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European Journal of Organic Chemistry

Volumn 2014, Issue 14, 2014, Pages 2956-2963

Electrophilicities of 1,2-disubstituted ethylenes

(2) Allgäuer, Dominik S a Mayr, Herbert a

a UNIVERSITY OF MUNICH (Germany)

Author keywords

Alkenes; Cycloaddition; Electrophilicity; Kinetics; Linear free energy relationships; Ylides

Indexed keywords

EID: 84899974085 PISSN: 1434193X EISSN: 10990690 Source Type: Journal
DOI: 10.1002/ejoc.201301779 Document Type: Article

Times cited : (41)

References (101)

1
- 84899930042
- For reviews, see
- For reviews, see

2
- 0002179569
- (Eds.:, S. Patai, Z. Rappoport), Wiley, New York
- S. Patai, Z. Rappoport, in: The Chemistry of Alkenes (Eds.:, S. Patai, Z. Rappoport), Wiley, New York, 1964, p. 469-584.
- (1964) The Chemistry of Alkenes , pp. 469-584
- Patai, S.¹ Rappoport, Z.²

3
- 0002922998
- (Eds.:, S. Patai, Z. Rappoport), Wiley, London
- C. Bianchi, C. De Micheli, R. Gandolfi, in: The Chemistry of Double-Bonded Functional Groups, vol. 1 (Eds.:, S. Patai, Z. Rappoport), Wiley, London, 1977, p. 369-533.
- (1977) The Chemistry of Double-Bonded Functional Groups , vol.1 , pp. 369-533
- Bianchi, C.¹ De Micheli, C.² Gandolfi, R.³

4
- 85050550551
- (Eds.:, E. L. Eliel, S. H. Wilen), Wiley-Interscience, Hoboken, NJ
- D. A. Oare, C. H. Heathcock, in: Topics in Stereochemistry, vol. 20 (Eds.:, E. L. Eliel, S. H. Wilen), Wiley-Interscience, Hoboken, NJ, 1991, p. 87-170.
- (1991) Topics in Stereochemistry , vol.20 , pp. 87-170
- Oare, D.A.¹ Heathcock, C.H.²

5
- 80555151463
- (Ed.:, J. Cossy), Thieme, Stuttgart, Germany
- I. Chataigner, A. Harrison-Marchand, J. Maddaluno, in: Science of Synthesis, vol. 26 (Ed.:, J. Cossy), Thieme, Stuttgart, Germany, 2005, p. 1123-1286.
- (2005) Science of Synthesis , vol.26 , pp. 1123-1286
- Chataigner, I.¹ Harrison-Marchand, A.² Maddaluno, J.³

6
- 84899935083
- (Ed.:, A. de Meijere), Thieme, Stuttgart, Germany
- F. Fringuelli, O. Piermatti, F. Pizzo, L. Vaccaro, in: Science of Synthesis, vol. 47b (Ed.:, A. de Meijere), Thieme, Stuttgart, Germany, 2010, p. 561-722.
- (2010) Science of Synthesis , vol.47 , pp. 561-722
- Fringuelli, F.¹ Piermatti, O.² Pizzo, F.³ Vaccaro, L.⁴

7
- 84899976340
- For reviews on conjugate additions, see
- For reviews on conjugate additions, see

8
- 0000146934
- W. Nagata, M. Yoshioka, Org. React. 1977, 25, 255-476.
- (1977) Org. React. , vol.25 , pp. 255-476
- Nagata, W.¹ Yoshioka, M.²

9
- 0037518546
- (Ed.:, J. E. Baldwin) Pergamon, Oxford, UK
- P. Perlmutter, in: Conjugate Addition Reactions in Organic Synthesis Tetrahedron Organic Chemistry Series, vol. 9 (Ed.:, J. E. Baldwin) Pergamon, Oxford, UK, 1992.
- (1992) Conjugate Addition Reactions in Organic Synthesis Tetrahedron Organic Chemistry Series , vol.9
- Perlmutter, P.¹

10
- 84891579278
- Wiley-VCH, Weinheim, Germany
- A. Cõrdova, Catalytic Asymmetric Conjugate Reactions, Wiley-VCH, Weinheim, Germany, 2010.
- (2010) Catalytic Asymmetric Conjugate Reactions
- Cõrdova, A.¹

