Skip to main content
Log in

Formylation of polyhydroxy flavones and chromones

  • Published:
Proceedings of the Indian Academy of Sciences - Section A Aims and scope Submit manuscript

Abstract

In the case of nor-wogonin and 5:7:8-trihydroxy-2-methylchromone, Gattermann method is efficient in yielding the corresponding aldehydes, whereas with their 8-methyl ethers hexamine method works satisfactorily.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  1. Schönberget al...J. Amer. Chem. Soc., 1953,75, 4992.

    Article  Google Scholar 

  2. Chakravortyet al...Proc. Ind. Acad. Sci., 1952,35 A, 34.

    Google Scholar 

  3. Mukerjee ..Ph.D. Thesis (Delhi University, 1953).

  4. Sastri and Seshadri..Proc. Ind. Acad. Sci., 1946,24 A, 243.

    Google Scholar 

  5. Shahet al. ..J. Chem. Soc., 1938, 1555.

  6. Geissman..J. Amer. Chem. Soc., 1951,73, 3514.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Murti, V.V.S., Seshadri, T.R., Sundaresan, V. et al. Formylation of polyhydroxy flavones and chromones. Proc. Indian Acad. Sci. 50, 192–195 (1959). https://doi.org/10.1007/BF03048852

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF03048852

Keywords

Navigation