213315-02-7Relevant academic research and scientific papers
Total Synthesis of (?)-Indoxamycins A and B
Hu, Naifeng,Dong, Changming,Zhang, Cuifang,Liang, Guangxin
, p. 6659 - 6662 (2019/04/13)
The concise total syntheses of (?)-indoxamycins A and B is reported. The chemistry features a seven-step preparation of a highly congested [5.5.6] tricyclic advanced common intermediate from a readily available R-carvone derivative. Key steps involve a Pa
Enantioselective synthesis of a key A-ring intermediate for the preparation of 1α,25-dihydroxyvitamin D3
Chen, Yan,Ju, Tong
supporting information; experimental part, p. 86 - 89 (2011/04/12)
A novel approach to the key A-ring α, β-unsaturated aldehyde 1, an important intermediate for the preparation of 1α,25-dihydroxyvitamin D3, has been developed. The strategy started from the inexpensive starting material (R)-carvone with an ene reaction serving as the key step toward the potential synthesis of vitamin D3 analogues bearing the modification at the C-2 position.
Carvone based approaches to chiral functionalised C-ring derivatives of taxanes
Srikrishna,Kumar, P. Praveen,Reddy, T. Jagadeeswar
, p. 5815 - 5818 (2007/10/03)
Enantiospecific synthesis of functionalised chiral C-ring derivatives of taxanes, starting from R-carvone, is described.
