SCOPUS 정보 검색 플랫폼

Volumn , Issue 42, 2008, Pages 5324-5326

Highly enantioselective carbon-carbon bond formation by Cu-catalyzed asymmetric [2,3]-sigmatropic rearrangement: Application to the syntheses of seven-membered oxacycles and six-membered carbocycles

(6) Kumaraswamy, Gullapalli a Sadaiah, Kadivendi a Ramakrishna, Duggirala Subrahmanya a Police, Naresh a Sridhar, Balasubramanian a Bharatam, Jagadeesh a

a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY (India)

Author keywords

[No Author keywords available]

Indexed keywords

COPPER;

ARTICLE; CATALYSIS; CHEMICAL BOND; CHEMICAL STRUCTURE; CHIRALITY; ENANTIOSELECTIVITY; REACTION ANALYSIS; SYNTHESIS;

EID: 55349087243 PISSN: 13597345 EISSN: None Source Type: Journal
DOI: 10.1039/b810770j Document Type: Article

Times cited : (30)

References (31)

1
- 33748336920
- R. M. Wilson S. J. Danishefsky Acc. Chem. Res. 2006 39 539
- (2006) Acc. Chem. Res. , vol.39 , pp. 539
- Wilson, R.M.¹ Danishefsky, S.J.²

2
- 0034122087
- M. Murata T. Yasumoto Nat. Prod. Rep. 2000 17 293
- (2000) Nat. Prod. Rep. , vol.17 , pp. 293
- Murata, M.¹ Yasumoto, T.²

3
- 0031718549
- A. Ameri Prog. Neurobiol. 1998 56 211
- (1998) Prog. Neurobiol. , vol.56 , pp. 211
- Ameri, A.¹

4
- 26444621024
- F. J. Schmitz S. P. Gunasekera G. Yalamanchili M. B. Hossain D. J. Van der Helm J. Am. Chem. Soc. 1984 106 7251
- (1984) J. Am. Chem. Soc. , vol.106 , pp. 7251
- Schmitz, F.J.¹ Gunasekera, S.P.² Yalamanchili, G.³ Hossain, M.B.⁴ Van Der Helm, D.J.⁵

5
- 0001156916
- N. Fusetani T. Sugawara S. Matsunaga J. Org. Chem. 1991 56 4971
- (1991) J. Org. Chem. , vol.56 , pp. 4971
- Fusetani, N.¹ Sugawara, T.² Matsunaga, S.³

6
- 33947243286
- S. E. Denmark C. S. Regens T. Kobayashi J. Am. Chem. Soc. 2007 129 2774
- (2007) J. Am. Chem. Soc. , vol.129 , pp. 2774
- Denmark, S.E.¹ Regens, C.S.² Kobayashi, T.³

7
- 0021979081
- A. A. E. El-Zayat N. R. Ferrighi T. G. McKenzie R. S. Byrn J. M. Cassady C.-J. Chang J. L. McLaughlin Tetrahedron Lett. 1985 26 955
- (1985) Tetrahedron Lett. , vol.26 , pp. 955
- El-Zayat, A.A.E.¹ Ferrighi, N.R.² McKenzie, T.G.³ Byrn, R.S.⁴ Cassady, J.M.⁵ Chang, C.-J.⁶ McLaughlin, J.L.⁷

8
- 36749086370
- K. C. Nicolaou K. P. Cole M. O. Frederick R. J. Aversa R. M. Deton Angew. Chem., Int. Ed. 2007 45 8875
- (2007) Angew. Chem., Int. Ed. , vol.45 , pp. 8875
- Nicolaou, K.C.¹ Cole, K.P.² Frederick, M.O.³ Aversa, R.J.⁴ Deton, R.M.⁵

9
- 0031004214
- R. Sakai H. Kamiya M. Murata K. Shimamoto J. Am. Chem. Soc. 1997 119 4112
- (1997) J. Am. Chem. Soc. , vol.119 , pp. 4112
- Sakai, R.¹ Kamiya, H.² Murata, M.³ Shimamoto, K.⁴

10
- 0035902232
- R. Sakai T. Koike M. Sasaki K. Shimamoto C. Oiwa A. Yano K. Suzuki K. Tachibana H. Kamiya Org. Lett. 2001 3 1479
- (2001) Org. Lett. , vol.3 , pp. 1479
- Sakai, R.¹ Koike, T.² Sasaki, M.³ Shimamoto, K.⁴ Oiwa, C.⁵ Yano, A.⁶ Suzuki, K.⁷ Tachibana, K.⁸ Kamiya, H.⁹

11
- 30744476469
- M. Inoue Chem. Rev. 2005 105 4379
- (2005) Chem. Rev. , vol.105 , pp. 4379
- Inoue, M.¹

12
- 2942557280
- I. Nakamura Y. Yamamoto Chem. Rev. 2004 104 2127
- (2004) Chem. Rev. , vol.104 , pp. 2127
- Nakamura, I.¹ Yamamoto, Y.²

13
- 17844362961
- K. Fujiwara A. Goto D. Sato H. Kawai T. Suzuki Tetrahedron Lett. 2005 46 3465
- (2005) Tetrahedron Lett. , vol.46 , pp. 3465
- Fujiwara, K.¹ Goto, A.² Sato, D.³ Kawai, H.⁴ Suzuki, T.⁵

14
- 0037463721
- T. Saitoh T. Suzuki N. Onodera H. Sekiguchi H. Hagiwara T. Hoshi Tetrahedron Lett. 2003 44 2709
- (2003) Tetrahedron Lett. , vol.44 , pp. 2709
- Saitoh, T.¹ Suzuki, T.² Onodera, N.³ Sekiguchi, H.⁴ Hagiwara, H.⁵ Hoshi, T.⁶

