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Sanini$c1 v.$d GRB NAR II 41$e GR 0000034975 B 1 v.$fT $h20120313$i20120313 977 $a 56$a 63$a 75$a AP$a CZ$a GR 996 $aMoneta di ferro$91485697 997 $aUNISANNIO LEADER 03437nam 2200601 a 450 001 9910461489703321 005 20210916150752.0 010 $a1-280-58131-X 010 $a9786613611093 010 $a0-12-415884-6 035 $a(CKB)2670000000147354 035 $a(EBL)872587 035 $a(OCoLC)781260639 035 $a(SSID)ssj0000629765 035 $a(PQKBManifestationID)12266045 035 $a(PQKBTitleCode)TC0000629765 035 $a(PQKBWorkID)10743058 035 $a(PQKB)11604290 035 $a(MiAaPQ)EBC872587 035 $a(PPN)170607178 035 $a(Au-PeEL)EBL872587 035 $a(CaPaEBR)ebr10537915 035 $a(CaONFJC)MIL361109 035 $a(EXLCZ)992670000000147354 100 $a20010606d2011 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aOrganic synthesis$b[electronic resource] /$fMichael B. Smith 205 $a3rd ed. 210 $a[Boston] $cAcademic Press, an imprint of Elsevier$d[2011] 215 $a1 online resource (1536 p.) 300 $aDescription based upon print version of record. 311 $a1-890661-40-6 320 $aIncludes bibliographical references and indexes. 327 $aFront Cover; Organic Synthesis; Copyright Page; About the Author; Table of Contents; Preface to the 3rd edition; Preface to the 1st edition. Why I wrote this book!; Common Abbreviations; Chapter 1: Retrosynthesis, Stereochemistry, and Conformations; 1.1. Introduction; 1.2. The Disconnection Protocol; 1.3. Bond Proximity and Implications for Chemical Reactions; 1.4. Stereochemistry; 1.5. Conformations; 1.6. Conclusion; Homework; Chapter 2: Acids, Bases and Functional Group Exchange Reactions; 2.1. Introduction; 2.2. Brønsted-Lowry Acids and Bases; 2.3. Lewis Acids 327 $a4.6. Borane, Aluminum Hydride, and Derivatives4.7. Stereoselectivity in Reductions; 4.8. Catalytic Hydrogenation; 4.9. Dissolving Metal Reductions; 4.10. Nonmetallic Reducing Agents; 4.11. Conclusion; Homework; Chapter 5 : Hydroboration; 5.1. Introduction; 5.2. Preparation of Alkyl and Alkenyl Boranes; 5.3. Synthetic Transformations; 5.4. Formation of Oxygen-Containing Functional Groups; 5.5. Amines and Sulfides via Hydroboration; 5.6. Conclusion; Homework; Chapter 6 : Stereocontrol and Ring Formation; 6.1. Introduction; 6.2. Stereocontrol in AcyclIc Systems 327 $a8.5. OrganoLithium Reagents (C-Li) 330 $aA reactions oriented course is a staple of most graduate organic programs, and synthesis is taught either as a part of that course or as a special topic. Ideally, the incoming student is an organic major, who has a good working knowledge of basic reactions, stereochemistry and conformational principles. In fact, however, many (often most) of the students in a first year graduate level organic course have deficiencies in their undergraduate work, are not organic majors and are not synthetically inclined. 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