SCOPUS 정보 검색 플랫폼

Beilstein Journal of Organic Chemistry

Volumn 8, Issue , 2012, Pages 1819-1824

Asymmetric Brønsted acid-catalyzed aza-Diels-Alder reaction of cyclic C-acylimines with cyclopentadiene

(2) Rueping, Magnus a Raja, Sadiya a

a RWTH AACHEN UNIVERSITY (Germany)

Author keywords

BINOL phosphate; 4 + 2 cycloaddition; Diels Alder reaction; Organocatalysis

Indexed keywords

EID: 84868352724 PISSN: None EISSN: 18605397 Source Type: Journal
DOI: 10.3762/bjoc.8.208 Document Type: Article

Times cited : (40)

References (56)

1
- 0003497902
- Wiley VCH: Weinheim, Germany
- Kobayashi, S.; Jørgensen, K. A., Eds. Cycloaddition Reactions in Organic Synthesis; Wiley-VCH: Weinheim, Germany, 2002.
- (2002) Cycloaddition Reactions in Organic Synthesis
- Kobayashi, S.¹ Jørgensen, K.A.²

2
- 0030602266
- Recent progress in the synthesis of 1,2,3,4-tetrahydroquinolines
- DOI 10.1016/S0040-4020(96)00911-8, PII S0040402096009118
- Katritzky, A. R.; Rachwal, S.; Rachwal, B. Tetrahedron 1996, 52, 15031-15070. doi:10.1016/S0040-4020(96)00911-8 (Pubitemid 26389007)
- (1996) Tetrahedron , vol.52 , Issue.48 , pp. 15031-15070
- Katritzky, A.R.¹ Rachwal, S.² Rachwal, B.³

3
- 53849120603
- doi:10.1002/chem.200800473
- Isambert, N.; Lavilla, R. Chem.-Eur. J. 2008, 14, 8444-8454. doi:10.1002/chem.200800473
- (2008) Chem.-Eur. J. , vol.14 , pp. 8444-8454
- Isambert, N.¹ Lavilla, R.²

4
- 80755126169
- doi:10.1021/cr100307m
- Sridharan, V.; Suryavanshi, P. A.; Menéndez, J. C. Chem. Rev. 2011, 111, 7157-7259. doi:10.1021/cr100307m
- (2011) C. Chem. Rev. , vol.111 , pp. 7157-7259
- Sridharan, V.¹ Suryavanshi, P.A.² Menéndez, J.³

5
- 80051739502
- Handbook of Cyclization Reactions; Ma, S., Ed.; Wiley-VCH: Weinheim, Germany
- Yamashita, Y.; Kobayashi, S. Catalytic Asymmetric Aza Diels-Alder Reactions. In Handbook of Cyclization Reactions; Ma, S., Ed.; Wiley-VCH: Weinheim, Germany, 2010; Vol. 1, pp 59-85.
- (2010) Catalytic Asymmetric Aza Diels-Alder Reactions , vol.1 , pp. 59-85
- Yamashita, Y.¹ Kobayashi, S.²

6
- 84988099752
- doi:10.1055/s-1993-22374
- Hattori, K.; Yamamoto, H. Synlett 1993, 129-130. doi:10.1055/s-1993-22374
- (1993) Synlett , pp. 129-130
- Hattori, K.¹ Yamamoto, H.²

7
- 0027392950
- doi:10.1016/S0040-4020(01)80532-9
- Hattori, K.; Yamamoto, H. Tetrahedron 1993, 49, 1749-1760. doi:10.1016/S0040-4020(01)80532-9
- (1993) Tetrahedron , vol.49 , pp. 1749-1760
- Hattori, K.¹ Yamamoto, H.²

8
- 0000656506
- doi:10.1021/ja00102a019
- Ishihara, K.; Miyata, M.; Hattori, K.; Tada, T.; Yamamoto, H. J. Am. Chem. Soc. 1994, 116, 10520-10524. doi:10.1021/ja00102a019
- (1994) J. Am. Chem. Soc. , vol.116 , pp. 10520-10524
- Ishihara, K.¹ Miyata, M.² Hattori, K.³ Tada, T.⁴ Yamamoto, H.⁵