11
- 0035126119
- N. Krause, A. Hoffmann-Röder, Synthesis 2001, 171-196.
- (2001) Synthesis , pp. 171-196
- Krause, N.¹ Hoffmann-Röder, A.²

12
- 0034612973
- M. P. Sibi, S. Manyem, Tetrahedron 2000, 56, 8033-8061.
- (2000) Tetrahedron , vol.56 , pp. 8033-8061
- Sibi, M.P.¹ Manyem, S.²

13
- 17244375162
- R. Ballini, G. Bosica, D. Fiorini, A. Palmieri, M. Petrini, Chem. Rev. 2005, 105, 933-972.
- (2005) Chem. Rev. , vol.105 , pp. 933-972
- Ballini, R.¹ Bosica, G.² Fiorini, D.³ Palmieri, A.⁴ Petrini, M.⁵

14
- 0026561424
- J. d'Angelo, D. Desmaële, F. Dumas, A. Guingant, Tetrahedron: Asymmetry 1992, 3, 459-505.
- (1992) Tetrahedron: Asymmetry , vol.3 , pp. 459-505
- D'Angelo, J.¹ Desmaële, D.² Dumas, F.³ Guingant, A.⁴

15
- 0004101860
- John Wiley & Sons, New York
- A. Padwa, 1,3-Dipolar Cycloaddition Chemistry, John Wiley & Sons, New York, 1985.
- (1985) 1,3-Dipolar Cycloaddition Chemistry
- Padwa, A.¹

16
- 84899923996
- For reviews on 1,3-dipolar cycloadditions, see
- For reviews on 1,3-dipolar cycloadditions, see

17
- 36749014055
- 1963, Angew. Chem. 75, 604-637
- R. Huisgen, Angew. Chem. Int. Ed. Engl. 1963, 2, 565-598; Angew. Chem. 1963, 75, 604-637.
- (1963) Angew. Chem. Int. Ed. Engl. , vol.2 , pp. 565-598
- Huisgen, R.¹

18
- 0000299952
- 1963, Angew. Chem. 75, 742-754
- R. Huisgen, Angew. Chem. Int. Ed. Engl. 1963, 2, 633-645; Angew. Chem. 1963, 75, 742-754.
- (1963) Angew. Chem. Int. Ed. Engl. , vol.2 , pp. 633-645
- Huisgen, R.¹

19
- 33847799231
- R. Huisgen, J. Org. Chem. 1976, 41, 403-419.
- (1976) J. Org. Chem. , vol.41 , pp. 403-419
- Huisgen, R.¹

20
- 33751433159
- G. Pandey, P. Banerjee, S. R. Gadre, Chem. Rev. 2006, 106, 4484-4517.
- (2006) Chem. Rev. , vol.106 , pp. 4484-4517
- Pandey, G.¹ Banerjee, P.² Gadre, S.R.³

21
- 33947231700
- H. Pellissier, Tetrahedron 2007, 63, 3235-3285.
- (2007) Tetrahedron , vol.63 , pp. 3235-3285
- Pellissier, H.¹

22
- 51049094424
- L. M. Stanley, M. P. Sibi, Chem. Rev. 2008, 108, 2887-2902.
- (2008) Chem. Rev. , vol.108 , pp. 2887-2902
- Stanley, L.M.¹ Sibi, M.P.²

23
- 0004092363
- Wiley, Chichester, UK
- F. Fringuelli, A. Taticchi, The Diels-Alder Reaction: Selected Practical Methods, Wiley, Chichester, UK, 2002.
- (2002) The Diels-Alder Reaction: Selected Practical Methods
- Fringuelli, F.¹ Taticchi, A.²

24
- 84899902911
- For reviews on Diels-Alder reactions, see
- For reviews on Diels-Alder reactions, see

25
- 84943701775
- R. Sustmann, Pure Appl. Chem. 1974, 40, 569-593.
- (1974) Pure Appl. Chem. , vol.40 , pp. 569-593
- Sustmann, R.¹

