萘烷

Quinoline catalytic cracking was studied on a fixed-bed microactivity test unit by using toluene, cetane, and tetralin as solvent.

采用固定床微反活性实验装置，以甲苯、十六烷、四氢萘为溶剂，研究了碱性含氮化合物喹啉的催化裂化转化规律。

S-1-phenylethanol was obtained in up to 19%ee in toluene at 0℃.(4)A series of C_2-symmetric chiralβ-amino alcoholsⅣ-5were synthesized in several steps from natural amino acid L-proline,and applied in the asymmetric borane reduction of prochiral ketones.

4以天然L-脯氨酸为起始原料，经过几步转化合成了以萘环为母体的C_2-对称的手性β-氨基醇Ⅳ-5，将其应用于硼烷对前手性酮的不对称还原反应中，同样，我们也观测到温度影(来源：Ac1BC论文网www.abclunwen.com)响产物构型的现象。

Asymmetric catalytic activity of chiral spiroborate esters,- or-1,1′-bi-2-naphthoxyboric acid-proline anhydride [-1 or-1], toward borane reduction of prochiral imine s has been ob- served.

手性螺硼酸酯-或-1，1'-联-2-萘酚硼酸--脯氨酸酐[-1或-1]对前手性亚胺硼烷还原的不对称催化活性被观察到。

Alkylbenzene, normal alkanes and alkylcyclohexane on the pyrolysates of P. Boryanum at 300℃ had uniform distribution and the relative content of them was similar, indicating that they originated from same precursors. Fatty acids, alcohol and ketone in algal cell are the possible precursors. For example, the precursor of relatively abundant C〓 alkylbenzene and alkylbenzene with C〓 side chain perhaps related with palmitic acid. N-alkylnaphthalene in pyrolysates at 300℃ probably derived from alkylation of cleavage products of aromatic steranes and terpanes.

在盘星藻300℃热解产物中，烷基苯、正烷烃和烷基环己烷碳数分布一致、各化合物的相对含量接近，表明它们有相同的来源，藻类体内的脂肪酸、醇和酮及细胞壁等物质可能是其母质，相对含量较高的碳数为16及侧链碳数为16的烷基苯类化合物，其前身物可能与软脂酸有关。300℃热解产物中的正烷基萘类化合物，可能由芳香甾、萜类的降解产物与直链烃类加成烷基化而形成。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。