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Volumn , Issue 30, 2006, Pages 3226-3228

3-Hydroxypyrrolidines from epoxysulfonamides and dimethylsulfoxonium methylide

Author keywords

[No Author keywords available]

Indexed keywords

PYRROLIDINE DERIVATIVE; SULFONAMIDE; SULFUR DERIVATIVE;

ARTICLE; CHEMICAL REACTION;

EID: 33746464910 PISSN: 13597345 EISSN: None Source Type: Journal
DOI: 10.1039/b606583j Document Type: Article

Times cited : (22)

References (27)

1
- 0004052642
- A.-F. M. Rizk, CRC Press, Boca Raton, pp. 1-89
- A.-F. M. Rizk, in Naturally occurring pyrrolizidine alkaloids, ed., A.-F. M. Rizk,, CRC Press, Boca Raton, 1991, pp. 1-89
- (1991) Naturally Occurring Pyrrolizidine Alkaloids, Ed.
- Rizk In, A.-F.M.¹

2
- 23844546994
- Detoxin A1:
- S. G. Pyne M. Tang Curr. Org. Chem. 2005 9 1393 1418
- (2005) Curr. Org. Chem. , vol.9 , pp. 1393-1418
- Pyne, S.G.¹ Tang, M.²

3
- 0012891220
- Anisomycin:
- W.-R. Li S.-Y. Han M. M. Joullié Heterocycles 1993 36 359 388
- (1993) Heterocycles , vol.36 , pp. 359-388
- Li, W.-R.¹ Han, S.-Y.² Joullié, M.M.³

4
- 1642461692
- Barnidipine:
- E. M. Rosser S. Morton K. S. Ashton P. Cohen A. N Hulme Org. Biomol. Chem. 2004 2 142 149
- (2004) Org. Biomol. Chem. , vol.2 , pp. 142-149
- Rosser, E.M.¹ Morton, S.² Ashton, K.S.³ Cohen, P.⁴ Hulme, A.N.⁵

5
- 0022993160
- DX-9065a:
- K. Tamazawa H. Arima T. Kojima Y. Isomura M. Okada S. Fujita T. Furuya T. Takenaka O. Inagaki M. Terai J. Med. Chem. 1986 29 2504 2511
- (1986) J. Med. Chem. , vol.29 , pp. 2504-2511
- Tamazawa, K.¹ Arima, H.² Kojima, T.³ Isomura, Y.⁴ Okada, M.⁵ Fujita, S.⁶ Furuya, T.⁷ Takenaka, T.⁸ Inagaki, O.⁹ Terai, M.¹⁰

6
- 0028265990
- T. Nagahara Y. Yokoyama K. Inamura S. Katakura S. Komoriya H. Yamaguchi T. Hara M. Iwamoto J. Med. Chem. 1994 37 1200 1207
- (1994) J. Med. Chem. , vol.37 , pp. 1200-1207
- Nagahara, T.¹ Yokoyama, Y.² Inamura, K.³ Katakura, S.⁴ Komoriya, S.⁵ Yamaguchi, H.⁶ Hara, T.⁷ Iwamoto, M.⁸

7
- 0035861695
- For a review, see:
- Z. Li H.-J. Feiten D. Chang W. A. Duetz J. B. van Beilen B. Witholt J. Org. Chem. 2001 66 8424 8430
- (2001) J. Org. Chem. , vol.66 , pp. 8424-8430
- Li, Z.¹ Feiten, H.-J.² Chang, D.³ Duetz, W.A.⁴ Van Beilen, J.B.⁵ Witholt, B.⁶

8
- 0345109734
- For more recent selected approaches, see:
- D. M. Flanagan M. M. Joullié Heterocycles 1987 26 2247 2265
- (1987) Heterocycles , vol.26 , pp. 2247-2265
- Flanagan, D.M.¹ Joullié, M.M.²

9
- 0345428104
- Y. Tamaru S. Kawamura T. Bando K. Tanaka M. Hojo Z. Yoshida J. Org. Chem. 1988 53 5491 5509
- (1988) J. Org. Chem. , vol.53 , pp. 5491-5509
- Tamaru, Y.¹ Kawamura, S.² Bando, T.³ Tanaka, K.⁴ Hojo, M.⁵ Yoshida, Z.⁶

10
- 33751157525
- S. E. Denmark M. E. Schnute J. Org. Chem. 1994 59 4576 4595
- (1994) J. Org. Chem. , vol.59 , pp. 4576-4595
- Denmark, S.E.¹ Schnute, M.E.²

11
- 23044453120
- D. M. Hodgson M. J. Fleming S. J. Stanway Org. Lett. 2005 7 3295 3298
- (2005) Org. Lett. , vol.7 , pp. 3295-3298
- Hodgson, D.M.¹ Fleming, M.J.² Stanway, S.J.³

12
- 6444221482
- J. M. Schomaker V. R. Pulgam B. Borhan J. Am. Chem. Soc. 2004 126 13600 13601
- (2004) J. Am. Chem. Soc. , vol.126 , pp. 13600-13601
- Schomaker, J.M.¹ Pulgam, V.R.² Borhan, B.³

13
- 33947485009
- For a recent review of sulfur ylide chemistry, see:
- E. J. Corey M. Chaykovsky J. Am. Chem. Soc. 1965 87 1353 1364
- (1965) J. Am. Chem. Soc. , vol.87 , pp. 1353-1364
- Corey, E.J.¹ Chaykovsky, M.²

