943586-77-4Relevant academic research and scientific papers
A rapid and efficient enantiospecific synthesis of the functionalized ABC-ring system of tetranortriterpene dumsins and their analogues
Srikrishna, Adusumilli,Pardeshi, Vijendra H.,Thriveni, Pinnu
, p. 1392 - 1396 (2008)
A rapid and enantiospecific synthesis of the ABC ring system of tetranortriterpene dumsin and its analogues, starting from the readily available monoterpene (R)-carvone employing two RCM reactions as key steps, is described.
Enantiospecific approaches to bicyclic vibsanes: a ring-closing metathesis reaction-based strategy to functionalized bicyclo[4.3.1]decanes
Srikrishna, Adusumilli,Pardeshi, Vijendra H.,Satyanarayana, Gedu
, p. 1984 - 1991 (2008/12/22)
An enantiospecific synthesis of functionalized bicyclo[4.3.1]decane, the bicyclic core system present in some bi- and tricyclic vibsane diterpenoids, for example, vibsanin E, via an RCM reaction of 2,6-diallylcarvone derivatives is described. It has been further extended to the synthesis of tricyclo[6.4.1.01,5]tridecanes starting from 2,6,6-triallylcarvones.
A rapid enantiospecific synthesis of the (6,6,5)-tricyclic ring system of the elisabethane diterpenes
Srikrishna,Pardeshi, Vijendra H.,Satyanarayana
, p. 4087 - 4090 (2008/02/03)
A rapid enantiospecific stereoselective synthesis of the 6,6,5-ring system of the novel tricyclic elisabethin diterpenes, starting from (R)-carvone, employing a ROM-RCM sequence as the key step, has been accomplished.
