PdCl2-promoted reactions of diaryl-substituted methylenecyclopropanes

Dalton Transactions

Volumn 39, Issue 37, 2010, Pages 8829-8834

  Qi, Ming Hui ^a   Shao, Li Xiong ^b   Shi, Min ^a,c  

^a EAST CHINA UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^b WENZHOU UNIVERSITY   (China)

^c SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

DIARYL SUBSTITUENTS; GOOD YIELD; METHYLENECYCLOPROPANES; MILD REACTION CONDITIONS; MINOR PRODUCTS; N ,N-DIMETHYLACETAMIDE; N ,N-DIMETHYLFORMAMIDE; PRESENCE OF WATER; TERMINAL DOUBLE BONDS; TOTAL YIELD; X RAY CRYSTAL STRUCTURES;

CRYSTAL STRUCTURE; DIMETHYLFORMAMIDE; PROPANE;

ORGANIC SOLVENTS;

EID: 77956492343     PISSN: 14779226     EISSN: 14779234     Source Type: Journal    
DOI: 10.1039/c0dt00059k     Document Type: Article

References (34)

1. A. Brandi A. Goti Chem. Rev. 1998 98 589
2. Carbocyclic Three-Membered Ring Compounds, in Houben-Weyl, Vol. E17a-c, (Ed.:, A. de Meijere,), Thieme, Stuttgart, 1996
3. P. Binger H. M. Buech Top. Curr. Chem. 1987 135 77
4. W. A. Donaldson Adv. Met. Org. Chem. 1991 2 269
5. M. Lautens Y. Ren P. Delanghe P. Chiu S. Ma J. Colucci Can. J. Chem. 1995 73 1251
6. I. Nakamura Y. Yamamoto Adv. Synth. Catal. 2002 344 111
7. M. Rubin M. Rubina V. Gevorgyan Chem. Rev. 2007 107 3117
8. L.-X. Shao M. Shi Curr. Org. Chem. 2007 11 1135
9. M. Shi L.-X. Shao B. Xu Org. Lett. 2003 5 579
10. L.-X. Shao M. Shi Adv. Synth. Catal. 2003 345 963
11. M. Shi B. Xu J.-W. Huang Org. Lett. 2004 6 1175
12. L.-X. Shao B. Xu J.-W. Huang M. Shi Chem.-Eur. J. 2006 12 510
13. B. K. Dallas R. P. Hughes J. Organomet. Chem. 1980 184 C67
14. P. R. Clemens R. P. Gughes L. D. Margerum J. Am. Chem. Soc. 1981 103 2428
15. T. A. Albright P. R. Clemens R. P. Hughes D. E. Hunton L. D. Margerum J. Am. Chem. Soc. 1982 104 5369
16. B. K. Dallas R. P. Hughes K. Schumann J. Am. Chem. Soc. 1982 104 5380
17. R. P. Hughes C. S. Day Organometallics 1982 1 1221
18. M. Green R. P. Hughes J. Chem. Soc., Dalton Trans. 1976 1880
19. M. Green R. P. Hughes J. Chem. Soc., Dalton Trans. 1976 1890
20. R. P. Hughes D. E. Hunton K. Schumann J. Organomet. Chem. 1979 169 C37
21. R. Noyori H. Takaya J. Chem. Soc., Chem. Commun. 1969 525
22. Y.-W. Yang X. Huang Synlett 2008 1825
23. M. Shi Y. Chen B. Xu Org. Lett. 2003 5 1225
24. M. Shi B.-Y. Wang J.-W. Huang J. Org. Chem. 2005 70 5606
25. M. Shi L.-P. Liu J. Tang J. Am. Chem. Soc. 2006 128 7430
26. M. Shi B.-Y. Wang Synlett 2006 3158
27. M. Shi B.-Y. Wang L.-X. Shao Synlett 2007 909
28. G.-Q. Tian Z.-L. Yuan Z.-B. Zhu M. Shi Chem. Commun. 2008 2668
29. M. Shi G.-Q. Tian J. Li Tetrahedron 2009 65 3404
30. M. Jiang M. Shi Organometallics 2009 28 5600
31. X.-X. Gu F.-J. Wang M.-H. Qi L.-X. Shao M. Shi Organometallics 2009 28 1569 1574
32. J.-M. Rosset M. P. Glenn J. D. Cotton A. C. Willis C. H. L. Kennard K. A. Byriel B. H. Riches W. Kitching Organometallics 1998 17 1968
33. The crystal data of 3a have been deposited in CCDC with number The crystal data of 4a have been deposited in CCDC with number The crystal data of 3b have been deposited in CCDC with number The crystal data of 6 have been deposited in CCDC with number
34. N. Marion O. Navarro J.-G. Mei E. D. Stevens N. M. Scott S. P. Nolan J. Am. Chem. Soc. 2006 128 4101