ScholarMate
客服热线:400-1616-289

Bioinspired syntheses of cryptoflavanones C and D, oboflavanones A and B, and cryptoyunnanones G and H enabled by an acid-triggered cascade sequence

Zheng, Anquan; Wang, Sasa; Zhou, Tingting; Chen, Yan; Ke, Xin; Chen, Huiyu*; Tan, Haibo*
Science Citation Index Expanded
中国科学院

摘要

We herein present a concise synthetic route for the collective total syntheses of six flavanones named oboflavanones A and B, cryptoflavanones C and D, and cryptoyunnanones G and H, which were all isolated from the genus Cryptocarya. The key strategy of these syntheses involves a bioinspired acid-triggered olefin isomerization/hemiacetalization/dehydration/Friedel-Crafts alkylative formal [3 + 3]-type cycloaddition cascade process.

关键词

STEREOSELECTIVE TOTAL-SYNTHESIS BIOMIMETIC TOTAL SYNTHESES CRYPTOCARYA-CHINENSIS CYTOTOXIC FLAVONOIDS INHIBITORY-ACTIVITY ALPHA-PYRONES FLAVANONES ALKALOIDS LEAVES CONSTRUCTION