26
- 0342713055
- Angew. Chem. 1980, 92, 773-801
- J. Sauer, R. Sustmann, Angew. Chem. Int. Ed. Engl. 1980, 19, 779-807; Angew. Chem. 1980, 92, 773-801.
- (1980) Angew. Chem. Int. Ed. Engl. , vol.19 , pp. 779-807
- Sauer, J.¹ Sustmann, R.²

27
- 4244033876
- H. B. Kagan, O. Riant, Chem. Rev. 1992, 92, 1007-1019.
- (1992) Chem. Rev. , vol.92 , pp. 1007-1019
- Kagan, H.B.¹ Riant, O.²

28
- 0036259981
- 2002, Angew. Chem. 114, 1742-1773
- K. C. Nicolaou, S. A. Snyder, T. Montagnon, G. Vassilikogiannakis, Angew. Chem. Int. Ed. 2002, 41, 1668-1698; Angew. Chem. 2002, 114, 1742-1773.
- (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 1668-1698
- Nicolaou, K.C.¹ Snyder, S.A.² Montagnon, T.³ Vassilikogiannakis, G.⁴

29
- 33845376451
- D. L. Boger, Chem. Rev. 1986, 86, 781-793.
- (1986) Chem. Rev. , vol.86 , pp. 781-793
- Boger, D.L.¹

30
- 0039930587
- U. Pindur, G. Lutz, C. Otto, Chem. Rev. 1993, 93, 741-761.
- (1993) Chem. Rev. , vol.93 , pp. 741-761
- Pindur, U.¹ Lutz, G.² Otto, C.³

31
- 0034583305
- J. B. F. N. Engberts
- S. Otto, J. B. F. N. Engberts, Pure Appl. Chem. 2000, 72, 1365-1372.
- (2000) Pure Appl. Chem. , vol.72 , pp. 1365-1372
- Otto, S.¹

32
- 0000713226
- (Eds.:, E. L. Eliel, S. H. Wilen), Wiley-Interscience, New York
- D. A. Oare, C. H. Heathcock, in: Topics in Stereochemistry, vol. 18 (Eds.:, E. L. Eliel, S. H. Wilen), Wiley-Interscience, New York, 1989, p. 227-407.
- (1989) Topics in Stereochemistry , vol.18 , pp. 227-407
- Oare, D.A.¹ Heathcock, C.H.²

33
- 0000097153
- (Eds.:, E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Berlin
- D. A. Evans, J. S. Johnson, in: Comprehensive Asymmetric Catalysis I-III, vol. 3 (Eds.:, E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Berlin, 1999, p. 1177-1235.
- (1999) Comprehensive Asymmetric Catalysis I-III , vol.3 , pp. 1177-1235
- Evans, D.A.¹ Johnson, J.S.²

34
- 33846594443
- W. Zeng, G.-Y. Chen, Y.-G. Zhou, Y.-X. Li, J. Am. Chem. Soc. 2007, 129, 750-751.
- (2007) J. Am. Chem. Soc. , vol.129 , pp. 750-751
- Zeng, W.¹ Chen, G.-Y.² Zhou, Y.-G.³ Li, Y.-X.⁴

35
- 33847021540
- I. Lõpez, G. Silvero, M. J. Arévalo, R. Babiano, J. C. Palacios, J. L. Bravo, Tetrahedron 2007, 63, 2901-2906.
- (2007) Tetrahedron , vol.63 , pp. 2901-2906
- Lõpez, I.¹ Silvero, G.² Arévalo, M.J.³ Babiano, R.⁴ Palacios, J.C.⁵ Bravo, J.L.⁶

36
- 0001040147
- B. E. Rossiter, N. M. Swingle, Chem. Rev. 1992, 92, 771-806.
- (1992) Chem. Rev. , vol.92 , pp. 771-806
- Rossiter, B.E.¹ Swingle, N.M.²

37
- 34249095816
- J. Christoffers, G. Koripelly, A. Rosiak, M. Rössle, Synthesis 2007, 1279-1300.
- (2007) Synthesis , pp. 1279-1300
- Christoffers, J.¹ Koripelly, G.² Rosiak, A.³ Rössle, M.⁴

38
- 0036263839
- 2002, Angew. Chem. 114, 1724-1741
- E. J. Corey, Angew. Chem. Int. Ed. 2002, 41, 1650-1667; Angew. Chem. 2002, 114, 1724-1741.
- (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 1650-1667
- Corey, E.J.¹

