{"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":27,"n_cols":5,"rows_kept":27,"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],[15,2,15,3],[16,2,16,3],[19,2,19,3]],"flags":["formulas_cached_only"]}
[null,"1.","Record Nr.",null,"UNINA9910133857603321"]
[null,null,"Autore",null,"Christmann Mathias"]
[null,null,"Titolo",null,"Asymmetric Synthesis II [[electronic resource] ] : More Methods and Applications"]
[null,null,"Pubbl/distr/stampa",null,"Weinheim, : Wiley, 2013"]
[null,null,"ISBN",null,"3-527-65223-X"]
[{"$nulls":4},"3-527-65225-6"]
[{"$nulls":4},"1-299-47604-X"]
[{"$nulls":4},"3-527-65226-4"]
[null,null,"Descrizione fisica",null,"1 online resource (432 p.)"]
[null,null,"Disciplina",null,"541.39"]
[null,null,"Soggetti",null,"Asymmetric synthesis"]
[{"$nulls":4},"Chemistry"]
[{"$nulls":4},"Physical Sciences & Mathematics"]
[{"$nulls":4},"Organic Chemistry"]
[{"$nulls":4},"Electronic books."]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Description based upon print version of record."]
[null,null,"Nota di contenuto",null,"Asymmetric Synthesis; Contents; List of Contributors; 1 Catalytic Enantioselective Alkylation of Prochiral Ketone Enolates; Background; Strategy and Results; Asymmetric Allylic Alkylation in Total Synthesis; Conclusions; CV of Corey M. Reeves; CV of Brian M. Stoltz; References; 2 Point-to-Planar Chirality Transfer in Total Synthesis: Scalable and Programmable Synthesis of Haouamine A and Its Atropisomer; Introduction; Synthetic Strategy Featuring Point-to-Planar Chirality Transfer; Programmable Synthesis of Haouamine A and Its Atropisomer; CV of Noah Z. Burns; CV of Phil S. Baran; References"]
[{"$nulls":4},"3 Tethered AminohydroxylationIntroduction and Background; Tethered Aminohydroxylation; a) First Generation of Reoxidants; b) N-Sulfonyloxy Carbamates; c) Carbonyloxycarbamates as Reoxidants for Osmium; Amide-Based Reoxidants; Evidence for the Mechanism of the TA Reaction; Applications in Organic Synthesis; Conclusion and Future Work; CV of Timothy J. Donohoe; CV of Stefanie Mesch; References; 4 Organocatalyzed Transformations of a, b-Unsaturated Carbonyl Compounds through Iminium Ion Intermediates; CV of Nicholas C. O. Tomkinson; CV of Julian H. Rowley; References"]
[{"$nulls":4},"5 The Renaissance of Silicon-Stereogenic Silanes: A Personal "]
[{"$nulls":4},"AccountBackground; Results; a) Intermolecular Chirality Transfer from Silicon to Carbon: Diastereoselective Palladium(II)-Catalyzed C-Si Bond Formation; b) Silicon-Stereogenic Silane as Stereochemical Probe: B(C6F5)3-Catalyzed Carbonyl Reduction; c) Kinetic Resolution with Silicon-Stereogenic Silanes: Cu-H-Catalyzed Diastereoselective Si-O Coupling; Conclusion; CV of Martin Oestreich; CV of Andreas Weickgenannt; References; 6 Asymmetric Dienamine Activation; Introduction; Historic Background; Results; Conclusion"]
[{"$nulls":4},"CV of Mathias ChristmannReferences; 7 Asymmetric Brønsted Acid Catalysis; Introduction and Background; Strategy; Results; Summary; CV of Iuliana Atodiresei; CV of Uxue Uria; CV of Magnus Rueping; References; 8 Quaternary Stereogenic Centers by Enantioselective b-Carbon Eliminations from tert-Cyclobutanols; Background; Objective: Enantioselective Formation of Quaternary Stereogenic Centers in Combination with Reactive Alkyl-Rhodium Intermediates; Selective Generation of the Alkyl-Rhodium Species and Its Downstream Reactivities; CV of Nicolai Cramer; CV of Tobias Seiser; References"]
[{"$nulls":4},"9 Total Synthesis of Oseltamivir and ABT-341 Using One-Pot TechnologyIntroduction; Results; a) Total Synthesis of (-)-Oseltamivir via Two One-Pot Processes; b) Total Synthesis of ABT-341 by One-Pot Sequence; Conclusions; CV of Yujiro Hayashi; CV of Hayato Ishikawa; References; 10 Enantioselective Annulations with Chiral N-Mesityl N-Heterocyclic Carbenes; Introduction; Catalytic Generation of Chiral Enolate Equivalents; Catalytic Generation of Homoenolate Equivalents; Enantioselective Cascade Reactions Catalyzed by Chiral N-Heterocyclic Carbenes"]
[{"$nulls":4},"Catalytic Annulations via a, b-Unsaturated Acyl Azoliums"]
[null,null,null,"Sommario/riassunto","Continuing the proven and successful concept of the well-received textbook \"\"Asymmetric Synthesis - The Essentials\"\", this is a brief and timely update on the latest developments in asymmetric synthesis and selected applications in natural product synthesis, chemical industry and materials science. As such, it covers a broad range of topics in all important areas, including metal catalysis, organocatalysis, physical organic chemistry, and analytical chemistry.Each contribution is similarly structured, while the short biographies of the experts are a useful tool for students selecting t"]