-
1
-
-
84855328667
-
Palladium-catalyzed carbonylation reactions of alkenes and alkynes
-
Brennführer, A., Neumann, H. & Beller, M. Palladium-catalyzed carbonylation reactions of alkenes and alkynes. ChemCatChem 1, 28-41 (2009).
-
(2009)
Chemcatchem
, vol.1
, pp. 28-41
-
-
Brennführer, A.1
Neumann, H.2
Beller, M.3
-
2
-
-
84898855064
-
Transition-metal-catalyzed carbonylation reactions of olefins and alkynes: A personal account
-
Wu, X.-F. et al. Transition-metal-catalyzed carbonylation reactions of olefins and alkynes: a personal account. Acc. Chem. Res. 47, 1041-1053 (2014).
-
(2014)
Acc. Chem. Res.
, vol.47
, pp. 1041-1053
-
-
Wu, X.-F.1
-
3
-
-
77951145972
-
-
(eds Beller, M. & Bolm, C.), Wiley-VCH
-
Ali, B. E. & Alper, H., in Transition Metals for Organic Synthesis (eds Beller, M. & Bolm, C.) 113-132 (Wiley-VCH, 2008).
-
(2008)
In Transition Metals for Organic Synthesis
, pp. 113-132
-
-
Ali, B.E.1
Alper, H.2
-
4
-
-
0035498330
-
Palladium-catalyzed Reppe carbonylation
-
Kiss, G. Palladium-catalyzed Reppe carbonylation. Chem. Rev. 101, 3435-3456 (2001).
-
(2001)
Chem. Rev.
, vol.101
, pp. 3435-3456
-
-
Kiss, G.1
-
5
-
-
84902258984
-
Carbonylations of alkenes with CO surrogates
-
Wu, L., Liu, Q., Jackstell, R. & Beller, M. Carbonylations of alkenes with CO surrogates. Angew. Chem. Int. Ed. 53, 6310-6320 (2014).
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 6310-6320
-
-
Wu, L.1
Liu, Q.2
Jackstell, R.3
Beller, M.4
-
6
-
-
84966267415
-
The development and application of two-chamber reactors and carbon monoxide precursors for safe carbonylation reactions
-
Friis, S. D., Lindhardt, A. T. & Skrydstrup, T. The development and application of two-chamber reactors and carbon monoxide precursors for safe carbonylation reactions. Acc. Chem. Res. 49, 594-605 (2016).
-
(2016)
Acc. Chem. Res.
, vol.49
, pp. 594-605
-
-
Friis, S.D.1
Lindhardt, A.T.2
Skrydstrup, T.3
-
7
-
-
84894144483
-
Ruthenium-catalysed alkoxycarbonylation of alkenes with carbon dioxide
-
Wu, L., Liu, Q., Fleischer, I., Jackstell, R. & Beller, M. Ruthenium-catalysed alkoxycarbonylation of alkenes with carbon dioxide. Nat. Commun 5, 3091 (2014).
-
(2014)
Nat. Commun
, vol.5
, pp. 3091
-
-
Wu, L.1
Liu, Q.2
Fleischer, I.3
Jackstell, R.4
Beller, M.5
-
8
-
-
79954532428
-
Ex situ generation of stoichiometric and substoichiometric 12CO and 13CO and its efficient incorporation in palladium catalyzed aminocarbonylations
-
Hermange, P. et al. Ex situ generation of stoichiometric and substoichiometric 12CO and 13CO and its efficient incorporation in palladium catalyzed aminocarbonylations. J. Am. Chem. Soc. 133, 6061-6071 (2011).
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 6061-6071
-
-
Hermange, P.1
-
9
-
-
8444233969
-
Evolution of carbonylation catalysis: No need for carbon monoxide
-
Morimoto, T. & Kakiuchi, K. Evolution of carbonylation catalysis: no need for carbon monoxide. Angew. Chem. Int. Ed. 43, 5580-5588 (2004).
