摘要
从原料百菌清出发 ,经过氟交换、氨解、水解、脱羧和酰化反应 ,合成得到 1 2个新型双苯甲酰基脲类几丁质抑制剂衍生物 ,总收率超过 3 0 %~5 0 %。
Twelve novel bis-benzoylphenylurea chitin inhibitor derivatives have been synthesized in over 30~50% yield from chlorothalonil via sequential fluorine exchange, nitrile hydrolysis, decarboxylation and acylation reactions.
出处
《合成化学》
CAS
CSCD
2004年第2期117-119,共3页
Chinese Journal of Synthetic Chemistry
基金
YunnanProvincialNaturalScienceFoundation( 99B0 0 0 5M)
OpenFoundationofStateKeyLaboratoryofElemento OrganicChemistry
NankaiUniversity( 2 0 0 2 0 6)