39
- 61949336768
- S. B. Reymond, J. Cossy, Chem. Rev. 2008, 108, 5359-5406.
- (2008) Chem. Rev. , vol.108 , pp. 5359-5406
- Reymond, S.B.¹ Cossy, J.²

40
- 47749122232
- Wiley-VCH, Weinheim, Germany
- A. Berkessel, H. Gröger, Asymmetric Organocatalysis, Wiley-VCH, Weinheim, Germany, 2005.
- (2005) Asymmetric Organocatalysis
- Berkessel, A.¹ Gröger, H.²

41
- 77950280363
- (Ed.:, B. List), Springer, Berlin
- A. Ting, J. M. Goss, N. T. McDougal, S. E. Schaus, in: Asymmetric Organocatalysis, Top. Curr. Chem., vol. 291 (Ed.:, B. List), Springer, Berlin, 2010, p. 145-201.
- (2010) Asymmetric Organocatalysis, Top. Curr. Chem. , vol.291 , pp. 145-201
- Ting, A.¹ Goss, J.M.² McDougal, N.T.³ Schaus, S.E.⁴

42
- 84872539386
- RSC Publ., Cambridge, UK
- J. L. Vicario, D. Badía, L. Carrillo, E. Reyes, Organocatalytic Enantioselective Conjugate Addition Reactions-A Powerful Tool for the Stereocontrolled Synthesis of Complex Molecules, RSC Catalysis Series, vol. 5, RSC Publ., Cambridge, UK, 2010.
- (2010) Organocatalytic Enantioselective Conjugate Addition Reactions-A Powerful Tool for the Stereocontrolled Synthesis of Complex Molecules, RSC Catalysis Series , vol.5
- Vicario, J.L.¹ Badía, D.² Carrillo, L.³ Reyes, E.⁴

43
- 34547198987
- J. L. Vicario, D. Badía, L. Carrillo, Synthesis 2007, 2065-2092.
- (2007) Synthesis , pp. 2065-2092
- Vicario, J.L.¹ Badía, D.² Carrillo, L.³

44
- 33847623075
- D. Almasi, D. A. Alonso, C. Nájera, Tetrahedron: Asymmetry 2007, 18, 299-365.
- (2007) Tetrahedron: Asymmetry , vol.18 , pp. 299-365
- Almasi, D.¹ Alonso, D.A.² Nájera, C.³

45
- 84872350942
- Z.-W. Ma, Y. Wu, B. Sun, H.-L. Du, W.-M. Shi, J.-C. Tao, Tetrahedron: Asymmetry 2013, 24, 7-13.
- (2013) Tetrahedron: Asymmetry , vol.24 , pp. 7-13
- Ma, Z.-W.¹ Wu, Y.² Sun, B.³ Du, H.-L.⁴ Shi, W.-M.⁵ Tao, J.-C.⁶

46
- 33847623075
- D. Almaşi, D. A. Alonso, C. Nájera, Tetrahedron: Asymmetry 2007, 18, 299-365.
- (2007) Tetrahedron: Asymmetry , vol.18 , pp. 299-365
- Almaşi, D.¹ Alonso, D.A.² Nájera, C.³

47
- 34547623607
- H. Pellissier, Tetrahedron 2007, 63, 9267-9331.
- (2007) Tetrahedron , vol.63 , pp. 9267-9331
- Pellissier, H.¹

48
- 75749143504
- P. Merino, E. Marqués-Lõpez, T. Tejero, R. P. Herrera, Synthesis 2010, 1-26.
- (2010) Synthesis , pp. 1-26
- Merino, P.¹ Marqués-Lõpez, E.² Tejero, T.³ Herrera, R.P.⁴

49
- 0000923627
- W. Bihlmaier, R. Huisgen, H.-U. Reissig, S. Voss, Tetrahedron Lett. 1979, 20, 2621-2624.
- (1979) Tetrahedron Lett. , vol.20 , pp. 2621-2624
- Bihlmaier, W.¹ Huisgen, R.² Reissig, H.-U.³ Voss, S.⁴

