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Angewandte Chemie - International Edition

Volumn 56, Issue 12, 2017, Pages 3319-3323

Alkyl−(Hetero)Aryl Bond Formation via Decarboxylative Cross-Coupling: A Systematic Analysis

(5) Sandfort, Frederik a O'Neill, Matthew J a Cornella, Josep a Wimmer, Laurin a Baran, Phil S a

a SCRIPPS RESEARCH INSTITUTE (United States)

Author keywords

decarboxylative cross coupling; iron catalysis; nickel catalysis; redox active esters

Indexed keywords

AMIDES; CARBOXYLIC ACIDS; CATALYSIS; COUPLING AGENTS; ESTERS; METALS; ORGANOMETALLICS; REDOX REACTIONS;

ALKYL CARBOXYLIC ACIDS; AMIDE BOND FORMATION; CROSS-COUPLINGS; DESIGNED EXPERIMENTS; IRON CATALYSIS; NICKEL CATALYSIS; REDOX-ACTIVE; SYSTEMATIC ANALYSIS;

CHEMICAL BONDS;

AMIDE; CARBOXYLIC ACID; HALOGENATED HYDROCARBON; ORGANOMETALLIC COMPOUND;

CHEMICAL STRUCTURE; CHEMISTRY; DECARBOXYLATION; OXIDATION REDUCTION REACTION; SYNTHESIS;

AMIDES; CARBOXYLIC ACIDS; DECARBOXYLATION; HYDROCARBONS, HALOGENATED; MOLECULAR STRUCTURE; ORGANOMETALLIC COMPOUNDS; OXIDATION-REDUCTION;

EID: 85012081867 PISSN: 14337851 EISSN: 15213773 Source Type: Journal
DOI: 10.1002/anie.201612314 Document Type: Article

Times cited : (84)

References (33)

1
- 0003397781
- Wiley-VCH, Weinheim
- F. Diederich, P. J. Stang, Metal-catalyzed Cross-coupling Reactions, Wiley-VCH, Weinheim, 1998.
- (1998) Metal-catalyzed Cross-coupling Reactions
- Diederich, F.¹ Stang, P.J.²

2
- 84959450281
- J. Cornella, J. T. Edwards, T. Qin, S. Kawamura, J. Wang, C.-M. Pan, R. Gianatassio, M. Schmidt, M. D. Eastgate, P. S. Baran, J. Am. Chem. Soc. 2016, 138, 2174;
- (2016) J. Am. Chem. Soc. , vol.138 , pp. 2174
- Cornella, J.¹ Edwards, J.T.² Qin, T.³ Kawamura, S.⁴ Wang, J.⁵ Pan, C.-M.⁶ Gianatassio, R.⁷ Schmidt, M.⁸ Eastgate, M.D.⁹ Baran, P.S.¹⁰

3
- 84964558188
- T. Qin, J. Cornella, C. Li, L. Malins, J. T. Edwards, S. Kawamura, B. D. Maxwell, M. D. Eastgate, P. S. Baran, Science 2016, 352, 801;
- (2016) Science , vol.352 , pp. 801
- Qin, T.¹ Cornella, J.² Li, C.³ Malins, L.⁴ Edwards, J.T.⁵ Kawamura, S.⁶ Maxwell, B.D.⁷ Eastgate, M.D.⁸ Baran, P.S.⁹

4
- 84986230272
- F. Toriyama, J. Cornella, L. Wimmer, T.-G. Chen, D. D. Dixon, G. Creech, P. S. Baran, J. Am. Chem. Soc. 2016, 138, 11132.
- (2016) J. Am. Chem. Soc. , vol.138 , pp. 11132
- Toriyama, F.¹ Cornella, J.² Wimmer, L.³ Chen, T.-G.⁴ Dixon, D.D.⁵ Creech, G.⁶ Baran, P.S.⁷

5
- 84979074178
- J. Wang, T. Qin, T.-G. Chen, L. Wimmer, J. T. Edwards, J. Cornella, B. Vokits, S. A. Shaw, P. S. Baran, Angew. Chem. Int. Ed. 2016, 55, 9676;
- (2016) Angew. Chem. Int. Ed. , vol.55 , pp. 9676
- Wang, J.¹ Qin, T.² Chen, T.-G.³ Wimmer, L.⁴ Edwards, J.T.⁵ Cornella, J.⁶ Vokits, B.⁷ Shaw, S.A.⁸ Baran, P.S.⁹

