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Synthesis of Apogalanthamine Analogues as α-Adrenergic Blocking Agents. XIII. Syntheses of Phenolic 8-Hydroxy-5, 6, 7, 8-tetrahydrodibenzc, eazocines

机译：作为α-肾上腺素能阻断剂的α-肾上腺素类似物的合成。 XIII。合成酚8-羟基-5,6,7,8-四氢二苯并C，E紫红素

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Masaru KIHARA; Suwanna VANGVERAVONG; Kuniyoshi OHNISHI; Yasuhiro IMAKURA; Shigeru KOBAYASHI;
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年度 1989
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2. Generation of a Small Library of Highly Electron-Rich 2-(Hetero)Aryl-Substituted Phenethylamines by the Suzuki-Miyaura Reaction:A Short Synthesis of an Apogalanthamine Analogue [J] . Prasad Appukkuttan, Amparo Baiget Orts, R.Prakash Chandran, European journal of organic chemistry . 2004,第15期

机译：铃木-Miyaura反应生成高电子含量的2-（杂）芳基取代的苯乙胺的小文库：Apogalanthamine类似物的简短合成
3. Synthesis of some newer analogues of substituted dibenzoyl phenol as potent anti-inflammatory agents. [J] . Khanum SA, D VT, Shashikanth S, Bioorganic and Medicinal Chemistry Letters . 2004,第21期

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4. SYNTHESIS OF A FLUORINATED ANALOGUE OF PHENOLIC GLYCOLIPID I [C] . Tokarski M., Holemann A. International Carbohydrate Symposium . 2013

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5. Part I. Asymmetric synthesis of bicyclic analogues of risedronate as molecular probes of the mechanism of action of bisphosphonate antiosteoporotic drugs and potentially more efficacious antiosteoporotic agents. Part II. Facile preparation and functionalization of chiral stabilized ylides from common chiral auxiliaries using the Bestmann ylide and their use in Wittig reactions. Part III. Asymmetric organocatalysis: 1. An investigation of alpha-hydroxylation of aldehydes; 2. Synthesis of a novel camphor-based alpha-aminotetrazole organocatalyst. [D] . Song, Xinyi. 2007

机译：第一部分：利塞膦酸盐双环类似物的不对称合成，作为双膦酸盐类抗骨质疏松药和潜在更有效的抗骨质疏松药作用机理的分子探针。第二部分使用Bestmann内酯从常见手性助剂轻松制备和官能化手性稳定化的叶基及其在Wittig反应中的用途。第三部分不对称有机催化：1.醛的α-羟基化研究； 2.合成新的基于樟脑的α-氨基四唑有机催化剂。
6. Extra-vesicular binding of noradrenaline and guanethidine in the adrenergic neurones of the rat heart: a proposed site of action of adrenergic neurone blocking agents. [O] . A Giachetti, R A Hollenbeck 1976

机译：去甲肾上腺素和胍乙啶在大鼠心脏的肾上腺素能神经元的囊泡外结合：拟议的肾上腺素能神经元阻断剂的作用部位。
7. Syntheses of Apogalanthamine Analogues as α-Adrenergic Blocking Agents. XII. : Syntheses and Stereochemistry of Methoxy and Methylenedioxy Derivatives of 8-Hydroxy-5, 6, 7, 8-tetrahydrodibenz-c, eazocines [O] . Masaru KIHARA, Kuniyoshi OHNISHI, Suwanna VANGVERAVONG, 1989

机译：作为α-肾上腺素能阻断剂的α-肾上腺素类似物的合成。 XII。：8-羟基-5，6,7,8-四氢二苯肼-C，E紫红素的合成和立体化学甲氧基和甲基二氧基衍生物
8. Synthesis of Qinghaosu Analogues as Potential Antiparasitic Agents. Phase 1 [R] . Mazur, D. J. 1990

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Synthesis of Apogalanthamine Analogues as α-Adrenergic Blocking Agents. XIII. Syntheses of Phenolic 8-Hydroxy-5, 6, 7, 8-tetrahydrodibenzc, eazocines

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