberts, and A.D. Smith Org. Biomol. Chem. 6 2008 1655
82. E. Abraham, E.A. Brock, J.I. Candela-Lena, S.G. Davies, M. Georgiou, R.L. Nicholson, J.H. Perkins, P.M. Roberts, A.J. Russell, E.M. Sánchez- Fernández, P.M. Scott, A.D. Smith, and J.E. Thomson Org. Biomol. Chem. 6 2008 1665
83. S.G. Davies, A.C. Garner, P.M. Roberts, A.D. Smith, M.J. Sweet, and J.E. Thomson Org. Biomol. Chem. 4 2006 2753
84. E. Abraham, J.I. Candela-Lena, S.G. Davies, M. Georgiou, R.L. Nicholson, P.M. Roberts, A.J. Russell, E.M. Sánchez-Fernández, A.D. Smith, and J.E. Thomson Tetrahedron: Asymmetry 18 2007 2510
85. For the established anti-alkylation preference of β-amino enolates, see: S.G. Davies, and I.A.S. Walters J. Chem. Soc., Perkin Trans. 1 1994 1129
86. S.G. Davies, O. Ichihara, and I.A.S. Walters J. Chem. Soc., Perkin Trans. 1 1994 1141
87. S.G. Davies, A.J. Edwards, and I.A.S. Walters Recl. Trav. Chim. Pays-Bas 114 1995 175
88. D.A. Price Synlett 1999 1919
89. M. Baenziger, L. Gobbi, B.P. Riss, R.F. Schaefer, and A. Vaupel Tetrahedron: Asymmetry 11 2000 2231
90. S.G. Davies, N.M. Gariddo, O. Ichihara, and I.A.S. Walters Chem. Commun. 1993 1153
91. T. Cailleau, J.W.B. Cooke, S.G. Davies, K.B. Ling, A. Naylor, R.L. Nicholson, P.D. Price, P.M. Roberts, A.J. Russell, A.D. Smith, and J.E. Thomson Org. Biomol. Chem. 5 2007 3922
92. S.G. Davies, P.M. Roberts, and A.D. Smith Org. Biomol. Chem. 5 2007 1405
93. S.G. Davies, P.M. Roberts, and A.D. Smith Org. Biomol. Chem. 5 2007 3717
94. N.M. Garrido, D. Díez, S.H. Domínguez, M. García, M.R. Sánchez, and S.G. Davies Tetrahedron: Asymmetry 1 2006 2183
95. For the one-pot conjugate addition of the lithium amide derived from (-)-47, followed by intramolecular cyclisation or aldol reactions, see: M. Ozeki, S. Ochi, N. Hayama, S. Hosoi, T. Kajimoto, and M. Node J. Org. Chem. 75 2010 4201
96. A.B. Holmes, A.L. Smith, S.F. Williams, L.R. Hughes, Z. Lidert, and C. Swithenbank J. Org. Chem. 56 1991 1393
97. S.G. Davies, N. Mujtaba, P.M. Roberts, A.D. Smith, and J.E. Thomson Org. Lett. 11 2009 1959
98. J.E. Beddow, S.G. Davies, A.D. Smith, and A.J. Russell Chem. Commun. 2004 2778
99. J.E. Beddow, S.G. Davies, K.B. Ling, P.M. Roberts, A.J. Russell, A.D. Smith, and J.E. Thomson Org. Biomol. Chem. 5 2007 2812
100. S.G. Davies, R.L. Nicholson, P.D. Price, P.M. Roberts, A.J. Russell, E.D. Savory, A.D. Smith, and J.E. Thomson Tetrahedron: Asymmetry 20 2009 758
101. E.A. Brock, S.G. Davies, J.A. Lee, P.M. Roberts, and J.E. Thomson Org. Lett. 13 2011 1594
102. S.G. Davies, R. Huckvale, T.J.A. Lorkin, P.M. Roberts, and J.E. Thomson Tetrahedron: Asymmetry 22 2011 1591
103. S.G. Davies, J.A. Lee, P.M. Roberts, J.E. Thomson, and C.J. West Tetrahedron Lett. 52 2011 6477
104. S. Takano, K. Hiroya, and K. Ogawasara Chem. Lett. 12 1983 255
