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Chemical Communications

Volumn 47, Issue 30, 2011, Pages 8512-8514

Three-component coupling using arynes and DMF: Straightforward access to coumarins via ortho-quinone methides

(3) Yoshida, Hiroto a Ito, Yu a Ohshita, Joji a

a HIROSHIMA UNIVERSITY (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

2 QUINONE METHIDE; ANION; COUMARIN DERIVATIVE; ESTER; QUINONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CYCLOADDITION; STRUCTURE ANALYSIS;

EID: 79960542254 PISSN: 13597345 EISSN: 1364548X Source Type: Journal
DOI: 10.1039/c1cc11955a Document Type: Article

Times cited : (116)

References (28)

1
- 0030122802
- P. Wan B. Barker L. Diao M. Fischer Y. Shi C. Yang Can. J. Chem. 1996 74 465
- (1996) Can. J. Chem. , vol.74 , pp. 465
- Wan, P.¹ Barker, B.² Diao, L.³ Fischer, M.⁴ Shi, Y.⁵ Yang, C.⁶

2
- 0036642529
- R. W. Van De Water T. R. R. Pettus Tetrahedron 2002 58 5367
- (2002) Tetrahedron , vol.58 , pp. 5367
- Van De Water, R.W.¹ Pettus, T.R.R.²

3
- 0037191616
- T. Rosenau A. Potthast T. Elder P. Kosma Org. Lett. 2002 4 4285
- (2002) Org. Lett. , vol.4 , pp. 4285
- Rosenau, T.¹ Potthast, A.² Elder, T.³ Kosma, P.⁴

4
- 0030833252
- S. R. Angle J. D. Rainier C. Woytowicz J. Org. Chem. 1997 62 5884
- (1997) J. Org. Chem. , vol.62 , pp. 5884
- Angle, S.R.¹ Rainier, J.D.² Woytowicz, C.³

5
- 8744281396
- For other examples on the reactions of o-QMs derived from arynes and aldehydes, see:
- H. Yoshida M. Watanabe H. Fukushima J. Ohshita A. Kunai Org. Lett. 2004 6 4049
- (2004) Org. Lett. , vol.6 , pp. 4049
- Yoshida, H.¹ Watanabe, M.² Fukushima, H.³ Ohshita, J.⁴ Kunai, A.⁵

6
- 37049115883
- H. Heaney C. T. McCarty Chem. Commun. 1970 123
- (1970) Chem. Commun. , pp. 123
- Heaney, H.¹ McCarty, C.T.²

7
- 37049119472
- H. Heaney J. M. Jablonski C. T. McCarty J. Chem. Soc., Perkin Trans. 1 1972 2903
- (1972) J. Chem. Soc., Perkin Trans. 1 , pp. 2903
- Heaney, H.¹ Jablonski, J.M.² McCarty, C.T.³

8
- 8744294978
- For selected reports on the synthesis of coumarins, see:
- J. Nakayama M. Yoshida O. Simamura Chem. Lett. 1973 451
- (1973) Chem. Lett. , pp. 451
- Nakayama, J.¹ Yoshida, M.² Simamura, O.³

9
- 0035944980
- M. K. Potdar S. S. Mohile M. M. Salunkhe Tetrahedron Lett. 2001 42 9285
- (2001) Tetrahedron Lett. , vol.42 , pp. 9285
- Potdar, M.K.¹ Mohile, S.S.² Salunkhe, M.M.³

10
- 33746895130
- J. Oyamada T. Kitamura Tetrahedron 2006 62 6918
- (2006) Tetrahedron , vol.62 , pp. 6918
- Oyamada, J.¹ Kitamura, T.²

11
- 60949099341
- Y. Yamamoto N. Kirai Org. Lett. 2008 10 5513
- (2008) Org. Lett. , vol.10 , pp. 5513
- Yamamoto, Y.¹ Kirai, N.²

12
- 0025272382
- D. Opherk G. Schuler W. Waas R. Dietz W. Kubler Eur. Heart J. 1990 11 342
- (1990) Eur. Heart J. , vol.11 , pp. 342
- Opherk, D.¹ Schuler, G.² Waas, W.³ Dietz, R.⁴ Kubler, W.⁵

13
- 70450186312
- J. J. Magadula P. Etasto Nat. Prod. Rep. 2009 26 1535
- (2009) Nat. Prod. Rep. , vol.26 , pp. 1535
- Magadula, J.J.¹ Etasto, P.²

14
- 33846441300
- Y. G. Cao X. Q. Liu Y. C. Chen K. Hao G. J. Wang Eur. J. Pharm. Sci. 2007 30 175
- (2007) Eur. J. Pharm. Sci. , vol.30 , pp. 175
- Cao, Y.G.¹ Liu, X.Q.² Chen, Y.C.³ Hao, K.⁴ Wang, G.J.⁵

