127969-63-5Relevant academic research and scientific papers
Carbanion cyclisation of esters. Part 2: Enantiospecific construction of the tricyclic framework of the marine sesquiterpenes, spirodysins
Srikrishna,Ravi Kumar,Ramasastry
, p. 383 - 386 (2004)
Enantiospecific construction of the bicyclo[4.3.0]nonan-8-one 17 employing a lithium and liquid ammonia mediated carbanion cyclisation of the δ-methyl-δ,ε-unsaturated ester 13, and its elaboration to the tricyclic framework of the marine sesquiterpenes sp
Enantiospecific synthesis of the tricyclic core structure of lippifolianes
Srikrishna, Adusumilli,Ramesh Babu,Beeraiah, Baire
scheme or table, p. 719 - 724 (2010/08/03)
An enantiospecific synthesis of the [6.6.3]-tricyclic carbon framework, 2,6,6,9-tetra-methyltricyclo[5.4.0.02,4]undecane, present in the sesquiterpenes lippifolianes and the diterpenes cyclosclareol, metasequoic acids and parguerols, starting f
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,
