-
16
-
-
0000323136
-
-
E. Wenkert, L.L. Davis, B.L. Mylari, M.F. Solomon, R.R. da Silva, S. Shulman, R.J. Warnet, P. Ceccherelli, M. Curini, and R. Pellicciari J. Org. Chem. 47 1982 3242 3247
-
(1982)
J. Org. Chem.
, vol.47
, pp. 3242-3247
-
-
Wenkert, E.1
Davis, L.L.2
Mylari, B.L.3
Solomon, M.F.4
Da Silva, R.R.5
Shulman, S.6
Warnet, R.J.7
Ceccherelli, P.8
Curini, M.9
Pellicciari, R.10
-
18
-
-
0001051581
-
-
M.P. Doyle, A. van Oeveren, L.J. Westrum, M.N. Protopopova, and T.W. Clayton Jr. J. Am. Chem. Soc. 113 1991 8982 8984
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 8982-8984
-
-
Doyle, M.P.1
Van Oeveren, A.2
Westrum, L.J.3
Protopopova, M.N.4
Clayton, Jr.T.W.5
-
19
-
-
0000562208
-
-
M.P. Doyle, A.B. Dyatkin, G.H.P. Roos, F. Cañas, D.A. Pierson, A. van Basten, P. Müller, and P. Polleux J. Am. Chem. Soc. 116 1994 4507 4508
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 4507-4508
-
-
Doyle, M.P.1
Dyatkin, A.B.2
Roos, G.H.P.3
Cañas, F.4
Pierson, D.A.5
Van Basten, A.6
Müller, P.7
Polleux, P.8
-
21
-
-
33845532561
-
-
references cited therein
-
M.P. Doyle J. Org. Chem. 71 2006 9253 9260 and references cited therein
-
(2006)
J. Org. Chem.
, vol.71
, pp. 9253-9260
-
-
Doyle, M.P.1
-
24
-
-
84890940790
-
-
references cited therein
-
K.M. Chepiga, Y. Feng, N.A. Brunelli, C.W. Jones, and H.M.L. Davies Org. Lett. 15 2013 6136 6139 and references cited therein
-
(2013)
Org. Lett.
, vol.15
, pp. 6136-6139
-
-
Chepiga, K.M.1
Feng, Y.2
Brunelli, N.A.3
Jones, C.W.4
Davies, H.M.L.5
-
25
-
-
0000090692
-
-
4-catalyzed enantioselective intramolecular C-H insertion reactions, see
-
4-catalyzed enantioselective intramolecular C-H insertion reactions, see: H.M.L. Davies, M.V.A. Grazini, and E. Aouad Org. Lett. 3 2001 1475 1477
-
(2001)
Org. Lett.
, vol.3
, pp. 1475-1477
-
-
Davies, H.M.L.1
Grazini, M.V.A.2
Aouad, E.3
-
26
-
-
0027209354
-
-
S. Hashimoto, N. Watanabe, T. Sato, M. Shiro, and S. Ikegami Tetrahedron Lett. 34 1993 5109 5112
-
(1993)
Tetrahedron Lett.
, vol.34
, pp. 5109-5112
-
-
Hashimoto, S.1
Watanabe, N.2
Sato, T.3
Shiro, M.4
Ikegami, S.5
-
29
-
-
0032726846
-
-
M. Anada, O. Mita, H. Watanabe, S. Kitagaki, and S. Hashimoto Synlett 1999 1775 1777
-
(1999)
Synlett
, pp. 1775-1777
-
-
Anada, M.1
Mita, O.2
Watanabe, H.3
Kitagaki, S.4
Hashimoto, S.5
-
30
-
-
0035823392
-
-
T. Takahashi, H. Tsutsui, M. Tamura, S. Kitagaki, M. Nakajima, and S. Hashimoto Chem. Commun. 2001 1604 1605
-
(2001)
Chem. Commun.
, pp. 1604-1605
-
-
Takahashi, T.1
Tsutsui, H.2
Tamura, M.3
Kitagaki, S.4
Nakajima, M.5
Hashimoto, S.6
-
31
-
-
0012630744
-
-
H. Saito, H. Oishi, S. Kitagaki, S. Nakamura, M. Anada, and S. Hahimoto Org. Lett. 4 2002 3887 3890
-
(2002)
Org. Lett.
