This unusual collection of 49 essays gives an overview of the trends and accomplishments of synthetic organic chemistry in recent years. Unique in its approach, it deals with almost every aspect of modern synthesis. The first part of the book describes methods and reagents, with particular emphasis on rapidly developing organometallic and biooriented procedures. In the second part, these tools are applied to the syntheses of interesting target compounds and natural compounds with remarkable physiological properties. Mechanistic discussions and retrosynthetic analyses are included. More than 1000 up-to-date references help the reader to pursue the topics highlighted here. This book gives both the active researcher and the advanced student insight into the competitive atmosphere, creativity, and resourcefulness so characteristic of organic synthesis today.

More than 15 years have passed since publication of the last monograph on anthracyclineantibiotics,theACSSymposium Series574,edited byW.Priebe. However, anthracycline antibiotics continue to be one of the most applied antitumor agents, mostly in combination therapy. In addition, a number of exciting new developments such as prodrug development or new synthetic, semi-synthetic, or biosynthetic derivatives have emerged in spite of a certain decrease in synthetic activity. With this background in mind, I accepted the invitation of Prof. J. Thiem to edit an updated collection of reviews on - thracyclineantibiotics. Infact,thistaskturnedouttobeanexciting endeavor andinsteadoftheinitiallyplannedsinglevolume,thenumerouscontributions frommany experts in this exciting ?eld had to be collected into two volumes. Thelast decadehasprovidedamuchgreater amountofnewinformationthen initially anticipated and these volumes represent a condensed review of this data derived fromjournals representing quite different ?elds. The ?rst volume is dedicated to biological occurrence and biosynthesis as well as the synthesis and chemistry of anthracyclines. Since the pioneering review of H.Brockmann on naturally occurring anthracyclines in 1963, no systematic overview has appeared and this volume will provide a review of the latest information. This topic is closely related to biosynthesis and the intriguing progress in biotechnology to produce biosynthetic anthracycline variants is presented. The part of the volume covering synthesis comprises an updated overview on asymmetric synthesis, combinatorial synthesis using the Diels-Alder reaction, synthesis of ?uorinated anthracyclines, the sugar moieties, non-natural glycosyl anthraquinones as DNA binding and pho- cleaving agents, and ?nally of anthracyclines and fredericamycin A via strong base-induced cycloadditionreaction.

This series presents critical reviews of the present position and future trends in modern chemical research. It contains short and concise reports on chemistry, each written by the world renowned experts. The series is still valid and useful after five or ten years. More information as well as the electronic version of the whole content is available at: springerlink.com.

This unusual collection of 49 essays gives an overview of the trends and accomplishments of synthetic organic chemistry in recent years. Unique in its approach, it deals with almost every aspect of modern synthesis. The first part of the book describes methods and reagents, with particular emphasis on rapidly developing organometallic and biooriented procedures. In the second part, these tools are applied to the syntheses of interesting target compounds and natural compounds with remarkable physiological properties. Mechanistic discussions and retrosynthetic analyses are included. More than 1000 up-to-date references help the reader to pursue the topics highlighted here. This book gives both the active researcher and the advanced student insight into the competitive atmosphere, creativity, and resourcefulness so characteristic of organic synthesis today.

More than 15 years have passed since publication of the last monograph on anthracyclineantibiotics,theACSSymposium Series574,edited byW.Priebe. However, anthracycline antibiotics continue to be one of the most applied antitumor agents, mostly in combination therapy. In addition, a number of exciting new developments such as prodrug development or new synthetic, semi-synthetic, or biosynthetic derivatives have emerged in spite of a certain decrease in synthetic activity. With this background in mind, I accepted the invitation of Prof. J. Thiem to edit an updated collection of reviews on - thracyclineantibiotics. Infact,thistaskturnedouttobeanexciting endeavor andinsteadoftheinitiallyplannedsinglevolume,thenumerouscontributions frommany experts in this exciting ?eld had to be collected into two volumes. Thelast decadehasprovidedamuchgreater amountofnewinformationthen initially anticipated and these volumes represent a condensed review of this data derived fromjournals representing quite different ?elds. The ?rst volume is dedicated to biological occurrence and biosynthesis as well as the synthesis and chemistry of anthracyclines. Since the pioneering review of H.Brockmann on naturally occurring anthracyclines in 1963, no systematic overview has appeared and this volume will provide a review of the latest information. This topic is closely related to biosynthesis and the intriguing progress in biotechnology to produce biosynthetic anthracycline variants is presented. The part of the volume covering synthesis comprises an updated overview on asymmetric synthesis, combinatorial synthesis using the Diels-Alder reaction, synthesis of ?uorinated anthracyclines, the sugar moieties, non-natural glycosyl anthraquinones as DNA binding and pho- cleaving agents, and ?nally of anthracyclines and fredericamycin A via strong base-induced cycloadditionreaction.

This series presents critical reviews of the present position and future trends in modern chemical research. It contains short and concise reports on chemistry, each written by the world renowned experts. The series is still valid and useful after five or ten years. More information as well as the electronic version of the whole content is available at: springerlink.com.