加成化合物

Thiazolidiane-4-carboxylic acid was prepared and used as the aid catalyst that has strengthened the catalytic effect of chloroplatinic acid, greatly improved the yield of the hydrosilylation of methyldichlorosilane with allychloride, and made the yield get to 64.9%.

通过比较，选用自制的含硫化合物4-羧基-1，3-噻唑烷作助催化剂，大大增强了氯铂酸的催化活性，使甲基二氯硅烷与氯丙烯的加成反应以较高产率得到γ-氯丙基甲基二氯硅烷，产率可达64.9%。

Firstly, 3-ethylthiobutanal was prepared from crotonaldehyde reacting with ethanehiol in triethylamine with high yield. Secondly, methyl acetoacetate was converted to 6-ethylthiohept-3-en-2-one by three steps via hydrolysis, condensation with 3-ethyltio-butanal and dehydration, then 6-ethylthiohept-3-en-2-one was cycloco ndensed with dimethyl malonate by Michael addition and Claisen condensation, followed by saponification and decarboxylation to give the intermediate of 5-(2-ethylthiopropyl)-cyclohexane-1,3-dione.

首先，以巴豆醛与乙硫醇为原料，在三乙胺的催化作用下高收率制得3-乙硫基丁醛；然后从乙酰乙酸甲酯出发，通过碱水解、与3-乙硫基丁醛缩合、脱水三步反应合成6-乙硫基-3-烯-2-庚酮，接着6-乙硫基-3-烯-2-庚酮与丙二酸二甲酯通过Michael加成和Claisen缩合成环，再通过皂化和脱羧反应生成中间体5-[2-丙基]-1，3-环己二酮；再与丙酸酐反应丙酰化，最后与0-3-氯-2-丙烯基羟胺肟化，得到目标化合物烯草酮。

A second group includes those compositions, which include an organic polymeric binding material, eg, mixed cellulose esters of monobasic or dibasic acids such as cellulose acetate succinate; an addition-polymerizable ethylenically unsaturated compound, eg, vinylidene and vinyl monomers, preferably of the acrylic or alkacrylic ester type; eg, triethylene glycol diacrylate; and an addition-polymerization initiator which forms radicals under the influence of actinic radiation, eg, anthraquinone.

第二组包括那些作品，其中包括有机聚合物具有约束力的物质，例如，对一元或二元酸混合纤维素酯，如醋酸纤维素琥珀酸； 1此外，聚合ethylenically不饱和化合物，例如，偏和乙烯基单体，丙烯酸最好的或alkacrylic酯类型，如，三乙二醇二丙烯酸酯；和加成聚合引发剂的形式下光化辐射的影响自由基，例如，蒽醌。

The possibility of 1,4-asymmetric induction in some nucleophilic addition reactions of chiralγ-amino Z-enals 7 with organolithium compounds was investigated.

本文研究了在手性的顺式-γ-氨基-α，β-不饱和醛(7)与有机锂化合物的亲核加成反应中的1，4-不对称诱导效应。

Generally, these compounds are derived from accessible α–oxoketen dithioacetals and the common methods of preparation involve regioselective sodium borohydride 1,2-reduce of α–oxoketen dithioacetals, 1,2-nucleophilic addition of organomatals such as organomagnesium, organolithium, Reformatsky regent to α–oxoketen dithioacetals, Baylis-Hillman reaction between polarized ketene dithioacetals and aldehydes.

主要方法包括：使用硼氢化钠1，2-选择性还原α-羰基二硫缩烯酮；利用有机金属化合物（如有机镁试剂，有机锂试剂，Reformatsky试剂等）对α-羰基二硫缩烯酮进行1，2-亲核加成；通过α-羰基二硫缩烯酮与芳醛进行Baylis-Hillman反应等获得。

The recent advancement of the asymmetric addition of organozinc reagent s to ketones and α-ketoesters is reviewed according to the type of the chiral ligands, with an emphasis on the introduction of the ligands with high efficiency and high selectivity.

按照手性配体的结构类型分类，综述了近年来有机锌试剂对酮、α-酮酯等化合物的不对称加成反应的研究进展，对高效、高选择性的手性配体在该类反应中的应用进行了重点评述。

Mehods Commercially available glycine ethyl ester hydrochloride was used as starting material to give the target compound via addition, protection with BOC, Dieckmann cyclation, reduction with NaBH4 and LiAlH4, protection, oxidation, oximation and deprotection.

以甘氨酸乙酯盐酸盐为原料，依次经加成、BOC保护氨基、Dieckmann环化、NaBH4还原羰基、LiAlH4还原氰基、BOC保护氨甲基、氧化、肟化、脱BOC保护等9步反应制得目标化合物。

For flavonoids containing 2,3-doublebond in their C ring, peroxyl radicals mainly add on the double bond, and the adductsmay transfer to the final products through short chain reactions, which results in theincrease of G values of hydrogen peroxide.

根据实验结果我们认为黄酮类化合物与过氧自由基的反应是加成与电子转移的混合反应。

Addition of metallated terminal alkynes to carbonyls is considered as an effective route for the synthesis of chiral propargyl alcohols and has gained considerable significance in recent years.

末端炔对羰基化合物的不对称加成反应是构建手性炔丙醇的重要方法之一，其产生的光学活性炔丙醇是很多天然产物，精细化学品及药物分子的重要合成砌块。

The asymmetric alkynylation of carbonyls is proved to be one of the most powerful procedures for organic synthetic chemistry,where the formation of one carbon-carbon bond and one chiral center of propargylic alcohol can be achieved in one step,and has attracted organic chemists\' most attentions.Plenty of works have been reported in recent years.

由于催化末端炔对羰基化合物的不对称加成在制备手性炔丙醇的同时，能够构建一个碳碳键和一个手性中心，因而该领域的研究受到了研究者的广泛关注，有大量的研究工作见报道。

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。