-
1
-
-
1442360753
-
-
Wiley-VCH Verlag GmbH and Co.: Weinheim, Germany
-
Grubbs, R. H. Handbook of Metathesis; Wiley-VCH Verlag GmbH and Co.: Weinheim, Germany, 2003.
-
(2003)
Handbook of Metathesis
-
-
Grubbs, R.H.1
-
4
-
-
0001040853
-
-
(a) Hashiguchi, S.; Fujii, A.; Takehara, J.; Ikariya, T.; Noyori, R. J. Am. Chem. Soc. 1995, 117, 7562-7563.
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 7562-7563
-
-
Hashiguchi, S.1
Fujii, A.2
Takehara, J.3
Ikariya, T.4
Noyori, R.5
-
5
-
-
34547158082
-
-
(a) Hamid, M. H. S. A.; Slatford, P. A.; Williams, J. M. J. Adv. Synth. Catal. 2007, 349, 1555-1575.
-
(2007)
J. Adv. Synth. Catal.
, vol.349
, pp. 1555-1575
-
-
Hamid, M.H.S.A.1
Slatford, P.A.2
Williams, J.M.3
-
6
-
-
58249100133
-
-
(b) Bower, J. F.; Kim, I. S.; Patman, R. L.; Krische, M. J. Angew. Chem., Int. Ed. 2009, 48, 34-36.
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 34-36
-
-
Bower, J.F.1
Kim, I.S.2
Patman, R.L.3
Krische, M.J.4
-
7
-
-
77949593456
-
-
(c) Guillena, G.; Ramon, D. J.; Yus, M. Chem. Rev. 2010, 110, 1611-1641.
-
(2010)
Chem. Rev.
, vol.110
, pp. 1611-1641
-
-
Guillena, G.1
Ramon, D.J.2
Yus, M.3
-
8
-
-
84944736946
-
-
(d) Leonard, J.; Blacker, A. J.; Marsden, S. P.; Jones, M. F.; Mulholland, K. R.; Newton, R. Org. Process Res. Dev. 2015, 19, 1400-1410.
-
(2015)
Org. Process Res. Dev.
, vol.19
, pp. 1400-1410
-
-
Leonard, J.1
Blacker, A.J.2
Marsden, S.P.3
Jones, M.F.4
Mulholland, K.R.5
Newton, R.6
-
11
-
-
4544298013
-
-
Beller, M.; Seayad, J.; Tillack, A.; Jiao, H. Angew. Chem., Int. Ed. 2004, 43, 3368-3398.
-
(2004)
Angew. Chem., Int. Ed.
, vol.43
, pp. 3368-3398
-
-
Beller, M.1
Seayad, J.2
Tillack, A.3
Jiao, H.4
-
12
-
-
34447129755
-
-
Corma, A.; Iborra, S.; Velty, A. Chem. Rev. 2007, 107, 2411-2502.
-
(2007)
Chem. Rev.
, vol.107
, pp. 2411-2502
-
-
Corma, A.1
Iborra, S.2
Velty, A.3
-
14
-
-
84886773605
-
-
Some recent exciting catalytic methodologies proceeding through formal group transfer from activated cyclohexadienes or dihydropyridines have not been included because the mechanism by which the donor is activated is likely not applicable to the reverse reaction. For transfer hydrosilylation, see: (a) Simonneau, A.; Oestreich, M. Angew. Chem., Int. Ed. 2013, 52, 11905-11907.
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 11905-11907
-
-
Simonneau, A.1
Oestreich, M.2
-
16
-
-
79955585053
-
-
(c) Chou, C.-M.; Guin, J.; Muck-Lichtenfeld, C.; Grimme, S.; Studer, A. Chem. - Asian J. 2011, 6, 1197-1209.
-
(2011)
Chem. - Asian J.
, vol.6
, pp. 1197-1209
-
-
Chou, C.-M.1
Guin, J.2
Muck-Lichtenfeld, C.3
Grimme, S.4
Studer, A.5
-
17
-
-
38349003056
-
-
(e) Guin, J.; Frohlich, R.; Studer, A. Angew. Chem., Int. Ed. 2008, 47, 779-782.
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 779-782
-
-
Guin, J.1
Frohlich, R.2
Studer, A.3
-
18
-
-
34247130947
-
-
(f) Guin, J.; Muck-Lichtenfeld, C.; Grimme, S.; Studer, A. J. Am. Chem. Soc. 2007, 129, 4498-4503. For a review of transfer reactions using cyclohexadienes, see
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 4498-4503
-
-
Guin, J.1
Muck-Lichtenfeld, C.2
Grimme, S.3
Studer, A.4
-
20
-
-
84969962379
-
-
For recent examples of metal-catalyzed transamidations, see: (a) Baker, E. L.; Yamano, M. M.; Zhou, Y.; Anthony, S. M.; Garg, N. K. Nat. Commun. 2016, 7, 11554.
