Textbooks, of Organic

Basic Organic Chemistry , J. M. Tedder, A. Nechvatal, and others, Wiley, 5 volumes 1966-1976. A complete textbook of organic chemistry. Explains all the reactions used in the programme and describes many syntheses in detail. 

A. Gero, Textbook of Organic Chemist, ]ohxi Wiley Sons, Inc., New York, 1963. 

L. E. Eiesei and M. Eiesei, Textbook of Organic Chemistry, D. C. Heath, Boston, Mass., 1950. 

Tiwari, K.S., and Vishmoi, S.N. (1999J A Textbook of Organic Chemistry, Sangam Books. 

Thus Ph3P=CH2 is triphenylphosphonium methylide (see pp. 274-304 of reference 2, or textbooks of organic chemistry for a fuller treatment of the Wittig reaction). 

One of the most popular of the semi-empirical LCAO methods is that of Hfickel. It is applicable to planar molecules which have n -electron systems. The delocalization of these systems, as treated by this method, has particular chemical significance. The traditional application is to the benzene molecule. Historically, different structures of this molecule were suggested by K6kuI6+ and by Dewar that are described in virtually all textbooks of organic chemistry. These structures represented the first efforts to represent the delocalization of the 3r orbitals in such systems. In the present context the delocalization can be better specified with the use of the method of Hilckel. 

Beale JM Jr (2004) Antibacterial antibiotics. In Block JH, Beale JM Jr (eds) Wilson and Gisvold s textbook of organic medicinal and pharmaceutical chemistry, 11th edn. Lippincott, Williams Wilkins, Philadelphia p 299... 

Textbook of Organic Medicinal and Pharmaceutical Chemistry", Lippincott, Philadelphia, 1966, pp. 4-64... 

In this book, rather than producing a textbook of organic chemistry, we hope to be able to show the science and art of organic chemistry in action. 

Almost every elementary textbook of organic chemistry provides a systematic description of properties of functional groups and their characteristic reactivity for example,... 

At first glance, there appear to be an infinite number of different chemical reactions, all of which will have to be remembered. A cursory look through any textbook of organic chemistry does little to dispel this fear. However, the beauty and strength of... 

Optical isomerism is the result of a dissymmetry in molecular suhstitution. The basic aspects of optical isomerism are discussed in various textbooks of organic chemistry. Optical isomers (enantiomers) may have different physiological activities from each other provided that their interaction with a receptor or some other effector structure involves the asymmetric carbon atom of the enantiomeric molecule and that the three different substituents on this carbon atom interact with the receptor. The Easson-Stedman hypothesis assumes that a three-point interaction ensures stereospecificity, since only one of the enantiomers will fit the other one is capable of a two-point attachment only, as shown in figure 1.13 for the reaction with a hypothetical planar receptor. However, it is reasonable to assume that receptor stereospecificity can also undergo a change when the receptor conformation is altered by a receptor-drug interaction. 

J. N. Delgado, W. A. Remers (1998). Wilson and Gisvold s Textbook of Organic, Medicinal and Pharmaceutical Chemistry, 10th ed. New York Lippincott, Williams and Wilkins. 

Only a couple of weeks later, the first two of a large number of other researchers, J.F. Norris and W.W. Sanders, made their views on Gomberg s discovery public," and Gomberg soon found himself embroiled in a lively discussion of his proposal. Over a period of 15 years, he published some 30 papers in defense of the free radical concept, and in the end it prevailed. He has since been quoted as the discoverer of the first free radical in almost every textbook of organic chemistry and, in retrospect, one can see this discovery as one of the most important in 20th century chemistry, theoretically as well as practically. 

Reusch, William. Virtual Textbook of Organic Chemistry, 1999 A comprehensive online text of organic chemistry. 

Methanediamine (NH2CH2NH2) is hardly mentioned in standard textbooks of organic chemistry and at least one casts doubts on its existence. Despite this, salts of the diamine are quite stable and easily prepared (equation l).149150 The potential of this diamine to act as a ligand has yet to be exploited. 

Most textbooks of organic chemistry include sections introducing pericyclic reactions. Earlier textbooks specifically covering pericyclic reactions are T. L. Gilchrist and R. C. Storr, Organic Reactions and Orbital Symmetry, CUP, Cambridge, 2nd Edn., 1979 A. P. Marchand and R. E. Lehr, Orbital Symmetry, Academic Press, New York, 1972. 

This technique, called bromine titration method , was extensively used by K.H. Meyer in the early twentieth century.18 It was later extended to determine the enol content of simple ketones using faster flow methods combined with more sensitive potentiometric measurements of bromine uptake, but this technique sometimes produced apparent enol contents that were far too high, such as the enol content of acetone of 2.5 x 10 4% that is frequently quoted in older textbooks of organic chemistry. The excessive values so obtained have been attributed to the presence of small amounts of impurities reacting with bromine. 

The Sn2 reaction involves the attack of a nucleophile from the side opposite the leaving group and proceeds with exclusive inversion of configuration in a concerted manner. In contrast to the popular bimolecular nucleophilic substitution at the aliphatic carbon atom, the SN2 reaction at the vinylic carbon atom has been considered to be a high-energy pathway. Textbooks of organic chemistry reject this mechanism on steric grounds [175]. 

Let us take a look at the back cover of Cram and Hammond s Textbook of organic chemistry, where a number of dream molecules are depicted. Truncated tetra-hedrane, or heptacyclo[5.5.0.02 12.03 5.041. 06 8.0911]dodecane, C12Hi2 (2) appears to offer a possibility of its cyclopropane bonds with high p-character to interact over the surface of the molecule. Structure 2 has eight faces and is formally obtained by truncating four vertices of tetrahedron (3) it is also the target of synthesis by several research groups (Woodward 1970). 

P. Karrer, Lehrbuch der organischen Chemie [Textbook of Organic Chemistry], 9th Ed., Thieme, Leipzig, 1943 pp. 610-612. . Houben-Weyl, Methoden der organischen Chemie [Methods of Organic Chemistry], 4th Ed., Vol. VII/3b, Chinone [Quinones], Part II (1979). 

Reusch, W. (1999). Virtual Textbook of Organic Chemistry Visible and Ultraviolet Spectroscopy. http //www.cem.msu.edU/ reusch/VirtualText/Spectrpy/UV-Vis/spectrum.htm uvl. Accessed April 22, 2009. 

---