9
- 0030573985
- Catalytic asymmetric aza Diels-Alder reactions using a chiral lanthanide Lewis acid. Enantioselective synthesis of tetrahydroquinoline derivatives using a catalytic amount of chiral source
- DOI 10.1016/0040-4039(96)01655-3
- Ishitani, H.; Kobayashi, S. Tetrahedron Lett. 1996, 37, 7357-7360. doi:10.1016/0040-4039(96)01655-3 (Pubitemid 26326327)
- (1996) Tetrahedron Letters , vol.37 , Issue.41 , pp. 7357-7360
- Ishitani, H.¹ Kobayashi, S.²

10
- 0032569819
- doi:10.1016/S0040-4039(98)01947-9
- Bromidge, S. W.; Whiting, P. C. Tetrahedron Lett. 1998, 39, 8905-8908. doi:10.1016/S0040-4039(98)01947-9
- (1998) Tetrahedron Lett , vol.39 , pp. 8905-8908
- Bromidge, S.W.¹ Whiting, P.C.²

11
- 0031980938
- doi:10.1002/(SICI)1521-3773(19980420)37:7<979::AID-ANIE979>3.0. CO;2-5
- Kobayashi, S.; Komiyama, S.; Ishitani, H. Angew. Chem. 1998, 110, 1026-1028. doi:10.1002/(SICI)1521-3757(19980403)110:7<1026::AID-ANGE1026> 3.0.CO;2-G Angew. Chem., Int. Ed. 1998, 110, 1026-1028. doi:10.1002/(SICI)1521- 3773(19980420)37:7<979::AID-ANIE979>3.0. CO;2-5
- (1998) Angew. Chem. , vol.110 , pp. 1026-1028
- Kobayashi, S.¹ Komiyama, S.² Ishitani, H.³

12
- 0000186325
- doi:10.1021/ol005656b
- Kobayashi, S.; Kusakabe, K.-i.; Ishitani, H. Org. Lett. 2000, 2, 1225-1227. doi:10.1021/ol005656b
- (2000) Org. Lett. , vol.2 , pp. 1225-1227
- Kobayashi, S.¹ Kusakabe, K.-I.² Ishitani, H.³

13
- 13944269207
- Catalytic asymmetric aza Diels-Alder reactions of hydrazones using a chiral zirconium catalyst
- DOI 10.1016/j.tetlet.2005.01.111
- Yamashita, Y.; Mizuki, Y.; Kobayashi, S. Tetrahedron Lett. 2005, 46, 1803-1806. doi:10.1016/j.tetlet.2005.01.111 (Pubitemid 40269178)
- (2005) Tetrahedron Letters , vol.46 , Issue.11 , pp. 1803-1806
- Yamashita, Y.¹ Mizuki, Y.² Kobayashi, S.³

14
- 0037427326
- Efficient and practical Ag-catalyzed cycloadditions between arylimines and the Danishefsky diene
- DOI 10.1021/ja030033p
- Josephsohn, N. S.; Snapper, M. L.; Hoveyda, A. H. J. Am. Chem. Soc. 2003, 125, 4018-4019. doi:10.1021/ja030033p (Pubitemid 36512274)
- (2003) Journal of the American Chemical Society , vol.125 , Issue.14 , pp. 4018-4019
- Josephsohn, N.S.¹ Snapper, M.L.² Hoveyda, A.H.³

15
- 0034600913
- doi:10.1002/1521-3765(20000703)6:13<2435::AID-CHEM2435>3.0.C O;2-Z
- Yao, S.; Saaby, S.; Hazell, R. G.; Jørgensen, K. A. Chem.-Eur. J. 2000, 6, 2435-2448. doi:10.1002/1521-3765(20000703)6:13<2435::AID- CHEM2435>3.0.C O;2-Z
- (2000) Chem.-Eur. J. , vol.6 , pp. 2435-2448
- Yao, S.¹ Saaby, S.² Hazell, R.G.³ Jørgensen, K.A.⁴

16
- 0347717646
- Chiral Copper Complexes of Phosphino Sulfenyl Ferrocenes as Efficient Catalysts for Enantioselective Formal Aza Diels-Alder Reactions of N-Sulfonyl Imines
- DOI 10.1021/ja038494y
- Mancheño, O. G.; Arrayás, R. G.; Carretero, J. C. J. Am. Chem. Soc. 2004, 126, 456-457. doi:10.1021/ja038494y (Pubitemid 38084613)
- (2004) Journal of the American Chemical Society , vol.126 , Issue.2 , pp. 456-457
- Mancheno, O.G.¹ Arrayas, R.G.² Carretero, J.C.³

17
- 38349189109
- doi:10.1021/cr068374j
- Akiyama, T. Chem. Rev. 2007, 107, 5744-5758. doi:10.1021/cr068374j
- (2007) Chem. Rev. , vol.107 , pp. 5744-5758
- Akiyama, T.¹

