萘并

The high purity of 2-mercapto-β-naphthothiazole was obtained with α-naphthylamine as raw material via reaction of seal glass tube, alkaline extraction, vapor distillation, acidification of acetic acid and ethanol recrystallization.

以α-萘胺为起始原料，通过封管反应、碱提取、水蒸气蒸馏、乙酸酸化和乙醇重结晶，取得了纯度较高的2-巯基－β-萘并噻唑。

N-Methyl-3,3-dimethyl spiroindoline-2,3'[3H] naphthaline [2,1-b] [1,4] oxazine was synthesized by 1,3,3-trimethyl-2-methylene indoline and 1-nitroso-2-naphthol, its UV and IR spectra and elemental analysis were carried out, and the photochromism and main influencing factors such as temperature, solvent and pH were studied.

以1，3，3-三甲基－2-亚甲基吲哚啉和1-亚硝基－2-萘酚为原料合成了N-甲基－3，3-二甲基螺吲哚啉-2，3'[3H]萘并[2，1-b][1，4]恶嗪，对其进行了紫外和红外光谱以及元素分析，并对其光致变色性质以及主要影响因素温度、溶剂和pH进行了研究。

In view of their versatile applications, the crystal structures of two naphthopyrone derivatives were for the first time undertaken. The planarity and rigidity are their most important structural features

萘并吡喃酮具有多方面的用途，为深入研究结构与性能的关系，首次测得了两种萘并吡喃酮的单晶分子结构，平面刚性是它们最为重要的分子结构特征。

Study on Surface Enhanced Raman Scattering of Piperidine;2. Using piperidine as catalyst and ethanol as solvent, a series of new 2-amino-3-cyano-4-aryl-6-methoxy-1,4,9,10-tetrahydronaphtho[2,1-b]pyran derivatives were synthesized by one-pot reaction of aromatic aldehydes, malononitrile and 7-methoxy-1,2,3,4-tetrahydronaphthalen-2-one at room temperature in good yields.

以芳醛、丙二腈和 7 甲氧基 1，2 ，3 ，4 四氢萘 2 酮为原料，在六氢吡啶催化下以乙醇为溶剂，在室温合成了一系列新的 2 氨基 3 氰基 4 芳基 6 甲氧基 1，4，9，10 四氢萘并 [2 ，1 b]吡喃衍生物，反应条件温和，产率较高，并通过IR ，1HNMR和元素分析表征产物的结构，还通过单晶X射线衍射分析确证产物的构

They are 4-(2- hydroxy-3-butynlenoxy) benzoic acid (1, WA), 5-chloro-7, 8-dihydroxy-7-methyl- 6-oxo-3- [ -3, 4-dihydroxy-3, 5-dimethyl-l-heptylene] -1H-8, 8a-dihydrobenzo [2, 3-c] pyran (2, WB),-2-(2-methyl-2-dibutene diamido)-2-butenoic acid (3, B5262), 3, 4-dihydro-9, 10-dihydroxy-7-methoxy-3-methyl-1H-naphtho [2, 3- c] pyran-1-one (4, A73 semi-Vioxanthin), 8, 8'-bis (6, 9-dioxo-3,4-dihydro-10- hydroxy-7-methoxy-3-methyl-1H-naphtho [2, 3-c] pyran-1-one)(5, A122 Xanthomegnin), 2, 5-dioxo-3a-hydroxymethyl-3, 3a, 6, 6a-tetrahydro-furo [2, 3-b] furan (6, 1003-2), 7-acety1-5-chloro-6, 8-dioxo-7-methyl-3- [ -3, 5-dimethyl-1, 3- diheptylene] -4aH-benzo [2, 3-c] pyran (7, M2-2 sclerotiorin), respectively.

它们分别被命名为4-（2-羟基-3-丁炔氧基）苯甲酸（1，WA）、5-氯-7，8-二羟基-7-甲基-6-氧代-3-[-3，4-二羟基-3，5-二甲基-1-庚烯基]-1H-8，8a-二氢苯并[2，3-c]吡喃（2，WB）、-2-（2-甲基-2-丁烯二酰亚胺基）-2-丁烯酸（3，B5262）、3，4-氢-9，10-二羟基-7-甲氧基-3-甲基-1H-萘并［2，3-c］吡喃-1-酮（semi-Vioxanthin，4，A73）、8，8'-双（6，9-二氧代-3，4-二氢-10-羟基-7-甲氧基-3-甲基-1H-萘并［2，3-c］吡喃-1-酮）（Xanthomegnin，5，A122）、2，5-二氧代-3a-羟甲基-3，3a，6，6a-四氢-呋喃并［2，3-b］呋喃（6，1003-2），7-乙酰基-5-氯-6，8-二氧代-7-甲基-3-［-3，5-二甲基-1，3-庚二烯基］-4aH-苯并2，3-c］吡喃（Sclerotiorin，7，M2-2）。

Chloro-5,12-naphthacenequinone was synthesized from 2-(1-hydroxy-2-naphthyl)carbonylbenzoic acid by chlorination reaction using a mixture of phosphorus pentachloride and phosphorus oxychloride as a chlorating agent and then by ring-closing reaction using sulfuric acid as a dehydrating agent.

以2-[(1-羟基-2-萘基)羰基]苯甲酸为原料、五氯化磷/三氯氧磷为氯化剂进行氯化反应，然后用浓硫酸脱水环化，合成了6-氯-5，12-萘并萘醌，优化了反应条件，总收率达68.2%。

Detailed studies on their photochromic properties were made out and the relation between molecular structure and properties were studies.

此外对萘并吡喃的掺杂在高分子膜中的抗疲劳性质也进行了研究，结果表明所合成的萘并吡喃衍生物具有较好的抗疲劳性质。

In this thesis, the design, synthesis and application of substituted 1,8-naphthalimides and napthopyrones conjugated with uridine, substituted 1,3,5-triazine, 1,2-dibromoethane, ethyl bromoacetate have been studied.

本论文研究了取代l，8-萘酰亚胺和萘并吡喃酮与尿苷、取代均三嗪、二溴乙烷、溴乙酸乙酯偶合和双l，8-萘酰亚胺之间偶合的设计、合成及应用。

Finally, N ethey[3,3 dimethyl spiralindoline naphthoxazine]was synthesized by the addition of 1 nitroso 2 naphthol also,the photochromic mechanism of the substance and its photochromic phenomenon in ethanol were studied.

报道了以苯肼和 3 甲基 2 丁酮为原料首先合成 2 ，3 ，3 三甲基吲哚，吲哚再与碘乙烷亲核取代，碱化得费舍尔碱，最后与 1 亚硝基 2 萘酚作用合成N 乙基 [3 ，3 二甲基螺吲哚啉萘并恶嗪 ]的全过程，并研究了该物质的变色机理以及在乙醇溶剂中的光致变色现

The ten target compounds from alkyl substituent to aryl substituent that have not yet been reported,which was obtained by dehydration, Subsequently treated with sodium nitrite resulting nitroso compounds and then reduced.

本论文以2-羟基-3-萘酸和邻巯基苯胺为原料，通过分子脱水、亚硝化、还原等反应合成了10个不同取代基团的4-苯并噻唑基-[1，2-d]萘并噁唑衍生物，并优化了合成的工艺条件。

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。