50
- 0001448788
- R. Huisgen, L. Xingya, Tetrahedron Lett. 1983, 24, 4185-4188.
- (1983) Tetrahedron Lett. , vol.24 , pp. 4185-4188
- Huisgen, R.¹ Xingya, L.²

51
- 0001640279
- B. Blankenburg, H. Fiedler, M. Hampel, H. G. Hauthal, G. Just, K. Kahlert, J. Korn, K. H. Müller, W. Pritzkow, Y. Reinhold, M. Röllig, E. Sauer, D. Schnurpfeil, G. Zimmermann, J. Prakt. Chem. 1974, 316, 804-816.
- (1974) J. Prakt. Chem. , vol.316 , pp. 804-816
- Blankenburg, B.¹ Fiedler, H.² Hampel, M.³ Hauthal, H.G.⁴ Just, G.⁵ Kahlert, K.⁶ Korn, J.⁷ Müller, K.H.⁸ Pritzkow, W.⁹ Reinhold, Y.¹⁰ Röllig, M.¹¹ Sauer, E.¹² Schnurpfeil, D.¹³ Zimmermann, G.¹⁴

52
- 84899927387
- For reviews, see
- For reviews, see

53
- 33749141140
- 1994, Angew. Chem. 106, 990-1010
- H. Mayr, M. Patz, Angew. Chem. Int. Ed. Engl. 1994, 33, 938-957; Angew. Chem. 1994, 106, 990-1010.
- (1994) Angew. Chem. Int. Ed. Engl. , vol.33 , pp. 938-957
- Mayr, H.¹ Patz, M.²

54
- 0035802329
- H. Mayr, T. Bug, M. F. Gotta, N. Hering, B. Irrgang, B. Janker, B. Kempf, R. Loos, A. R. Ofial, G. Remennikov, H. Schimmel, J. Am. Chem. Soc. 2001, 123, 9500-9512.
- (2001) J. Am. Chem. Soc. , vol.123 , pp. 9500-9512
- Mayr, H.¹ Bug, T.² Gotta, M.F.³ Hering, N.⁴ Irrgang, B.⁵ Janker, B.⁶ Kempf, B.⁷ Loos, R.⁸ Ofial, A.R.⁹ Remennikov, G.¹⁰ Schimmel, H.¹¹

55
- 0037016457
- 2002, Angew. Chem. 114, 97-102
- R. Lucius, R. Loos, H. Mayr, Angew. Chem. Int. Ed. 2002, 41, 91-95; Angew. Chem. 2002, 114, 97-102.
- (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 91-95
- Lucius, R.¹ Loos, R.² Mayr, H.³

56
- 0037241494
- H. Mayr, B. Kempf, A. R. Ofial, Acc. Chem. Res. 2003, 36, 66-77.
- (2003) Acc. Chem. Res. , vol.36 , pp. 66-77
- Mayr, H.¹ Kempf, B.² Ofial, A.R.³

57
- 28544449432
- H. Mayr, A. R. Ofial, Pure Appl. Chem. 2005, 77, 1807-1821.
- (2005) Pure Appl. Chem. , vol.77 , pp. 1807-1821
- Mayr, H.¹ Ofial, A.R.²

58
- 46949092914
- H. Mayr, A. R. Ofial, J. Phys. Org. Chem. 2008, 21, 584-595.
- (2008) J. Phys. Org. Chem. , vol.21 , pp. 584-595
- Mayr, H.¹ Ofial, A.R.²

59
- 84866281848
- H. Mayr, S. Lakhdar, B. Maji, A. R. Ofial, Beilstein J. Org. Chem. 2012, 8, 1458-1478.
- (2012) Beilstein J. Org. Chem. , vol.8 , pp. 1458-1478
- Mayr, H.¹ Lakhdar, S.² Maji, B.³ Ofial, A.R.⁴

60
- 84899909025
- N, and electrophilicity parameters E, see
- N, and electrophilicity parameters E, see: http://www.cup.lmu.de/oc/ mayr/.