18
- 33745683617
- Recent progress in chiral Bronsted acid catalysis
- DOI 10.1002/adsc.200606074
- Akiyama, T.; Itoh, J.; Fuchibe, K. Adv. Synth. Catal. 2006, 348, 999-1010. doi:10.1002/adsc.200606074 (Pubitemid 44000157)
- (2006) Advanced Synthesis and Catalysis , vol.348 , Issue.9 , pp. 999-1010
- Akiyama, T.¹ Itoh, J.² Fuchibe, K.³

19
- 33646468489
- doi:10.1002/ange.200503132 Angew. Chem., Int. Ed. 2006, 45, 1520-1543 doi101002/anie200503132
- Taylor, M. S.; Jacobsen, E. N. Angew. Chem. 2006, 118, 1550-1573. doi:10.1002/ange.200503132 Angew. Chem., Int. Ed. 2006, 45, 1520-1543. doi:10.1002/anie.200503132
- (2006) Angew. Chem. , vol.118 , pp. 1550-1573
- Taylor, M.S.¹ Jacobsen, E.N.²

20
- 84891509470
- Acids, H-bond donors and combined acid systems in asymmetric catalysis
- Pihko, P. M., Ed.; Wiley-VCH: Weinheim, Germany
- Yamamoto, H.; Payette, N. Brønsted Acids, H-Bond Donors, and Combined Acid Systems in Asymmetric Catalysis. In Hydrogen Bonding in Organic Synthesis; Pihko, P. M., Ed.; Wiley-VCH: Weinheim, Germany, 2009; pp 73-140.
- (2009) Hydrogen Bonding in Organic Synthesis; , pp. 73-140
- Yamamoto, H.¹ Brønsted, P.N.²

21
- 77950248809
- doi:10.1007/128-2009-1
- Kampen, D.; Reisinger, C. M.; List, B. Top. Curr. Chem. 2009, 291, 395-456. doi:10.1007/128-2009-1
- (2009) Top. Curr. Chem. , vol.291 , pp. 395-456
- Kampen, D.¹ Reisinger, C.M.² List, B.³

22
- 77953261329
- doi:10.1055/s-0029-1218801
- Terada, M. Synthesis 2010, 1929-1982. doi:10.1055/s-0029-1218801
- (2010) Synthesis , pp. 1929-1982
- Terada, M.¹

23
- 80053992962
- doi:10.1039/c1cs15087a
- Rueping, M.; Kuenkel, A.; Atodiresei, I. Chem. Soc. Rev. 2011, 40, 4539-4549. doi:10.1039/c1cs15087a
- (2011) Chem. Soc. Rev. , vol.40 , pp. 4539-4549
- Rueping, M.¹ Kuenkel, A.² Atodiresei, I.³

24
- 33846157409
- doi:10.1021/ol062499t
- Liu, H.; Cun, L.-F.; Mi, A.-Q.; Jiang, Y.-Z.; Gong, L.-Z. Org. Lett. 2006, 8, 6023-6026. doi:10.1021/ol062499t
- (2006) Org. Lett. , vol.8 , pp. 6023-6026
- Liu, H.¹ Cun, L.-F.² Mi, A.-Q.³ Jiang, Y.-Z.⁴ Gong, L.-Z.⁵

25
- 33845329553
- doi:10.1002/ange.200603199 Angew. Chem., Int. Ed. 2006, 45, 7832-7835 doi101002/anie200603199
- Rueping, M.; Azap, C. Angew. Chem. 2006, 118, 7996-7999. doi:10.1002/ange.200603199 Angew. Chem., Int. Ed. 2006, 45, 7832-7835. doi:10.1002/anie.200603199
- (2006) Angew. Chem. , vol.118 , pp. 7996-7999
- Rueping, M.¹ Azap, C.²

26
- 33746801098
- doi:10.1002/ange.200601345 Angew. Chem., Int. Ed. 2006, 45, 4796-4798 doi101002/anie200601345
- Itoh, J.; Fuchibe, K.; Akiyama, T. Angew. Chem. 2006, 118, 4914-4916. doi:10.1002/ange.200601345 Angew. Chem., Int. Ed. 2006, 45, 4796-4798. doi:10.1002/anie.200601345
- (2006) Angew. Chem. , vol.118 , pp. 4914-4916
- Itoh, J.¹ Fuchibe, K.² Akiyama, T.³

