Functionalization double bond

A. F. Cockerill and R. G. Harrison, The Chemistry of Double-Bonded Functional Groups, Part 1, S. Patai, ed., John Wiley Sons, New York, 1977, Chapter 4. 

Supplement A The chemistry of double-bonded functional groups (2 parts) Supplement B The chemistry of acid derivatives (2 parts) Supplement C The chemistry of triple-bonded functional groups (2 parts) Supplement D The chemistry of halides, pseudo-halides and azides (2 parts) Supplement E The chemistry of ethers, crown ethers, hydroxyl groups and their sulphur analogues (2 parts)... 

Supplement A The Chemistry of Double-bonded Functional Groups (two parts)... 

For comprehensive reviews of 1,3-dipolar cycloaddition reactions, see R. Huisgen, R. Grashey and J. Sauer in The Chemistry of Alkenes, S. Patai, ed., Interscience London, 1965, pp. 806-878 G. Bianchi, C. DeMicheli, and R. Gandolfi, in The Chemistry of Double Bonded Functional Groups, Part I, Supplement A, S. Patai, ed., Wiley-Interscience, New York, 1977, pp. 369-532 A. Padwa, ed., 1,3-Dipolar Cycloaddition Chemistry, Wiley, New York, 1984. 

Bartok, M., and Molnar, A., Supplement A3 The Chem. of Double-bonded Functional Groups, Patai, S., (Ed.), Wiley, Chichester, 1997, pp. 843-908. 

Marchand, A. P. in Thechemistry of double-bonded functional groups(Patai, S. (ed.)) Suppl. A, Part 1, Chapter 7 Wiley, London (1977)... 

Supplement A The chemistry of double-bonded functional groups (2 volumes, 4 parts) Supplement B The chemistry of acid derivatives (2 volumes, 4 parts)... 

S. Patai (Ed.), The Chemistry of Functional Groups, Supplement A The Chemistry of Double-bonded Functional Groups, Vol.2. (esp. pp.1-52) Wiley, Chichester, 1989 F. Hartley and S. Patai (Eds.), The Chemistry of the Metal-carbon Bond, Wiley, Chichester, 1982 P. A. Cusack, P. J. Smith, J. D. Donaldson and S. M. Grimes, A Bibliography of X-Ray Crystal Structures of Tin Compounds, International Tin Research Institute Publication 588, 1981 Organotin Cluster Chemistry, R. R. Holmes, Acct. Chem. Research, 22, 190 (1989). 

Transition metals can display selectivities for either carbonyls or olefins (Table 20.3). RuCl2(PPh3)3 (24) catalyzes reduction of the C-C double bond function in the presence of a ketone function (Table 20.3, entries 1-3). With this catalyst, reaction rates of the reduction of alkenes are usually higher than for ketones. This is also the case with various iridium catalysts (entries 6-14) and a ruthenium catalyst (entry 15). One of the few transition-metal catalysts that shows good selectivity towards the ketone or aldehyde function is the nickel catalyst (entries 4 and 5). Many other catalysts have never been tested for their selectivity for one particular functional group. 

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