REACTIVIDAD Y SÍNTESIS

REACCIONES ORGÁNICAS CON NOMBRE PROPIO

 

NAMED ORGANIC REACTION

Tutorial de Oxford University que permite analizar los mecanismos de muchas reacciones orgánicas.

Reaction Name

Aldol - Acid Catalysed

Aldol - Base Catalysed

Baeyer-Villiger

Balz-Schiemann

Beckmann

Bischler-Napieralski

Cannizzaro

Chichibabin Amination

Claisen

Darzens

Dieckmann

Favorskii

Fischer

Friedel-Crafts Acylation

Friedel-Crafts Alkylation

Gabriel

Gatterman-Koch

Hantzsch Pyridine Synthesis

Hantzsch Thiazole Synthesis

Hell-Volhard-Zelinsky

Hofmann

Knoevenagel

Knorr

Kornblum

Mannich

Meerwein-Pondorf-Verley

Mitsunobu

Nametkin

Paal-Knorr Furan Synthesis

Paal-Knorr Pyrrole Synthesis

Paal-Knorr Thiophene Synthesis

Payne

Perkin

Peterson - Acid Catalysed

Peterson - Base Catalysed

Pictet-Spengler

Pinacol

Pummerer

Ramberg-Backlund

Reformatsky

Robinson Ring Annulation

Robinson-Gabriel

Semi-Pinacol

Simmons-Smith

Skraup

Stobbe

Strecker

Swern

Thorpe

Tiffeneau-Demjanov

Vilsmeier

Wagner-Meerwein

Williamson

Wittig

Wolff-Kischner

Difficulty

2

2

4

1

3

4

2

3

2

3

3

3

5

2

2

3

2

5

3

3

4

3

4

2

4

3

3

2

3

3

3

2

3

3

3

4

2

3

2

3

3

3

3

3

3

3

3

3

4

4

4

2

1

2

3

Reactant

Aldehyde

Aldehyde

Ketone

Diazo

Oxime

Amide

2 x Aldehyde

Pyridine

2 x Ester

a-Halo Ester + Aldehyde / Ketone

Diester

a-Halogeno Carbonyl / Alkoxide

Aryl Hydrazine + Ketone

Arene

Arene

Haloalkane

Arene

2 x Ketone + Aldehyde

a-Chloroketone

Carboxylic Acid

Amide

Malonic Acid

Ketone + a-Aminoketone

Alkyl Halide

Thiophene / Pyrrole / Alkyl-Fuan

Ketone

Alcohol

Terpene

1, 4-Diketone

1, 4-Diketone

1, 4-Diketone

2, 3-Epoxy Alcohol

Acid Anhydride

Carbonyl

Carbonyl

b-Arylethylamine + Aldehyde

1, 2-Diol

Sulphoxide

a-halosulphone

a-Haloester

b-Ketoalkene + a, g-Diketone

a-Aminoketone + Acid Chloride

b-Amino Alcohol

Alkene

Aniline + Glycerol

Diester

Aldehyde

Alcohol

2 x Nitrile

Ketone

Reactive Aromatic + Amide

Alcohol

Alcohol

Carbonyl

Carbonyl

Product

Aldol + Dehydrated Product

Aldol + Dehydrated Product

Ester

Aromatic Fluoride

Amide

Isoquinoline

Alcohol + Carboxylic Acid

2-Aminopyridine

b-Ketoester

a-Epoxide Ester

Cyclic b-Ketoester

Ester

Indole

Acylated Arene

Alkylated Arene

Amine

Formylated Arene

Pyridine

Thiazole

b-Bromo Carboxylic Acid

Isocyanate

E-Alkenoic Acid

Pyrrole

Carbonyl

Aminomethyl Heterocycle

Alcohol

Nu- Substituted Alkane

Rearranged Hydroxy-Terpene

Furan

Pyrrole

Thiophene

1, 2-Epoxy Alcohol

a, b-Unsaturated Carboxylic Acid

Alkene

Alkene

Tetrahydroisoquinoline

Carbonyl

a-acyloxythioether

Alkene

b-Hydroxyester

Fused Rings

Oxazole

Carbonyl

Cyclopropane

Quinoline

Unsaturated Ester Carboxylate

Amino Acid

Carbonyl

Aminonitrile

Ring-Expanded Ketone

Substituted Aromatic Carbonyl

Alkene

Ether

Alkene

Alkane




Practicando con Virtual Text – Curly Arrows 1

Practicando con Virtual Text – Curly Arrows 2

Practicando con Organic Chemistry Direct: OCOL- mecanismos