15
- 0033576445
- M. T. Crimmins K. A. Emmitte Org. Lett. 1999 1 2029
- (1999) Org. Lett. , vol.1 , pp. 2029
- Crimmins, M.T.¹ Emmitte, K.A.²

16
- 0030841278
- J. W. Burton J. S. Clark S. Derrer T. C. Stork J. G. Bendall A. B. Holmes J. Am. Chem. Soc. 1997 119 7483
- (1997) J. Am. Chem. Soc. , vol.119 , pp. 7483
- Burton, J.W.¹ Clark, J.S.² Derrer, S.³ Stork, T.C.⁴ Bendall, J.G.⁵ Holmes, A.B.⁶

17
- 31144436305
- G. Kumaraswamy M. Padmaja B. Markondaiah N. Jena B. Sridhar M. Udaya Kiran J. Org. Chem. 2006 71 337
- (2006) J. Org. Chem. , vol.71 , pp. 337
- Kumaraswamy, G.¹ Padmaja, M.² Markondaiah, B.³ Jena, N.⁴ Sridhar, B.⁵ Udaya Kiran, M.⁶

18
- 36849051367
- G. Kumaraswamy K. Ankamma A. Pitchaiah J. Org. Chem. 2007 72 9822
- (2007) J. Org. Chem. , vol.72 , pp. 9822
- Kumaraswamy, G.¹ Ankamma, K.² Pitchaiah, A.³

19
- 33846331228
- S. V. Pansare V. A. Adsool Org. Lett. 2006 8 5897
- (2006) Org. Lett. , vol.8 , pp. 5897
- Pansare, S.V.¹ Adsool, V.A.²

20
- 38349172460
- B. Schmidt A. Biernat Org. Lett. 2008 10 105
- (2008) Org. Lett. , vol.10 , pp. 105
- Schmidt, B.¹ Biernat, A.²

21
- 0036026808
- M. C. Elliott J. Chem. Soc., Perkin Trans. 1 2002 2301
- (2002) J. Chem. Soc., Perkin Trans. 1 , pp. 2301
- Elliott, M.C.¹

22
- 38849199901
- H. Kiyota, Springer-Verlag, Berlin, p. 97
- K. Fujiwara, in Marine Natural Products (Topics in Heterocyclic Chemistry), ed., H. Kiyota,, Springer-Verlag, Berlin, 2006, vol. 5, p. 97
- (2006) Marine Natural Products (Topics in Heterocyclic Chemistry), Ed.
- Fujiwara In, K.¹

23
- 0000100584
- M. P. Doyle D. C. Forbes Chem. Rev. 1998 98 911
- (1998) Chem. Rev. , vol.98 , pp. 911
- Doyle, M.P.¹ Forbes, D.C.²

24
- 0030797298
- M. P. Doyle C. S. Peterson Tetrahedron Lett. 1997 38 5265
- (1997) Tetrahedron Lett. , vol.38 , pp. 5265
- Doyle, M.P.¹ Peterson, C.S.²

25
- 0030819975
- M. P. Doyle C. S. Peterson M. N. Protopopova A. B. Marnett D. L. Parker, Jr D. G. Ene V. Lynch J. Am. Chem. Soc. 1997 119 8826
- (1997) J. Am. Chem. Soc. , vol.119 , pp. 8826
- Doyle, M.P.¹ Peterson, C.S.² Protopopova, M.N.³ Marnett, A.B.⁴ Parker Jr., D.L.⁵ Ene, D.G.⁶ Lynch, V.⁷

26
- 0029838575
- M. P. Doyle C. S. Peterson D. L. Parker, Jr Angew. Chem., Int. Ed. Engl. 1996 35 1324
- (1996) Angew. Chem., Int. Ed. Engl. , vol.35 , pp. 1324
- Doyle, M.P.¹ Peterson, C.S.² Parker Jr., D.L.³

27
- 0000431832
- M. P. Doyle V. Bagheri N. K. Harn Tetrahedron Lett. 1988 38 5119
- (1988) Tetrahedron Lett. , vol.38 , pp. 5119
- Doyle, M.P.¹ Bagheri, V.² Harn, N.K.³

28
- 55349142053
- 4, and CuI, but none gave the observed product
- 4, and CuI, but none gave the observed product

29
- 33750305620
- A. A. Scholte M. H. An M. L. Snapper Org. Lett. 2006 8 4759
- (2006) Org. Lett. , vol.8 , pp. 4759
- Scholte, A.A.¹ An, M.H.² Snapper, M.L.³

30
- 0029895814
- The preferential conformations of 15, 16, 17, 18, 21, 22 [compounds generated using the (R,R)-diol], 6a″, 7a″, 15″ and 17″ [compounds generated using the (S,S)-diol], have been characterised by NMR data (see ESI)
- A. Yanagisawa H. Nakashima A. Ishiba H. Yamamoto J. Am. Chem. Soc. 1996 118 4723
- (1996) J. Am. Chem. Soc. , vol.118 , pp. 4723
- Yanagisawa, A.¹ Nakashima, H.² Ishiba, A.³ Yamamoto, H.⁴

31
- 46849088854
- M. Shibasaki M. Kanai Eur. J. Org. Chem. 2008 1839
- (2008) Eur. J. Org. Chem. , pp. 1839
- Shibasaki, M.¹ Kanai, M.²

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