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Paperback. Demonstrates the wide scope of cycloaddition reactions, including the Diels-Alder reaction, the ene reaction, 1,3-dipolar cycloadditions and [2]2] cycloadditions in organic synthesis. The author, a leading exponent of the subject, illustrates the ways in which they can be employed in the synthesis of a wide range of carbocyclic and heterocyclic compounds, including a variety of natural products of various types. Special attention is given to intramolecular reactions, which often provide a rapid and efficient route to polycyclic compounds, and to the stereochemistry of the reactions, including recent and developing work on enantioselective synthesis.
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Steven Dornacker
reviewed Enantioselective synthesis of tetracyclic quassinoid intermediates via a diene transmissive diels-alder strategy on April 09, 2014
Enantioselective synthesis of tetracyclic quassinoid intermediates via a diene transmissive diels-al
It took me 21 months to read this third volume. When Maupin comes up with a totally unbelievable plot line involving a resurrected Jim Jones, his kidnapping of two four-year-old children from an Alaskan cruise and then perhaps through Little Diomedes (a US island) to Big Diomedes (a Russian island) and then on to Nome which is "over eleven hundred miles from here [Diomedes]" Mary Ann says, right off the top of her head, the last half of this volume turns into a ridiculously thriller. And not even a drug-induced one via Mrs. Mardigal's magical backyard plants! Finally, Maupin returns to form by having Jon (Micheal's ex-doctor/lover) show up at 28 Barbary Lane while Father Paddy and Officer Rivera enjoy an afternoon delight behind park shrubbery. I'll read the rest of this series but I hope Maupin sticks to what he does best: love, sex, and lovesexdrugsdisco in San Francisco of the 1980s.
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