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Advanced Organic Chemistry:<br />
Reaction Mechanisms<br />
R. Bruckner, Academic Press, Orlando, FL,<br />
2001, 512pp. Hardcover. A best-selling<br />
mechanistic organic chemistry text in<br />
Germany, this text's translation into English<br />
fills a long-existing need for a modern,<br />
thorough, and accessible treatment of<br />
reaction mechanisms for students of organic<br />
chemistry.<br />
Z51,372-5<br />
High-Throughput Synthesis<br />
I. Sucholeiki, Ed., Marcel Dekker, New York,<br />
NY, 2001, 365pp. Hardcover. This reference<br />
text presents how-to methods, novel<br />
materials, and catalyst developments for<br />
creating new compounds. Background<br />
material on combinatorial chemistry is<br />
combined with cookbook-style directions and<br />
detailed case studies that emphasize the<br />
potential for reproducing experiments.<br />
Z51,376-8<br />
Chiral Drugs<br />
C.A. Challener, Ed., Ashgate Publishing Co.,<br />
Burlington, VT, 2001, 672pp. Hardcover. Part<br />
one provides an introduction to the types of<br />
sources and methods currently in use for<br />
obtaining chiral molecules, while part two<br />
gives a comprehensive listing of over 2,500<br />
chiral drugs and includes structures and<br />
physical properties for each entry in the listing.<br />
Z51,357-1<br />
Chiral Intermediates<br />
C.A. Challener, Ed., Ashgate Publishing Co.,<br />
Burlington, VT, 2001, 832pp. Hardcover.<br />
Chiral Intermediates is an invaluable resource<br />
for information on available chiral molecules.<br />
Presents 4,700 commercially available<br />
chiral compounds with structures, physical<br />
properties, applications, manufacturers, and<br />
suppliers for each listing. Indexes, including a<br />
master index of names and synonyms and an<br />
index of custom manufacturing services for<br />
chiral compounds, are appended.<br />
Z51,356-3<br />
Save over 15% when you order both Chiral<br />
Drugs and Chiral Intermediates together!<br />
2-Volume Set<br />
Z51,359-8<br />
From<br />
the<br />
<strong>Aldrich</strong><br />
Bookshelf<br />
Combinatorial Library Design and<br />
Evaluation: Principles, Software Tools,<br />
and Applications in Drug Discovery<br />
A.K. Ghose and V.N. Viswanadhan, Eds.,<br />
Marcel Dekker, New York, NY, 2001, 648pp.<br />
Hardcover. This book traces the latest<br />
advances in rational drug discovery and<br />
combinatorial library design, covering basic<br />
principles, design strategies, methodologies,<br />
software tools and algorithms, and<br />
applications. Specific topics include fast<br />
continuum electrostatics methods for<br />
structure-based ligand design, knowledgebased<br />
approaches for the design of smallmolecule<br />
libraries for drug discovery, relative<br />
and absolute diversity analyses of<br />
combinatorial libraries, and design of<br />
combinatorial libraries that mimic biological<br />
motifs.<br />
Z51,373-3<br />
Fenaroli's Handbook of Flavor<br />
Ingredients<br />
4th ed., G.A. Burdock, CRC Press, Boca<br />
Raton, FL, 2001, 1,864pp. Hardcover. With a<br />
new format and twice the information found in<br />
the third edition, it gives you easy access to<br />
synonyms, international codes, sensory<br />
information, permitted uses of ingredients,<br />
international regulations, and more. The<br />
handbook puts together the "wish lists" of food<br />
scientists, regulatory and safety officers,<br />
pharmacologists, and toxicologists to provide<br />
a one-stop source for both GRAS and non-<br />
GRAS flavoring substances.<br />
Z51,367-9<br />
Crystallization<br />
4th ed., J.W. Mullin, Butterworth-Heinemann,<br />
Stoneham, MA, 2001, 600pp. Hardcover.<br />
Incorporates all the recent developments and<br />
applications of crystallization technology.<br />
Provides clear accounts of underlying<br />
principles, a review of the past and current<br />
research themes, and guidelines for<br />
equipment and process design. This new<br />
edition introduces and enlarges upon such<br />
subjects as: separation of polymorphs and<br />
chiral crystals, micro- and macromixing, and<br />
seeding and secondary nucleation in batch<br />
crystallization processes.<br />
Z51,368-7<br />
The Diels–Alder Reaction: Selected<br />
Practical Methods<br />
F. Fringuelli and A. Taticchi, John Wiley &<br />
Sons, New York, NY, 2002, 350pp. Hardcover.<br />
This is the first book to collect together 70<br />
years worth of experimental procedures that<br />
have been developed to perform the<br />
Diels–Alder reaction. It begins with the<br />
fundamental principles and contains<br />
numerous graphical abstracts to present the<br />
basic concepts in a concise and pictorial way.<br />
Covers theory and synthetic applications of<br />
the experimental methods, and includes<br />
reports on industrial applications.<br />
Z51,385-7<br />
Handbook of Organopalladium<br />
Chemistry for Organic Synthesis<br />
Ei-ichi Negishi, John Wiley & Sons, New York,<br />
NY, 2002, 3,300pp. Hardcover. 2-vol. set. This<br />
handbook is the most comprehensive and<br />
authoritative reference available on organopalladium<br />
reagents and catalysts. The material is<br />
organized according to reaction type, rather<br />
than type of organopalladium compound.<br />
Z51,386-5<br />
Nomenclature of Organic<br />
Compounds: Principles and Practice<br />
2nd ed., R.B. Fox and W.H. Powell, Eds.,<br />
Oxford University Press, New York, NY, 2001,<br />
464pp. Hardcover. The book is divided into<br />
two parts. The first is a general overview of<br />
organic nomenclature, the second uses<br />
concepts from the first part to answer the<br />
question "How do I name this compound?".<br />
Individual chapters are concerned with almost<br />
every class of organic derivative, stressing the<br />
relationship between structure and names.<br />
Z51,355-5<br />
The Nitro Group in Organic Synthesis<br />
N. Ono, John Wiley & Sons, New York, NY,<br />
2001, 392pp. Hardcover. This book focuses<br />
on reactions that proceed under mild<br />
conditions, important functional groups that<br />
can be synthesized by the conversion of nitro<br />
groups, and the stereoselectivity of reactions<br />
of nitro compounds. Emphasizes environmentally<br />
friendly methods for nitration, the<br />
importance of aliphatic nitro compounds, and<br />
modern preparations of nitro compounds.<br />
Z51,365-2<br />
Search, browse, and order books online at www.sigma-aldrich.com/books<br />
Available May<br />
2002!