A two-step biomimetic synthesis of antimalarial robustadials A and B
摘要:
The antimalarial robustadials A and B have been synthesized in two steps starting from commercially available phloroglucinol comprising a key biomimetic three-component reaction that involves in situ generation of an o-quinone methide via Knoevenagel condensation and subsequent Diels-Alder cycloaddition with (-)-beta-pinene. @ 2006 Elsevier Ltd. All rights reserved.
A two-step biomimetic synthesis of antimalarial robustadials A and B
作者:Sandip B. Bharate、Inder Pal Singh
DOI:10.1016/j.tetlet.2006.07.113
日期:2006.9
The antimalarial robustadials A and B have been synthesized in two steps starting from commercially available phloroglucinol comprising a key biomimetic three-component reaction that involves in situ generation of an o-quinone methide via Knoevenagel condensation and subsequent Diels-Alder cycloaddition with (-)-beta-pinene. @ 2006 Elsevier Ltd. All rights reserved.