, vol.4
, pp. 3887-3890
-
-
Saito, H.1
Oishi, H.2
Kitagaki, S.3
Nakamura, S.4
Anada, M.5
Hahimoto, S.6
-
32
-
-
33947694406
-
-
Y. Natori, M. Anada, S. Nakamura, H. Nambu, and S. Hashimoto Heterocycles 70 2006 635 646
-
(2006)
Heterocycles
, vol.70
, pp. 635-646
-
-
Natori, Y.1
Anada, M.2
Nakamura, S.3
Nambu, H.4
Hashimoto, S.5
-
33
-
-
66249093147
-
-
Y. Natori, H. Tsutsui, N. Sato, S. Nakamura, H. Nambu, M. Shiro, and S. Hashimoto J. Org. Chem. 74 2009 4418 4421
-
(2009)
J. Org. Chem.
, vol.74
, pp. 4418-4421
-
-
Natori, Y.1
Tsutsui, H.2
Sato, N.3
Nakamura, S.4
Nambu, H.5
Shiro, M.6
Hashimoto, S.7
-
34
-
-
84892436243
-
-
M. Ito, R. Namie, J. Krishnamurthi, H. Miyamae, K. Takeda, H. Nambu, and S. Hashimoto Synlett 25 2014 288 292
-
(2014)
Synlett
, vol.25
, pp. 288-292
-
-
Ito, M.1
Namie, R.2
Krishnamurthi, J.3
Miyamae, H.4
Takeda, K.5
Nambu, H.6
Hashimoto, S.7
-
38
-
-
27544502534
-
-
K. Minami, H. Saito, H. Tsutsui, H. Nambu, M. Anada, and S. Hashimoto Adv. Synth. Catal. 347 2005 1483 1487
-
(2005)
Adv. Synth. Catal.
, vol.347
, pp. 1483-1487
-
-
Minami, K.1
Saito, H.2
Tsutsui, H.3
Nambu, H.4
Anada, M.5
Hashimoto, S.6
-
39
-
-
84880638817
-
-
4-catalyzed intermolecular C-H insertion of α-alkyl-α-diazo esters, see
-
4-catalyzed intermolecular C-H insertion of α-alkyl-α-diazo esters, see: T. Goto, T. Onozuka, Y. Kosaka, M. Anada, K. Takeda, and S. Hashimoto Heterocycles 86 2012 1647 1659
-
(2012)
Heterocycles
, vol.86
, pp. 1647-1659
-
-
Goto, T.1
Onozuka, T.2
Kosaka, Y.3
Anada, M.4
Takeda, K.5
Hashimoto, S.6
-
40
-
-
33747216251
-
-
4 is a highly effective catalyst for intra- and intermolecular C-H insertion reactions. See: (a)
-
4 is a highly effective catalyst for intra- and intermolecular C-H insertion reactions. See: (a) R.P. Reddy, G.H. Lee, and H.M.L. Davies Org. Lett. 8 2006 3437 3440
-
(2006)
Org. Lett.
, vol.8
, pp. 3437-3440
-
-
Reddy, R.P.1
Lee, G.H.2
Davies, H.M.L.3
-
43
-
-
2942567899
-
-
references cited therein
-
D.F. Taber, and P.V. Joshi J. Org. Chem. 69 2004 4276 4278 and references cited therein
-
(2004)
J. Org. Chem.
, vol.69
, pp. 4276-4278
-
-
Taber, D.F.1
Joshi, P.V.2
-
50
-
-
0035809956
-
-
F. Estevan, K. Herbst, P. Lahuerta, M. Barberis, and J. Pérez-Prieto Organometallics 20 2001 950 957
-
(2001)
Organometallics
, vol.20
, pp. 950-957
-
-
Estevan, F.1
Herbst, K.2
Lahuerta, P.3
Barberis, M.4
Pérez-Prieto, J.5
-
53
-
-
0141534438
-
-
For recent reports on total synthesis of natural products using 1,6-C-H insertion, see: (a)
-
For recent reports on total synthesis of natural products using 1,6-C-H insertion, see: (a) A. Hinman, and J. Du Bois J. Am. Chem. Soc. 125 2003 11510 11511
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 11510-11511
-
-
Hinman, A.1
Du Bois, J.2
-
54
-
-
58149148291
-
-
K.C. Nicolaou, A.F. Stepan, T. Lister, A. Li, A. Montero, G.S. Tria, C.I. Turner, Y. Tang, J. Wang, R.M. Denton, and D.J. Edmonds J. Am. Chem. Soc. 130 2008 13110 13119
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 13110-13119
-
-
Nicolaou, K.C.1
Stepan, A.F.2
Lister, T.3
Li, A.4
Montero, A.5
Tria, G.S.6
Turner, C.I.7
Tang, Y.8
Wang, J.9
Denton, R.M.10
Edmonds, D.J.11
-
55
-
-
0001691695
-
-
J. Adams, M.-A. Poupart, L. Grenier, C. Schaller, N. Ouimet, and R. Frenette Tetrahedron Lett. 30 1989 1749 1752
-
(1989)
Tetrahedron Lett.
