Development of a Novel Approach to Formation of a Pyrrole Ring: Synthesis of 2,3,5-Substituted 1-[2-(Vinyloxy)ethyl]pyrroles

Reaction of 2-(vinyloxy)ethylisothiocyanate with unsaturated carbanions generated in situ from propargyl ethers and amines when treated with superbases, after S-alkylation and cyclization of the adducts in the presence of CuBr, leads to the previously unknown 2,3,5-substituted 1-[2-(vinyloxy)ethyl]pyrroles.     

Synthesis of diaminohydroxyethersvia 3-(ω-haloalkoxy)-2-hydroxypropyl sulfamates

Reactions of 3-(ω-haloalkoxy)-2-hydroxypropyl sulfamates with amines or ammonia followed by acid hydrolysis give the corresponding diaminohydroxyethers. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1663–1665, August, 1998.     

Synthesis and Some Transformations of 2-(3-Amino-1-Phenylpropyl)furan

A preparative method was developed for the synthesis of ethyl furfurylidenecyanoacetate. Its condensation with phenylmagnesium bromide gave ethyl α-cyano-β-(2-furyl)hydrocinnamate, the decarboxylation of which led to β-(2-furyl)hydrocinnamonitrile. Reduction of this nitrile with lithium aluminum hydride gave 2-(3-amino-1-phenylpropyl)furan. Some of its transformations were studied.__________Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 517–521, April, 2005.     

Structure-Activity Relationship of Insecticidal Steroids. III. Δ4,7-6-Ketosteroids

The toxicity of steroids 1-11 for colorado beetle (Leptinotarsa decemlineata Say.) larvae was studied by contact-intestinal treatment. Active insect-growth regulators were found among the studied compounds.     

A simple synthesis of (±)-2,6-dimethylocta-5(<Emphasis Type="Italic">Z</Emphasis>),7-diene-4-ol and its attractant activity for the bark beetle <Emphasis Type="Italic">Ips typographus</Emphasis>

A simple method for the synthesis of (±)-2,6-dimethylocta-5(Z),7-diene-4-ol possessing a high pheromone activity for the bark beetle Ips typographus was developed.__________Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 2245–2247, October, 2004.     

LC-MS法分析鸡肝中的玉米赤霉醇

玉米赤霉醇(Zeranol)是一种非甾体类激素,具有促进家畜蛋白质合成和增重的作用。由于其在动物组织中残留,目前在欧盟被禁用。2002年4月我国农业部第193号公告和2002年11月农业部、国家药品监督管理局第227号公告中规定禁止使用玉米赤霉醇,但由于玉米赤霉醇作为畜禽增重剂效果好、经济回报高,仍有一些不法饲养业主受利益驱使而违法使用。为保证动物源性食品安全,维护人民身体健康,必须建立一种适用、可行、规范的残留检测方法以适应当前加入WTO的形势需要。本实验建立了高效液相色谱-质谱联用法(LC-MS)测定鸡肝中玉米赤霉醇,旨在为政府监控禽类产品中的玉米赤霉醇提供准确可靠的检测方法。     

(R)-4-Menthenone in the synthesis of optically pure sex pheromone of the peach leafminer moth (Lyonetia clerkella)

The synthesis of (14S)-methyloctadec-1-ene, sex pheromone of the peach leafminer moth (Lyonetia clerkella), is described to demonstrate a new potential of the synthetic use of (R)-4-menthenone.     

A novel heterocyclic system — dihydro-2H-1,5,2,4-dioxadiazine. 2,4-Dimethyldihydro-2H-1,5,2,4-dioxadiazine hydrochloride: synthesis and NMR study

The first representative of a novel heterocyclic system, namely, 2,4-dimethyldihydro-2H-1,5,2,4-dioxadiazine hydrochloride, was synthesized.     

Synthesis of 3β,20S-dihydroxydammar-24-en-12-one 3,20-di-O-β-D-glucopyranoside (chikusetsusaponin-LT8), a glycoside from Panax japonicus

A method for preparative production of 3β,20S-dihydroxydammar-24-en-12-one 3,20-di-O-β-D-glucopyranoside (1), a glycoside from Panax japonicus, chikusetsusaponin-LT₈ was developed. Chemical transformation of betulafolientriol, a component of Betula leaves extract, produced the 12-keto-20S-protopanaxadiol (3β,20S-dihydroxydammar-24-en-12-one) (2), exhaustive glycosylation of which by 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosylbromide (3) under Koenigs—Knorr reaction conditions with subsequent removal of protecting groups formed 3β,20S-dihydroxydammar-24-en-12-one 3,20-di-O-β-D-glucopyranoside (1). The principal glycosylation product was 3β,20S-dihydroxydammar-24-en-12-one 3-O-β-D-glucopyranoside if equimolar amounts of (2) and (3) were used. __________ Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 44–48, January–February, 2006.     

2-(N'-乙基咔唑-3'-烯基)-8-羟基喹啉的合成及理论研究

设计合成了2-(N'-乙基咔唑-3'-烯基)-8-羟基喹啉. 以UV-Vis, ¹H NMR, FT-IR, 元素分析和MS进行了结构表征, 并测定了产物的光致发光(PL)性质. 运用Gaussian98量子化学程序包, 采用B3LYP密度泛函(DFT)的方法, 在6-31G(d,p)水平上对分子的几何构型进行结构优化; 预测目标产物的振动光谱, 结果表明与实验值相符.