Chemistry of Natural Compounds

, Volume 15, Issue 6, pp 695–699 | Cite as

Structure and configuration of a new diterpenoid lactone fromLagochilus hirsutissimus

  • M. P. Nurmatova
  • U. N. Zainutdinov
  • F. G. Kamaev
  • Kh. A. Aslanov


The epigeal part of the plantLagochilus hirsutissimus has yielded a new diterpenoid lactone — lagohirsidin, C22H34O5, mp 144–145°C, [α] D 22 − 17.5° (c 1; ethanol). Reduction with LiAlH4 has yielded a diol C22H38O5, mp 165–166°C [α] D 20 −1.2 (c 0.6; ethanol). Acid hydrolysis of the diol has led to the formation of lagochilin, C20H36O5, mp 167–168°C, [α] D 20 −3.9° (c 1; ethanol). The synthesis of lagohirsidin from lagochilin has been effected.


Lactone Sesquiterpene Lactone Lactone Ring Epigeal Part Nuclear Overhauser Effect 


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Copyright information

© Plenum Publishing Corporation 1980

Authors and Affiliations

  • M. P. Nurmatova
  • U. N. Zainutdinov
  • F. G. Kamaev
  • Kh. A. Aslanov

There are no affiliations available

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