, vol.30
, pp. 1749-1752
-
-
Adams, J.1
Poupart, M.-A.2
Grenier, L.3
Schaller, C.4
Ouimet, N.5
Frenette, R.6
-
61
-
-
79953690184
-
-
A. Rosales, I. Rodríguez-García, C. López-Sánchez, M. Álvarez-Corral, and M. Muñoz-Dorado Tetrahedron 67 2011 3071 3075
-
(2011)
Tetrahedron
, vol.67
, pp. 3071-3075
-
-
Rosales, A.1
Rodríguez-García, I.2
López-Sánchez, C.3
Álvarez-Corral, M.4
Muñoz-Dorado, M.5
-
62
-
-
84885097810
-
-
2-catalyzed reactions of α-aryl-α-diazo ketones led to the preferential formation of cyclohexanones via a 1,6-C-H insertion into electron-rich methine or benzylic C-H bonds. See
-
2-catalyzed reactions of α-aryl-α-diazo ketones led to the preferential formation of cyclohexanones via a 1,6-C-H insertion into electron-rich methine or benzylic C-H bonds. See: D.F. Taber, C.M. Paquette, P. Gu, and W. Tian J. Org. Chem. 78 2013 9772 9780
-
(2013)
J. Org. Chem.
, vol.78
, pp. 9772-9780
-
-
Taber, D.F.1
Paquette, C.M.2
Gu, P.3
Tian, W.4
-
63
-
-
33846406906
-
-
Recently, Rh(II)-catalyzed 1,6-C-H insertion reactions of diazosulfonates and diazosulfones were reported independently by Novikov and Du Bois. See: (a)
-
Recently, Rh(II)-catalyzed 1,6-C-H insertion reactions of diazosulfonates and diazosulfones were reported independently by Novikov and Du Bois. See: (a) J.P. John, and A.V. Novikov Org. Lett. 9 2007 61 63
-
(2007)
Org. Lett.
, vol.9
, pp. 61-63
-
-
John, J.P.1
Novikov, A.V.2
-
66
-
-
84865838463
-
-
For a recent review on C-H functionalization in natural products synthesis, see
-
For a recent review on C-H functionalization in natural products synthesis, see: J. Yamaguchi, A.D. Yamaguchi, and K. Itami Angew. Chem., Int. Ed. 51 2012 8960 9009
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 8960-9009
-
-
Yamaguchi, J.1
Yamaguchi, A.D.2
Itami, K.3
-
67
-
-
84874303999
-
-
For a recent review on Rh(II)-catalyzed tandem oxonium ylide formation-rearrangement, see
-
For a recent review on Rh(II)-catalyzed tandem oxonium ylide formation-rearrangement, see: G.K. Murphy, C. Stewart, and F.G. West Tetrahedron 69 2013 2667 2686
-
(2013)
Tetrahedron
, vol.69
, pp. 2667-2686
-
-
Murphy, G.K.1
Stewart, C.2
West, F.G.3
-
70
-
-
0026481190
-
-
N. McCarthy, M.A. McKervey, T. Ye, M. McCann, E. Murphy, and M.P. Doyle Tetrahedron Lett. 33 1992 5983 5986
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 5983-5986
-
-
McCarthy, N.1
McKervey, M.A.2
Ye, T.3
McCann, M.4
Murphy, E.5
Doyle, M.P.6
-
71
-
-
0035801851
-
-
S. Kitagaki, Y. Yanamoto, H. Tsutsui, M. Anada, M. Nakajima, and S. Hashimoto Tetrahedron Lett. 42 2001 6361 6364
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 6361-6364
-
-
Kitagaki, S.1
Yanamoto, Y.2
Tsutsui, H.3
Anada, M.4
Nakajima, M.5
Hashimoto, S.6
-
72
-
-
0001357910
-
-
H. Tsutsui, M. Matsuura, K. Makino, S. Nakamura, M. Nakajima, S. Kitagaki, and S. Hashimoto Isr. J. Chem. 41 2001 283 295
-
(2001)
Isr. J. Chem.
, vol.41
, pp. 283-295
-
-
Tsutsui, H.1
Matsuura, M.2
Makino, K.3
Nakamura, S.4
Nakajima, M.5
Kitagaki, S.6
Hashimoto, S.7
-
73
-
-
67650345243
-
-
N. Shimada, S. Nakamura, M. Anada, M. Shiro, and S. Hashimoto Chem. Lett. 38 2009 488 489
-
(2009)
Chem. Lett.
