-
1
-
-
32144461175
-
-
For reviews on α-oxo ketene (S,S)-acetals, see: (a)
-
For reviews on α-oxo ketene (S,S)-acetals, see: (a) Dieter, R. K. Tetrahedron 1986, 42, 3029.
-
(1986)
Tetrahedron
, vol.42
, pp. 3029
-
-
Dieter, R.K.1
-
2
-
-
0001453067
-
-
(b) Junjappa, H.; Ila, H.; Asokan, C. V. Tetrahedron 1990, 46, 5423.
-
(1990)
Tetrahedron
, vol.46
, pp. 5423
-
-
Junjappa, H.1
Ila, H.2
Asokan, C.V.3
-
4
-
-
58549087741
-
-
Selected examples for C-C bond-forming reactions at the α-position of functionalized ketene (S,S)-acetals: (a)
-
Selected examples for C-C bond-forming reactions at the α-position of functionalized ketene (S,S)-acetals: (a) Yuan, H.-J.; Wang, M.; Liu, Y.-J.; Liu, Q. Adv. Synth. Catal. 2009, 351, 112.
-
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 112
-
-
Yuan, H.-J.1
Wang, M.2
Liu, Y.-J.3
Liu, Q.4
-
5
-
-
65249111209
-
-
(b) Ma, Y.; Wang, M.; Li, D.; Bekturhun, B.; Liu, J.; Liu, Q. J. Org. Chem. 2009, 74, 3116.
-
(2009)
J. Org. Chem.
, vol.74
, pp. 3116
-
-
Ma, Y.1
Wang, M.2
Li, D.3
Bekturhun, B.4
Liu, J.5
Liu, Q.6
-
6
-
-
53049097221
-
-
(c) Fu, Z.; Wang, M.; Ma, Y.; Liu, Q.; Liu, J. J. Org. Chem. 2008, 73, 7625.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 7625
-
-
Fu, Z.1
Wang, M.2
Ma, Y.3
Liu, Q.4
Liu, J.5
-
7
-
-
35948940824
-
-
Selected examples of intramolecular anti-Michael addition: (a) Domino reaction
-
Selected examples of intramolecular anti-Michael addition: (a) Bi, X.; Zhang, J.; Liu, Q.; Tan, J.; Li, B. Adv. Synth. Catal. 2007, 349, 2301. Domino reaction:
-
(2007)
Adv. Synth. Catal.
, vol.349
, pp. 2301
-
-
Bi, X.1
Zhang, J.2
Liu, Q.3
Tan, J.4
Li, B.5
-
8
-
-
33749350169
-
-
[5C + 1N] annulations
-
(b) Liang, F.; Zhang, J.; Tan, J.; Liu, Q. Adv. Synth. Catal. 2006, 348, 1986. [5C + 1N] annulations:
-
(2006)
Adv. Synth. Catal.
, vol.348
, pp. 1986
-
-
Liang, F.1
Zhang, J.2
Tan, J.3
Liu, Q.4
-
9
-
-
29944435631
-
-
(c) Dong, D.; Bi, X.; Liu, Q.; Cong, F. Chem. Commun. 2005, 3580.
-
(2005)
Chem. Commun.
, pp. 3580
-
-
Dong, D.1
Bi, X.2
Liu, Q.3
Cong, F.4
-
10
-
-
41849134378
-
-
[5C + 1S] and [5C + 1Se] annulations
-
(d) Hu, J.; Zhang, Q.; Yuan, H.; Liu, Q. J. Org. Chem. 2008, 73, 2442. [5C + 1S] and [5C + 1Se] annulations:
-
(2008)
J. Org. Chem.
, vol.73
, pp. 2442
-
-
Hu, J.1
Zhang, Q.2
Yuan, H.3
Liu, Q.4
-
11
-
-
29944434374
-
-
(e) Bi, X.; Dong, D.; Li, Y.; Liu, Q. J. Org. Chem. 2005, 70, 10886.
-
(2005)
J. Org. Chem.
, vol.70
, pp. 10886
-
-
Bi, X.1
Dong, D.2
Li, Y.3
Liu, Q.4
-
12
-
-
46649089366
-
-
(f) Li, D.; Xu, X.; Liu, Q.; Dong, S. Synthesis 2008, 1895.
-
(2008)
Synthesis
, pp. 1895
-
-
Li, D.1
Xu, X.2
Liu, Q.3
Dong, S.4
-
13
-
-
16844377947
-
-
Selected examples for [5C + 1C] annulations: (a)
-
Selected examples for [5C + 1C] annulations: (a) Bi, X.; Dong, D.; Liu, Q.; Pan, W.; Zhao, L.; Li, B. J. Am. Chem. Soc. 2005, 127, 4578.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 4578
-
-
Bi, X.1
Dong, D.2
Liu, Q.3
Pan, W.4
Zhao, L.5
Li, B.6
-
14
-
-
60849107309
-
-
(b) Zhang, L.; Liang, F.; Cheng, X.; Liu, Q. J. Org. Chem. 2009, 74, 899.
