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Preparation of syn-d-Hydroxyl-b-Amino Esters via an Intramolecular Hydrogen Bond Directed Diastereoselective Hydrogenation. Total Synthesis of (3S, 4aS, 6R, 8S)-Hyperaspine

机译：通过分子内氢键指向的非对映选择性氢化制备SYN-D-羟基-B-氨基酯。（3S，4A，6R，8S）的总合成

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1. Preparation of syn-δ-Hydroxy-β-amino Esters via an Intramolecular Hydrogen Bond Directed Diastereoselective Hydrogenation. Total Synthesis of (3S,4aS,6R,8S)-Hyperaspine [J] . Wei Zhu, Dawei Ma Organic letters . 2003,第26期

机译：通过分子内氢键定向非对映选择性加氢制备合成-δ-羟基-β-氨基酯。（3S，4aS，6R，8S）-Hyperaspine的全合成
2. Preparation of Enantiopure Norbornane Ligands Bearing Both (2S,3S)-Bis(phosphinomethyl) and 7-syn-Oxygen Functional Groups and an Application to Rhodium-Catalyzed Asymmetric Hydrogenation. [J] . Morimoto T, Yamazaki A, Achiwa K Chemical and Pharmaceutical Bulletin . 2004,第11期

机译：带有（2S，3S）-双（膦甲基）和7-合成氧官能团的对映体纯降冰片烷配体的制备及其在铑催化的不对称加氢中的应用。
3. Synthesis of (3S,6RS)- and (3RS,6RS)-analogs of component AI of the Aonidiella aurantii sex pheromone by stepwise alkylation of acetoacetic ester [J] . Ishmuratov GY, Kharisov RY, Yakovleva MP, Chemistry of Natural Compounds . 2005,第6期

机译：通过乙酰乙酸酯的逐步烷基化合成Aonidiella aurantii性信息素的组分（3S，6RS）-和（3RS，6RS）-类似物
4. First direct observation of C=O o o o H-N intramolecular hydrogen bonds in 3_(10)-helical peptides [C] . Mario Rainaldi, Massimo Bellanda, Stefano Mammi International Peptide Symposium;European Peptide Symposium . 2005

机译：第一次直接观察C = O O O H-N在3_（10） - 尿布中的分子内氢键
5. Part One. Synthesis of optically active tryptophan derivatives with potential activity as indoleamine 2,3-dioxygenase inhibitors: An approach via asymmetric catalytic hydrogenation. Part Two. Design, synthesis and pharmacology of selective ligands for alpha1-containing GABA(A)/benzodiazepine receptor subtypes: SAR studies of beta-carbolines at positions -3 and -6 and their corresponding bivalent ligands. Part Three. First enantiospecific total synthesis of the important biogenetic intermediates, (+)-polyneuridine and (+)-polyneuridine aldehyde, as well as 16-epi-vellosimine and macusine A. [D] . Yin, Wenyuan. 2007

机译：第一部分。具有吲哚胺2,3-二加氧酶抑制剂潜在活性的旋光色氨酸衍生物的合成：一种通过不对称催化氢化的方法。第二部分。含α1的GABA（A）/苯并二氮杂receptor受体亚型的选择性配体的设计，合成和药理作用：位于-3和-6位的β-咔啉及其相应的二价配体的SAR研究。第三部分。重要生物遗传中间体，（+）-聚神经氨酸和（+）-聚神经氨酸醛，以及16-表-维西辛和Macusine A的首次对映体全合成。
6. Diastereoselective Synthesisof Highly SubstitutedTetrahydrofurans by Pd-Catalyzed Tandem Oxidative Cyclization–RedoxRelay Reactions Controlled by Intramolecular Hydrogen Bonding [O] . JoshuaL. Brooks, Liping Xu, Olaf Wiest, -1

机译：非对映选择性合成高度替代钯催化串联氧化环化氧化还原四氢呋喃分子内氢键控制的接力反应
7. Preparation of syn-d-Hydroxyl-b-Amino Esters via an Intramolecular Hydrogen Bond Directed Diastereoselective Hydrogenation. Total Synthesis of (3S, 4aS, 6R, 8S)-Hyperaspine [O] . -1

机译：通过分子内氢键指向的非对映选择性氢化制备SYN-D-羟基-B-氨基酯。（3S，4A，6R，8S）的总合成

Preparation of syn-d-Hydroxyl-b-Amino Esters via an Intramolecular Hydrogen Bond Directed Diastereoselective Hydrogenation. Total Synthesis of (3S, 4aS, 6R, 8S)-Hyperaspine

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