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Chemical Communications

Volumn , Issue 6, 2008, Pages 730-732

Towards the total synthesis of FD-838: Modular enantioselective assembly of the core

(2) Orellana, Arturo a,b Rovis, Tomislav a

a Department of Environmental and Radiological Health Sciences (United States)

b YORK UNIVERSITY (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBIOTIC AGENT; AZASPIRENE; CEPHALIMYSIN A; FD 838; NATURAL PRODUCT; SYNERAZOL; TETRACYCLINE DERIVATIVE; UNCLASSIFIED DRUG;

ADDITION REACTION; ARTICLE; BROMINATION; CHEMICAL REACTION; DRUG STRUCTURE; DRUG SYNTHESIS; ELIMINATION REACTION; ENANTIOSELECTIVITY; OXIDATION; SYNTHESIS;

EID: 38649119429 PISSN: 13597345 EISSN: None Source Type: Journal
DOI: 10.1039/b716445a Document Type: Article

Times cited : (55)

References (31)

1
- 4944259975
- Eur. Pat. Appl. EP 216607, J. P. Appl. 205278, 1987; Chem. Abstr.
- K. Mizoue, T. Okazaki, K. Hanada, T. Amamoto, M. Yamagashi and S. Omura, Eur. Pat. Appl. EP 216607, J. P. Appl. 205278, 1987; Chem. Abstr., 1987, 107, 132627x
- (1987) Chem. Abstr. , vol.107
- Mizoue, K.¹ Okazaki, T.² Hanada, K.³ Amamoto, T.⁴ Yamagashi, M.⁵ Omura, S.⁶

2
- 0000879865
- Y. Asami H. Kakeya R. Onose A. Yoshida H. Matsuzaki H. Osada Org. Lett. 2002 4 2845
- (2002) Org. Lett. , vol.4 , pp. 2845
- Asami, Y.¹ Kakeya, H.² Onose, R.³ Yoshida, A.⁴ Matsuzaki, H.⁵ Osada, H.⁶

3
- 0025829101
- O. Ando H. Satake M. Nakajina A. Sato T. Nakamura T. Kinoshita K. Furuya T. Haneishi J. Antibiot. 1991 44 382
- (1991) J. Antibiot. , vol.44 , pp. 382
- Ando, O.¹ Satake, H.² Nakajina, M.³ Sato, A.⁴ Nakamura, T.⁵ Kinoshita, T.⁶ Furuya, K.⁷ Haneishi, T.⁸

4
- 34547684833
- Reported syntheses:
- T. Yamada E. Imai K. Nakatuji A. Numata R. Tanaka Tetrahedron Lett. 2007 48 6294
- (2007) Tetrahedron Lett. , vol.48 , pp. 6294
- Yamada, T.¹ Imai, E.² Nakatuji, K.³ Numata, A.⁴ Tanaka, R.⁵

5
- 0037120884
- Y. Hayashi M. Shoji J. Yamaguchi K. Sato S. Yamaguchi T. Mukaiyama K. Sakai Y. Asami H. Kakeya H. Osada J. Am. Chem. Soc. 2002 124 12078
- (2002) J. Am. Chem. Soc. , vol.124 , pp. 12078
- Hayashi, Y.¹ Shoji, M.² Yamaguchi, J.³ Sato, K.⁴ Yamaguchi, S.⁵ Mukaiyama, T.⁶ Sakai, K.⁷ Asami, Y.⁸ Kakeya, H.⁹ Osada, H.¹⁰

6
- 0141741600
- Y. Hayashi M. Shoji S. Yamaguchi T. Mukaiyama J. Yamaguchi H. Kakeya H. Osada Org. Lett. 2003 5 2287
- (2003) Org. Lett. , vol.5 , pp. 2287
- Hayashi, Y.¹ Shoji, M.² Yamaguchi, S.³ Mukaiyama, T.⁴ Yamaguchi, J.⁵ Kakeya, H.⁶ Osada, H.⁷