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 5580-5588
-
-
Morimoto, T.1
Kakiuchi, K.2
-
10
-
-
67650531072
-
Rh(I)-catalyzed CO gas-free carbonylative cyclization reactions of alkynes with 2-bromophenylboronic acids using formaldehyde
-
Morimoto, T. et al. Rh(I)-catalyzed CO gas-free carbonylative cyclization reactions of alkynes with 2-bromophenylboronic acids using formaldehyde. Org. Lett. 11, 1777-1780 (2009).
-
(2009)
Org. Lett.
, vol.11
, pp. 1777-1780
-
-
Morimoto, T.1
-
11
-
-
85003749611
-
Alkyl bromides as mild hydride sources in Ni-catalyzed hydroamidation of alkynes with isocyanates
-
Wang, X., Nakajima, M., Serrano, E. & Martin, R. Alkyl bromides as mild hydride sources in Ni-catalyzed hydroamidation of alkynes with isocyanates. J. Am. Chem. Soc. 138, 15531-15534 (2016).
-
(2016)
J. Am. Chem. Soc.
, vol.138
, pp. 15531-15534
-
-
Wang, X.1
Nakajima, M.2
Serrano, E.3
Martin, R.4
-
12
-
-
84882257765
-
Diaminophosphine oxide ligand enabled asymmetric nickel-catalyzed hydrocarbamoylations of alkenes
-
Donets, P. A. & Cramer, N. Diaminophosphine oxide ligand enabled asymmetric nickel-catalyzed hydrocarbamoylations of alkenes. J. Am. Chem. Soc. 135, 11772-11775 (2013).
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 11772-11775
-
-
Donets, P.A.1
Cramer, N.2
-
13
-
-
84927737338
-
Palladium-catalyzed carbonylative esterification of primary alcohols with aryl chlorides through dehydroxymethylative C-C bond cleavage
-
Park, H.-S., Kim, D.-S. & Jun, C.-H. Palladium-catalyzed carbonylative esterification of primary alcohols with aryl chlorides through dehydroxymethylative C-C bond cleavage. ACS Catal. 5, 397-401 (2015).
-
(2015)
ACS Catal
, vol.5
, pp. 397-401
-
-
Park, H.-S.1
Kim, D.-S.2
Jun, C.-H.3
-
17
-
-
84994246457
-
Stereoselective synthesis of methylene oxindoles via palladium(II)-catalyzed intramolecular cross-coupling of carbamoyl chlorides
-
Le, C. M. et al. Stereoselective synthesis of methylene oxindoles via palladium(II)-catalyzed intramolecular cross-coupling of carbamoyl chlorides. J. Am. Chem. Soc. 138, 14441-14448 (2016).
-
(2016)
J. Am. Chem. Soc.
, vol.138
, pp. 14441-14448
-
-
Le, C.M.1
-
18
-
-
84887815121
-
A palladium-catalyzed carbonylation approach to acid chloride synthesis
-
Quesnel, J. S. & Arndtsen, B. A. A palladium-catalyzed carbonylation approach to acid chloride synthesis. J. Am. Chem. Soc. 135, 16841-16844 (2013).
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 16841-16844
-
-
Quesnel, J.S.1
Arndtsen, B.A.2
-
19
-
-
84934933946
-
Acid chloride synthesis by the palladium-catalyzed chlorocarbonylation of aryl bromides
-
Quesnel, J. S., Kayser, L. V., Fabrikant, A. & Arndtsen, B. A. Acid chloride synthesis by the palladium-catalyzed chlorocarbonylation of aryl bromides. Chem. Eur. J. 21, 9550-9555 (2015).
-
(2015)
Chem. Eur. J
, vol.21
, pp. 9550-9555
-
-
Quesnel, J.S.1
Kayser, L.V.2
Fabrikant, A.3
Arndtsen, B.A.4
-
20
-
-
67749145466
-
Multicatalytic synthesis of α-pyrrolidinyl ketones via a tandem palladium(II)/indium(III)-catalyzed aminochlorocarbonylation/Friedel-Crafts acylation reaction
-
Cernak, T. A. & Lambert, T. H. Multicatalytic synthesis of α-pyrrolidinyl ketones via a tandem palladium(II)/indium(III)-catalyzed aminochlorocarbonylation/Friedel-Crafts acylation reaction. J. Am. Chem. Soc. 131, 3124-3125 (2009).
