1) Oxa-Diels-Alder reaction
Oxa-Diels-Alder反应
1.
In this context, we document the organocatalytic asymmetric Aldol reactions as well as Oxa-Diels-Alder reactions.
本文研究了用脯胺酰胺催化的不对称Aldol反应和吡咯烷催化的Oxa-Diels-Alder反应来合成四氢吡喃酮类化合物，取得了满意的结果。
2) Diels-Alder reaction
Diels-Alder反应
1.
Asymmetric Diels-Alder reaction catalyzed by Mg(ClO_4)_2;
高氯酸镁催化不对称Diels-Alder反应
2.
The application of Diels-Alder reaction to syntheses of terpenoids;
Diels-Alder反应在萜类化合物合成中的应用
3.
Modeling the Diels-Alder reaction of the spontaneous initiation of the polymerization of n-butyl acrylate;
丙烯酸正丁酯聚合的Diels-Alder反应机理理论研究(英文)
3) Diels-Alder reaction
Diels-Alder 反应
1.
Diels-Alder reaction has a huge applied value as their high regional selectivity and st.
Diels-Alder 反应,因其很高的区位和立体选择性而具有巨大的应用价值。
4) retro-Diels-Alder reaction
逆Diels-Alder反应
5) hetero-Diels-Alder reaction
杂Diels-Alder反应
1.
Application of hetero-Diels-Alder reaction in synthesis of piperidine derivatives;
杂Diels-Alder反应在合成哌啶衍生物中的应用
2.
The hetero-Diels-Alder reactions between methyl pyridinedithiocarboxylates and butadienes have been investigated theoretically using density functional theory at the B3LYP/6-31G(d) level, in which the influences of catalysts, solvents and substituent groups on the mechanisms and activation barriers of these reactions have been involved.
采用密度泛函理论方法在B3LYP/6-31G(d)水平上对吡啶二硫代酯与丁二烯的杂Diels-Alder反应的反应机理进行了理论计算研究,并且也考虑了催化效应、溶剂化效应及取代基效应对反应机理和反应位垒的影响。
3.
Four hetero-Diels-Alder reactions between phosphonodithioformate and 1-acetoxybutadiene have been studied theoretically with density functional theory at B3LYP/6-31G(d) level.
采用密度泛函理论方法在B3LYP/6-31G(d)水平上对膦酰基二硫代甲酸酯与1-乙酰氧基丁二烯的4种可能的杂Diels-Alder反应进行了理论计算研究。
6) hetero Diels-Alder reaction
杂Diels-Alder反应
1.
Theoretical study on the hetero Diels-Alder reaction between 1,3-butadiene and silyleneimine;
1,3-丁二烯与硅甲基亚胺杂Diels-Alder反应的理论研究
2.
During the hetero Diels-Alder reaction (HAD) between 4-(4-methoxyphenyl)-1-phenyl-3- (trimethylsilyloxy)-2-aza-butadiene (2-ABDE) and hexanone, a unimolecular [2+2] cyclization of 2-ABDE forming a four-membered monocyclic β-lactam took place.
研究了不同的Lewis酸催化剂、温度、微波等条件下,4-(4-甲氧苯基)-1-苯基-3-三甲基硅氧基-2-氮杂-1,3-丁二烯(2-ABDE)和亲二烯体环己酮发生杂Diels-Alder反应生成[4+2]的六元环合产物噁嗪酮衍生物,伴随的2-ABDE的[2+2]单分子环合,生成单环β-内酰胺衍生物。
补充资料：2,2,4-trimethyl-1-Oxa-4-aza-2-silicacyclohexane
CAS: 10196-49-3
分子式:C6H15NOSi
中文名称: 2,2,4-三甲基-1-氧杂-4-氮杂-2-硅杂环己烷
英文名称: 2,2,4-trimethyl-1-Oxa-4-aza-2-silacyclohexane；2,2,4-trimethyl-1-Oxa-4-aza-2-silicacyclohexane；2,2,4-trimethyl-1-oxa-4-aza-2-silacyclohexan
分子式:C6H15NOSi
中文名称: 2,2,4-三甲基-1-氧杂-4-氮杂-2-硅杂环己烷
英文名称: 2,2,4-trimethyl-1-Oxa-4-aza-2-silacyclohexane；2,2,4-trimethyl-1-Oxa-4-aza-2-silicacyclohexane；2,2,4-trimethyl-1-oxa-4-aza-2-silacyclohexan
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
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