Introduction to strategies for organic synthesis / Laurie S. Starkey, California State Polytechnic University, Pomona, CA, USA

Von:

Starkey, Laurie Shaffer, 1969- [VerfasserIn]

Resource type: Ressourcentyp: Buch (Online)Buch (Online)Sprache: Englisch Verlag: Hoboken, NJ : John Wiley & Sons, 2018Auflage: Second editionBeschreibung: 1 Online-RessourceISBN:

1119347211
9781119347217
1119347238
9781119347231

Schlagwörter:

Andere physische Formen: 9781119347248. | Erscheint auch als: Introduction to strategies for organic synthesis. Druck-Ausgabe Second edition. Hoboken, NJ : Wiley, 2018. xxi, 399 SeitenRVK: RVK: VK 5501 | VK 5500LOC-Klassifikation:

QD262

Online-Ressourcen:

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Zusammenfassung: 1.2.4 PROTECTION OF AMINESAmide Protective Groups for Amines; Carbamate Protective Groups for Amines; CHAPTER 1 PROBLEMS: PROTECTIVE GROUPS; CHAPTER 2 SYNTHETIC TOOLBOX 2: OVERVIEW OF ORGANIC TRANSFORMATIONS; CHAPTER 2.1 NUCLEOPHILES AND ELECTROPHILES; 2.1.1 COMMON NUCLEOPHILES; Ionic and Other Commercially Available Nucleophiles; Metal-Stabilized Nucleophiles; Resonance-Stabilized Nucleophiles; 2.1.2 COMMON ELECTROPHILES; CHAPTER 2.2 OXIDATION AND REDUCTION REACTIONS; 2.2.1 OVERVIEW OF OXIDATIONS AND REDUCTIONS; General Chemistry Examples of Redox ReactionsZusammenfassung: CHAPTER 3 SYNTHESIS OF MONOFUNCTIONAL TARGET MOLECULES (1-FG TMs)CHAPTER 3.1 SYNTHESIS OF ALCOHOLS (ROH) AND PHENOLS (ArOH); 3.1.1 SYNTHESIS OF ALCOHOLS BY FUNCTIONAL GROUP INTERCONVERSION (FGI); Acetate as a Synthetic Equivalent of Hydroxide; Retrosynthesis of Alcohols (FGI); PRACTICE PROBLEM 3.1A: ALCOHOL SYNTHESIS BY FGI; 3.1.2 SYNTHESIS OF ALCOHOLS BY THE GRIGNARD REACTION; Preparation of a Grignard Reagent (RMgX); Examples of Grignard Reagents; Synthesis of Alcohols (Grignard); Mechanism of the Grignard Reaction; Retrosynthesis of an Alcohol (Grignard)Zusammenfassung: Intro; TITLE PAGE; COPYRIGHT PAGE; CONTENTS; PREFACE; ACKNOWLEDGMENTS; CHAPTER 1 SYNTHETIC TOOLBOX 1: RETROSYNTHESIS AND PROTECTIVE GROUPS; CHAPTER 1.1 RETROSYNTHETIC ANALYSIS; 1.1.1 RETROSYNTHESIS BY FUNCTIONAL GROUP INTERCONVERSION (FGI); Choice of Reagents; 1.1.2 RETROSYNTHESIS BY MAKING A DISCONNECTION; What Makes a Good Synthesis?; CHAPTER 1.2 PROTECTIVE GROUPS; 1.2.1 PROTECTION OF KETONES AND ALDEHYDES; 1.2.2 PROTECTION OF ALCOHOLS; Ether Protective Groups for Alcohols; Ester Protective Groups for Alcohols; Acetal Protective Groups for Alcohols; 1.2.3 PROTECTION OF CARBOXYLIC ACIDSZusammenfassung: Reaction of a Grignard with an EsterMechanism of the Grignard Reaction with an Ester; Retrosynthesis of an Alcohol Containing Two Identical Groups; Reaction of a Grignard with an Epoxide; Mechanism of an Epoxide Ring-Opening Reaction with a Grignard; Alternate Retrosynthesis of an Alcohol; EXAMPLE: ALCOHOL TM; 3.1.3 SYNTHESIS OF PROPARGYLIC ALCOHOLS (RCaCCH2OH); Preparation of Alkynyl Nucleophiles (RCaCNa); PRACTICE PROBLEM 3.1B: ALCOHOL RETROSYNTHESIS; 3.1.4 SYNTHESIS OF PHENOL DERIVATIVES (ArOH); CHAPTER 3.2 SYNTHESIS OF ALKYL (RX) AND ARYL HALIDES (ArX)PPN: PPN: 102620805XPackage identifier: Produktsigel: ZDB-4-NLEBK

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