61
- 84885613746
- D. S. Allgäuer, P. Mayer, H. Mayr, J. Am. Chem. Soc. 2013, 135, 15216-15224.
- (2013) J. Am. Chem. Soc. , vol.135 , pp. 15216-15224
- Allgäuer, D.S.¹ Mayer, P.² Mayr, H.³

62
- 77955166010
- R. Appel, H. Mayr, Chem. Eur. J. 2010, 16, 8610-8614.
- (2010) Chem. Eur. J. , vol.16 , pp. 8610-8614
- Appel, R.¹ Mayr, H.²

63
- 78650269582
- R. Appel, N. Hartmann, H. Mayr, J. Am. Chem. Soc. 2010, 132, 17894-17900.
- (2010) J. Am. Chem. Soc. , vol.132 , pp. 17894-17900
- Appel, R.¹ Hartmann, N.² Mayr, H.³

64
- 84899920549
- For reviews on pyridinium ylide chemistry, see
- For reviews on pyridinium ylide chemistry, see

65
- 0003487195
- McGraw-Hill, New York
- I. Zugravescu, M. Petrovanu, N-Ylid Chemistry, McGraw-Hill, New York, 1976.
- (1976) N-Ylid Chemistry
- Zugravescu, I.¹ Petrovanu, M.²

66
- 2442698345
- A. G. Mikhailovskii, V. S. Shklyaev, Chem. Heterocycl. Compd. 1997, 33, 243-265.
- (1997) Chem. Heterocycl. Compd. , vol.33 , pp. 243-265
- Mikhailovskii, A.G.¹ Shklyaev, V.S.²

67
- 79958233010
- J. Jacobs, E. Van Hende, S. Claessens, N. De Kimpe, Curr. Org. Chem. 2011, 15, 1340-1362.
- (2011) Curr. Org. Chem. , vol.15 , pp. 1340-1362
- Jacobs, J.¹ Van Hende, E.² Claessens, S.³ De Kimpe, N.⁴

68
- 84864129277
- A. Kakehi, Heterocycles 2012, 85, 1529-1577.
- (2012) Heterocycles , vol.85 , pp. 1529-1577
- Kakehi, A.¹

69
- 21644447978
- O. Tsuge, S. Kanemasa, S. Takenaka, Bull. Chem. Soc. Jpn. 1985, 58, 3137-3157.
- (1985) Bull. Chem. Soc. Jpn. , vol.58 , pp. 3137-3157
- Tsuge, O.¹ Kanemasa, S.² Takenaka, S.³

70
- 33947317869
- R. A. Firestone, J. Org. Chem. 1968, 33, 2285-2290.
- (1968) J. Org. Chem. , vol.33 , pp. 2285-2290
- Firestone, R.A.¹

71
- 0001057190
- R. A. Firestone, J. Org. Chem. 1972, 37, 2181-2191.
- (1972) J. Org. Chem. , vol.37 , pp. 2181-2191
- Firestone, R.A.¹

72
- 0001640615
- R. Huisgen, J. Org. Chem. 1968, 33, 2291-2297.
- (1968) J. Org. Chem. , vol.33 , pp. 2291-2297
- Huisgen, R.¹

73
- 0001485086
- A.-H. Li, L.-X. Dai, V. K. Aggarwal, Chem. Rev. 1997, 97, 2341-2372.
- (1997) Chem. Rev. , vol.97 , pp. 2341-2372
- Li, A.-H.¹ Dai, L.-X.² Aggarwal, V.K.³

74
- 77953098576
- S. L. Riches, C. Saha, N. F. Filgueira, E. Grange, E. M. McGarrigle, V. K. Aggarwal, J. Am. Chem. Soc. 2010, 132, 7626-7630.
- (2010) J. Am. Chem. Soc. , vol.132 , pp. 7626-7630
- Riches, S.L.¹ Saha, C.² Filgueira, N.F.³ Grange, E.⁴ McGarrigle, E.M.⁵ Aggarwal, V.K.⁶

75
- 29544442212
- V. K. Aggarwal, E. Grange, Chem. Eur. J. 2006, 12, 568-575.
- (2006) Chem. Eur. J. , vol.12 , pp. 568-575
- Aggarwal, V.K.¹ Grange, E.²

76
- 0001138538
- C. R. Johnson, C. W. Schroeck, J. Am. Chem. Soc. 1968, 90, 6852-6854.
- (1968) J. Am. Chem. Soc. , vol.90 , pp. 6852-6854
- Johnson, C.R.¹ Schroeck, C.W.²