7
- 0345828942
- S. Aoki T. Oi K. Shimizu R. Shiraki K. Takao K. Tadano Heterocycles 2004 62 161
- (2004) Heterocycles , vol.62 , pp. 161
- Aoki, S.¹ Oi, T.² Shimizu, K.³ Shiraki, R.⁴ Takao, K.⁵ Tadano, K.⁶

8
- 4944222149
- S. Aoki T. Oi K. Shimizu R. Shiraki K. Takao K. Tadano Bull. Chem. Soc. Jpn. 2004 77 1703
- (2004) Bull. Chem. Soc. Jpn. , vol.77 , pp. 1703
- Aoki, S.¹ Oi, T.² Shimizu, K.³ Shiraki, R.⁴ Takao, K.⁵ Tadano, K.⁶

9
- 22144441375
- Synthetic Studies:
- Y. Hayashi M. Shoji T. Mukaiyama H. Gotoh S. Yamaguchi M. Nakata H. Kakeya H. Osada J. Org. Chem. 2005 70 5643
- (2005) J. Org. Chem. , vol.70 , pp. 5643
- Hayashi, Y.¹ Shoji, M.² Mukaiyama, T.³ Gotoh, H.⁴ Yamaguchi, S.⁵ Nakata, M.⁶ Kakeya, H.⁷ Osada, H.⁸

10
- 0029081305
- Z. Su C. Tamm Tetrahedron 1995 51 11177
- (1995) Tetrahedron , vol.51 , pp. 11177
- Su, Z.¹ Tamm, C.²

11
- 29144532995
- Biosynthetic studies:
- J. M. Mitchell N. S. Finney Org. Biomol. Chem. 2005 3 4274
- (2005) Org. Biomol. Chem. , vol.3 , pp. 4274
- Mitchell, J.M.¹ Finney, N.S.²

12
- 10044251967
- Y. Igarashi Y. Yabuta A. Sekine K. Fujii K. Harada T. Oikawa M. Sato T. Furumai T. Oki J. Antibiot. 2004 57 748
- (2004) J. Antibiot. , vol.57 , pp. 748
- Igarashi, Y.¹ Yabuta, Y.² Sekine, A.³ Fujii, K.⁴ Harada, K.⁵ Oikawa, T.⁶ Sato, M.⁷ Furumai, T.⁸ Oki, T.⁹

13
- 38649108858
- L. A. Paquette, Wiley, New York, p. 407
- H. Stetter and H. Kuhlmann, Organic Reactions, ed., L. A. Paquette,, Wiley, New York, 1991, vol. 40, p. 407
- (1991) Organic Reactions, Ed.
- Stetter, H.¹ Kuhlmann, H.²

14
- 84982510866
- H. Stetter H. Kuhlmann Chem. Ber. 1976 109 2890
- (1976) Chem. Ber. , vol.109 , pp. 2890
- Stetter, H.¹ Kuhlmann, H.²

15
- 84982417601
- H. Stetter Angew. Chem., Int. Ed. Engl. 1976 15 639
- (1976) Angew. Chem., Int. Ed. Engl. , vol.15 , pp. 639
- Stetter, H.¹

16
- 0037019628
- M. S. Kerr J. Read de Alaniz T. Rovis J. Am. Chem. Soc. 2002 124 10298
- (2002) J. Am. Chem. Soc. , vol.124 , pp. 10298
- Kerr, M.S.¹ Read De Alaniz, J.² Rovis, T.³

17
- 0142059744
- M. S. Kerr T. Rovis Synlett 2003 1934
- (2003) Synlett , pp. 1934
- Kerr, M.S.¹ Rovis, T.²

18
- 3242812738
- M. S. Kerr T. Rovis J. Am. Chem. Soc. 2004 126 8876
- (2004) J. Am. Chem. Soc. , vol.126 , pp. 8876
- Kerr, M.S.¹ Rovis, T.²

