{"text_format":"2","workbook":"xls","n_sheets":1,"sheets":["report2"],"not_rendered":{"charts":0,"images":0,"macros":0,"external_links":1,"defined_names":1,"comments":0,"pivot_tables":0},"unopened":[],"bounds":{"document_bytes":16777216,"sheet_cells":100000,"run_cost":"one","rows_first":2000,"rows_last":500,"rows_between":2000,"halvings":0,"cell_chars":16384,"cell_head_chars":4096},"cells_cut":0,"cells_raw":0,"read":"whole","date_system":"1900","formulas":"cached_only"}

{"sheet":"report2","index":0,"n_rows":28,"n_cols":5,"rows_kept":28,"cut":false,"hidden":false,"merged":[[0,2,0,3],[0,4,0,5],[1,2,1,3],[1,4,1,5],[2,2,2,3],[2,4,2,5],[3,2,3,3],[4,2,4,3],[8,2,8,3],[9,2,9,3],[10,2,10,3],[12,2,12,3],[15,2,15,3],[16,2,16,3],[20,2,20,3]],"flags":["formulas_cached_only"]}
[null,"1.","Record Nr.",null,"UNISA996202135403316"]
[null,null,"Autore",null,"Nógrádi M"]
[null,null,"Titolo",null,"Stereoselective synthesis [[electronic resource] ] : a practical approach / / Mihály Nógrádi ; foreword by A.I. Meyers"]
[null,null,"Pubbl/distr/stampa",null,"Weinheim ; ; New York, : VCH, 1995"]
[null,null,"ISBN",null,"1-281-75874-4"]
[{"$nulls":4},"9786611758745"]
[{"$nulls":4},"3-527-61569-5"]
[{"$nulls":4},"3-527-61568-7"]
[null,null,"Edizione",null,"[2nd, thoroughly rev. and updated ed.]"]
[null,null,"Descrizione fisica",null,"1 online resource (390 p.)"]
[null,null,"Disciplina",null,"541.223"]
[{"$nulls":4},"541.39"]
[null,null,"Soggetti",null,"Stereochemistry"]
[{"$nulls":4},"Stereoisomers"]
[{"$nulls":4},"Organic compounds - Synthesis"]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Description based upon print version of record."]
[null,null,null,"Nota di bibliografia","Includes bibliographical references (p. [315]-358) and index."]
[null,null,"Nota di contenuto",null,"Stereoselective Synthesis; Contents; List of Symbols and Abbreviations; Introduction; 1 General Concepts of Stereoselective Synthesis; 1.1 Principles of Differentiating Molecules; 1.2 Characterization of Stereoisomers. Conformation and Configuration; 1.3 Intramolecular Symmetry. Topicity and Prochirality; 1.4 Selectivity in Chemistry; 1.4.1 Substrate Selectivity; 1.4.1.1 Substrate Diastereoselectivity (Diastereomer Selectivity); 1.4.1.2 Substrate Enantioselectivity (Enantiomer Selectivity). Kinetic Resolution; 1.4.2 Product Selectivity; 1.4.2.1 Formation of Stereoisomers"]
[{"$nulls":4},"1.4.2.2 Conditions Necessary for Stereoselectivity1.4.2.3 Concept of Stereodifferentiation; 1.4.2.4 Methods for Inducing Stereoselectivity; 1.4.3 Stereoselective Synthetic Strategies; 1.4.3.1 Enantioconvergent Synthesis; 1.4.3.2 Selective Preparation of Both Enantiomers from a Single Substrate; 1.5 Kinetics and Thermodynamics of Stereoselective Reactions; 2 Stereoselective Catalytic Reductions; 2.1 Stereoselective Homogeneous Hydrogenations with Rhodium-, Ruthenium- and Iridium-Phosphine Catalysts; 2.1.1 Hydrogenation of Olefinic Bonds; 2.1.1.1 Chiral Phosphorus Containing Ligands"]
[{"$nulls":4},"2.1.2 Enantioselective Catalytic Hydrogenation of Ketones and Imines2.1.3 Diastereoselective Hydrogenations in Homogeneous Phase; 2.2 "]
[{"$nulls":4},"Catalytic Hydrosilylation; 2.3 Heterogeneous Stereoselective Catalytic Hydrogenations; 2.3.1 Enantioselective Heterogeneous Catalytic Hydrogenations; 2.3.2 Diastereoselective Heterogeneous Catalytic Hydrogenations; 3 Stereoselective Non-Catalytic Reductions; 3.1 Enantioselective Reductions; 3.1.1 Chiral Lithium Aluminum Hydrides; 3.1.1.1 Reduction of Carbonyl Groups; 3.1.1.2 Reduction of C=N and C=C Bonds; 3.1.2 Chirally Modified Hydridoborates"]
[{"$nulls":4},"3.1.3 Chiral Boranes and Boronates3.1.4 Enantioselective Reductions with Hydride Transfer from Carbon; 3.1.4.1 Chiral Trialkylboranes; 3.1.4.2 Chiral Metal Alkyls; 3.1.4.3 Chiral Metal Alkoxides; 3.1.4.4 Chiral 1 ,4-Dihydropyridines; 3.1.5 Correlation of Substrate Constitution and Enantioselectivity; 3.2 Diastereoselective Reductions of Carbonyl Groups; 3.2.1 Stereochemistry of Diastereoselective Ketone Reductions; 3.2.2 Practical Aspects of Diastereoselective Ketone Reductions; 4 Stereoselective Oxidations; 4.1 Enantioselective Oxidations; 4.1.1 Epoxidation with Chiral Oxidants"]
[{"$nulls":4},"4.1.2 Oxidations in the Presence of Chiral Catalysts4.2 Diastereoselective Oxidations; 4.2.1 Diastereoselective Epoxidation; 4.2.2 Various Diastereoselective Oxidations; 5 Stereoselective Carbon-Carbon Bond Forming Reactions by Nucleophilic Addition to Carbonyl Groups; 5.1 Addition of Simple Nucleophiles to Carbonyl Compounds; 5.1.1 Enantioselective Additions; 5.1.2 Diastereoselective Additions; 5.1.3 Additions to C=N Bonds; 5.2 Additions Involving Allylmetal and Allylboron Compounds; 5.2.1 General Aspects of Allylmetal Addition; 5.2.2 Addition of Allylboron Compounds"]
[{"$nulls":4},"5.2.3 Addition of Allyltitanium Compounds"]
[null,null,null,"Sommario/riassunto","The state-of-the-art in stereoselective synthesis!Thoroughly revised and updated, this enlarged second edition offers a plethora of valuable information on methods and reagents in stereoselective synthesis. Methods have been selected for high efficiency and selectivity; mechanistic aspects are treated succinctly, with a strong emphasis on practical applications. For this new edition, material has been added on* homogeneous diastereoselective hydrogenations* enantioselective oxidations* novel, efficient chiral auxiliariesMuch of the information given is presented in figu"]