✍ Scribed by Chusheng Huang; Shuhua Li; Liming Hou; Yulin Li; Ying Li
No coin nor oath required. For personal study only.
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## Abstract A facile approach for the first total synthesis of two naturally occurring geranylated flavonoids, (±)‐puyanin (**1**) and (±)‐4′‐__O__‐methylbonannione (**2**) has been obtained with total yields of 27% and 17.8%, respectively. The key steps were regioselective cyclization of geranylat
Total Syntheses of O4,9-Dimethyl Stealthins A and C. -Using the Suzuki coupling reaction of (I) and (II) as key step gives the target compound (IV) which serves as substrate for the O-methylated and -acylated analogues (V) and (VI) of stealthin C and A, radical scavengers produced by Streptomyces vi
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v