Understanding the domino reaction between 3-chloroindoles and methyl coumalate yielding carbazoles. A DFT study-Reference-Cited by-同舟云学术

Understanding the domino reaction between 3-chloroindoles and methyl coumalate yielding carbazoles. A DFT study

Author:

Domingo Luis R.¹²³⁴,Sáez José A.⁵⁶⁴,Emamian Saeed R.⁷⁸⁹¹⁰¹¹

Affiliation:

1. Departamento de Química Orgánica

2. Universidad de Valencia

3. E-46100 Burjassot

4. Spain

5. Instituto de Tecnología Química UPV-CSIC

6. 46022 Valencia

7. Chemistry Department

8. Shahrood Branch

9. Islamic Azad University

10. Shahrood

11. Iran

Abstract

The elimination of HCl and CO₂ in the corresponding cycloadducts makes the unfavourable polar Diels–Alder reaction of 3-chloroindole irreversible.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

Reference55 articles.

1. W. Carruthers , Some Modern Methods of Organic Synthesis, Cambridge University Press, Cambridge, 2nd edn, 1978

2. W. Carruthers , Cycloaddition Reactions in Organic Synthesis, Pergamon, Oxford, 1990

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