-
(2009)
J. Org. Chem.
, vol.74
, pp. 899
-
-
Zhang, L.1
Liang, F.2
Cheng, X.3
Liu, Q.4
-
15
-
-
33846045228
-
-
(c) Zhang, Q.; Sun, S.; Hu, J.; Liu, Q.; Tan, J. J. Org. Chem. 2007, 72, 139.
-
(2007)
J. Org. Chem.
, vol.72
, pp. 139
-
-
Zhang, Q.1
Sun, S.2
Hu, J.3
Liu, Q.4
Tan, J.5
-
16
-
-
46149083746
-
-
For a review of applications of nitroalkanes in the synthesis of benzene derivatives, see
-
For a review of applications of nitroalkanes in the synthesis of benzene derivatives, see: Ballini, R.; Palmieri, A.; Barboni, L. Chem. Commun. 2008, 2975.
-
(2008)
Chem. Commun.
, pp. 2975
-
-
Ballini, R.1
Palmieri, A.2
Barboni, L.3
-
17
-
-
70349783700
-
-
Tan, J.; Xu, X.; Zhang, L.; Li, Y.; Liu, Q. Angew. Chem., Int. Ed. 2009, 48, 2868.
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 2868
-
-
Tan, J.1
Xu, X.2
Zhang, L.3
Li, Y.4
Liu, Q.5
-
18
-
-
11244348930
-
-
For selective reports on the Michael reactions of α-oxo ketene (S,S)- acetals with acetophenones, see: (a)
-
For selective reports on the Michael reactions of α-oxo ketene (S,S)- acetals with acetophenones, see: (a) Potts, K. T.; Cipullo, M. J.; Ralli, P.; Theodoridis, G. J. Am. Chem. Soc. 1981, 103, 3584.
-
(1981)
J. Am. Chem. Soc.
, vol.103
, pp. 3584
-
-
Potts, K.T.1
Cipullo, M.J.2
Ralli, P.3
Theodoridis, G.4
-
19
-
-
0000542050
-
-
(b) Potts, K. T.; Cipullo, M. J.; Ralli, P.; Theodoridis, G. J. Am. Chem. Soc. 1981, 103, 3585.
-
(1981)
J. Am. Chem. Soc.
, vol.103
, pp. 3585
-
-
Potts, K.T.1
Cipullo, M.J.2
Ralli, P.3
Theodoridis, G.4
-
20
-
-
84986492798
-
-
(c) Tinggaard, M.; Hansen, P.; Mogensen, P. K.; Simonsen, O.; Becher, J. J. Heterocycl. Chem. 1989, 26, 439.
-
(1989)
J. Heterocycl. Chem.
, vol.26
, pp. 439
-
-
Tinggaard, M.1
Hansen, P.2
Mogensen, P.K.3
Simonsen, O.4
Becher, J.5
-
21
-
-
34547943871
-
-
(d) Kumar, S.; Ila, H.; Junjappa, H. Tetrahedron 2007, 63, 10067.
-
(2007)
Tetrahedron
, vol.63
, pp. 10067
-
-
Kumar, S.1
Ila, H.2
Junjappa, H.3
-
22
-
-
0000159773
-
-
For reports on inter- and intramolecular Michael addition of an 1,5- electrophilic double Michael acceptor and certain nucleophilic addend, see: (a)
-
For reports on inter- and intramolecular Michael addition of an 1,5- electrophilic double Michael acceptor and certain nucleophilic addend, see: (a) Bergmann, E. D.; Ginsburg, D.; Pappo, R. Org. React. 1959, 10, 179.
-
(1959)
Org. React.
, vol.10
, pp. 179
-
-
Bergmann, E.D.1
Ginsburg, D.2
Pappo, R.3
-
24
-
-
0029796652
-
-
(c) Gómez-Bengoa, E.; Cuerva, J. M.; Mateo, C.; Echavarren, A. M. J. Am. Chem. Soc. 1996, 118, 8553.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 8553
-
-
Gómez-Bengoa, E.1
Cuerva, J.M.2
Mateo, C.3
Echavarren, A.M.4
-
25
-
-
0028940129
-
-
(d) Rule, N. G.; Detty, M. R.; Kaeding, J. E.; Sinicropi, J. A. J. Org. Chem. 1995, 60, 1665.
-
(1995)
J. Org. Chem.
, vol.60
, pp. 1665
-
-
Rule, N.G.1
Detty, M.R.2
Kaeding, J.E.3
Sinicropi, J.A.4
-
30
-
-
5644277805
-
-
For reports on intermolecular double Michael additions of methyl ketones to electron-deficient alkenes, see: (a)
-
For reports on intermolecular double Michael additions of methyl ketones to electron-deficient alkenes, see: (a) Basu, B.; Das, P.; Hossain, I. Synlett 2004, 2224.
