Unusual catalysis with nickel(0) complexes

Journal of the Chemical Society, Chemical Communications

Volumn , Issue 5, 1973, Pages 157-158

  De Pasquale, Ralph J ^a,b  

^a SHELL GLOBAL SOLUTIONS INTERNATIONAL B V   (United States)

^b PCR Inc ^*

Author keywords

[No Author keywords available]

Indexed keywords

EID: 37049131440     PISSN: 00224936     EISSN: None     Source Type: Journal    
DOI: 10.1039/C39730000157     Document Type: Article

References (16)

1. G. P. Chuisoli and L. Cassar, Angew. Chem. Internat. Edn., 1967, 6, 124.
2. P. Heimbach, P. W. Jolly, and G. Wilke, Adv. Organometallic Chem., 1970, 8, 48.
3. G. C. Bailey, Catalysis Rev., 1969, 3, 37.
4. J. P. Candlin, A. W. Parkins, and K. A. Taylor, Ann. Reports, 1970, 67B, 314.
5. transition-metal catalysis with aldehydes and ketones, P. Heimbach, P. W. Jolly, and G. Wilke, Adv. Organometallic Chem., 1970, 8, p. 39.
6. for transition-metal epoxide activation see E. J. Corey and M. F. Semmelhack, J. Amer. Chem. Soc., 1967, 89, 2755.
7. A. J. Chalk, Chem. Comm., 1970, 847.
8. S. Fukuoka, M. Ryang, and S. Tsutsumi, J. Org. Chem., 1970, 35, 3184.
9. The nickel(O) complexes were prepared by the sodium amalgam reduction of the corresponding bis-tertiary-phosphinenickel dihalide complexes.
10. R. J. De Pasquale, J. Organometallic Chem., 1971, 32, 381.
11. P. P. McClellan, U.S.P. 1959, 2, 873, 282 (Chem. Abs., 1959, 15987i).
12. A. L. Shapiro, S. Z. Levin, and V. P. Chekhovskaya, Zhur. org. Khim., 1968, 4, 2065, and references cited therein.
13. Similar transition-metal-carbon dioxide complexes have been isolated.
14. P. W. Jolly, K. Jonas, C. Krüger, and Y. H. Tsay, J. Organometallic Chem., 1971, 33, 109.
15. G. G. Aleksandrov, Yu. T. Struckhov, and M. E. Vol’pin, Chem. Comm., 1971, 972. Intermediates (I)-(III) might be zwitterions.
16. H. Ulrich, ‘Cycloaddition Reactions of Heterocumulenes,’ Academic Press, New York, London, 1967.