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From the Back Cover: This book discusses important reactions not usually covered in introductory courses, including pericyclic reactions, formation and reactions of carbenes, migrations to electron-deficient centers, and rearrangements of carbanions and free radicals. It covers symmetry conservation rules and linear free energy relationships.
The text is written in an easily understandable, conversational style and at a level suitable for graduate students or undergraduates who have taken a year-long course in organic chemistry.
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- Strong coverage of heterocyclic chemistry – a vitally important subject not traditionally covered in introductory courses.
- Includes many exercises with a wide range of difficulty — some of which will challenge, and delight, the most talented students.
- Clear explanations of the thought processes involved in proposing mechanisms for complex reactions.
- New chapter on Organophosphorus and Organosulphur Chemistry.
- New chapter on Photochemistry.
Among the rewards I've reaped for having written, Advanced Organic Chemistry: Reactions and Mechanisms, are the conversations and correspondence I've had with the users (or perhaps just perusers) of this text.
I greatly appreciate the contributions from those of you who have taken the time to inform me of misprints in the first edition. (No errors of fact, I'm happy to say.) The publisher and I have tried to correct those errors in later printings.
I'm also grateful for your suggestions of additional subjects to incorporate into the second edition. (I appreciate your faith that there would be a second edition.) Several of you were rightfully indignant that I had skipped so briefly over photochemistry, aside from pericylic photochemical reactions. The complaint is a valid one, and I have tried to make up for the earlier lapse by including a chapter on photochemistry in this edition.
A smaller number of readers offered a suggestion that I had thought of as well: the great and increasing importance of synthetic reagents incorporating phosphorus and sulfur atoms makes a discussion of the mechanisms by which those reagents act imperative. I have therefore added a chapter on those reactions to the text of this edition.
Of course, a principal purpose of a second edition is to bring the subject matter up-to-date. This edition includes material (and many problems) from the literature through the summer of 2002.
I can't really claim that our understanding of organic reaction mechanisms has been revolutionized in the past half-decade, but there have been some fascinating examples of applications of known processes. There have been notable advances in some areas, such as the dehydro Diels-Alder reaction and the Bergman and Meyers-Saito reactions, and in perhaps my favorite example (because of its elegant simplicity), Bakke's demonstration, contradicting a century of experience that pyridime can be easily nitrated in high yield and under mild conditions—provided you know how.
I am looking forward to hearing from you in regard to this latest version of my text. I can be reached at [email protected].
Bernard Miller
Amherst, MA
Amherst, MA
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