首页> 外文OA文献 >Stereochemical studies. XLI. Asymmetric synthesis of optically active 4a-methyl-4,4a,9,10-tetrahydro-2(3H)-phenanthrone derivatives, key intermediates for total syntheses of optically active diterpenes and steroids.

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Stereochemical studies. XLI. Asymmetric synthesis of optically active 4a-methyl-4,4a,9,10-tetrahydro-2(3H)-phenanthrone derivatives, key intermediates for total syntheses of optically active diterpenes and steroids.

机译：立体化学研究。 XLI。光学活性4a-甲基-4,4a，9,10-四羟基-2（3h） - 苯蒽酮衍生物的不对称合成，用于光学活性的替代萜和类固醇的总合成的关键中间体。

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TAKANORI SONE; SHIRO TERASHIMA; SHUNICHI YAMADA;
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年度 1976
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1. Efficient Synthesis of Optically Active 2-N-Boc (or Cbz)-amino-l-arylethanols as Key Intermediates for Synthesis of Chiral Drugs via Asymmetric Reduction [J] . Byung Tae Cho, Sung Hye Shin Bulletin of the Korean Chemical Society . 2004,第5期

机译：高效合成光学活性的2-N-Boc（或Cbz）-氨基-1-芳基乙醇作为通过不对称还原合成手性药物的关键中间体
2. Efficient Synthesis of Optically Active 2-N-Boc (or Cbz)-amino-1-arylethanols as Key Intermediates for Synthesis of Chiral Drugs via Asymmetric Reduction [J] . Byung Tae Cho, Sung Hye Shin Bulletin of the Korean Chemical Society . 2004,第5期

机译：有效合成旋光性2-N-Boc（或Cbz）-氨基-1-芳基乙醇作为通过不对称还原合成手性药物的关键中间体
3. Synthesis of Optically Active #alpha#-Furfuryl Amine Derivatives and Application to the Asymmetric Syntheses [J] . Wei-Shan Zhou, Zhi-Hui Lu, Yi-Ming Xu, Tetrahedron . 1999,第41期

机译：光学活性＃α＃-糠胺衍生物的合成及其在不对称合成中的应用
4. Catalytic Asymmetric Synthesis of α-Amino Acid Derivatives: Approaches toward Green Sustainable Methodology for Preparation of Optically Active Amino Acids [C] . Yasuhiro Yamashita, Shu Kobayashi Asymmetric synthesis and application of α-amino acids . 2007

机译：催化不对称合成α-氨基酸衍生物：绿色可持续方法制备光学活性氨基酸的方法
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. A Convenient Enzymatic Route to Optically Active l-Aminoindan-2-ol: Versatile Ligands for HIV-1 Protease Inhibitors and Asymmetric Syntheses [O] . Arun K. Ghosh, John F. Kincaid, Michael G. Haske -1

机译：光学活性l-Aminoindan-2-ol的便捷酶途径：HIV-1蛋白酶抑制剂和不对称合成的多功能配体。
7. Stereochemical studies. XXXVIII. Asymmetric synthesis of the key compounds for the synthesis of optically active diterpenes. Asymmetric synthesis of optically active 1,2,3,4,5,6-7,8,8a-octahydro-8a-methyl-3,8-naphthalenedione derivatives with L-proline derivatives. [O] . KUNIO HIROI, SHUNICHI YAMADA 1975

机译：立体化学研究。 xxxviii。用于合成光学活性脱萜的关键化合物的不对称合成。具有L-脯氨酸衍生物的光学活性1,2,3,4,5,6-7,8,8-萘二硫醚衍生物的不对称合成。
8. Sterically controlled syntheses of optically active organic compounds. 13: Catalytic hydrogenation of symmetric substrates in the presence of asymmetric molecules [R] . Yoshida, T. 1971

机译：空间控制的光学活性有机化合物的合成。图13：在不对称分子存在下对称底物的催化氢化

Stereochemical studies. XLI. Asymmetric synthesis of optically active 4a-methyl-4,4a,9,10-tetrahydro-2(3H)-phenanthrone derivatives, key intermediates for total syntheses of optically active diterpenes and steroids.

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