-
(2016)
Nat. Commun.
, vol.7
, pp. 11554
-
-
Baker, E.L.1
Yamano, M.M.2
Zhou, Y.3
Anthony, S.M.4
Garg, N.K.5
-
21
-
-
67651208251
-
-
(b) Stephenson, N. A.; Zhu, J.; Gellman, S. H.; Stahl, S. S. J. Am. Chem. Soc. 2009, 131, 10003-10008.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 10003-10008
-
-
Stephenson, N.A.1
Zhu, J.2
Gellman, S.H.3
Stahl, S.S.4
-
22
-
-
33646152127
-
-
(c) Hoerter, J. M.; Otte, K. M.; Gellman, S. H.; Stahl, S. S. J. Am. Chem. Soc. 2006, 128, 5177-5183.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 5177-5183
-
-
Hoerter, J.M.1
Otte, K.M.2
Gellman, S.H.3
Stahl, S.S.4
-
23
-
-
34250618375
-
-
(a) Jun, C.-H.; Jo, E.-A.; Park, J.-W. Eur. J. Org. Chem. 2007, 2007, 1869-1881.
-
(2007)
Eur. J. Org. Chem.
, vol.2007
, pp. 1869-1881
-
-
Jun, C.-H.1
Jo, E.-A.2
Park, J.-W.3
-
25
-
-
77349099246
-
-
(c) Willis, M. C. Chem. Rev. 2010, 110, 725-748.
-
(2010)
Chem. Rev.
, vol.110
, pp. 725-748
-
-
Willis, M.C.1
-
27
-
-
40549088216
-
-
(b) Park, Y. J.; Park, J.-W.; Jun, C.-H. Acc. Chem. Res. 2008, 41, 222-234.
-
(2008)
Acc. Chem. Res.
, vol.41
, pp. 222-234
-
-
Park, Y.J.1
Park, J.-W.2
Jun, C.-H.3
-
28
-
-
0035948514
-
-
(c) Jun, C.-H.; Lee, D.-Y.; Kim, Y.-H.; Lee, H. Organometallics 2001, 20, 2928-2931.
-
(2001)
Organometallics
, vol.20
, pp. 2928-2931
-
-
Jun, C.-H.1
Lee, D.-Y.2
Kim, Y.-H.3
Lee, H.4
-
29
-
-
0035977634
-
-
(d) Jun, C.-H.; Lee, H.; Lim, S.-G. J. Am. Chem. Soc. 2001, 123, 751-752.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 751-752
-
-
Jun, C.-H.1
Lee, H.2
Lim, S.-G.3
-
30
-
-
31544451018
-
-
(e) Ahn, J.-A.; Chang, D.-H.; Park, Y. J.; Yon, Y. R.; Loupy, A.; Jun, C.-H. Adv. Synth. Catal. 2006, 348, 55-58.
-
(2006)
Adv. Synth. Catal.
, vol.348
, pp. 55-58
-
-
Ahn, J.-A.1
Chang, D.-H.2
Park, Y.J.3
Yon, Y.R.4
Loupy, A.5
Jun, C.-H.6
-
31
-
-
84867957605
-
-
Franke, R.; Selent, D.; Borner, A. Chem. Rev. 2012, 112, 5675-5732.
-
(2012)
Chem. Rev.
, vol.112
, pp. 5675-5732
-
-
Franke, R.1
Selent, D.2
Borner, A.3
-
32
-
-
33846387040
-
-
Lepesheva, G. I.; Waterman, M. R. Biochim. Biophys. Acta, Gen. Subj. 2007, 1770, 467-477.
-
(2007)
Biochim. Biophys. Acta, Gen. Subj.
, vol.1770
, pp. 467-477
-
-
Lepesheva, G.I.1
Waterman, M.R.2
-
33
-
-
84922481413
-
-
(a) Murphy, S. K.; Park, J.-W.; Cruz, F. A.; Dong, V. M. Science 2015, 347, 56-60.
-
(2015)
Science
, vol.347
, pp. 56-60
-
-
Murphy, S.K.1
Park, J.-W.2
Cruz, F.A.3
Dong, V.M.4
-
34
-
-
84922479719
-
-
(b) Landis, C. R. Science 2015, 347, 29-30. For an acceptor-free dehydroformylation see
-
(2015)
Science
, vol.347
, pp. 29-30
-
-
Landis, C.R.1
-
35
-
-
84941757411
-
-
(c) Kusumoto, S.; Tatsuki, T.; Nozaki, K. Angew. Chem., Int. Ed. 2015, 54, 8458-8461.
