By Noboru Ono
The main worthwhile reactions of organonitro compounds in natural synthesis Compounds containing nitro teams are valuable intermediates for the synthesis of usual items and different complicated natural molecules. The Nitro team in natural Synthesis specializes in reactions that continue less than light stipulations, vital practical teams that may be synthesized through conversion of nitro teams, and the stereoselectivity of reactions of nitro compounds. those matters are of serious significance to working towards researchers in latest pharmaceutical, agrochemical, and wonderful chemical industries. The Nitro staff in natural Synthesis additionally emphasizes environmentally-friendly equipment for nitration, the significance of aliphatic nitro compounds, and smooth coaching of nitro compounds. different subject matters mentioned comprise:
- Henry reaction
- Asymmetric Michael addition
- Alkylation, acylation, halogenation, and comparable reactions of RNO2
- Substitution and removing of NO2 and RNO2 The Nitro staff in natural Synthesis is an invaluable source for researchers and scholars in natural and medicinal chemistry.
Read or Download The Nitro Group in Organic Synthesis PDF
Similar organic chemistry books
HardPress vintage Books sequence
Derived from the popular, Encyclopedia of Reagents for natural Synthesis (EROS), the comparable editors have created a brand new guide which makes a speciality of chiral reagents utilized in uneven synthesis and is designed for the chemist on the bench. This new guide follows an identical structure because the Encyclopedia, together with an creation and an alphabetical association of the reagents.
- Semimicro and macro organic chemistry;: A laboratory manual
- Introduction to Organic Chemistry (5th Edition)
- Oxidation and antioxidants in organic chemistry and biology
- Organic Syntheses An annual publication of satisfactory methods
Extra resources for The Nitro Group in Organic Synthesis
Segnitz. 10/1 ed. by E. Mulleer, George Thieme Verlag, Stutttgart, 1969, p, 310. 38c. Coomers, R. G. In Comprehensive Organic Chemistry, Vol. 2 ed. by I. O. Sutherland, Pergamon Press, Oxford, p. 326 (1979). 38d. Feuer, H. The Chemistry of Amino, Nitroso and Nitro Compounds and Their Derivatives, Supplemental F; . ed. by S. Patai, John Wiley and Sons; New York, 1982, p. 805848. 39a. , and J. P. Lawrence. J. Org. , 37, 3662 (1972). 39b. , and H. Friedman. J. Org. , 40, 187 (1975). 40a. , J. W. Shepherd, and C.
Org. , 61, 9097 (1996). 100. Evans, D. , D. H. B. Ripin, D. Halstead, and K. R. Campos. J. Am. Chem. , 121, 6816 (1999). 101. Grossman, R. , R. H. Rasne, and B. O. Patrick. J. Org. , 64, 7173 (1999). 102. , T. Eguichi, H. Uno, and N. Ono. J. Org. , 64, 6518 (1999). 103. , G. Bisica, and G. Rafaiani. Helv. Chim. Acta, 78, 879 (1995). 104. , N. Kumagai, K. Uotsu, T. Oshima, and M. Shibasaki. , 41, 509 (2000). 105. , S. Saito, and J. Kumanotani. Chem. , 1677 (1981). 106. Schneider, H. , and R. Busch.
Chem. , 74, 3052 (1952). 49e. Bordwell, F. , and E. W. Garbisch, Jr. J. Am. Chem. , 82, 3588 (1960). 50. Borisenko, A. A. , V. Nikulin, S. Wolfe, N. S. Zefirov, and Z. V. Zyk. J. Am Chem. , 106, 1074 (1984). 51. McMurray, J. , J. H. Musser, I. Fleming, J. Fortunak and C. Nubling. Org. Synth. Coll. 6, 799 (1988). 52. Seifert, W. K. Org. Synth. Coll. Vol. 6, 837 (1988). 53a. , E. Hata, and T. Yamada. Chem. , 1395 (1995). 53b. , T. Yamada, and T. Mukaiyama. Bull. Chem. Soc. , 68, 3269 (1995). 54. , R.
The Nitro Group in Organic Synthesis by Noboru Ono