27
- 33749522044
- Chiral Bronsted acid-catalyzed inverse electron-demand aza Diels-Alder reaction
- DOI 10.1021/ja064676r
- Akiyama, T.; Morita, H.; Fuchibe, K. J. Am. Chem. Soc. 2006, 128, 13070-13071. doi:10.1021/ja064676r (Pubitemid 44527674)
- (2006) Journal of the American Chemical Society , vol.128 , Issue.40 , pp. 13070-13071
- Akiyama, T.¹ Morita, H.² Fuchibe, K.³

28
- 30544453001
- doi:10.1055/s-2005-922773
- Akiyama, T.; Tamura, Y.; Itoh, J.; Morita, H.; Fuchibe, K. Synlett 2006, 141-143. doi:10.1055/s-2005-922773
- (2006) Synlett , pp. 141-143
- Akiyama, T.¹ Tamura, Y.² Itoh, J.³ Morita, H.⁴ Fuchibe, K.⁵

29
- 67749110116
- doi:10.1021/ja900806q
- Liu, H.; Dagousset, G.; Masson, G.; Retailleau, P.; Zhu, J. P. J. Am. Chem. Soc. 2009, 131, 4598-4599. doi:10.1021/ja900806q
- (2009) J. Am. Chem. Soc. , vol.131 , pp. 4598-4599
- Liu, H.¹ Dagousset, G.² Masson, G.³ Retailleau, P.⁴ Zhu, J.P.⁵

30
- 84862583275
- doi:10.1021/ol301251h
- He, L.; Bekkaye, M.; Retailleau, P.; Masson, G. Org. Lett. 2012, 14, 3158-3161. doi:10.1021/ol301251h
- (2012) Org. Lett. , vol.14 , pp. 3158-3161
- He, L.¹ Bekkaye, M.² Retailleau, P.³ Masson, G.⁴

31
- 0242432417
- Single enantiomers from a chiral-alcohol catalyst
- DOI 10.1038/424146a
- Huang, Y.; Unni, A. K.; Thadani, A. N.; Rawal, V. H. Nature 2003, 424, 146. doi:10.1038/424146a (Pubitemid 36868971)
- (2003) Nature , vol.424 , Issue.6945 , pp. 146
- Huang, Y.¹ Unni, A.K.² Thadani, A.N.³ Rawal, V.H.⁴

32
- 13444265956
- Axially chiral biaryl diols catalyze highly enantioselective hetero-diels-alder reactions through hydrogen bonding
- DOI 10.1021/ja044076x
- Unni, A. K.; Takenaka, N.; Yamamoto, H.; Rawal, V. H. J. Am. Chem. Soc. 2005, 127, 1336-1337. doi:10.1021/ja044076x (Pubitemid 40207498)
- (2005) Journal of the American Chemical Society , vol.127 , Issue.5 , pp. 1336-1337
- Unni, A.K.¹ Takenaka, N.² Yamamoto, H.³ Rawal, V.H.⁴

33
- 33746654536
- Design of chiral N-triflyl phosphoramide as a strong chiral Bronsted acid and its application to asymmetric Diels-Alder reaction
- DOI 10.1021/ja062508t
- Nakashima, D.; Yamamoto, H. J. Am. Chem. Soc. 2006, 128, 9626-9627. doi:10.1021/ja062508t See for a pioneering work in the field of chiral BINOL-based N-triflylphosphoramides. (Pubitemid 44147935)
- (2006) Journal of the American Chemical Society , vol.128 , Issue.30 , pp. 9626-9627
- Nakashima, D.¹ Yamamoto, H.²

34
- 79960219398
- doi:10.1002/anie.201100169
- Rueping, M.; Nachtsheim, B. J.; Ieawsuwan, W.; Atodiresei, I. Angew. Chem., Int. Ed. 2011, 50, 6706-6720. doi:10.1002/anie.201100169
- (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 6706-6720
- Rueping, M.¹ Nachtsheim, B.J.² Ieawsuwan, W.³ Atodiresei, I.⁴

35
- 79952744547
- doi:10.1021/ja110213t
- Rueping, M.; Uria, U.; Lin, M.-Y.; Atodiresei, I. J. Am. Chem. Soc. 2011, 133, 3732-3735. doi:10.1021/ja110213t
- (2011) J. Am. Chem. Soc. , vol.133 , pp. 3732-3735
- Rueping, M.¹ Uria, U.² Lin, M.-Y.³ Atodiresei, I.⁴

