pericyclic reactions (py-303).pdf

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Pericyclic Reactions

by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 1 of 24

Reactions of Organic Compounds

A pericyclic reaction, a reaction that occurs as a result of

reorganizing the electrons in the reactant(s)

by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 2 of 24

Pericyclic Reaction I

An intramolecular reaction in which a new s bond is

formed between the ends of a conjugated p system by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 3 of 24

Electrocyclic Reactions Are Reversible

by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 4 of 24

Pericyclic Reaction II

Two different p bond-containing molecules react to form

a cyclic compound by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 5 of 24

Pericyclic Reaction III

A s bond is broken in the reactant, a new s bond is

formed in the product, and the p bonds rearrange by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 6 of 24

by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 7 of 24

• The electrocyclic reactions and sigmatropic

rearrangements are intramolecular reactions

Note

• The cycloaddition reactions are usually intermolecular

reactions

Common features among the three pericyclic reactions

• are concerted reactions

• are highly stereoselective

• are not affected by catalysts by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 8 of 24

The configuration of the product formed depends on:

• the configuration of the reactant

• the number of conjugated double bonds or pairs of

electrons in the reacting system

• whether the reaction is a thermal or a photochemical

reaction

A photochemical reaction takes place when a reactant absorbs light

A thermal reaction takes place without the absorption of light by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 9 of 24

An electrocyclic reaction is completely stereoselective

by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 10 of 24

by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 11 of 24

by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 12 of 24

by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 13 of 24

A symmetry-allowed pathway is one in which in-phase

orbitals overlap

If a reaction is symmetry-forbidden, it cannot take place

by a concerted pathway

The symmetry of the HOMO of the compound undergoing

ring closure controls the stereochemical outcome of an

electrocyclic reaction

by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 14 of 24

Cycloadditions are classified according to the number of

p electrons that interact in the reaction

by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 15 of 24

A [2 + 2] Cycloaddition Reaction

by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 16 of 24

Table 29.3

by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 17 of 24

Sigmatropic Rearrangements

by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 18 of 24

by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 19 of 24

Table 29.4

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by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 23 of 24

by Gaurav Kayal, Assistant Professor, Pharmaceutical Chemistry Page 24 of 24

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