15
- 12444257779
- L. Piazzi A. Rampa A. Bisi S. Gobbi F. Belluti A. Cavalli M. Bartolini V. Andrisano P. Valenti M. Recanatini J. Med. Chem. 2003 46 2279
- (2003) J. Med. Chem. , vol.46 , pp. 2279
- Piazzi, L.¹ Rampa, A.² Bisi, A.³ Gobbi, S.⁴ Belluti, F.⁵ Cavalli, A.⁶ Bartolini, M.⁷ Andrisano, V.⁸ Valenti, P.⁹ Recanatini, M.¹⁰

16
- 0002977163
- Y. Himeshima T. Sonoda H. Kobayashi Chem. Lett. 1983 1211
- (1983) Chem. Lett. , pp. 1211
- Himeshima, Y.¹ Sonoda, T.² Kobayashi, H.³

17
- 22544456259
- For other C-C bond cleavage reactions using arynes, see:
- H. Yoshida M. Watanabe J. Ohshita A. Kunai Chem. Commun. 2005 3292
- (2005) Chem. Commun. , pp. 3292
- Yoshida, H.¹ Watanabe, M.² Ohshita, J.³ Kunai, A.⁴

18
- 17644362249
- U. K. Tambar B. M. Stoltz J. Am. Chem. Soc. 2005 127 5340
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 5340
- Tambar, U.K.¹ Stoltz, B.M.²

19
- 23944440375
- H. Yoshida M. Watanabe J. Ohshita A. Kunai Tetrahedron Lett. 2005 46 6729
- (2005) Tetrahedron Lett. , vol.46 , pp. 6729
- Yoshida, H.¹ Watanabe, M.² Ohshita, J.³ Kunai, A.⁴

20
- 33748480130
- U. K. Tambar D. C. Ebner B. M. Stoltz J. Am. Chem. Soc. 2006 128 11752
- (2006) J. Am. Chem. Soc. , vol.128 , pp. 11752
- Tambar, U.K.¹ Ebner, D.C.² Stoltz, B.M.³

21
- 34147156607
- H. Yoshida M. Watanabe T. Morishita J. Ohshita A. Kunai Chem. Commun. 2007 1505
- (2007) Chem. Commun. , pp. 1505
- Yoshida, H.¹ Watanabe, M.² Morishita, T.³ Ohshita, J.⁴ Kunai, A.⁵

22
- 56749164601
- H. Yoshida T. Kishida M. Watanabe J. Ohshita Chem. Commun. 2008 5963
- (2008) Chem. Commun. , pp. 5963
- Yoshida, H.¹ Kishida, T.² Watanabe, M.³ Ohshita, J.⁴

23
- 0000264238
- For a review on nucleophilic coupling with arynes, see ed., B. M. Trost, and, I. Flemming, Pergamon Press, Oxford
- For a review on nucleophilic coupling with arynes, see: S. V. Kessar, in Comprehensive Organic Synthesis, ed., B. M. Trost, and, I. Flemming, Pergamon Press, Oxford, 1991, vol. 4, pp. 483-515
- (1991) Comprehensive Organic Synthesis , vol.4 , pp. 483-515
- Kessar, S.V.¹

24
- 0037244549
- C. Su Z.-C. Chen Q.-G. Zhen Synthesis 2003 555
- (2003) Synthesis , pp. 555
- Su, C.¹ Chen, Z.-C.² Zhen, Q.-G.³

25
- 33748374224
- For the generation of salicylaldehyde by the reaction of arynes with DMF in the presence of water, see:
- B. C. Ranu R. Jana Eur. J. Org. Chem. 2006 3767
- (2006) Eur. J. Org. Chem. , pp. 3767
- Ranu, B.C.¹ Jana, R.²

26
- 50549200091
- S. Yaroslavsky Tetrahedron Lett. 1965 6 1503
- (1965) Tetrahedron Lett. , vol.6 , pp. 1503
- Yaroslavsky, S.¹

27
- 77951914957
- E. Yoshioka S. Kohtani H. Miyabe Org. Lett. 2010 12 1956
- (2010) Org. Lett. , vol.12 , pp. 1956
- Yoshioka, E.¹ Kohtani, S.² Miyabe, H.³

28
- 79952651032
- K. Okuma A. Nojima Y. Nakamura N. Matsunaga N. Nagahora K. Shioji Bull. Chem. Soc. Jpn. 2011 84 328
- (2011) Bull. Chem. Soc. Jpn. , vol.84 , pp. 328
- Okuma, K.¹ Nojima, A.² Nakamura, Y.³ Matsunaga, N.⁴ Nagahora, N.⁵ Shioji, K.⁶

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