Download Comprehensive Organic Name Reactions and Reagents by Zerong Wang PDF

By Zerong Wang

With its assurance of 701 natural identify reactions and reagents, this three-volume set is the biggest, most recent significant reference paintings of its sort. It bargains scholars chemists a helpful source for undertaking experiments and acting a extensive variety of purposes, from prescribed drugs to plastics to insecticides. each one response directory is obviously geared up into uniform sections that permit readers to speedy assemble the knowledge they should behavior their very own experimental procedures

Comprehensive natural identify Reactions and Reagents deals numerous gains that aid readers assemble info speedy and behavior their experiments successfully:

  • Chemical abbreviations checklist the abbreviation, the chemical's complete identify, its constitution, and web page references
  • Schematic response index bargains a short review of every reaction
  • Reaction summaries supply simple information regarding every one identify reaction
  • Reaction sort summaries categorize and arrange all similar identify reactions in response to the kind of transformation (e.g., oxidation, relief, synthesis of alkenes, etc.)

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Extra info for Comprehensive Organic Name Reactions and Reagents

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Am. Chem. , 2002, 124, 8198. (d) Trost, B. ; Probst, G. D. , J. Am. Chem. , 1998, 120, 9228. (e) Trost, B. M. , J. Am. Chem. , 1996, 118, 6625. (f) Johannsen, M. and Jørgensen, K. , J. Org. , 1995, 60, 5757. (g) Trost, B. M. and M¨uller, T. J. , J. Am. Chem. , 1994, 116, 4985. ; Mallakpour, S. E. and Butler, G. , J. Org. , 1985, 50, 4378. 11 Alder-Rickert Reaction A. 1 It is the extension of the Diels-Alder Reaction in which the Diels-Alder cycloadducts extrude the cleavable groups to give even more stable aromatic compounds2 under thermal conditions or in the presence of either acid or base.

2006, 260, 235. (cc) Schramm, O. G. and Mueller, T. J. , Synlett, 2006, 1841. ; Dong, D. ; Zhang, J. , Tetrahedron, 2006, 62, 10111. ; Pehk, T. , Synlett, 2006, 1699. -I. , 2006, 47, 6433. ; Miura, H. , J. Mol. Catal. , 2006, 255, 117. (hh) Li, J. ; Tai, J. R. and Davis, R. , Catal. Today, 2006, 116, 226. -C. , J. Am. Chem. , 2006, 128, 9661. ; Hita, M. del C. , Tetrahedron: Asymmetry, 2006, 17, 1027. (kk) Barrett, C. ; Chheda, J. ; Huber, G. W. and Dumesic, J. , Appl. Catal. , 2006, 66, 111.

And Howell, A. , Org. , 2007, 9, 1699. ; Arseniyadis, S. , Org. , 2007, 9, 1695. (f) Storcken, R. P. ; van Delft, F. ; Broxterman, Q. ; Schoemaker, H. E. and Rutjes, F. P. J. , Adv. Synth. , 2007, 349, 161. (g) Tischer, S. , Adv. Synth. , 2007, 349, 147. (h) Fomine, S. and Tlenkopatchev, M. , J. Organomet. , 2006, 691, 5189. 12. (a) Zhang, X. ; Hsung, R. P. and Li, H. , Chem. , 2007, 2420. (b) Murray, A. ; Parsons, P. J. , Tetrahedron, 2007, 63, 6485. (c) Wojtkielewicz, A. and Morzycki, J. , Steroids, 2007, 72, 552.

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