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Highly Stereoselective Michael Addition Reactions of CamTHP*-Desymmetrized Glycinamide for the Synthesis of Functionally Dense Amino Acid Derivatives

机译：高度立体选择性的迈克尔加法ChamTh * -desymetized甘氨酸的反应，用于合成功能致密氨基酸衍生物

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1. Highly Stereoselective Michael Addition Reactions of CamTHP*-Desymmetrized Glycinamide for the Synthesis of Functionally Dense Amino Acid Derivatives [J] . Darren J.Dixon, Richard A.J.Horan, Nathaniel J.T.Monck Organic letters . 2004,第24期

机译：CamTHP *不对称的甘氨酰胺的高度立体选择性迈克尔加成反应，用于合成功能密集的氨基酸衍生物
2. Highly Diastereoselective Michael Addition Reations of Butane-2,3-diacetal Desymmetrize Glycolic Acid. Preparation of #alpha#-Hydroxy-#gamma#-amino Acid Derivatives [J] . Darren J. Dixon, Steven V. Ley, Felix Rodriguez Organic letters . 2001,第23期

机译：丁烷-2,3-二缩醛对称乙醇酸的非对映选择性迈克尔加成反应。＃alpha＃-羟基-＃gamma＃-氨基酸衍生物的制备
3. Highly Diastereoselective Michael Addition Reactions between Nucleophilic Glycine Equivalents and β-substituted-α,β-Unsaturated Carboxylic acid Derivatives a General Approach to the Stereochemically Defined and Sterically χ-Constrained α-Amino Acids [J] . Vadim A. Soloshonok Current Organic Chemistry . 2002,第4期

机译：亲核甘氨酸当量与β-取代的α，β-不饱和羧酸衍生物之间的高度非对映选择性Michael加成反应立体化学定义和立体χ约束的α-氨基酸的一般方法
4. Michael Addition Reactions between Nucleophilic GlycineEquivalents and Acrylic Acid Derivatives as a Practicaland Generalized Approach to the Asymmetric Synthesisof II-Substituted-a-Amino Acids [C] . Vadim A. Soloshonok, Hisanori Ueki, Trevor K. Ellis ACS symposium asymmetric synthesis and application of α-amino acids . 2009

机译：亲核糖糖糖尿剂与丙烯酸衍生物之间的迈克尔添加反应作为不对称合成的不对称 - A-氨基酸的不对称方法的普遍化方法
5. Michael–Heck Approach towards the Synthesis of Highly Functionalized Polyalkyl Furans and Application of the Vinylogous Michael–Heck Reaction towards the Total Synthesis of Furanosesquiterpenes and Furanoeremophilanes [D] . Chen, Yi-Jang Violet. 2021

机译：迈克尔 - Heck探讨了高官能化聚烷基呋喃的合成及乙烯基迈克尔 - Heck反应对呋喃孢素Quiterpenes和呋喃胺磷酸的总合成
6. Michael Addition Reactions between Chiral Equivalents of a Nucleophilic Glycine and (S)- or (R)-3-(E)-Enoyl-4-phenyl-13-oxazolidin-2-ones as a General Method for Efficient Preparation of β-Substituted Pyroglutamic Acids. Case of Topographically Controlled Stereoselectivity [O] . Vadim A. Soloshonok*, Chaozhong Cai, Takeshi Yamada, -1

机译：亲核甘氨酸与（S）-或（R）-3-（E）-烯丙基 -4-苯基-13-恶唑烷-2-酮的手性当量之间的迈克尔加成反应作为有效制备的一般方法β-取代的焦谷氨酸地形控制立体选择性的情况
7. Highly Stereoselective Michael Addition Reactions of CamTHP*-Desymmetrized Glycinamide for the Synthesis of Functionally Dense Amino Acid Derivatives [O] . -1

机译：高度立体选择性的迈克尔加法ChamTh * -desymetized甘氨酸的反应，用于合成功能致密氨基酸衍生物

Highly Stereoselective Michael Addition Reactions of CamTHP*-Desymmetrized Glycinamide for the Synthesis of Functionally Dense Amino Acid Derivatives

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