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 3124-3125
-
-
Cernak, T.A.1
Lambert, T.H.2
-
21
-
-
85051258636
-
-
US patent 3,065,242
-
Alderson, T. & Engelhardt, V. A. Production of acyl halides, carboxylic acids and lactones. US patent 3,065,242 (1962).
-
(1962)
Production of Acyl Halides, Carboxylic Acids and Lactones
-
-
Alderson, T.1
Engelhardt, V.A.2
-
23
-
-
84958999478
-
Catalytic reversible alkene-nitrile interconversion through controllable transfer hydrocyanation
-
Fang, X., Yu, P. & Morandi, B. Catalytic reversible alkene-nitrile interconversion through controllable transfer hydrocyanation. Science 351, 832-836 (2016).
-
(2016)
Science
, vol.351
, pp. 832-836
-
-
Fang, X.1
Yu, P.2
Morandi, B.3
-
24
-
-
85003740087
-
Catalytic transfer functionalization through shuttle catalysis
-
Bhawal, B. N. & Morandi, B. Catalytic transfer functionalization through shuttle catalysis. ACS Catal. 6, 7528-7535 (2016).
-
(2016)
ACS Catal
, vol.6
, pp. 7528-7535
-
-
Bhawal, B.N.1
Morandi, B.2
-
25
-
-
84922481413
-
Rh-catalyzed C-C bond cleavage by transfer hydroformylation
-
Murphy, S. K., Park, J.-W., Cruz, F. A. & Dong, V. M. Rh-catalyzed C-C bond cleavage by transfer hydroformylation. Science 347, 56-60 (2015).
-
(2015)
Science
, vol.347
, pp. 56-60
-
-
Murphy, S.K.1
Park, J.-W.2
Cruz, F.A.3
Dong, V.M.4
-
26
-
-
84922479719
-
Construction and deconstruction of aldehydes by transfer hydroformylation
-
Landis, C. R. Construction and deconstruction of aldehydes by transfer hydroformylation. Science 347, 29-30 (2015).
-
(2015)
Science
, vol.347
, pp. 29-30
-
-
Landis, C.R.1
-
27
-
-
40549088216
-
Metal-organic cooperative catalysis in C-H and C-C bond activation and its concurrent recovery
-
Park, Y. J., Park, J.-W. & Jun, C.-H. Metal-organic cooperative catalysis in C-H and C-C bond activation and its concurrent recovery. Acc. Chem. Res. 41, 222-234 (2008).
-
(2008)
Acc. Chem. Res.
, vol.41
, pp. 222-234
-
-
Park, Y.J.1
Park, J.-W.2
Jun, C.-H.3
-
28
-
-
0035200787
-
Wide bite angle diphosphines: Xantphos ligands in transition metal complexes and catalysis
-
Kamer, P. C. J., van Leeuwen, P. W. N. M. & Reek, J. N. H. Wide bite angle diphosphines: Xantphos ligands in transition metal complexes and catalysis. Acc. Chem. Res. 34, 895-904 (2001).
-
(2001)
Acc. Chem. Res.
, vol.34
, pp. 895-904
-
-
Kamer, P.C.J.1
Van Leeuwen, P.W.N.M.2
Reek, J.N.H.3
-
29
-
-
0035781198
-
Metal-catalyzed living radical polymerization
-
Kamigaito, M., Ando, T. & Sawamoto, M. Metal-catalyzed living radical polymerization. Chem. Rev. 101, 3689-3746 (2001).
-
(2001)
Chem. Rev.
, vol.101
, pp. 3689-3746
-
-
Kamigaito, M.1
Oza, T.2
Sawamoto, M.3
-
30
-
-
51549101998
-
Room temperature ICl-induced dehydration/iodination of 1-acyl-5-hydroxy-4,5-dihydro-1H-pyrazoles. A selective route to substituted 1-acyl-4-iodo-1H-pyrazoles
-
Waldo, J. P., Mehta, S. & Larock, R. C. Room temperature ICl-induced dehydration/iodination of 1-acyl-5-hydroxy-4,5-dihydro-1H-pyrazoles. A selective route to substituted 1-acyl-4-iodo-1H-pyrazoles. J. Org. Chem. 73, 6666-6670 (2008).