6
- 85007043414
- Angew. Chem. 2016, 128, 9828.
- (2016) Angew. Chem. , vol.128 , pp. 9828

7
- 84930002266
- Apple Publishing Group, New York
- Y. Ishihara, A. Montero, P. S. Baran, The Portable Chemist's Consultant, Apple Publishing Group, New York, 2013.
- (2013) The Portable Chemist's Consultant
- Ishihara, Y.¹ Montero, A.² Baran, P.S.³

8
- 80054968939
- For the use of aromatic carboxy groups in decarboxylative strategies, see
- For the use of aromatic carboxy groups in decarboxylative strategies, see: N. Rodríguez, L. J. Goossen, Chem. Soc. Rev. 2011, 40, 5030.
- (2011) Chem. Soc. Rev. , vol.40 , pp. 5030
- Rodríguez, N.¹ Goossen, L.J.²

9
- 85043884925
- For the use of aromatic carboxy groups in decarbonylative C−C bond formation, see
- For the use of aromatic carboxy groups in decarbonylative C−C bond formation, see:

10
- 84934325537
- K. Muto, J. Yamaguchi, D. G. Musaev, K. Itami, Nat. Commun. 2015, 6, 7508;
- (2015) Nat. Commun. , vol.6 , pp. 7508
- Muto, K.¹ Yamaguchi, J.² Musaev, D.G.³ Itami, K.⁴

11
- 84865430497
- K. Amaike, K. Muto, J. Yamaguchi, K. Itami, J. Am. Chem. Soc. 2012, 134, 13573.
- (2012) J. Am. Chem. Soc. , vol.134 , pp. 13573
- Amaike, K.¹ Muto, K.² Yamaguchi, J.³ Itami, K.⁴

12
- 85043840411
- For the use of alkylcarboxy groups in Ni-catalysis in conjunction with photoinduced electron transfer (PET) chemistry, see
- For the use of alkylcarboxy groups in Ni-catalysis in conjunction with photoinduced electron transfer (PET) chemistry, see:

13
- 84904797499
- Z. Zuo, D. T. Ahneman, L. Chu, J. A. Terrett, A. G. Doyle, D. W. C. MacMillan, Science 2014, 345, 437;
- (2014) Science , vol.345 , pp. 437
- Zuo, Z.¹ Ahneman, D.T.² Chu, L.³ Terrett, J.A.⁴ Doyle, A.G.⁵ MacMillan, D.W.C.⁶

14
- 84930268175
- L. Chu, J. M. Lipshultz, D. W. C. MacMillan, Angew. Chem. Int. Ed. 2015, 54, 7929;
- (2015) Angew. Chem. Int. Ed. , vol.54 , pp. 7929
- Chu, L.¹ Lipshultz, J.M.² MacMillan, D.W.C.³

15
- 85013291262
- Angew. Chem. 2015, 127, 8040.
- (2015) Angew. Chem. , vol.127 , pp. 8040

16
- 84966292281
- For the use of redox-active esters in reductive cross-couplings, see
- For the use of redox-active esters in reductive cross-couplings, see: K. M. M. Huihui, J. A. Caputo, Z. Melchor, A. M. Olivares, A. M. Spiewak, K. A. Johnson, T. A. DiBenedetto, S. Kim, L. K. G. Ackerman, D. J. Weix, J. Am. Chem. Soc. 2016, 138, 5016.
- (2016) J. Am. Chem. Soc. , vol.138 , pp. 5016
- Huihui, K.M.M.¹ Caputo, J.A.² Melchor, Z.³ Olivares, A.M.⁴ Spiewak, A.M.⁵ Johnson, K.A.⁶ DiBenedetto, T.A.⁷ Kim, S.⁸ Ackerman, L.K.G.⁹ Weix, D.J.¹⁰

17
- 84881498225
- in, Springer, Berlin, Heidelberg
- Y. Nishihara, in Applied Cross-Coupling Reactions, Springer, Berlin, Heidelberg, 2013.
- (2013) Applied Cross-Coupling Reactions
- Nishihara, Y.¹

