SCOPUS 정보 검색 플랫폼 - 논문 보기

메뉴 건너뛰기

Chemical Communications

Volumn , Issue 43, 2008, Pages 5526-5528

Tandem conjugate addition-elimination reaction promoted by chiral pyrrolidinyl sulfonamide (CPS)

(6) Xu, Junye a Fu, Xiao a Low, Ruijuan a Goh, Yong Peng a Jiang, Zhiyong a Tan, Choon Hong a

a NATIONAL UNIVERSITY OF SINGAPORE (Singapore)

Author keywords

[No Author keywords available]

Indexed keywords

1,3 DICARBONYL; ALLYL COMPOUND; BROMIDE; CARBONYL DERIVATIVE; CHIRAL PYRROLIDINYL SULFONAMIDE; SULFONAMIDE; UNCLASSIFIED DRUG;

ADDITION REACTION; ARTICLE; CHEMICAL STRUCTURE; CHIRALITY; CONJUGATE; ELIMINATION REACTION; ENANTIOMER; ENANTIOSELECTIVITY; STRUCTURE ANALYSIS;

EID: 56049115182 PISSN: 13597345 EISSN: None Source Type: Journal
DOI: 10.1039/b810905m Document Type: Article

Times cited : (18)

References (24)

1
- 0001731115
- R. Tamura K.-i. Watabe N. Ono Y. Yamamoto J. Org. Chem. 1992 57 4895
- (1992) J. Org. Chem. , vol.57 , pp. 4895
- Tamura, R.¹ Watabe, K.-I.² Ono, N.³ Yamamoto, Y.⁴

2
- 0001614606
- K. Fuji M. Node H. Nagasawa Y. Naniwa T. Taga K. Machida G. Snatzke J. Am. Chem. Soc. 1989 111 7921
- (1989) J. Am. Chem. Soc. , vol.111 , pp. 7921
- Fuji, K.¹ Node, M.² Nagasawa, H.³ Naniwa, Y.⁴ Taga, T.⁵ MacHida, K.⁶ Snatzke, G.⁷

3
- 0037049208
- J. N. Kim H. J. Lee J. H. Gong Tetrahedron Lett. 2002 43 9141
- (2002) Tetrahedron Lett. , vol.43 , pp. 9141
- Kim, J.N.¹ Lee, H.J.² Gong, J.H.³

4
- 2942519744
- Y. Du X. Han X. Lu Tetrahedron Lett. 2004 45 4967
- (2004) Tetrahedron Lett. , vol.45 , pp. 4967
- Du, Y.¹ Han, X.² Lu, X.³

5
- 2542448981
- C.-W. Cho J.-R. Kong M. J. Krische Org. Lett. 2004 6 1337
- (2004) Org. Lett. , vol.6 , pp. 1337
- Cho, C.-W.¹ Kong, J.-R.² Krische, M.J.³

6
- 26044441701
- P. V. Ramachandran S. Madhi L. Bland-Berry M. V. R. Reddy M. J. O'Donnell J. Am. Chem. Soc. 2005 127 13450
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 13450
- Ramachandran, P.V.¹ Madhi, S.² Bland-Berry, L.³ Reddy, M.V.R.⁴ O'Donnell, M.J.⁵

7
- 18244387510
- H. M. R. Hoffmann J. Rabe J. Org. Chem. 1985 50 3849
- (1985) J. Org. Chem. , vol.50 , pp. 3849
- Hoffmann, H.M.R.¹ Rabe, J.²

8
- 23944497647
- H.-Y. Chen L. N. Patkar S.-H. Ueng C.-C. Lin A. S.-Y. Lee Synlett. 2005 13 2035
- (2005) Synlett. , vol.13 , pp. 2035
- Chen, H.-Y.¹ Patkar, L.N.² Ueng, S.-H.³ Lin, C.-C.⁴ Lee, A.S.-Y.⁵

9
- 0035903871
- D. Basavaiah N. Kumaragurubaran D. S. Sharada R. M. Reddy Tetrahedron 2001 57 8167
- (2001) Tetrahedron , vol.57 , pp. 8167
- Basavaiah, D.¹ Kumaragurubaran, N.² Sharada, D.S.³ Reddy, R.M.⁴

10
- 30344441213
- W. Ye D. Leow S. L. M. Goh C.-T. Tan C.-H. Chian C.-H. Tan Tetrahedron Lett. 2006 47 1007
- (2006) Tetrahedron Lett. , vol.47 , pp. 1007
- Ye, W.¹ Leow, D.² Goh, S.L.M.³ Tan, C.-T.⁴ Chian, C.-H.⁵ Tan, C.-H.⁶

11
- 0000039618
- B. M. Kim S. M. So H. J. Choi Org. Lett. 2002 4 949
- (2002) Org. Lett. , vol.4 , pp. 949
- Kim, B.M.¹ So, S.M.² Choi, H.J.³