105. M.G. Ranasinghe, and P.L. Fuchs Synth. Commun. 18 1988 227
106. The high stereocontrol exerted upon protonation of an enolate anti to an adjacent heteroatom is also well documented, see: H.M.L. Davies, L.M. Hodges, and T.M. Gregg J. Org. Chem. 66 2001 7898
107. L. Banfi, and G. Guanti Tetrahedron: Asymmetry 10 1999 439
108. J.R. Mohrig, R.E. Rosenberg, J.W. Apostol, M. Bastienaansen, J.W. Evans, S.J. Franklin, C.D. Frisbie, S.S. Fu, M.L. Hamm, C.B. Hirose, D.A. Hunstad, T.L. James, R.W. King, C.J. Larson, H.A. Latham, D.A. Owen, K.A. Stein, and R. Warnet J. Am. Chem. Soc. 119 1997 479
109. G. Vavon, and A. Antonini Searces. Acad. Sci. Ser. C 230 1950 1870
110. K. Harada, and K. Matsumoto J. Org. Chem. 31 1966 2985
111. A. Horeau, H.B. Kagan, and J.P. Vigneron Bull. Soc. Chim. Fr. 1968 3795
112. S. Masamune, and W. Choy Aldrichim. Acta 15 1982 47
113. S. Masamune Heterocycles 21 1984 107
114. A.N. Chernega, S.G. Davies, C.J. Goodwin, D. Hepworth, W. Kurosawa, P.M. Roberts, and J.E. Thomson Org. Lett. 11 2009 3254
115. S.G. Davies, C.J. Goodwin, D. Hepworth, P.M. Roberts, and J.E. Thomson J. Org. Chem. 75 2010 1214
116. A.N. Chernega, S.G. Davies, A.M. Fletcher, C.J. Goodwin, D. Hepworth, R.S. Prasad, P.M. Roberts, E.D. Savory, A.D. Smith, and J.E. Thomson Tetrahedron 66 2010 4167
117. J. Etxebarria, J.L. Vicario, D. Badia, L. Carrillo, and N. Ruiz J. Org. Chem. 70 2005 8790
118. Z. Szakonyi, A. Balázs, T.A. Martinek, and F. Fülöp Tetrahedron: Asymmetry 21 2010 2498
119. For kinetic resolution of 3-alkyl-cyclopent-1-ene-carboxylates, see: S. Bailey, S.G. Davies, A.D. Smith, and J.M. Withey Chem. Commun. 2002 2910
120. M.E. Bunnage, A.M. Chippindale, S.G. Davies, R.M. Parkin, A.D. Smith, and J.M. Withey Org. Biomol. Chem. 1 2003 3698
121. M.E. Bunnage, S.G. Davies, R.M. Parkin, P.M. Roberts, A.D. Smith, and J.M. Withey Org. Biomol. Chem. 2 2004 3337
122. For parallel kinetic resolution of 3-alkyl-cyclopent-1-ene-carboxylates, see: S.G. Davies, A.C. Garner, M.J.C. Long, A.D. Smith, M.J. Sweet, and J.M. Withey Org. Biomol. Chem. 2 2004 3355
123. For kinetic and parallel kinetic resolution of 5-alkyl-cyclopent-1-ene- carboxylates, see: S.G. Davies, D. Díez, M.M. El Hammouni, A.C. Garner, N.M. Garrido, M.J.C. Long, R.M. Morrison, A.D. Smith, M.J. Sweet, and J.M. Withey Chem. Commun. 2003 2410
124. S.G. Davies, A.C. Garner, M.J.C. Long, R.M. Morrison, P.M. Roberts, E.D. Savory, A.D. Smith, M.J. Sweet, and J.M. Withey Org. Biomol. Chem. 3 2005 2762
125. D.H. Appella, L.A. Christianson, I.L. Karle, D.R. Powell, and S.H. Gellman J. Am. Chem. Soc. 118 1996 13071
126. J.J. Barchi Jr., X. Huang, D.H. Appella, L.A. Christianson, S.R. Durell, and S.H. Gellman J. Am. Chem. Soc. 122 2000 2711
127. H. Nohira, K. Ehara, and A. Miyashita Bull. Chem. Soc. Jpn. 43 1970 2230
