41198-02-1Relevant academic research and scientific papers
A PROCESS FOR THE SYNTHESIS ANTHRANILIC DIAMIDE COMPOUNDS AND INTERMEDIATES THEREOF
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Page/Page column 21; 22; 25; 26, (2020/09/08)
The present invention disclosed a process for the synthesis of anthranilic diamide compound of formula (I), wherein, R1, R2, R3a, R3b, R3c, R4, R5, R6 and Z are as defined in the detailed description. The process comprising the step of obtaining a mono- or dicyano substituted aniline compound of formula (IV) which is then converted to an anthranilic acid compound of formula (V) or an anthranilic amide compound of formula (Va). Further, the compound of formula (VI) can be optionally synthesized from compound of formula (IV or V or Va).
Amide derivative and preparation method and application thereof
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Paragraph 0050-0057, (2019/10/23)
The invention relates to an amide derivative and a preparation method and application thereof. The compound is an amide derivative containing 3-bromo-5-chloro (bromo) phenyl units, has obvious insecticidal activity, and can be used for killing various bio
QUINAZOLINE DERIVATIVES USED TO TREAT HIV
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Paragraph 0283, (2016/07/27)
Described herein are compounds of Formula (I) and tautomers and pharmaceutical salts thereof, compositions and formulations containing such compounds, and methods of using and making such compounds.
HYDRAZIDE COMPOUND AND PESTICIDAL USE OF THE SAME
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Page/Page column 511-512, (2008/06/13)
A hydrazide compound represented by the formula (1): has excellent pesticidal activity.
An anion-induced regio- and chemoselective acylation and its application to the synthesis of an anticancer agent
Poirier, Marc,Chen, Frank,Bernard, Charles,Wong, Yee-Shing,Wu, George G.
, p. 3795 - 3798 (2007/10/03)
Figure presented An efficient Grignard- and organolithium-induced regio- and chemoselective anionic acylation is reported. A number of tricyclic ketones are prepared in good to excellent yields via this method. This method is complementary to the Frieldel-Crafts acylation for electron-deficient substrates. A novel anisole-based Grignard reagent was developed to effect the cyclization of sterically hindered substrates. This novel reagent has been successfully applied to the synthesis of Sch 66336, a candidate for oncologic treatment.