-
(2004)
Synlett
, pp. 2224
-
-
Basu, B.1
Das, P.2
Hossain, I.3
-
31
-
-
34548767600
-
-
(b) DeGraffenreid, M. R.; Bennett, S.; Caille, S.; Turiso, F. G.-L.; Hungate, R. W.; Julian, L. D.; Kaizeman, J. A.; McMinn, D. L.; Rew, Y.; Sun, D.; Yan, X.; Powers, J. P. J. Org. Chem. 2007, 72, 7455.
-
(2007)
J. Org. Chem.
, vol.72
, pp. 7455
-
-
DeGraffenreid, M.R.1
Bennett, S.2
Caille, S.3
Turiso, F.G.-L.4
Hungate, R.W.5
Julian, L.D.6
Kaizeman, J.A.7
McMinn, D.L.8
Rew, Y.9
Sun, D.10
Yan, X.11
Powers, J.P.12
-
32
-
-
53049088095
-
-
(c) Ishikawa, T.; Kudo, K.; Kuroyabu, K.; Uchida, S.; Kudoh, T.; Saito, S. J. Org. Chem. 2008, 73, 7498.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 7498
-
-
Ishikawa, T.1
Kudo, K.2
Kuroyabu, K.3
Uchida, S.4
Kudoh, T.5
Saito, S.6
-
33
-
-
17644361896
-
-
For selected recent reports of the synthetic applications of substituted 2-cyclohexenones, see: (a)
-
For selected recent reports of the synthetic applications of substituted 2-cyclohexenones, see: (a) Herzon, S. B.; Myers, A. G. J. Am. Chem. Soc. 2005, 127, 5342.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 5342
-
-
Herzon, S.B.1
Myers, A.G.2
-
34
-
-
33745669425
-
-
(b) Yang, J.; Dewal, M. B.; Shimizu, L. S. J. Am. Chem. Soc. 2006, 128, 8122.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 8122
-
-
Yang, J.1
Dewal, M.B.2
Shimizu, L.S.3
-
35
-
-
70349105794
-
-
(c) Paczkowski, R.; Maichle-Molssmer, C.; Maier, M. E. Org. Lett. 2006, 8, 151.
-
(2006)
Org. Lett.
, vol.8
, pp. 151
-
-
Paczkowski, R.1
Maichle-Molssmer, C.2
Maier, M.E.3
-
36
-
-
35048843654
-
-
(d) Linghu, X.; Kennedy-Smith, J. J.; Toste, F. D. Angew. Chem., Int. Ed. 2007, 46, 7671.
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 7671
-
-
Linghu, X.1
Kennedy-Smith, J.J.2
Toste, F.D.3
-
37
-
-
0037460172
-
-
For recent examples of the synthesis of substituted 2-cyclohexenones from acyclic precursors, see: (a)
-
For recent examples of the synthesis of substituted 2-cyclohexenones from acyclic precursors, see: (a) Pei, T.; Wang, X.; Widenhoefer, R. A. J. Am. Chem. Soc. 2003, 125, 648.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 648
-
-
Pei, T.1
Wang, X.2
Widenhoefer, R.A.3
-
38
-
-
1542287652
-
-
(b) Lee, S. I.; Park, J. H.; Chung, Y. K.; Lee, S. J. Am. Chem. Soc. 2004, 126, 2714.
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 2714
-
-
Lee, S.I.1
Park, J.H.2
Chung, Y.K.3
Lee, S.4
-
39
-
-
56449094610
-
-
(c) Seiser, T.; Cramer, N. Angew. Chem., Int. Ed. 2008, 47, 9294.
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 9294
-
-
Seiser, T.1
Cramer, N.2
-
40
-
-
53049088090
-
-
(d) Zhang, C.; Cui, D.; Yao, L.; Wang, B.; Hu, Y.; Hayashi, T. J. Org. Chem. 2008, 73, 7811.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 7811
-
-
Zhang, C.1
Cui, D.2
Yao, L.3
Wang, B.4
Hu, Y.5
Hayashi, T.6
-
41
-
-
52449111844
-
-
(e) Sudo, Y.; Shirasaki, D.; Harada, S.; Nishida, A. J. Am. Chem. Soc. 2008, 130, 12588.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 12588
-
-
Sudo, Y.1
Shirasaki, D.2
Harada, S.3
Nishida, A.4
-
42
-
-
18744369601
-
-
(f) Murakami, M.; Ashida, S.; Matsuda, T. J. Am. Chem. Soc. 2005, 127, 6932.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 6932
-
-
Murakami, M.1
Ashida, S.2
Matsuda, T.3
-
43
-
-
1242269278
-
-
(a) Magomedov, N. A.; Ruggiero, P. L.; Tang, Y. J. Am. Chem. Soc. 2004, 126, 1624.
