Accedi

Cycloadditions are one of the most valuable and effective synthesis routes to form cyclic compounds. These are concerted pericyclic reactions between two unsaturated compounds resulting in a cyclic product with two new σ bonds formed at the expense of π bonds. The [4 + 2] cycloaddition, known as the Diels–Alder reaction, is the most common. The other example is a [2 + 2] cycloaddition.

Figure1

The feasibility of cycloaddition reactions under thermal and photochemical conditions can be predicted using a set of selection rules. If the total number of π electrons involved in the rearrangement is a multiple of 4n, the reaction is photochemically allowed. The reaction is thermally allowed if the total number of π electrons involved is 4n + 2.

Tags
CycloadditionPericyclic ReactionDiels Alder Reaction4 2 Cycloaddition2 2 CycloadditionThermal ConditionsPhotochemical ConditionsSelection RulesElectrons

Dal capitolo 16:

article

Now Playing

16.15 : Cycloaddition Reactions: Overview

Dienes, Conjugated Pi Systems, and Pericyclic Reactions

2.4K Visualizzazioni

article

16.1 : Struttura dei dieni coniugati

Dienes, Conjugated Pi Systems, and Pericyclic Reactions

4.2K Visualizzazioni

article

16.2 : Stabilità dei dieni coniugati

Dienes, Conjugated Pi Systems, and Pericyclic Reactions

3.1K Visualizzazioni

article

16.3 : π Orbitali molecolari dell'1,3-butadiene

Dienes, Conjugated Pi Systems, and Pericyclic Reactions

8.0K Visualizzazioni

article

16.4 : π Orbitali molecolari del catione allile e dell'anione

Dienes, Conjugated Pi Systems, and Pericyclic Reactions

3.9K Visualizzazioni

article

16.5 : π Orbitali molecolari del radicale allile

Dienes, Conjugated Pi Systems, and Pericyclic Reactions

3.2K Visualizzazioni

article

16.6 : Addizione elettrofila di 1,2 e 1,4 di HX a 1,3-butadiene

Dienes, Conjugated Pi Systems, and Pericyclic Reactions

4.6K Visualizzazioni

article

16.7 : Addizione elettrofila di X2 a 1,3-butadiene

Dienes, Conjugated Pi Systems, and Pericyclic Reactions

2.2K Visualizzazioni

article

16.8 : Addizione elettrofila di HX all'1,3-butadiene: controllo termodinamico vs controllo cinetico

Dienes, Conjugated Pi Systems, and Pericyclic Reactions

2.3K Visualizzazioni

article

16.9 : Spettroscopia UV-Vis di sistemi coniugati

Dienes, Conjugated Pi Systems, and Pericyclic Reactions

6.6K Visualizzazioni

article

16.10 : Spettroscopia UV-Vis: Regole di Woodward-Fieser

Dienes, Conjugated Pi Systems, and Pericyclic Reactions

22.5K Visualizzazioni

article

16.11 : Reazioni pericicliche: Introduzione

Dienes, Conjugated Pi Systems, and Pericyclic Reactions

7.1K Visualizzazioni

article

16.12 : Reazioni elettrocicliche termiche e fotochimiche: panoramica

Dienes, Conjugated Pi Systems, and Pericyclic Reactions

2.2K Visualizzazioni

article

16.13 : Reazioni Elettrocicliche Termiche: Stereochimica

Dienes, Conjugated Pi Systems, and Pericyclic Reactions

1.9K Visualizzazioni

article

16.14 : Reazioni elettrocicliche fotochimiche: stereochimica

Dienes, Conjugated Pi Systems, and Pericyclic Reactions

1.7K Visualizzazioni

See More

JoVE Logo

Riservatezza

Condizioni di utilizzo

Politiche

Ricerca

Didattica

CHI SIAMO

Copyright © 2025 MyJoVE Corporation. Tutti i diritti riservati