دانلود کتاب سنتز آلی مدرن زوایفل ویرایش 1

Modern Organic Synthesis 1st Edition George S. Zweifel کتاب سنتز آلی مدرن ویرایش 1 کتاب سنتز آلی مدرن زوایفل ویرایش 1 اول Modern Organic Synthesis 1st Edition تالیف و نوشته George S. Zweifel , Michael H. Nantz از کتاب های تخصصی شیمی آلی که به بررسی و ارائه انواع روش و متدهای سنتز آلی مدرن پرداخته است . این کتاب توسط انتشارات Freeman به چاپ رسیده است و یکی از کتاب های پر طرفدار در زمینه سنتز آلی در بین دانشجویان و اساتید شیمی به حساب می آید.

مشخصات کتاب

• عنوان انگلیسی:  Modern Organic Synthesis
• عنوان فارسی : سنتز آلی مدرن
• فرمت فایل: PDF
• حجم فایل فشرده:  24 مگابایت
• ویرایش: 1
• سال انتشار: March 17, 2007
• زبان نوشتاری: انگلیسی
• شابک: 0716772663, 9780716772668
• نویسنده(ها):  George S. Zweifel | Michael H. Nantz
• تعداد صفحات: 486 صفحه
• تعداد فصل ها: 9 فصل
• نحوه دریافت : دریافت فوری و آنی لینک دانلود فایل بعد از پرداخت

فهرست مطالب و عناوین فصل های کتاب

• Synthetic Design
• 1.1 Retrosynthetic Analysis
• 1.2 Reversal of the Carbonyl Group Polarity (Umpolung)
• 1.3 Steps in Planning a Synthesis
• 1.4 Choice of SyntheticMethod
• 1.5 Domino Reactions (Cascade or Tandem Reactions)
• 1.6 Computer-Assisted Retrosynthetic Analysis
• References
• Stereochemical Considerations in Planning Syntheses
• 2.1 Conformational Analysis
• 2.2 Evaluation of Non-Bonded Interactions
• 2.3 Six-Membered Heterocyclic Systems
• 2.4 Polycyclic Ring Systems
• 2.5 Cyclohexyl Systems with sp2-Hybridized Atoms
• 2.6 Significant Energy Difference
• 2.7 Computer-Assisted Molecular Modeling
• 2.8 Reactivity and Product Determination as a Function of Conformation
• References
• The Concept of Protecting Functional Groups
• 3.1 Protection of N–H Groups
• 3.2 Protection of OH Groups
• 3.3 Protection of Diols as Acetals
• 3.4 Protection of Carbonyl Groups in Aldehydes and Ketones
• 3.5 Protection of the Carboxyl Group
• 3.6 Protection of Double Bonds
• 3.7 Protection of Triple Bonds
• References
• Functional Group Transformations
• 4.1 Oxidation of Alcohols to Aldehydes and Ketones
• 4.2 Reagents and Procedures for Alcohol Oxidation
• 4.3 Chemoselective Oxidizing Agents
• 4.4 Oxidation of Acyloins
• 4.5 Oxidation of Tertiary Allylic Alcohols
• 4.6 Oxidative Procedures to Carboxylic Acids
• 4.7 Allylic Oxidation of Alkenes
• 4.8 Terminology for Reduction of Carbonyl Compounds
• 4.9 Nucleophilic Reducing Agents
• 4.10 Electrophilic Reducing Agents
• 4.11 Regio- and Chemoselective Reductions
• 4.12 Diastereoselective Reductions of Cyclic Ketones
• 4.13 Inversion of Secondary Alcohol Stereochemistry
• 4.14 Diastereofacial Selectivity in Acyclic Systems
• 4.15 Enantioselective Reductions
• References
• Functional Group Transformations
• 5.1 Reactions of Carbon–Carbon Double Bonds
• 5.2 Reactions of Carbon–Carbon Triple Bonds
• References
• Formation of Carbon–Carbon Single Bonds via Enolate Anions
• 6.1 1,3-Dicarbonyl Compounds
• 6.2 Direct Alkylation of Enolates
• 6.3 Cyclization Reactions—Baldwin’s Rules for Ring Closure
• 6.4 Stereochemistry of Cyclic Ketone Alkylation
• 6.5 Imine and Hydrazone Anions
• 6.6 Enamines
• 6.7 The Aldol Reaction
• 6.8 Condensation Reactions of Enols and Enolates
• 6.9 Robinson Annulation
• References
• Formation of Carbon–Carbon Bonds via Organometallic Reagents
• 7.1 Organolithium Reagents
• 7.2 Organomagnesium Reagents
• 7.3 Organotitanium Reagents
• 7.4 Organocerium Reagents
• 7.5 Organocopper Reagents
• 7.6 Organochromium Reagents
• 7.7 Organozinc Reagents
• 7.8 Organoboron Reagents
• 7.9 Organosilicon Reagents
• 7.10 Organogold Chemistry
• References
• Palladium-Catalyzed Coupling Reactions
• 8.1 Palladium Oxidation State
• 8.2 Organic Synthesis with Palladium(0) Complexes
• 8.3 The Heck Reaction—Palladium(0)-Catalyzed Olefin Insertion Reactions
• 8.4 Palladium-Catalyzed Cross-Coupling with Organometallic Reagents
• 8.5 Cross-Coupling Reactions Involving sp-Carbons
• 8.6 The Trost–Tsuji Reaction
• References
• Formation of Carbon–Carbon ��-Bonds
• 9.1 Formation of Carbon–Carbon Double Bonds
• 9.2 Formation of Carbon–Carbon Triple Bonds
• References
• The Art of Synthesis