An informative look at the intricacies of today's drug development
process
Once a discovery organization has identified a potential new
drug candidate, it is the daunting task of synthetic organic
chemists to identify the chemical process suitable for preparation
of this compound in a highly regulated environment. Only through a
multi-layered chemical process that takes into account such factors
as safety, environmental considerations, freedom to operate and
cost-effectiveness can researchers begin to refine the drug in
terms of quality and yield.
This book covers both recent advances in the design and
synthesis of new drugs, as well as the myriad other issues facing a
new drug candidate as it moves through the development process.
Utilizing recent case studies, the authors provide valuable
insights into the complexities of the process, from designing new
synthetic methodologies and applying new automated techniques for
finding optimal reaction conditions to selecting the final drug
form and formulation.
Both novice and active researchers will appreciate the inclusion
of chapters on such diverse topics as: Cross-coupling methods
Asymmetric synthesis Automation Chemical Engineering Application of
radioisotopes Final form selection Formulations Intellectual
property
A wealth of real-world examples and contributions from leading
process scientists, engineers, and related professionals make this
book a valuable addition to the scientific literature.
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