{"product_id":"studies-in-natural-products-chemistry-stereoselective-synthesis-9780444893666","title":"Studies in Natural Products Chemistry: Stereoselective Synthesis","description":"\u003cp\u003e • Author(s): Atta-Ur Rahman\u003cbr\u003e • Publisher: Elsevier\u003cbr\u003e • Publisher Imprint: Elsevier\u003cbr\u003e • BISAC: Chemistry - Organic\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003e\u003cp\u003eStudies in Natural Products Chemistry Volume 12: Stereoselective Synthesis (Part H) reviews the stereoselective synthetic and mechanistic chemistry of bicyclomycin. It discusses chemical studies of the taxane diterpenes; the synthetic methodology for 2-amino alcohols of biological interest; and the synthesis and structure of hydroxylated indolizidines. Some of the topics covered in the book are the synthetic routes to the oxahydrindene subunit of the avermectin-milbemycin family of antiparasitic agents; isolation, structure elucidation, biosynthesis, and biological activity of the avermectins; two-stage coupling process of macrolide antibiotics synthesis; and synthesis of the rifamycin S ansa-chain compound. The complete synthesis of erythromycin A is also covered. The role of isocyanides in the synthesis of beta lactam antibiotics and the characteristics of the beta lactam antibiotics are discussed. The development of an A-Ring annulation strategy for taxane synthesis is also presented. A chapter is devoted to the advances in the synthesis of tumor-promoting diterpenes. The book can provide useful information to chemists, biologists, students, and researchers.\u003c\/p\u003e","brand":"Elsevier","offers":[{"title":"Hardcover","offer_id":45309980639383,"sku":"9780444893666","price":5446.0,"currency_code":"INR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0666\/3471\/1191\/files\/9780444893666.webp?v=1769286702","url":"https:\/\/atlanticbooks.com\/products\/studies-in-natural-products-chemistry-stereoselective-synthesis-9780444893666","provider":"Atlantic Books","version":"1.0","type":"link"}