Recherche PDF

CHIMIE 100%

ELECTROPHILES 4.1 Le proton 4.2 Les acides de Lewis 4.3 Certaines liaisons 4.4 Certaines liaison !

https://www.fichier-pdf.fr/2010/11/19/chimie/

19/11/2010 www.fichier-pdf.fr

Organic Chemistry-QuickStudy Fundamentals 90%

acceptor electrophiles Base aqueous OHproton acceptor electron-pr.

https://www.fichier-pdf.fr/2013/09/03/organic-chemistry-quickstudy-fundamentals/

03/09/2013 www.fichier-pdf.fr

ERRATUM N°3 (spécial chimie orga) 89%

https://www.fichier-pdf.fr/2015/12/20/erratum-n-3-special-chimie-orga/

20/12/2015 www.fichier-pdf.fr

Cours S3 SMC Chapitre IV 83%

Electrophiles et nucléophiles B- Réactivité chimique I.

https://www.fichier-pdf.fr/2016/12/02/cours-s3-smc-chapitre-iv/

02/12/2016 www.fichier-pdf.fr

Chapitre IV 82%

Electrophiles et nucléophiles B- Réactivité chimique I.

https://www.fichier-pdf.fr/2017/11/15/chapitre-iv/

15/11/2017 www.fichier-pdf.fr

The Disconnection Approach (Warren) 80%

267 List of Tables Table 2.1 One-carbon electrophiles for aromatic synthesis Table 2.2 Reagents for aromatic electrophilic substitution Table 2.3 Aromatic side chains by functional group interconversion Table 2.4 Aromatic compounds diazonium salts Table 3.1 Direction and activation in aromatic electrophiIic substitution Table 4.1 Hierarchy of reactivity for acid derivatives Table 4.2 Aliphatic compounds derived from alcohols Table 7.1 Synthons for I ,n-DiX synthesis Table 9.1 Protecting groups Table 10.1 One-group C-C disconnections Table 10.2 Oxidising agents for conversion of alcohols into aldehydes and ketones Table 10.3 Compounds derived from alcohols Table 11.1 Some readily available starting materials Table 11.2 Guidelines to good disconnections Table 12.1 Stereospecific reactions Table 18.1 Natural or logical synthons Table 18.2 Carbon acids and the bases used to ionise them Table 20.1 Reactivity of carbonyl compounds made by nucleophilic ix displacement of x Table 23.1 Alkenes as sources of 1,2-difunctionalised compounds Table 23.2 Available 1,2-difunctionalised Tabl~.1 Removal of functional groups Table 25.1 Available I ,4-difunctionalised Table 26.1 Double bond cleavage methods Table 29.1 Factors affecting ring formation Table 29.2 Available reagents containing two heteroatoms Table 38.1 Stereospecific reactions Table 38.2 Control of sp2 g~ometry Table 40.1 Molecules whose synthesis was designed to start from a readily available starting material Table 40.2 Some readily available starting materials Table 40.3 Starting materials available by simple routes from other cheap compounds compounds compounds

https://www.fichier-pdf.fr/2016/10/26/the-disconnection-approach-warren/

26/10/2016 www.fichier-pdf.fr

Ronéo Chimie Orga N°8 (1) 72%

https://www.fichier-pdf.fr/2013/11/16/roneo-chimie-orga-n-8-1/

16/11/2013 www.fichier-pdf.fr

07.09.15 8H30-10H30 INTRO WILLAND 70%

https://www.fichier-pdf.fr/2015/09/10/07-09-15-8h30-10h30-intro-willand/

10/09/2015 www.fichier-pdf.fr