36
- 78649261543
- doi:10.1002/chem.201001438
- Rueping, M.; Nachtsheim, B. J.; Koenigs, R. M.; Ieawsuwan, W. Chem.-Eur. J. 2010, 16, 13116-13126. doi:10.1002/chem.201001438
- (2010) Chem.-Eur. J. , vol.16 , pp. 13116-13126
- Rueping, M.¹ Nachtsheim, B.J.² Koenigs, R.M.³ Ieawsuwan, W.⁴

37
- 34250725648
- Chiral Brosted acids in the catalytic asymmetric nazarov cyclization - The first enantioselective organocatalytic electrocyclic reaction
- DOI 10.1002/anie.200604809
- Rueping, M.; Ieawsuwan, W.; Antonchick, A. P.; Nachtsheim, B. J. Angew. Chem., Int. Ed. 2007, 46, 2097-2100. doi:10.1002/anie.200604809 (Pubitemid 46973679)
- (2007) Angewandte Chemie - International Edition , vol.46 , Issue.12 , pp. 2097-2100
- Rueping, M.¹ Ieawsuwan, W.² Antonchick, A.P.³ Nachtsheim, B.J.⁴

38
- 53249085441
- doi:10.1002/anie.200705314
- Jiao, P.; Nakashima, D.; Yamamoto, H. Angew. Chem., Int. Ed. 2008, 47, 2411-2413. doi:10.1002/anie.200705314
- (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 2411-2413
- Jiao, P.¹ Nakashima, D.² Yamamoto, H.³

39
- 38949210780
- Asymmetric Bronsted acid catalysis: Enantioselective nucleophilic substitutions and 1,4-additions
- DOI 10.1002/anie.200703668
- Rueping, M.; Nachtsheim, B. J.; Moreth, S. A.; Bolte, M. Angew. Chem., Int. Ed. 2008, 47, 593-596. doi:10.1002/anie.200703668 (Pubitemid 351412350)
- (2008) Angewandte Chemie - International Edition , vol.47 , Issue.3 , pp. 593-596
- Rueping, M.¹ Nachtsheim, B.J.² Moreth, S.A.³ Bolte, M.⁴

40
- 53249117700
- doi:10.1002/anie.200802139
- Rueping, M.; Theissmann, T.; Kuenkel, A.; Koenigs, R. M. Angew. Chem., Int. Ed. 2008, 47, 6798-6801. doi:10.1002/anie.200802139
- (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 6798-6801
- Rueping, M.¹ Theissmann, T.² Kuenkel, A.³ Koenigs, R.M.⁴

41
- 57749121489
- doi:10.1002/anie.200803610
- Rueping, M.; Antonchick, A. P. Angew. Chem., Int. Ed. 2008, 47, 10090-10093. doi:10.1002/anie.200803610
- (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 10090-10093
- Rueping, M.¹ Antonchick, A.P.²

42
- 53549133122
- doi:10.1002/anie.200801354
- Enders, D.; Narine, A. A.; Toulgoat, F.; Bisschops, T. Angew. Chem., Int. Ed. 2008, 47, 5661-5665. doi:10.1002/anie.200801354
- (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 5661-5665
- Enders, D.¹ Narine, A.A.² Toulgoat, F.³ Bisschops, T.⁴

43
- 55049095133
- doi:10.1002/adsc.200800523
- Zeng, M.; Kang, Q.; He, Q.-L.; You, S.-L. Adv. Synth. Catal. 2008, 350, 2169-2173. doi:10.1002/adsc.200800523
- (2008) Adv. Synth. Catal. , vol.350 , pp. 2169-2173
- Zeng, M.¹ Kang, Q.² He, Q.-L.³ You, S.-L.⁴

44
- 58549085979
- doi:10.1002/adsc.200800623
- Rueping, M.; Ieawsuwan, W. Adv. Synth. Catal. 2009, 351, 78-84. doi:10.1002/adsc.200800623
- (2009) Adv. Synth. Catal. , vol.351 , pp. 78-84
- Rueping, M.¹ Ieawsuwan, W.²

45
- 77950795873
- doi:10.1002/chem.201000203
- Rueping, M.; Lin, M.-Y. Chem.-Eur. J. 2010, 16, 4169-4172. doi:10.1002/chem.201000203
- (2010) Chem.-Eur. J. , vol.16 , pp. 4169-4172
- Rueping, M.¹ Lin, M.-Y.²