18
- 79251600617
- D. S. Surry, S. L. Buchwald, Chem. Sci. 2011, 2, 27.
- (2011) Chem. Sci. , vol.2 , pp. 27
- Surry, D.S.¹ Buchwald, S.L.²

19
- 0037146041
- A. Fürstner, A. Leitner, M. Méndez, H. Krause, J. Am. Chem. Soc. 2002, 124, 13856;
- (2002) J. Am. Chem. Soc. , vol.124 , pp. 13856
- Fürstner, A.¹ Leitner, A.² Méndez, M.³ Krause, H.⁴

20
- 4544294922
- R. Martin, A. Fürstner, Angew. Chem. Int. Ed. 2004, 43, 3955;
- (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 3955
- Martin, R.¹ Fürstner, A.²

21
- 84929309569
- Angew. Chem. 2004, 116, 4045.
- (2004) Angew. Chem. , vol.116 , pp. 4045

22
- 84963522319
- A. A. Thomas, S. E. Denmark, Science 2016, 352, 329;
- (2016) Science , vol.352 , pp. 329
- Thomas, A.A.¹ Denmark, S.E.²

23
- 84880095538
- A. J. J. Lennox, G. C. Lloyd-Jones, Angew. Chem. Int. Ed. 2013, 52, 7362;
- (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 7362
- Lennox, A.J.J.¹ Lloyd-Jones, G.C.²

24
- 84900343425
- Angew. Chem. 2013, 125, 7506;
- (2013) Angew. Chem. , vol.125 , pp. 7506

25
- 79951832916
- B. P. Carrow, J. F. Hartwig, J. Am. Chem. Soc. 2011, 133, 2116.
- (2011) J. Am. Chem. Soc. , vol.133 , pp. 2116
- Carrow, B.P.¹ Hartwig, J.F.²

26
- 84858038469
- G. R. Dick, E. M. Woerly, M. D. Burke, Angew. Chem. Int. Ed. 2012, 51, 2667;
- (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 2667
- Dick, G.R.¹ Woerly, E.M.² Burke, M.D.³

27
- 84962945264
- Angew. Chem. 2012, 124, 2721.
- (2012) Angew. Chem. , vol.124 , pp. 2721

28
- 67650492323
- O. Vechorkin, V. Proust, X. Hu, J. Am. Chem. Soc. 2009, 131, 9756.
- (2009) J. Am. Chem. Soc. , vol.131 , pp. 9756
- Vechorkin, O.¹ Proust, V.² Hu, X.³

29
- 79953020974
- A. K. Steib, T. Thaler, K. Komeyama, P. Mayer, P. Knochel, Angew. Chem. Int. Ed. 2011, 50, 3303;
- (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 3303
- Steib, A.K.¹ Thaler, T.² Komeyama, K.³ Mayer, P.⁴ Knochel, P.⁵

30
- 85014893644
- Angew. Chem. 2011, 123, 3361;
- (2011) Angew. Chem. , vol.123 , pp. 3361

31
- 84939985642
- J. M. Hammann, D. Haas, A. K. Steib, P. Knochel, Synthesis 2015, 47, 1461.
- (2015) Synthesis , vol.47 , pp. 1461
- Hammann, J.M.¹ Haas, D.² Steib, A.K.³ Knochel, P.⁴

32
- 79953169089
- A. Krasovskiy, I. Thomé, J. Graff, V. Krasovskaya, P. Konopelski, C. Duplais, B. H. Lipshutz, Tetrahedron Lett. 2011, 52, 2203.
- (2011) Tetrahedron Lett. , vol.52 , pp. 2203
- Krasovskiy, A.¹ Thomé, I.² Graff, J.³ Krasovskaya, V.⁴ Konopelski, P.⁵ Duplais, C.⁶ Lipshutz, B.H.⁷

33
- 78650410560
- G. A. Molander, O. A. Argintaru, I. Aron, S. D. Dreher, Org. Lett. 2010, 12, 5783.
- (2010) Org. Lett. , vol.12 , pp. 5783
- Molander, G.A.¹ Argintaru, O.A.² Aron, I.³ Dreher, S.D.⁴

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