Advances in the Synthesis and Pharmacological Applications of Heterocyclic Scaffolds: Benzoxepine and Benzothiepine Derivatives

Authors

  • Sanjay K. Gautam Department of Chemistry, University of Lucknow, Lucknow. U.P. India, 226007 Author
  • Pushyamitra Mishra Department of Chemistry, Shri Lal Bahadur Shastri Degree College Gonda, Uttar Pradesh, India Author
  • Balendu K. Gupta Department of Chemistry, University of Lucknow, Lucknow. U.P. India, 226007 Author
  • Anoop K. Awasthi Lokmata Devi Ahilya Bai Holkar Rajkiya Engineering College, Mainpuri U.P. India. Author
  • Vishnu K. Tandon Department of Chemistry, University of Lucknow, Lucknow. U.P. India, 226007 Author

DOI:

https://doi.org/10.59828/ijsrmst.v2i7.127

Abstract

Paul Cagniant first reported the synthesis of benzoxepine which was named as homochroman 1.1 Since then a large number of substituted benzoxepine derivatives were prepared by various synthetic routes, the significant being (i) By rearrangement of anisylidine flavone epoxides;2 (ii) From dihydrobenzofuran-3-one;3 (iii) By PARHAM Cyclialkylation;4,5 (iv) From aryl oxazolines;6 (v) By ring closure of Isoprenyl terminal epoxides;7 

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Homochroman (1-Benzoxepine and 1-Benzothiepine)

(vi) By photocycloaddition of Benzo[b]furan derivatives to alkenes;8 and several other synthetic routes not being employed in common practice. The thia analog is known as benzothiepine 1a.

A review on Benzoxepines has described the synthetic routes reported in literature till 1990.9,10 The present review describes the synthetic routes, reactions, the naturally occurring 1-Benzoxepines, its derivatives and their pharmacological significance.

Keywords: Benzoxepine and Benzothiepine, synthetic routes, reactions, pharmacological significance.

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Published

2023-07-30

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How to Cite

Advances in the Synthesis and Pharmacological Applications of Heterocyclic Scaffolds: Benzoxepine and Benzothiepine Derivatives. (2023). International Journal of Scientific Research in Modern Science and Technology, 2(7), 34-53. https://doi.org/10.59828/ijsrmst.v2i7.127