-
(2008)
J. Org. Chem.
, vol.73
, pp. 6666-6670
-
-
Waldo, J.P.1
Mehta, S.2
Larock, R.C.3
-
31
-
-
0346690002
-
A convenient method for preparing aromatic α,β-unsaturated ketones from α,β-unsaturated acyl chlorides and arylboronic acids via Suzuki-Miyaura type coupling reaction
-
Urawa, Y., Nishiura, K., Souda, S. & Ogura, K. A convenient method for preparing aromatic α,β-unsaturated ketones from α,β-unsaturated acyl chlorides and arylboronic acids via Suzuki-Miyaura type coupling reaction. Synthesis 2882-2885 (2003).
-
(2003)
Synthesis
, pp. 2882-2885
-
-
Urawa, Y.1
Nishiura, K.2
Souda, S.3
Ogura, K.4
-
32
-
-
2442656574
-
Selective iron-catalyzed cross-coupling reactions of Grignard reagents with enol triflates, acid chlorides, and dichloroarenes
-
Scheiper, B., Bonnekessel, M., Krause, H. & Fürstner, A. Selective iron-catalyzed cross-coupling reactions of Grignard reagents with enol triflates, acid chlorides, and dichloroarenes. J. Org. Chem. 69, 3943-3949 (2004).
-
(2004)
J. Org. Chem.
, vol.69
, pp. 3943-3949
-
-
Scheiper, B.1
Bonnekessel, M.2
Krause, H.3
Fürstner, A.4
-
33
-
-
0242515860
-
Efficient synthesis of enantiomerically pure β2-amino acids via chiral isoxazolidinones
-
Lee, H.-S., Park, J.-S., Kim, B. M. & Gellman, S. H. Efficient synthesis of enantiomerically pure β2-amino acids via chiral isoxazolidinones. J. Org. Chem. 68, 1575-1578 (2003).
-
(2003)
J. Org. Chem.
, vol.68
, pp. 1575-1578
-
-
Lee, H.-S.1
Park, J.-S.2
Kim, B.M.3
Gellman, S.H.4
-
35
-
-
84942366983
-
Palladium-catalyzed decarbonylative dehydration for the synthesis of α -vinyl carbonyl compounds and total synthesis of (-)-aspewentins A, B, and C
-
Liu, Y., Virgil, S. C., Grubbs, R. H. & Stoltz, B. M., Palladium-catalyzed decarbonylative dehydration for the synthesis of α -vinyl carbonyl compounds and total synthesis of (-)-aspewentins A, B, and C. Angew. Chem. Int. Ed. 54, 11800-11803 (2015).
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 11800-11803
-
-
Liu, Y.1
Virgil, S.C.2
Grubbs, R.H.3
Stoltz, B.M.4
-
36
-
-
1842431563
-
A mild and efficient protocol for the conversion of carboxylic acids to olefins by a catalytic decarbonylative elimination reaction
-
Gooßen, L. J. & Rodriguez, N. A mild and efficient protocol for the conversion of carboxylic acids to olefins by a catalytic decarbonylative elimination reaction. Chem. Commun. 724-725 (2004).
-
(2004)
Chem. Commun.
, pp. 724-725
-
-
Gooßen, L.J.1
Rodriguez, N.2
-
37
-
-
0002694246
-
Organic syntheses by means of noble metal compounds. XXXIV. Carbonylation and decarbonylation reactions catalyzed by palladium
-
Tsuji, J. & Ohno, K. Organic syntheses by means of noble metal compounds. XXXIV. Carbonylation and decarbonylation reactions catalyzed by palladium. J. Am. Chem. Soc. 90, 94-98 (1968).
-
(1968)
J. Am. Chem. Soc.
, vol.90
, pp. 94-98
-
-
Tsuji, J.1
Ohno, K.2
|