14
- 33746442282
- A. Padwa and D. Bellus, Thieme, Stuttgart, pp. 21-104
- V. Aggarwal and J. Richardson, in Science of synthesis, ed., A. Padwa, and, D. Bellus,, Thieme, Stuttgart, 2004, vol. 27, pp. 21-104
- (2004) Science of Synthesis, Ed.
- Aggarwal, V.¹ Richardson In, J.²

15
- 0000991872
- K. Okuma Y. Tanaka S. Kaji H. Ohta J. Org. Chem. 1983 48 5133 5134
- (1983) J. Org. Chem. , vol.48 , pp. 5133-5134
- Okuma, K.¹ Tanaka, Y.² Kaji, S.³ Ohta, H.⁴

16
- 84986775450
- a of the trimethylsulfoxonium ion in DMSO at 25°C is 18.2
- A. O. Fitton J. Hill D. E. Jane R. Millar Synthesis 1987 1140 1142
- (1987) Synthesis , pp. 1140-1142
- Fitton, A.O.¹ Hill, J.² Jane, D.E.³ Millar, R.⁴

17
- 0003491250
- D. N. Jones, Pergamon Press, Oxford, pp. 247-260)
- C. R. Johnson, in Comprehensive Organic Chemistry, ed., D. N. Jones,, Pergamon Press, Oxford, 1979, vol. 3, pp. 247-260
- (1979) Comprehensive Organic Chemistry, Ed.
- Johnson In, C.R.¹

18
- 37049088477
- U. K. Nadir R. L. Sharma V. K. Koul J. Chem. Soc., Perkin Trans. 1 1991 2015 2019
- (1991) J. Chem. Soc., Perkin Trans. 1 , pp. 2015-2019
- Nadir, U.K.¹ Sharma, R.L.² Koul, V.K.³

19
- 0000315389
- T. Ibuka K. Nakai H. Habashita Y. Hotta A. Otaka H. Tamamura N. Fujii N. Mimura Y. Miwa T. Taga Y. Chounan Y. Yamamoto J. Org. Chem. 1995 60 2044 2058
- (1995) J. Org. Chem. , vol.60 , pp. 2044-2058
- Ibuka, T.¹ Nakai, K.² Habashita, H.³ Hotta, Y.⁴ Otaka, A.⁵ Tamamura, H.⁶ Fujii, N.⁷ Mimura, N.⁸ Miwa, Y.⁹ Taga, T.¹⁰ Chounan, Y.¹¹ Yamamoto, Y.¹²

20
- 0032365573
- T. Ibuka Chem. Soc. Rev. 1998 27 145 154
- (1998) Chem. Soc. Rev. , vol.27 , pp. 145-154
- Ibuka, T.¹

21
- 0000458209
- A. H. Hoveyda D. A. Evans G. C. Fu Chem. Rev. 1993 93 1307 1370
- (1993) Chem. Rev. , vol.93 , pp. 1307-1370
- Hoveyda, A.H.¹ Evans, D.A.² Fu, G.C.³

22
- 0346656525
- P. O'Brien A. C. Childs G. J. Ensor C. L. Hill J. P. Kirby M. J. Dearden S. J. Oxenford C. M. Rosser Org. Lett. 2003 5 4955 4957
- (2003) Org. Lett. , vol.5 , pp. 4955-4957
- O'Brien, P.¹ Childs, A.C.² Ensor, G.J.³ Hill, C.L.⁴ Kirby, J.P.⁵ Dearden, M.J.⁶ Oxenford, S.J.⁷ Rosser, C.M.⁸

23
- 0032527724
- J. U. Jeong B. Tao I. Sagasser H. Henniges K. B. Sharpless J. Am. Chem. Soc. 1998 120 6844 6845
- (1998) J. Am. Chem. Soc. , vol.120 , pp. 6844-6845
- Jeong, J.U.¹ Tao, B.² Sagasser, I.³ Henniges, H.⁴ Sharpless, K.B.⁵

24
- 33746401784
- Use of 5 equivalents of ylide 2 gave 3-hydroxypyrrolidine 8a in 13% yield
- Use of 5 equivalents of ylide 2 gave 3-hydroxypyrrolidine 8a in 13% yield

25
- 33746464293
- University of Oxford, During the preparation of this manuscript, the in situ process was reported:
- M. J. Fleming, D. Phil. thesis, University of Oxford, 2005
- (2005)
- Fleming, D.¹ Phil. Thesis, M.J.²

26
- 33746397386
- R. A. Jones, J. M. Schomaker and B. Borhan, Ylide-mediated expansion of 2,3-aziridin-1-ols to substituted pyrrolidines: Application to the syntheses of pyrrolizidine alkaloids, Abstracts of Papers, 231st ACS National Meeting, Atlanta, March 26-30, 2006, CHED-568
- Ylide-mediated Expansion of 2,3-aziridin-1-ols to Substituted Pyrrolidines: Application to the Syntheses of Pyrrolizidine Alkaloids, Abstracts of Papers, 231st ACS National Meeting, Atlanta, March 26-30, 2006, CHED-568
- Jones, R.A.¹ Schomaker, J.M.² Borhan, B.³

27
- 33746420405
- -1, 10663 reflections were measured, R = 0.0423, wR = 0.0507. CCDC 602881. For crystallographic data in CIF or other electronic format see DOI:
- 3S(O)Cl as a source of ylide 2 under these conditions gave an identical yield of 8a

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