128. R.P. Cheng, S.H. Gellman, and W.F. DeGrado Chem. Rev. 101 2001 3219
129. G.H.P. Van Daele, M.F.L. De Bruyn, F.M. Sommen, M. Janssen, J.M. Van Nueten, J.A.J. Schuurkes, C.J.E. Niemegeers, and J.E. Leysen Drug Dev. Res. 8 1986 225
130. N.M. Garrido, M. García, D. Díez, M.R. Sánchez, F. Santz, and J.G. Urones Org. Lett. 10 2008 1687
131. N.M. Garrido, M.R. Sánchez, D. Díez, F. Santz, and J.G. Urones Tetrahedron: Asymmetry 22 2011 872
132. D. Basavaiah, A.J. Rao, and T. Satyanarayana Chem. Rev. 103 2003 811
133. N.M. Garrido, M. García, M.R. Sánchez, D. Díez, F. Santz, and J.G. Urones Synlett 2010 387
134. For example, see: P. Roger, C. Monneret, J.-P. Fournier, P. Choay, R. Gagnet, C. Gosse, Y. Letourneux, G. Atassi, and A. Gouyette J. Med. Chem. 32 1989 16
135. I. Kovács, P. Herczegh, and J. Sztaricskai Tetrahedron 47 1991 7837
136. B. Renneberg, Y.-M. Ling, H. Laatsch, and H.-H. Fiebig Carbohydrate Res. 329 2000 861
137. W. Shi, R.S. Coleman, and T.L. Lowary Org. Biomol. Chem. 7 2009 3709
138. For example, see: M. Hirama, T. Shigemoto, and S. Itô J. Org. Chem. 52 1987 3342
139. A.W. Konradi, and S.F. Pedersen J. Org. Chem. 55 1990 4506
140. M. Hatanaka, and I. Ueda Chem. Lett. 20 1991 61
141. For example, see: P.M. Wovkulich, and M.R. Uskoković Tetrahedron 41 1985 3455
142. X. Ginesta, M. Pastó, M.A. Pericàs, and A. Riera Org. Lett. 5 2003 3001
143. M. Sugiura, K. Hirano, and S. Kobayashi J. Am. Chem. Soc. 126 2004 7182
144. Y. Matsushima, and J. Kino Tetrahedron Lett. 46 2005 8609
145. C. Aciro, T.D.W. Claridge, S.G. Davies, P.M. Roberts, A.J. Russell, and J.E. Thomson Org. Biomol. Chem. 6 2008 3751
146. C. Aciro, S.G. Davies, P.M. Roberts, A.J. Russell, A.D. Smith, and J.E. Thomson Org. Biomol. Chem. 6 2008 3762
147. C.W. Bond, A.J. Cresswell, S.G. Davies, A.M. Fletcher, W. Kurosawa, J.A. Lee, P.M. Roberts, A.J. Russell, A.D. Smith, and J.E. Thomson J. Org. Chem. 74 2009 6735
148. S.G. Davies, A.M. Fletcher, W. Kurosawa, J.A. Lee, G. Poce, P.M. Roberts, J.E. Thomson, and D.M. Williamson J. Org. Chem. 75 2010 7745
149. W. Kurosawa, P.M. Roberts, and S.G. Davies Yuki Gosei Kagaku Kyokaishi (J. Synth. Org. Chem. Jpn.) 68 2010 1295
150. We have also developed a protocol for the diastereoselective oxidation of an allylic tertiary amine N-oxide, see: C. Aciro, S.G. Davies, W. Kurosawa, P.M. Roberts, A.J. Russell, and J.E. Thomson Org. Lett. 11 2009 1333
151. J. Monfray, Y. Mialhe-Gelas, J.-C. Gramain, and R. Remuson Tetrahedron: Asymmetry 16 2005 1025
152. Y. Hayashi, T. Regnier, S. Nishiguchi, M.O. Sydnes, D. Hashimoto, J. Hasegawa, T. Katoh, T. Kajimoto, M. Shiozuka, R. Matsuda, M. Node, and Y. Kiso Chem. Commun. 2008 2379
153. S. Nishiguchi, M.O. Sydnes, A. Taguchi, T. Regnier, T. Kajimoto, M. Node, Y. Yamazaki, F. Yakushiji, Y. Kiso, and Y. Hayashi Tetrahedron 66 2010 314