46
- 77949904394
- doi:10.1055/s-0029-1218539
- Rueping, M.; Nachtsheim, B. J. Synlett 2010, 119-122. doi:10.1055/s-0029-1218539
- (2010) Synlett , pp. 119-122
- Rueping, M.¹ Nachtsheim, B.J.²

47
- 78449251697
- doi:10.1002/adsc.201000547
- Rueping, M.; Merino, E.; Koenigs, R. M. Adv. Synth. Catal. 2010, 352, 2629-2634. doi:10.1002/adsc.201000547
- (2010) Adv. Synth. Catal. , vol.352 , pp. 2629-2634
- Rueping, M.¹ Merino, E.² Koenigs, R.M.³

48
- 77953003770
- doi:10.1021/ol100233t
- Cheon, C. H.; Yamamoto, H. Org. Lett. 2010, 12, 2476-2479. doi:10.1021/ol100233t
- (2010) Org. Lett. , vol.12 , pp. 2476-2479
- Cheon, C.H.¹ Yamamoto, H.²

49
- 79959896382
- doi:10.1002/anie.201101385
- Fleischmann, M.; Drettwann, D.; Sugiono, E.; Rueping, M.; Gschwind, R. M. Angew. Chem., Int. Ed. 2011, 50, 6364-6369. doi:10.1002/anie.201101385
- (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 6364-6369
- Fleischmann, M.¹ Drettwann, D.² Sugiono, E.³ Rueping, M.⁴ Gschwind, R.M.⁵

50
- 79959521750
- doi:10.1021/ja203901h
- Hashimoto, T.; Nakatsu, H.; Yamamoto, K.; Maruoka, K. J. Am. Chem. Soc. 2011, 133, 9730-9733. doi:10.1021/ja203901h
- (2011) J. Am. Chem. Soc. , vol.133 , pp. 9730-9733
- Hashimoto, T.¹ Nakatsu, H.² Yamamoto, K.³ Maruoka, K.⁴

51
- 80053942941
- doi:10.1039/c1cc15289k
- Rueping, M.; Ieawsuwan, W. Chem. Commun. 2011, 47, 11450-11452. doi:10.1039/c1cc15289k
- (2011) Chem. Commun. , vol.47 , pp. 11450-11452
- Rueping, M.¹ Ieawsuwan, W.²

52
- 84868367956
- According to Mayr's nucleophilicity scale, which compares nucleophilictity relative to benzhydrylium ions, the nucleophilicity of the tested dienes decreases in the order: cyclopentadiene>1,3- pentadiene>2,3- dimethyl-1,3-butadiene>1,3- cyclo hexadiene
- According to Mayr's nucleophilicity scale, which compares nucleophilictity relative to benzhydrylium ions, the nucleophilicity of the tested dienes decreases in the order: cyclopentadiene>1,3-pentadiene>2,3- dimethyl-1,3-butadiene>1,3-cyclo hexadiene.

53
- 46949092914
- doi:10.1002/poc.1325
- Mayr, H.; Ofial, A. R. J. Phys. Org. Chem. 2008, 21, 584-595. doi:10.1002/poc.1325
- (2008) J. Phys. Org. Chem. , vol.21 , pp. 584-595
- Mayr, H.¹ Ofial, A.R.²

54
- 28544449432
- Kinetics of electrophile-nucleophile combinations: A general approach to polar organic reactivity
- DOI 10.1351/pac200577111807
- Mayr, H.; Ofial, A. R. Pure Appl. Chem. 2005, 77, 1807-1821. doi:10.1351/pac200577111807 (Pubitemid 41746286)
- (2005) Pure and Applied Chemistry , vol.77 , Issue.11 , pp. 1807-1821
- Mayr, H.¹ Ofial, A.R.²

55
- 0037241494
- doi:10.1021/ar020094c
- Mayr, H.; Kempf, B.; Ofial, A. R. Acc. Chem. Res. 2003, 36, 66-77. doi:10.1021/ar020094c
- (2003) Acc. Chem. Res. , vol.36 , pp. 66-77
- Mayr, H.¹ Kempf, B.² Ofial, A.R.³

56
- 0037427238
- Synthesis of 8-desbromohinckdentine A
- DOI 10.1021/ja021380m
- Liu, Y.; McWhorter, W. W., Jr. J. Am. Chem. Soc. 2003, 125, 4240-4252. doi:10.1021/ja021380m (Pubitemid 36512317)
- (2003) Journal of the American Chemical Society , vol.125 , Issue.14 , pp. 4240-4252
- Liu, Y.¹ McWhorter Jr., W.W.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.