A convenient new method to construct 1-alkynyl cyclopropanol and its synthetic application to prepare trisubstituted dienones

Tetrahedron Letters

Volumn 49, Issue 19, 2008, Pages 3124-3128

  An, Yan ^a   Liu, Jie ^a   Jiang, Hai Ying ^a   Wang, Yahui ^a   Chen, Zili ^a  

^a RENMIN UNIVERSITY OF CHINA   (China)

Author keywords

1 Alkynyl cyclopropanol; Cyclopropanone surrogate; Dienone; Palladium catalyzed process

Indexed keywords

1 ALKYNYL CYCLOPROPANOL; 1 ARYLSULFNYL CYCLOPROPANOL; 1 TOLUEN SULFONYL CYCLOPROPANOL; ALKADIENE; ARYL IODIDE; CYCLOPROPANE DERIVATIVE; IODINE DERIVATIVE; IODOBENZENE; LITHIUM ALKYNYLIDE; LITHIUM DERIVATIVE; PALLADIUM; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; SUBSTITUTION REACTION; SYNTHESIS;

EID: 41649089261     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.03.041     Document Type: Article

References (19)

1. De Puy C.H. Acc. Chem. Res. 1 (1968) 33
2. Gibson D.H., and De Puy C.H. Chem. Rev. 74 (1974) 605
3. Conia J.M., and Robson M.J. Angew. Chem. 87 (1975) 505
4. Conia J.M., and Robson M.J. Angew. Chem., Int. Ed. Engl. 14 (1975) 473
5. Salaün J. Top. Curr. Chem. 144 (1988) 1
6. Salaün J. In: Rappoport Z. (Ed). The Chemistry of the Cyclopropyl Group (1987), Wiley, London 809
7. Salaün J. Chem. Rev. 89 (1989) 1247
8. Kulinkovich O.G. Pol. J. Chem. 71 (1997) 849
9. Liu H.-U., and Walsh C.T. In: Rappoport Z. (Ed). The Chemistry of the Cyclopropyl Group (1987), Wiley, London 959
10. Salaün J., and Baird M.S. Curr. Med. Chem. 2 (1995) 511
11. Salaün J. Top. Curr. Chem. 207 (2000) 1
12. Iwasawa N., Matsuo T., Iwamoto M., and Ikeno T. J. Am. Chem. Soc. 120 (1998) 3903
13. Salaün J., Bennani F., Compain J.-C., Fadel A., and Oliver J. J. Org. Chem. 45 (1980) 4129
14. Markham J.P., Staben S.T., and Toste F.D. J. Am. Chem. Soc. 127 (2005) 9708
15. Liu J., An Y., Jiang H.-Y., and Chen Z. Tetrahedron Lett. 49 (2008) 490
16. +, 25), 129 (100), 115 (27), 103 (11), 78 (28), 55 (21).
17. The initial reaction condition was adopted from. Tian Q., and Larock R.C. Org. Lett. 2 (2000) 3329
18. The product in this condition is {A figure is presented}
19. 18O: 310.1358; found: 310.1352.