1)  hydrazines
杂环基醛腙
1.
Heterocycles as 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazines, imidazo[2,1-b]-1,3,4-thiadiazoles and hydrazines containing thiazole ring, have received considerable attention over the past years due to their wide range of versatile, significant bioactivities and pharmalogical activities as antiviral, antibacterial, antiparasitic, anticonvulsant, analgisic, anticancer, antiulcer, anti-tuberculosis etc.
杂环化合物如1,2,4-三唑[3,4-b]-1,3,4-噻二嗪、咪唑[2,1-b]-1,3,4-噻二唑、杂环基醛腙具有抗菌、驱虫、抗痉挛、止痛、抗癌、抗溃疡、抗肺结核等生物活性,因此近年来受到人们的广泛关注。
2)  heterocycle
杂环
1.
Synthesis and characterization of the derivatives of 1,8-naphthalimides containing thiadiazole heterocycle;
含噻二唑杂环的1,8-萘酰亚胺衍生物的合成与表征
2.
Theoretical design of high-spin biradical molecules with heterocycles as end groups;
以杂环做端基的高自旋双自由基分子的理论研究
3.
The design of novel biradicals with high spin ground state possessing heterocycles;
含杂环并具有高自旋基态的双自由基体系的理论设计
3)  heterocyclic
杂环
1.
Studies on the Acylaminothiosemicarbazides and the Related Heterocyclic Derivatives(ⅩⅩⅤ)——Synthesis of 1-(2,4-dichIorophenoxylacetyl)-4-aroylthiosemicarbazides and Studies on Its cyclization Behavior Under Basic Catalysis;
酰氨基硫脲及其相关杂环衍生物的研究(ⅩⅩⅤ)——1-(2,4-二氯苯氧乙酰基)-4-芳酰基氨基硫脲的合成及其碱催化环化行为的研究
2.
Study on N-heterocyclic carbene iron complex;
氮杂环卡宾铁配合物的研究
3.
Hexahydroxy N-containing heterocyclic compound without sulfur and phosphorus was synthesized and its structure was characterized.
合成了无硫、磷的六元含氮杂环化合物添加剂。
4)  heterocycles
杂环
1.
The research progress on carbonylation reactions of heterocycles (such as epoxides and aziridines) during the last 40 years is reviewed in the presence of transition metal complex catalysts.
综述了近 4 0年来杂环化合物和一氧化碳在金属络合物催化下的羰基化反应 ,详细讨论了不同类型反应的有关机理 ,并展望了该领域的研究前景。
5)  hetero-cyclo peptide
杂环肽
6)  N-heterocyclic
N-杂环
1.
Research on Enantioselective Benzoin Condensations Using N-heterocyclic Carbenes;
手性N-杂环卡宾催化不对称偶姻缩合研究进展
参考词条
补充资料:2-乙基己醛环乙二醇缩醛
分子式:
CAS号:

性质:为脂肪族醛的环状缩醛。无色液体。具强的清香,也有像菊花和栀子花香韵。沸点77~78℃(1.3kPa)。0.909~0.917。1.433~1.439。由2-乙基己醛和乙二醇在酸性催化剂存在下共沸脱水生成。主要用于香皂、合成洗涤剂等日用香精。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。