, vol.38
, pp. 488-489
-
-
Shimada, N.1
Nakamura, S.2
Anada, M.3
Shiro, M.4
Hashimoto, S.5
-
74
-
-
84899503919
-
-
references cited therein
-
J.S. Clark, and K.E. Hansen Chem. Eur. J. 20 2014 5454 5459 and references cited therein
-
(2014)
Chem. Eur. J.
, vol.20
, pp. 5454-5459
-
-
Clark, J.S.1
Hansen, K.E.2
-
75
-
-
35948970147
-
-
M. Anada, M. Tanaka, T. Washio, M. Yamawaki, T. Abe, and S. Hashimoto Org. Lett. 9 2007 4559 4562
-
(2007)
Org. Lett.
, vol.9
, pp. 4559-4562
-
-
Anada, M.1
Tanaka, M.2
Washio, T.3
Yamawaki, M.4
Abe, T.5
Hashimoto, S.6
-
76
-
-
0037164672
-
-
M. Yamawaki, H. Tsutsui, S. Kitagaki, M. Anada, and S. Hashimoto Tetrahedron Lett. 43 2002 9561 9564
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 9561-9564
-
-
Yamawaki, M.1
Tsutsui, H.2
Kitagaki, S.3
Anada, M.4
Hashimoto, S.5
-
77
-
-
54049087840
-
-
N. Shimada, M. Anada, S. Nakamura, H. Nambu, H. Tsutsui, and S. Hashimoto Org. Lett. 10 2008 3603 3606
-
(2008)
Org. Lett.
, vol.10
, pp. 3603-3606
-
-
Shimada, N.1
Anada, M.2
Nakamura, S.3
Nambu, H.4
Tsutsui, H.5
Hashimoto, S.6
-
78
-
-
82355160842
-
-
N. Shimada, T. Oohara, J. Krishnamurthi, H. Nambu, and S. Hashimoto Org. Lett. 13 2011 6284 6287
-
(2011)
Org. Lett.
, vol.13
, pp. 6284-6287
-
-
Shimada, N.1
Oohara, T.2
Krishnamurthi, J.3
Nambu, H.4
Hashimoto, S.5
-
79
-
-
84880903565
-
-
J. Krishnamurthi, H. Nambu, K. Takeda, M. Anada, A. Yamano, and S. Hashimoto Org. Biomol. Chem. 11 2013 5374 5382
-
(2013)
Org. Biomol. Chem.
, vol.11
, pp. 5374-5382
-
-
Krishnamurthi, J.1
Nambu, H.2
Takeda, K.3
Anada, M.4
Yamano, A.5
Hashimoto, S.6
-
81
-
-
77956914868
-
-
For the effective use of an immobilized catalyst based on Rh2(S-PTTL)4, see
-
For the effective use of an immobilized catalyst based on Rh2(S-PTTL)4, see: K. Takeda, T. Oohara, M. Anada, H. Nambu, and S. Hashimoto Angew. Chem., Int. Ed. 49 2010 6979 6983
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 6979-6983
-
-
Takeda, K.1
Oohara, T.2
Anada, M.3
Nambu, H.4
Hashimoto, S.5
-
85
-
-
84860356113
-
-
J. Hashida, M. Niitsuma, M. Iwatsuki, M. Mori, A. Ishiyama, M. Namatane, A. Nishihara-Tsukashima, A. Matsumoto, I. Ara, Y. Takahashi, H. Yamada, K. Otoguro, K. Shiomi, and S. Omura J. Antibiot. 65 2012 197 202
-
(2012)
J. Antibiot.
, vol.65
, pp. 197-202
-
-
Hashida, J.1
Niitsuma, M.2
Iwatsuki, M.3
Mori, M.4
Ishiyama, A.5
Namatane, M.6
Nishihara-Tsukashima, A.7
Matsumoto, A.8
Ara, I.9
Takahashi, Y.10
Yamada, H.11
Otoguro, K.12
Shiomi, K.13
Omura, S.14
-
86
-
-
36549007528
-
-
L. Yu, W. Zhang, T. Liu, X. Wang, J. Peng, S. Li, and Q. Jin J. Appl. Microbiol. 103 2007 2346 2352
-
(2007)
J. Appl. Microbiol.
, vol.103
, pp. 2346-2352
-
-
Yu, L.1
Zhang, W.2
Liu, T.3
Wang, X.4
Peng, J.5
Li, S.6
Jin, Q.7
|