-
(2015)
Angew. Chem., Int. Ed.
, vol.54
, pp. 8458-8461
-
-
Kusumoto, S.1
Tatsuki, T.2
Nozaki, K.3
-
36
-
-
33750510074
-
-
(a) Kreis, M.; Palmelund, A.; Bunch, L.; Madsen, R. Adv. Synth. Catal. 2006, 348, 2148-2154.
-
(2006)
Adv. Synth. Catal.
, vol.348
, pp. 2148-2154
-
-
Kreis, M.1
Palmelund, A.2
Bunch, L.3
Madsen, R.4
-
38
-
-
0033521183
-
-
Two examples of forward transfer hydroformylation are reported in the following
-
Two examples of forward transfer hydroformylation are reported in the following: Lenges, C. P.; Brookhart, M. Angew. Chem., Int. Ed. 1999, 38, 3533-3537.
-
(1999)
Angew. Chem., Int. Ed.
, vol.38
, pp. 3533-3537
-
-
Lenges, C.P.1
Brookhart, M.2
-
39
-
-
84927667614
-
-
For the use of paraformaldehyde in hydroformylation reactions, see: (a) Morimoto, T.; Fujii, T.; Miyoshi, K.; Makado, G.; Tanimoto, H.; Nishiyama, Y.; Kakiuchi, K. Org. Biomol. Chem. 2015, 13, 4632-4636.
-
(2015)
Org. Biomol. Chem.
, vol.13
, pp. 4632-4636
-
-
Morimoto, T.1
Fujii, T.2
Miyoshi, K.3
Makado, G.4
Tanimoto, H.5
Nishiyama, Y.6
Kakiuchi, K.7
-
40
-
-
84936990203
-
-
Catalytic irreversible CO transfer has been reported in a Pauson-Khand reaction
-
(b) Fuentes, J. A.; Pittaway, R.; Clarke, M. L. Chem. - Eur. J. 2015, 21, 10645-10649. Catalytic irreversible CO transfer has been reported in a Pauson-Khand reaction
-
(2015)
Chem. - Eur. J.
, vol.21
, pp. 10645-10649
-
-
Fuentes, J.A.1
Pittaway, R.2
Clarke, M.L.3
-
41
-
-
0037123291
-
-
(c) Morimoto, T.; Fuji, K.; Tsutsumi, K.; Kakiuchi, K. J. Am. Chem. Soc. 2002, 124, 3806-3807. For the in situ generation and two-chamber use of CO, see
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 3806-3807
-
-
Morimoto, T.1
Fuji, K.2
Tsutsumi, K.3
Kakiuchi, K.4
-
42
-
-
84966267415
-
-
(d) Friis, S. D.; Lindhardt, A. T.; Skrydstrup, T. Acc. Chem. Res. 2016, 49, 594-605. For a general review on CO surrogates, see
-
(2016)
Acc. Chem. Res.
, vol.49
, pp. 594-605
-
-
Friis, S.D.1
Lindhardt, A.T.2
Skrydstrup, T.3
-
43
-
-
84902258984
-
-
(e) Wu, L.; Liu, Q.; Jackstell, R.; Beller, M. Angew. Chem., Int. Ed. 2014, 53, 6310-6320.
-
(2014)
Angew. Chem., Int. Ed.
, vol.53
, pp. 6310-6320
-
-
Wu, L.1
Liu, Q.2
Jackstell, R.3
Beller, M.4
-
44
-
-
84958999478
-
-
(a) Fang, X.; Yu, P.; Morandi, B. Science 2016, 351, 832-836.
-
(2016)
Science
, vol.351
, pp. 832-836
-
-
Fang, X.1
Yu, P.2
Morandi, B.3
-
47
-
-
79952416827
-
-
(a) Bini, L.; Muller, C.; Vogt, D. ChemCatChem 2010, 2, 590-608.
-
(2010)
ChemCatChem
, vol.2
, pp. 590-608
-
-
Bini, L.1
Muller, C.2
Vogt, D.3
-
48
-
-
84959004061
-
Transition metalcatalyzed alkene and alkyne hydrocyanations
-
Beller, M., Bolm, C., Eds.; Wiley-VCH Verlag GmbH and Co.: Weinheim, Germany
-
(b) Casalnuovo, A. L.; Rajan Babu, T. V. Transition Metalcatalyzed Alkene and Alkyne Hydrocyanations. In Transition Metals for Organic Synthesis: Building Blocks and Fine Chemicals; Beller, M., Bolm, C., Eds.; Wiley-VCH Verlag GmbH and Co.: Weinheim, Germany, 2008; pp 149-156. For a method using in situ-generated HCN from TMSCN, see:.
