1) THPP
四氢吡啶戊二烯
2) 6,7-dihydro-5H-cyclopenteno[b]pyridine
6,7-二氢-5H-环戊烯并[b]吡啶
1.
6,7-Dihydro-5H-cyclopenteno[b]pyridine was prepared from 1-amino-2-cyanocyclopentene by acetylation, cyclization and chlorination to give 4-amino-2-chloro-6,7-dihydro-5H-cyclopenteno[b]pyridine, which was subjected to Sandmeyer bromination and then catalytic hydrogenated dehalogenation with an overall yield of about 61%.
1-氨基-2-氰基环戊烯经乙酰化、闭环和氯化反应制得4-氨基-2-氯-6,7-二氢-5H-环戊烯并[b]吡啶,再经Sandmeyer溴化和钯炭催化氢化脱卤制得6,7-二氢-5H-环戊烯并[b]吡啶,总收率为61%。
3) Tetrahydrocyclopentadiene
四氢二环戊二烯
4) tetrahydropyridine
四氢吡啶
1.
Functionalized tetrahydropyridine and piperidine ring systems are widely found in biologically active natural products and pharmaceuticals.
四氢吡啶和哌啶环结构是那些有生物活性和药用价值的天然产物中最常见的结构之一。
5) tetrahydrodicyclopentadiene
四氢双环戊二烯
1.
Study on Endo-to Exo-Isomerization of Tetrahydrodicyclopentadiene Catalyzed by Y Zeolites;
Y分子筛催化桥式四氢双环戊二烯异构化制备椅式四氢双环戊二烯
2.
Adamantane(ADH) was synthesized by isomerization of endo-tetrahydrodicyclopentadiene(endo-TCD) over supported AlCl_3 catalyst.
以固载化AlCl3为催化剂催化桥式四氢双环戊二烯(endo-TCD)异构化合成金刚烷。
3.
Exo-tetrahydrodicyclopentadiene(exo-THDCPD), the isomer of endo-tetrahydrodicyclopentadiene (endo-THDCPD), can be used as an excellent liquid fuel with high density, high heating value and low viscosity at low temperature.
采用无水AlCl3为催化剂,考察了使用不同溶剂对桥式四氢双环戊二烯(endo-THDCPD)异构化为挂式四氢双环戊二烯(exo-THDCPD)过程中反应速率、反应转化率、收率、选择性及杂质生成量的影响。
6) tetrahydrotricyclopentadiene
四氢三环戊二烯
1.
This dissertation is concerned with the approaches to a new high density liquid fuel, tetrahydrotricyclopentadiene (THTCPD), which can be synthesized with dicyclopentadiene (DCPD) as raw materials by three steps: Diels-Alder reaction, separation and hydrogenation.
本文以双环戊二烯(DCPD)为原料,通过双烯加成、分离、加氢反应得到目的产物——新型高密度液体燃料四氢三环戊二烯(THTCPD),主要研究内容包括: 1。
补充资料:四氢吡啶戊二烯
分子式:
CAS号:
性质:放线菌MD736-C6产生的一种兔肺N-甲基转移酶的非特异性抑制剂。THPP盐酸盐为无色晶体,熔点192℃,无旋光性,茚三酮反应显黄色。与色胺和S-腺苷基-L-蛋氨酸有竞争性作用,但不抑制儿茶酚-O-甲基转移酶。毒性大,小鼠静脉注射LD505.9mg/kg,无抗菌活性。
CAS号:
性质:放线菌MD736-C6产生的一种兔肺N-甲基转移酶的非特异性抑制剂。THPP盐酸盐为无色晶体,熔点192℃,无旋光性,茚三酮反应显黄色。与色胺和S-腺苷基-L-蛋氨酸有竞争性作用,但不抑制儿茶酚-O-甲基转移酶。毒性大,小鼠静脉注射LD505.9mg/kg,无抗菌活性。
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
参考词条