77
- 0000349588
- C. R. Johnson, C. W. Schroeck, J. Am. Chem. Soc. 1971, 93, 5303-5305.
- (1971) J. Am. Chem. Soc. , vol.93 , pp. 5303-5305
- Johnson, C.R.¹ Schroeck, C.W.²

78
- 0000571875
- C. R. Johnson, C. W. Schroeck, J. R. Shanklin, J. Am. Chem. Soc. 1973, 95, 7424-7431.
- (1973) J. Am. Chem. Soc. , vol.95 , pp. 7424-7431
- Johnson, C.R.¹ Schroeck, C.W.² Shanklin, J.R.³

79
- 77952394193
- Y. Liu, Y. Zhang, Y.-M. Shen, H.-W. Hua, J.-H. Xu, Org. Biomol. Chem. 2010, 8, 2449-2456.
- (2010) Org. Biomol. Chem. , vol.8 , pp. 2449-2456
- Liu, Y.¹ Zhang, Y.² Shen, Y.-M.³ Hua, H.-W.⁴ Xu, J.-H.⁵

80
- 0041373430
- O. Tsuge, S. Kanemasa, S. Takenaka, S. Kuraoka, Chem. Lett. 1984, 465-468.
- (1984) Chem. Lett. , pp. 465-468
- Tsuge, O.¹ Kanemasa, S.² Takenaka, S.³ Kuraoka, S.⁴

81
- 0001537796
- O. Tsuge, S. Kanemasa, S. Takenaka, Bull. Chem. Soc. Jpn. 1987, 60, 1489-1495.
- (1987) Bull. Chem. Soc. Jpn. , vol.60 , pp. 1489-1495
- Tsuge, O.¹ Kanemasa, S.² Takenaka, S.³

82
- 84884905570
- D. S. Allgäuer, H. Mayr, Eur. J. Org. Chem. 2013, 6379-6388.
- (2013) Eur. J. Org. Chem. , pp. 6379-6388
- Allgäuer, D.S.¹ Mayr, H.²

83
- 84899901167
- The kinetics of the reactions of sulfonium ylides 3c and 3d with 1b and 1c could not be investigated photometrically because of overlapping UV/Vis absorptions of the reactants and products
- The kinetics of the reactions of sulfonium ylides 3c and 3d with 1b and 1c could not be investigated photometrically because of overlapping UV/Vis absorptions of the reactants and products.

84
- 77957599924
- T. Kanzian, H. Mayr, Chem. Eur. J. 2010, 16, 11670-11677.
- (2010) Chem. Eur. J. , vol.16 , pp. 11670-11677
- Kanzian, T.¹ Mayr, H.²

85
- 34548328238
- S. T. A. Berger, F. H. Seeliger, F. Hofbauer, H. Mayr, Org. Biomol. Chem. 2007, 5, 3020-3026.
- (2007) Org. Biomol. Chem. , vol.5 , pp. 3020-3026
- Berger, S.T.A.¹ Seeliger, F.H.² Hofbauer, F.³ Mayr, H.⁴

86
- 84862074826
- Angew. Chem. 2012, 124, 5325-5329
- R. C. Samanta, B. Maji, S. De Sarkar, K. Bergander, R. Fröhlich, C. Mück-Lichtenfeld, H. Mayr, A. Studer, Angew. Chem. Int. Ed. 2012, 51, 5234-5238; Angew. Chem. 2012, 124, 5325-5329.
- (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 5234-5238
- Samanta, R.C.¹ Maji, B.² De Sarkar, S.³ Bergander, K.⁴ Fröhlich, R.⁵ Mück-Lichtenfeld, C.⁶ Mayr, H.⁷ Studer, A.⁸

87
- 84861559396
- H. Asahara, H. Mayr, Chem. Asian J. 2012, 7, 1401-1407.
- (2012) Chem. Asian J. , vol.7 , pp. 1401-1407
- Asahara, H.¹ Mayr, H.²