-
(2008)
Transition Metals for Organic Synthesis: Building Blocks and Fine Chemicals
, pp. 149-156
-
-
Casalnuovo, A.L.1
Rajan Babu, T.V.2
-
49
-
-
84872867223
-
-
(c) Falk, A.; Goderz, A.-L.; Schmalz, H.-G. Angew. Chem., Int. Ed. 2013, 52, 1576-1580. From acetone cyanohydrin, see
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 1576-1580
-
-
Falk, A.1
Goderz, A.-L.2
Schmalz, H.-G.3
-
50
-
-
58249097255
-
-
(d) de Greef, M.; Breit, B. Angew. Chem., Int. Ed. 2009, 48, 551-554.
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 551-554
-
-
De Greef, M.1
Breit, B.2
-
51
-
-
84893467790
-
-
Lo, J. C.; Yabe, Y.; Baran, P. S. J. Am. Chem. Soc. 2014, 136, 1304-1307.
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 1304-1307
-
-
Lo, J.C.1
Yabe, Y.2
Baran, P.S.3
-
52
-
-
0001030517
-
-
(a) Huang, J.; Haar, C. M.; Nolan, S. P.; Marcone, J. E.; Moloy, K. G. Organometallics 1999, 18, 297-299.
-
(1999)
Organometallics
, vol.18
, pp. 297-299
-
-
Huang, J.1
Haar, C.M.2
Nolan, S.P.3
Marcone, J.E.4
Moloy, K.G.5
-
53
-
-
33847633018
-
-
(b) Nakao, Y.; Yada, A.; Ebata, S.; Hiyama, T. J. Am. Chem. Soc. 2007, 129, 2428-2429.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 2428-2429
-
-
Nakao, Y.1
Yada, A.2
Ebata, S.3
Hiyama, T.4
-
55
-
-
84855710309
-
-
Shirakawa, E.; Ikeda, D.; Masui, S.; Yoshida, M.; Hayashi, T. J. Am. Chem. Soc. 2012, 134, 272-279.
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 272-279
-
-
Shirakawa, E.1
Ikeda, D.2
Masui, S.3
Yoshida, M.4
Hayashi, T.5
-
56
-
-
40149093861
-
-
Shirakawa, E.; Ikeda, D.; Yamaguchi, S.; Hayashi, T. Chem. Commun. 2008, 1214-1216.
-
(2008)
Chem. Commun.
, pp. 1214-1216
-
-
Shirakawa, E.1
Ikeda, D.2
Yamaguchi, S.3
Hayashi, T.4
-
58
-
-
84920772634
-
-
(b) Greenhalgh, M. D.; Jones, A. S.; Thomas, S. P. ChemCatChem 2015, 7, 190-222.
-
(2015)
ChemCatChem
, vol.7
, pp. 190-222
-
-
Greenhalgh, M.D.1
Jones, A.S.2
Thomas, S.P.3
-
59
-
-
84908626492
-
-
(c) Greenhalgh, M. D.; Kolodziej, A.; Sinclair, F.; Thomas, S. P. Organometallics 2014, 33, 5811-5819.
-
(2014)
Organometallics
, vol.33
, pp. 5811-5819
-
-
Greenhalgh, M.D.1
Kolodziej, A.2
Sinclair, F.3
Thomas, S.P.4
-
60
-
-
84912544495
-
-
(d) Jones, A. S.; Paliga, J. F.; Greenhalgh, M. D.; Quibell, J. M.; Steven, A.; Thomas, S. P. Org. Lett. 2014, 16, 5964-5967.
-
(2014)
Org. Lett.
, vol.16
, pp. 5964-5967
-
-
Jones, A.S.1
Paliga, J.F.2
Greenhalgh, M.D.3
Quibell, J.M.4
Steven, A.5
Thomas, S.P.6
-
63
-
-
0037077611
-
-
Cirakovic, J.; Driver, T. G.; Woerpel, K. A. J. Am. Chem. Soc. 2002, 124, 9370-9371.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 9370-9371
-
-
Cirakovic, J.1
Driver, T.G.2
Woerpel, K.A.3
-
65
-
-
33750002664
-
-
Corbett, P. T.; Leclaire, J.; Vial, L.; West, K. R.; Wietor, J.-L.; Sanders, J. K. M.; Otto, S. Chem. Rev. 2006, 106, 3652-3711.
-
(2006)
Chem. Rev.
, vol.106
, pp. 3652-3711
-
-
Corbett, P.T.1
Leclaire, J.2
Vial, L.3
West, K.R.4
Wietor, J.-L.5
Sanders, J.K.M.6
Otto, S.7
|