12
- 36749034757
- W. Ye Z. Jiang Y. Zhao S. L. M. Goh D. Leow Y.-T. Soh C.-H. Tan Adv. Synth. Catal. 2007 349 2454
- (2007) Adv. Synth. Catal. , vol.349 , pp. 2454
- Ye, W.¹ Jiang, Z.² Zhao, Y.³ Goh, S.L.M.⁴ Leow, D.⁵ Soh, Y.-T.⁶ Tan, C.-H.⁷

13
- 39749156976
- M. Agostinho Shū Kobayashi J. Am. Chem. Soc. 2008 130 2430
- (2008) J. Am. Chem. Soc. , vol.130 , pp. 2430
- Agostinho, M.¹ Shu, K.²

14
- 46049105895
- G. Lalic E. J. Corey Tetrahedron Lett. 2008 49 4894
- (2008) Tetrahedron Lett. , vol.49 , pp. 4894
- Lalic, G.¹ Corey, E.J.²

15
- 33845556313
- 3 catalysed Diels-Alder reactions, see:
- A. L. Gernal J.-L. Luche J. Am. Chem. Soc. 1981 103 5454
- (1981) J. Am. Chem. Soc. , vol.103 , pp. 5454
- Gernal, A.L.¹ Luche, J.-L.²

16
- 0026486293
- S. Kobayashi I. Hachiya T. Takahori M. Araki H. Ishitani Tetrahedron Lett. 1992 33 6815
- (1992) Tetrahedron Lett. , vol.33 , pp. 6815
- Kobayashi, S.¹ Hachiya, I.² Takahori, T.³ Araki, M.⁴ Ishitani, H.⁵

17
- 0037179188
- We assigned the exo stereochemistry according to the following report:
- J. H. Kim H.-K. Kim S. B. Jeon K.-H. Son E. H. Kim S. K. Kang N.-D. Sung B.-M. Kwon Tetrahedron Lett. 2002 43 6205
- (2002) Tetrahedron Lett. , vol.43 , pp. 6205
- Kim, J.H.¹ Kim, H.-K.² Jeon, S.B.³ Son, K.-H.⁴ Kim, E.H.⁵ Kang, S.K.⁶ Sung, N.-D.⁷ Kwon, B.-M.⁸

18
- 0010380718
- R. R. Sauers T. R. Henderson J. Org. Chem. 1974 39 1850
- (1974) J. Org. Chem. , vol.39 , pp. 1850
- Sauers, R.R.¹ Henderson, T.R.²

19
- 37549037472
- 2 at room temperature (see ESI)
- S. Cabrera J. Alemán P. Bolze S. Bertelsen K. A. Jørgensen Angew. Chem., Int. Ed. 2008 47 121
- (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 121
- Cabrera, S.¹ Alemán, J.² Bolze, P.³ Bertelsen, S.⁴ Jørgensen, K.A.⁵

20
- 0002539369
- Ethyl acetate was found to provide product with highest diastereoselectivity
- D. A. Evans C. L. Sims Tetrahedron Lett. 1973 47 4691
- (1973) Tetrahedron Lett. , vol.47 , pp. 4691
- Evans, D.A.¹ Sims, C.L.²

21
- 0001080242
- 3J = 10.1 Hz, which indicates a trans geometry according to the following report:
- E. Nakamura S. Matsuzawa Y. Horiguchi I. Kuwajima Tetrahedron Lett. 1986 27 4029
- (1986) Tetrahedron Lett. , vol.27 , pp. 4029
- Nakamura, E.¹ Matsuzawa, S.² Horiguchi, Y.³ Kuwajima, I.⁴

22
- 2442589745
- M. I. Donnoli P. Scafato M. Nardiello D. Casarini E. Giorgio C. Rosini Tetrahedron 2004 60 4975
- (2004) Tetrahedron , vol.60 , pp. 4975
- Donnoli, M.I.¹ Scafato, P.² Nardiello, M.³ Casarini, D.⁴ Giorgio, E.⁵ Rosini, C.⁶

23
- 0034699310
- The structure of the ammonium salt was determined by single crystal X-ray analyses (see ESI) as follows
- T. Perrard J.-C. Plaquevent J.-R. Desmurs D. Hébrault Org. Lett. 2000 2 2959
- (2000) Org. Lett. , vol.2 , pp. 2959
- Perrard, T.¹ Plaquevent, J.-C.² Desmurs, J.-R.³ Hébrault, D.⁴

24
- 27744501832
- W. Ye J. Xu C.-T. Tan C.-H. Tan Tetrahedron Lett. 2005 46 6875
- (2005) Tetrahedron Lett. , vol.46 , pp. 6875
- Ye, W.¹ Xu, J.² Tan, C.-T.³ Tan, C.-H.⁴

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.