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 1624
-
-
Magomedov, N.A.1
Ruggiero, P.L.2
Tang, Y.3
-
44
-
-
51449113436
-
-
(b) Lu, Z.; Chai, G.; Ma, S. Angew. Chem., Int. Ed. 2008, 47, 6045.
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 6045
-
-
Lu, Z.1
Chai, G.2
Ma, S.3
-
45
-
-
33751571805
-
-
(c) Carlone, A.; Marigo, M.; North, C.; Landa, A.; Jorgensen, K. A. Chem. Commun. 2006, 4928.
-
(2006)
Chem. Commun.
, pp. 4928
-
-
Carlone, A.1
Marigo, M.2
North, C.3
Landa, A.4
Jorgensen, K.A.5
-
47
-
-
59649123396
-
-
(a) Hayashi, Y.; Toyoshima, M.; Gotoh, H.; Ishikawa, H. Org. Lett. 2009, 11, 45.
-
(2009)
Org. Lett.
, vol.11
, pp. 45
-
-
Hayashi, Y.1
Toyoshima, M.2
Gotoh, H.3
Ishikawa, H.4
-
48
-
-
0033693443
-
-
(b) Inokuchi, T.; Okano, M.; Miyamoto, T.; Madon, H. B.; Takagi, M. Synlett 2000, 1549.
-
(2000)
Synlett
, pp. 1549
-
-
Inokuchi, T.1
Okano, M.2
Miyamoto, T.3
Madon, H.B.4
Takagi, M.5
-
49
-
-
70349094334
-
-
note
-
For experimental details, see Supporting Information.
-
-
-
-
50
-
-
70349083199
-
-
note
-
2 = 0.1112.
-
-
-
-
51
-
-
53849104644
-
-
For recent examples on the synthesis of benzophenones, see: (a)
-
For recent examples on the synthesis of benzophenones, see: (a) Srivastava, A. K.; Panda, G. Chem. - Eur. J. 2008, 14, 4675.
-
(2008)
Chem. - Eur. J.
, vol.14
, pp. 4675
-
-
Srivastava, A.K.1
Panda, G.2
-
52
-
-
55549109706
-
-
(b) Terzidis, M. A.; Tsoleridis, C. A.; Stephanidou-Stephanatou, J.; Terzis, A.; Raptopoulou, C. P.; Psycharis, V. Tetrahedron 2008, 64, 11611.
-
(2008)
Tetrahedron
, vol.64
, pp. 11611
-
-
Terzidis, M.A.1
Tsoleridis, C.A.2
Stephanidou-Stephanatou, J.3
Terzis, A.4
Raptopoulou, C.P.5
Psycharis, V.6
-
53
-
-
53049083816
-
-
and references therein
-
(c) Chuzel, O.; Roesch, A.; Genet, J.-P.; Darses, S. J. Org. Chem. 2008, 73, 7800 and references therein. .
-
(2008)
J. Org. Chem.
, vol.73
, pp. 7800
-
-
Chuzel, O.1
Roesch, A.2
Genet, J.-P.3
Darses, S.4
-
54
-
-
0028791580
-
-
Hegde, S. G.; Kassim, A. M.; Ingrum, A. I. Tetrahedron Lett. 1995, 36, 8395.
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 8395
-
-
Hegde, S.G.1
Kassim, A.M.2
Ingrum, A.I.3
-
55
-
-
0001031409
-
-
For recent examples of the synthetic applications of o-iodophenol derivatives, see: (a)
-
For recent examples of the synthetic applications of o-iodophenol derivatives, see: (a) Kadnikov, D. V.; Larock, R. C. Org. Lett. 2000, 2, 3643.
-
(2000)
Org. Lett.
, vol.2
, pp. 3643
-
-
Kadnikov, D.V.1
Larock, R.C.2
-
57
-
-
0038362007
-
-
(c) Bates, C. G.; Saejueng, P.; Murphy, J. M.; Venkataraman, D. Org. Lett. 2002, 4, 4727.
-
(2002)
Org. Lett.
, vol.4
, pp. 4727
-
-
Bates, C.G.1
Saejueng, P.2
Murphy, J.M.3
Venkataraman, D.4
-
60
-
-
34848888306
-
-
(f) Bi, H.; Liu, X.; Gou, F.; Guo, L.; Duan, X.; Shu, X.; Liang, Y. Angew. Chem., Int. Ed. 2007, 46, 7068.
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 7068
-
-
Bi, H.1
Liu, X.2
Gou, F.3
Guo, L.4
Duan, X.5
Shu, X.6
Liang, Y.7
|