1254784-76-3Relevant academic research and scientific papers
Enantiospecific total synthesis of aciphyllene
Srikrishna,Pardeshi, Vijendra H.
, p. 8160 - 8168 (2010)
Enantiospecific total synthesis of the sesquiterpene aciphyllene and its three epimers have been described starting from the readily available monoterpene (R)-limonene employing an intramolecular type II carbonyl ene reaction as the key step.
Enantiospecific synthesis and confirmation of the relative and absolute stereostructure of 11-hydroxyguaiadienes
Srikrishna, Adusumilli,Pardeshi, Vijendra H.,Mahesh, Konda
, p. 2830 - 2833 (2010)
Enantiospecific total synthesis of two epimeric sesquiterpenes 11-hydroxyguaiadienes has been accomplished starting from the readily available monoterpene (R)-limonene, which confirmed the structure and absolute configuration of the natural products.
Enantiospecific first total synthesis and confirmation of the relative and absolute stereostructure of isocalamusenone
Srikrishna, Adusumilli,Pardeshi, Vijendra H.,Mahesh, Konda
, p. 2512 - 2516 (2010)
The enantiospecific total synthesis of two epimers of the sesquiterpene isocalamusenone has been accomplished starting from the readily available monoterpene (R)-limonene, which of the natural product established the stereostructure and the absolute configuration.
