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Some six hundred structures of naturally occurring carbogenic molecules appe on the pages which follow, together with the name of each compound and references to the original literature of successful chemical synthesis. Thus, Part Three of this book is effectively a key to the literature of chemical synthesis as applied to the complex molecules of nature. The survey does not include oligomeric or polymeric structures, such as peptides, proteins, carbohydrates and polynucleotides, which fall outside the scope of this book because they can be assembled by repetitive procedures. 

Each question is accompanied by an answer, a paragraph explanation, and a specific page reference to an appropriate textbook. A bibliography listing sources can be found following the last chapter. 

Entries are indicated by volume and page numbers italic numbers indicate volumes numbers that follow colons indicate pages. Page references in bold type indicate primary articles. References followed by t indicate material in tables. 

In the pages which follow, this subject is treated separately for items used for nonmilitary and military purposes. As the subject is very extensive, it is separated into several sections. The references and additional references given at the end of this compilation apply to all sections... 

In summary, although there are no hard and fast rules in the construction of a perfume, there are certain principles that need to be adhered to. We will repeatedly refer to these principles in the pages that follow. 

Note Page numbers followed by f refer to figures, and page numbers followed by f refer to tables. Page numbers in bold type indicate the primary discussion of a topic. 

The Historical Glossary on the following pages refers to Refs. [1-3, 9, 10, 12, 73-83]. No comprehensive description of the history of organometallic chemistry is available as yet. A first review article was published in 1975 by Thayer [69],... 

In the following, parcnthctkal page references are to Wilson <1988). Citations within the cited passages are taken from contemporary records. 

Note The page numbers following each diagnosis refer the reader to the discussion in the text. 

The following tables appeared in previous editions of the CRC Handbook of Chemistry and Physics but have been removed, retitled, or rearranged in subsequent editions. In most cases, some or all of the information contained in the original table has been incorporated, in updated form, in a different table (or tables). In such cases the appropriate page references to the 90th Edition (2009-2010) are given in the last column, and the older table should be considered obsolete. The last edition in which the older table appeared is indicated. 

Therefore, while you study the sample spectra in the pages that follow, take notice of shapes and intensities. They are as important as the frequency at which an absorption occurs, and the eye must be trained to recognize these features. Often, when reading the literature of organic chemistry, you will find absorptions referred to as strong (s), medium (m), weak (w), broad, or sharp. The author is trying to convey some idea of what the peak looks like without actually drawing the spectrum. 

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