{"product_id":"9783527348312","title":"Amide Bond Activation Concepts and Reactions","description":"\u003ch1\u003eAmide Bond Activation\u003c\/h1\u003e\u003ch2\u003eConcepts and Reactions\u003c\/h2\u003e\u003ch3\u003eMichal Szostak\u003c\/h3\u003e\u003cdiv\u003e\u003cb\u003eScience \/ Chemistry \/ Organic\u003c\/b\u003e\u003c\/div\u003e\u003cbr\u003e\u003cdiv\u003e\n\u003cb\u003eAmide Bond Activation\u003c\/b\u003e \u003cp\u003e\u003cb\u003eComprehensive resource on the pivotal role of the amide bond in organic synthesis\u003c\/b\u003e \u003c\/p\u003e\n\u003cp\u003eThis book provides the reader with insight into the advances that have taken place in the field of amide bond activation. It focuses on both the fundamental structural properties of the amide bond and the synthetic reactions mediated by transition-metals. \u003c\/p\u003e\n\u003cp\u003eBy discussing amide bond activation in terms of modern organic synthesis, the reader is provided with a thorough overview of the area and its crucial role in forging carbon-carbon and carbon-heteroatom bonds. Sample topics discussed within the work include: \u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e Cross-coupling of amides\u003c\/li\u003e \u003cli\u003e Amide bond activation by twisting and nitrogen pyramidalization\u003c\/li\u003e \u003cli\u003e Electrophilic amide bond functionalization\u003c\/li\u003e \u003cli\u003e Transition metal-catalyzed radical reactions of amides\u003c\/li\u003e \u003cli\u003e Amide bond esterification, hydrolysis and transamidation\u003c\/li\u003e \u003cli\u003e Classical bridged lactams and anomeric amides\u003c\/li\u003e \u003cli\u003e Computational studies of amide C-N bond activation\u003c\/li\u003e \u003cli\u003eCross-coupling of esters by C-O activation\u003c\/li\u003e\n\u003c\/ul\u003e \u003cp\u003eThe book is immensely valuable to synthetic chemists in academia and the pharmaceutical industry who wish to gain an in-depth understanding of the concept of amide bond activation.\u003c\/p\u003e\n\u003c\/div\u003e\u003cdiv\u003e  \u003cp\u003e\u003ci\u003e\u003cb\u003eMichal Szostak\u003c\/b\u003e is currently a Professor of Chemistry at Rutgers University, Newark, USA. He received his Ph.D. from the University of Kansas (USA) with Prof. Jeffrey Aubé in 2009. After postdoctoral stints at Princeton University (USA) with Prof. David MacMillan and at the University of Manchester (UK) with Prof. David Procter, in 2014, he joined the faculty at Rutgers University. His research group is focused on the development of new synthetic methodology based on transition-metal-catalysis, amide bond activation, conformational preferences of amides, transition-metal-mediated free-radical chemistry, C-H activation, and application to the synthesis of biologically-active molecules. \u003c\/i\u003e \u003c\/p\u003e\n\u003c\/div\u003e\u003cbr\u003e\u003ctable\u003e\n\u003ctr\u003e\n\u003ctd\u003ePublication Date: \u003c\/td\u003e\n\u003ctd\u003e17 October 2022\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003ePublisher: \u003c\/td\u003e\n\u003ctd\u003eWiley\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eImprint: \u003c\/td\u003e\n\u003ctd\u003eWiley-VCH\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eISBN-13: \u003c\/td\u003e\n\u003ctd\u003e9783527348312\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eFormat: \u003c\/td\u003e\n\u003ctd\u003eHardback\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003ePage Count: \u003c\/td\u003e\n\u003ctd\u003e528\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eWeight (oz): \u003c\/td\u003e\n\u003ctd\u003e32.0\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/table\u003e","brand":"Wiley","offers":[{"title":"Default Title","offer_id":44315753971852,"sku":"9783527348312","price":189.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0710\/9545\/1788\/files\/9783527348312.jpg?v=1780617535","url":"https:\/\/fh90cf-fv.myshopify.com\/products\/9783527348312","provider":"Late Knight Books and Services, LLC","version":"1.0","type":"link"}