776306-92-4Relevant academic research and scientific papers
Enantiospecific synthesis of (+)-trans-α-himachalene via an intramolecular type II carbonyl ene reaction
Srikrishna,Kumar, P. Ravi
experimental part, p. 1414 - 1422 (2009/04/11)
Enantiospecific synthesis of (+)-trans-α-himachalene starting from (R)-carvone is described. An intramolecular type II carbonyl ene reaction has been employed as the key step for the construction of the bicyclo[5.4.0]undecane ring system.
Enantiospecific first total synthesis of (+)-trans-α-himachalene
Srikrishna,Ravi Kumar
, p. 6867 - 6870 (2007/10/03)
An enantiospecific first total synthesis of (+)-trans-α-himachalene, one of the eight male specific sesquiterpenes isolated from the crucifer flea beetle Phyllotreta cruciferae, starting from the readily and abundantly available monoterpene, (R)-carvone,