88
- 84859135572
- K. Troshin, P. Mayer, H. Mayr, Organometallics 2012, 31, 2416-2424.
- (2012) Organometallics , vol.31 , pp. 2416-2424
- Troshin, K.¹ Mayer, P.² Mayr, H.³

89
- 77957581327
- T. Kanzian, S. Nicolini, L. De Crescentini, O. A. Attanasi, A. R. Ofial, H. Mayr, Chem. Eur. J. 2010, 16, 12008-12016.
- (2010) Chem. Eur. J. , vol.16 , pp. 12008-12016
- Kanzian, T.¹ Nicolini, S.² De Crescentini, L.³ Attanasi, O.A.⁴ Ofial, A.R.⁵ Mayr, H.⁶

90
- 81055147770
- I. Zenz, H. Mayr, J. Org. Chem. 2011, 76, 9370-9378.
- (2011) J. Org. Chem. , vol.76 , pp. 9370-9378
- Zenz, I.¹ Mayr, H.²

91
- 79957757640
- R. Appel, H. Mayr, J. Am. Chem. Soc. 2011, 133, 8240-8251.
- (2011) J. Am. Chem. Soc. , vol.133 , pp. 8240-8251
- Appel, R.¹ Mayr, H.²

92
- 55049121808
- O. Kaumanns, R. Lucius, H. Mayr, Chem. Eur. J. 2008, 14, 9675-9682.
- (2008) Chem. Eur. J. , vol.14 , pp. 9675-9682
- Kaumanns, O.¹ Lucius, R.² Mayr, H.³

93
- 84899931011
- For previous theoretical approaches to electrophilicity and nucleophilicity parameters, as defined by Equation (1), see
- For previous theoretical approaches to electrophilicity and nucleophilicity parameters, as defined by Equation (1), see

94
- 0037067528
- P. Pérez, A. Toro-Labbé, A. Aizman, R. Contreras, J. Org. Chem. 2002, 67, 4747-4752.
- (2002) J. Org. Chem. , vol.67 , pp. 4747-4752
- Pérez, P.¹ Toro-Labbé, A.² Aizman, A.³ Contreras, R.⁴

95
- 4143091851
- L. R. Domingo, P. Pérez, R. Contreras, Tetrahedron 2004, 60, 6585-6591.
- (2004) Tetrahedron , vol.60 , pp. 6585-6591
- Domingo, L.R.¹ Pérez, P.² Contreras, R.³

96
- 58949103819
- E. Chamorro, M. Duque-Noreña, P. Pérez, THEOCHEM 2009, 896, 73-79.
- (2009) THEOCHEM , vol.896 , pp. 73-79
- Chamorro, E.¹ Duque-Noreña, M.² Pérez, P.³

97
- 62949202874
- E. Chamorro, M. Duque-Noreña, P. Pérez, THEOCHEM 2009, 901, 145-152.
- (2009) THEOCHEM , vol.901 , pp. 145-152
- Chamorro, E.¹ Duque-Noreña, M.² Pérez, P.³

98
- 77049118318
- C. Wang, Y. Fu, Q.-X. Guo, L. Liu, Chem. Eur. J. 2010, 16, 2586-2598.
- (2010) Chem. Eur. J. , vol.16 , pp. 2586-2598
- Wang, C.¹ Fu, Y.² Guo, Q.-X.³ Liu, L.⁴

99
- 84887694249
- L.-G. Zhuo, W. Liao, Z.-X. Yu, Asian J. Org. Chem. 2012, 1, 336-345.
- (2012) Asian J. Org. Chem. , vol.1 , pp. 336-345
- Zhuo, L.-G.¹ Liao, W.² Yu, Z.-X.³

100
- 84876289393
- S.-i. Kiyooka, D. Kaneno, R. Fujiyama, Tetrahedron 2013, 69, 4247-4258.
- (2013) Tetrahedron , vol.69 , pp. 4247-4258
- Kaneno, D.¹ Fujiyama, R.²

101
- 84875713347
- E. Chamorro, M. Duque-Noreña, R. Notario, P. Pérez, J. Phys. Chem. A 2013, 117, 2636-2643.
- (2013) J. Phys. Chem. A , vol.117 , pp. 2636-2643
- Chamorro, E.¹ Duque-Noreña, M.² Notario, R.³ Pérez, P.⁴

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