19
- 18244367138
- J. Read de Alaniz T. Rovis J. Am. Chem. Soc. 2005 127 6284
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 6284
- Read De Alaniz, J.¹ Rovis, T.²

20
- 20444450149
- N. T. Reynolds T. Rovis Tetrahedron 2005 61 6368
- (2005) Tetrahedron , vol.61 , pp. 6368
- Reynolds, N.T.¹ Rovis, T.²

21
- 33644661812
- Q. Liu T. Rovis J. Am. Chem. Soc. 2006 128 2552
- (2006) J. Am. Chem. Soc. , vol.128 , pp. 2552
- Liu, Q.¹ Rovis, T.²

22
- 33750440190
- J. L. Moore M. S. Kerr T. Rovis Tetrahedron 2006 62 11477
- (2006) Tetrahedron , vol.62 , pp. 11477
- Moore, J.L.¹ Kerr, M.S.² Rovis, T.³

23
- 35948961858
- Q. Liu T. Rovis Org. Process Res. Dev. 2007 11 598
- (2007) Org. Process Res. Dev. , vol.11 , pp. 598
- Liu, Q.¹ Rovis, T.²

24
- 0037236222
- M. J. Sahoo S. B. Mhaske N. P. Argade Synthesis 2003 346
- (2003) Synthesis , pp. 346
- Sahoo, M.J.¹ Mhaske, S.B.² Argade, N.P.³

25
- 0001345095
- M. E. Jung Y.-G. Pan M. W. Rathke D. F. Sullivan R. P. Woodbury J. Org. Chem. 1977 42 3961
- (1977) J. Org. Chem. , vol.42 , pp. 3961
- Jung, M.E.¹ Pan, Y.-G.² Rathke, M.W.³ Sullivan, D.F.⁴ Woodbury, R.P.⁵

26
- 84986955199
- I. Fleming I. Paterson Synthesis 1979 736
- (1979) Synthesis , pp. 736
- Fleming, I.¹ Paterson, I.²

27
- 33846027862
- M. A. Grundl A. Kaster E. D. Beaulieu D. Trauner Org. Lett. 2006 8 5429
- (2006) Org. Lett. , vol.8 , pp. 5429
- Grundl, M.A.¹ Kaster, A.² Beaulieu, E.D.³ Trauner, D.⁴

28
- 49549128736
- J.-R. Pougny P. Sinaÿ Tetrahedron Lett. 1976 17 4073
- (1976) Tetrahedron Lett. , vol.17 , pp. 4073
- Pougny, J.-R.¹ Sinaÿ, P.²

29
- 37049089952
- A. J. Ratcliffe B. Fraser-Reid J. Chem. Soc., Perkin Trans. 1 1990 747
- (1990) J. Chem. Soc., Perkin Trans. 1 , pp. 747
- Ratcliffe, A.J.¹ Fraser-Reid, B.²

30
- 0000300180
- Stereochemistry was assigned on the basis of extensive NOE experiments on an analogue bearing a vinyl group in place of the furan. Further support for this assignment was provided by a partially solved crystal structure of compound. 10 (a fully solved structure proved unattainable presumably due to crystal twinning)
- A. Marra J. Esnault A. Veyrieres P. Sinaÿ J. Am. Chem. Soc. 1992 114 6354
- (1992) J. Am. Chem. Soc. , vol.114 , pp. 6354
- Marra, A.¹ Esnault, J.² Veyrieres, A.³ Sinaÿ, P.⁴

31
- 0035966598
- Observed by-products invariably involved dihydrofuran ring opening. In no case did we observe formation of regioisomers
- S. Farcas J.-L. Namy Tetrahedron Lett. 2001 42 879
- (2001) Tetrahedron Lett. , vol.42 , pp. 879
- Farcas, S.¹ Namy, J.-L.²

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