Haku "Methods - Synthesis"

Chattopadhyay, Shital K. - Heterocycles in Natural Product Synthesis, e-kirja

Heterocycles in Natural Product Synthesis

Chattopadhyay, Shital K.

Alk. 180,30€

Filling a gap on the market, this handbook and ready reference is unique in its discussion of the usefulness of various heterocyclic systems in the synthesis of natural products.
Clearly structured for easy access to the information, each chapter is devoted to a certain class of heterocycle,

Chandrasekaran, Srinivasan - Click Reactions in Organic Synthesis, e-kirja

Click Reactions in Organic Synthesis

Chandrasekaran, Srinivasan


The first book on click reactions to focus on organic synthesis, this reference work describes the click concept and underlying mechanisms as well as the main applications in various fields. As such, the chapters cover green chemical synthesis, metal-free

Wang, Meixiang - Multicomponent Reactions in Organic Synthesis, e-kirja

Multicomponent Reactions in Organic Synthesis

Wang, Meixiang


In addition to carbene-promoted MCRs and frequently applied metal-catalyzed MCRs, it also covers recently developed catalytic enantioselective variants as well as MCR in drug discovery and for the synthesis of heterocyclic molecules and macrocycles.
Edited by the

Langer, Peter - Asymmetric Synthesis of Non-Proteinogenic Amino Acids, e-kirja

Asymmetric Synthesis of Non-Proteinogenic Amino Acids

Langer, Peter


Authored by two internationally recognized experts with an excellent track record, this much-needed reference summarizes latest research in the rapidly developing field of stereoselective synthesis of enantiomerically enriched amino acids, particularly of non-proteinogenic origin. It highlights

Bates, Roderick - Organic Synthesis Using Transition Metals, e-kirja

Organic Synthesis Using Transition Metals

Bates, Roderick


Transition metals open up new opportunities for synthesis, because their means of bonding and their reaction mechanisms differ from those of the elements of the s and p blocks. In the last two decades the subject has mushroomed - established reactions are seeing both technical improvements