A Diepoxide Belonging to the Rare C1 Point Group

2,6- and 2,7-Dimethylanthracenes were reduced seriatim with lithium in liquid ammonia and lithium in methylamine to their 1,4,5,8,9,10-hexahydro derivatives. Two-fold epoxidation of these tetraenes provided the cis and trans diepoxides resulting from electrophilic attack at the inner double bonds. Trans diepoxide 1 has the very unusual characteristic of lacking a σ plane of symmetry but possessing an inversion center. As a consequence, the ¹H NMR spectrum of C₁-symmetric 1 is simplified relative to those of its isomers 5, 9, and 10.     

取代对苯二酚醚化物的合成研究

本文从取代的对苯三酚３出发、利用Ｗｉｌｌｉａｍｓｏｎ醚化反应合成了一系列它的醚化产物４ａ－４Ｈ，给出了它们的核磁共振数据（氢谱和碳谱）。讨论了影响醚化反应的一些因素，比较了不同烷化剂发生醚化反应的活泼性。     

Formation of 2,6-dioxabicyclo[3.3.0]-octa-3,7-dienes or multiply substituted o-benzoquinones from reactions of 1,4-dilithio-1,3-dienes with dimethyl oxalate

Reactions of 1,4-dilithio-1,3-dienes with dimethyl oxalates afforded multiply substituted o-benzoquinones or stereodefined 2,6-dioxabicyclo[3.3.0]-octa-3,7-dienes in good yields.     

An efficient and facile one-step synthesis of highly substituted thiophenes

An efficient one-step method for the synthesis of fully substituted thiophenes, from thiomorpholides and α-halo ketones, was developed. A mechanism has also been proposed for the course of reaction.     

Expedient synthesis of substituted imidazoles from nitriles

Expedient and practical new methodology for the synthesis of substituted imidazoles was developed to provide a rapid access to a variety of 2-substituted, 1,2-disubstituted and 1,2,4-trisubstituted imidazoles by the direct CuCl-mediated reaction of nitriles with α-amino acetals in an intermolecular as well as intramolecular fashion.     

Base- and light-assisted synthesis of anthracenes from 3-allylnaphthalene-2-carbaldehydes

The synthesis of substituted anthracenes from naphthalene precursors is described. The key step involved heating ortho-allyl substituted naphthalene-2-carbaldehydes and potassium t-butoxide in DMF with concomitant irradiation from a high pressure mercury lamp to afford anthracenes in yields of 76-98%.     

CCl2(A1B1)被O2及取代甲烷类分子猝灭的动力学研究

对CCl4／Ar混合气体放电产生CCl2自由基，再用541.52nm激光将电子基态CCl2激发到激发态A^1B1（0，4，0）振动态k=0能级上，通过检测 激发态CCl2时间分辨荧光信号，测得室温下CCl2(A^1B1)被O2，CF4，CF2Cl，CH3NO2，CH2Br2等分子猝灭的实验结果，用改进的三能级模型分析处理实验数据，获得态分辨速常数KA和Ka值，并对实验结果进行了讨论。     

Stereoselective synthesis of the ABCD ring framework of azaspiracids

A stereoselective synthesis of the ABCD ring framework of azaspiracid-1 and azaspiracid-3 has been achieved using a tandem bis-spiroketalization protocol in the presence of a mild proton source from 1,4-diketone precursor. A tetrahydrofuran intermediate with the correct stereochemistry for the D ring of azaspiracids-1 and 3 was then taken through a linear sequence of reactions to afford the desired diketone precursor. The D-ring of azaspiracid-1 was then constructed by employing a Sharpless asymmetric dihydroxylation followed by etherification using a homoallyl derivative. The structure of the ABCD ring framework with four contiguous rings was established by extensive NMR analysis.     

取代苯系列衍生物电子结构与毒性关系的量子化学研究

取代苯系列衍生物电子结构与毒性关系的量子化学研究苏忠民，徐贤姬，李金昶（东北师范大学化学系，长春，１３００２４）赵宝忠，盛连喜（东北师范大学环科系，长春，１３００２４）关键词：取代苯衍生物，分子毒性，ＭＮＤＯ采用量子化学半经验ＡＭＩ、ＭＮＤＯ方法，从...     

New selective O-debenzylation of phenol with Mg/MeOH

Carboxylate-benzyl and nitro-benzyl groups used in phenols protection were selectively debenzylated with 3-25 equiv of Mg in methanol at room temperature. Good yields of the desired phenols were obtained within 3-10 h from a wide variety of O-(carboxylate-benzyl)- or O-(nitro-benzyl)-phenols. Selective O-debenzylation was possible in the presence of O-(carboxylate-benzyl)- or O-(nitro-benzyl)-phenols with Mg/MeOH.