SCOPUS 정보 검색 플랫폼

Synlett

Volumn , Issue 12, 2009, Pages 1951-1954

Synthesis of furo[3,4-c]furanones via DDQ treatment of furo[3,4-c]pyranone derivatives

(3) Meng, Tao a Fuhrer, Cyril A a Häner, Robert a

a UNIVERSITY OF BERN (Switzerland)

Author keywords

2,3 Dichloro 5,6 dicyano 1,4 benzoquinone (DDQ); Furo 3,4 c furanones; Furo 3,4 c pyranones

Indexed keywords

2,3 DICHLORO 5,6 DICYANO 1,4 BENZOQUINONE; BENZOQUINONE; FURANONE DERIVATIVE; FURO [3,4 C] FURANONE DERIVATIVE; FURO [3,4 C] PYRANONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; DRUG STRUCTURE; DRUG SYNTHESIS;

EID: 67651213442 PISSN: 09365214 EISSN: 14372096 Source Type: Journal
DOI: 10.1055/s-0029-1217525 Document Type: Article

Times cited : (2)

References (12)

1
- 84970568699
- Corrie, J. E. T.; Green, G. H.; Ritchie, E.; Taylor, W. C. Aust. J. Chem. 1970, 23, 133.
- (1970) Aust. J. Chem , vol.23 , pp. 133
- Corrie, J.E.T.¹ Green, G.H.² Ritchie, E.³ Taylor, W.C.⁴

2
- 0001615482
- Gonzalez, A. G.; Estevezreyes, R.; Mato, C. J. Nat. Prod. 1989, 52, 1139.
- (1989) J. Nat. Prod , vol.52 , pp. 1139
- Gonzalez, A.G.¹ Estevezreyes, R.² Mato, C.³

3
- 0006875845
- Cooper, R.; Gottlieb, H. E.; Lavie, D.; Levy, E. C. Tetrahedron 1979, 35, 861.
- (1979) Tetrahedron , vol.35 , pp. 861
- Cooper, R.¹ Gottlieb, H.E.² Lavie, D.³ Levy, E.C.⁴

4
- 0028587722
- Matsunaga, K.; Shibuya, M.; Ohizumi, Y. J. Nat. Prod. 1994, 57, 1734.
- (1994) J. Nat. Prod , vol.57 , pp. 1734
- Matsunaga, K.¹ Shibuya, M.² Ohizumi, Y.³

5
- 0030934346
- Tatlock, J. H.; Linton, M. A.; Hou, X. J.; Kissinger, C. R.; Pelletier, L. A.; Showalter, R. E.; Tempczyk, A.; Villafranca, J. E. Bioorg. Med. Chem. Lett. 1997, 7, 1007.
- (1997) Bioorg. Med. Chem. Lett , vol.7 , pp. 1007
- Tatlock, J.H.¹ Linton, M.A.² Hou, X.J.³ Kissinger, C.R.⁴ Pelletier, L.A.⁵ Showalter, R.E.⁶ Tempczyk, A.⁷ Villafranca, J.E.⁸

6
- 2342499889
- Fuhrer, C.; Messer, R.; Häner, R. Tetrahedron Lett. 2004, 45, 4297.
- (2004) Tetrahedron Lett , vol.45 , pp. 4297
- Fuhrer, C.¹ Messer, R.² Häner, R.³

7
- 47549119105
- Fuhrer, C. A.; Grüter, E.; Ruetz, S.; Häner, R. ChemMedChem 2007, 2, 441.
- (2007) ChemMedChem , vol.2 , pp. 441
- Fuhrer, C.A.¹ Grüter, E.² Ruetz, S.³ Häner, R.⁴

8
- 0005698715
- Nightingale, D. V.; Sukornick, B. J. Org. Chem. 1959, 24, 497.
- (1959) J. Org. Chem , vol.24 , pp. 497
- Nightingale, D.V.¹ Sukornick, B.²

9
- 0037462373
- Padwa, A.; Straub, C. S. J. Org. Chem. 2003, 68, 227.
- (2003) J. Org. Chem , vol.68 , pp. 227
- Padwa, A.¹ Straub, C.S.²

10
- 33344466047
- For example, see
- For example, see: Bharate, S. B. Synlett 2006, 496.
- (2006) Synlett , pp. 496
- Bharate, S.B.¹

11
- 67651247623
- Representative Analytical Data of Furo[3,4-c]furanones; Compound 2: pale-yellow solid; mp 172-175 °C. 1H NMR (300 MHz, DMSO-d6, δ, 8.13-8.16 (m, 2 H, 7.60-7.62 (m, 2 H, 7.47-7.51 (m, 2 H, 7.35 (m, 1 H, 7.11-7.13 (m, 2 H, 5.59 (s, 2 H, 3.83 (s, 3 H, 13C NMR (75 MHz, CDCl3, δ, 164.37 (C, 160.70 (C, 149.78 (C, 140.77 (C, 129.08 (2 × CH, 128.70 (C, 128.48 (C, 127.86 (CH, 127.17 (2 × CH, 123.79 (2 × CH, 120.62 (C, 114.70 (2 × CH, 114.15 (C, 65.85 (CH2, 55.38 (CH3, EI-MS: m/z, 306. HRMS (ESI, m/z [M, H, calcd for C 19H15O4: 307.0970; found: 307.0965. Detailed 1H, 13C NMR and 2D NMR (COSY, HSQC and HMQC) analysis were used for further structural assignment. The following NMR signals were observed: three sets of 12 aromatic carbons 9 of which are H-substitute
- 3: 372.9876; found: 372.9870. Compound 6g: yellow solid; mp 178-181 °C.

12
- 67651249873
- Reactions were carried out under an open atmosphere
- Reactions were carried out under an open atmosphere.

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