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Synthesis of Novel Pyrido1,2-cpyrimidine Derivatives with 6-Fluoro-3-(4-piperidynyl)-1,2-benzisoxazole Moiety as Potential SSRI and 5-HT1A Receptor Ligands

机译：具有6-氟-3-（4-哌啶基）-1,2-苯并异恶唑部分的新型吡啶1,2-C嘧啶衍生物的合成作为潜在的SsRI和5-HT1A受体配体

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Marek Król; Grzegorz Ślifirski; Jerzy Kleps; Szymon Ulenberg; Mariusz Belka; Tomasz Bączek; Agata Siwek; Katarzyna Stachowicz; Bernadeta Szewczyk; Gabriel Nowak; Beata Duszyńska; Franciszek Herold;
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1. Synthesis of new 5,6,7,8-tetrahydropyrido[1,2-c]pyrimidine derivatives with rigidized tryptamine moiety as potential SSRI and 5-HT1A receptor ligands [J] . Slifirski Grzegorz, Krol Marek, Kleps Jerzy, European Journal of Medicinal Chemistry: Chimie Therapeutique . 2019,第期

机译：用刚性的木粉胺部分合成新的5,6,7,8-四氢吡啶衍生物作为潜在的SSRI和5-HT1A受体配体
2. Synthesis of novel pyrido[1,2-c]pyrimidine derivatives with rigidized tryptamine moiety as potential SSRI and 5-HT1A receptor ligands [J] . Slifirski Grzegorz, Krol Marek, Kleps Jerzy, European Journal of Medicinal Chemistry: Chimie Therapeutique . 2019,第期

机译：用刚性的木瓜部分的新型吡啶[1,2-C]嘧啶衍生物的合成作为潜在的SSRI和5-HT1A受体配体
3. Synthesis of new hexahydro- and octahydropyrido(1,2-c)pyrimidine derivatives with an arylpiperazine moiety as ligands for 5-HT1A and 5-HT2A receptors. Part 4. [J] . Herold F, Krol M, Kleps J, European Journal of Medicinal Chemistry: Chimie Therapeutique . 2006,第1期

机译：合成具有芳基哌嗪部分作为5-HT1A和5-HT2A受体配体的六氢-和八氢吡啶并（1,2-c）嘧啶衍生物。第4部分
4. SYNTHESIS OF IMIDAZO1,2-cPYRIMIDINE DERIVATIVES [C] . Florentina Georgescu, Emilian Georgescu, Pauia C. Iuhas, 12th Romanian International Conference on Chemistry and Chemical Engineering Sep 13-15, 2001 Bucharest, Romania . 2001

机译：咪唑并1,2-c嘧啶衍生物的合成
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. Synthesis of Conformationally Constrained Aryl- or Heteroaryl-piperazinyl Derivatives of Selected Imides as 5-HT1A Receptor Ligands [O] . Jerzy Kossakowski, Mariola Krawiecka, Bożena Kuran 2006

机译：合成的5-酰亚胺（5-HT1A受体配体）的酰亚胺的构象受限的芳基-或杂芳基-哌嗪基衍生物的合成
7. Synthesis and Insecticidal Activity of Mesoionic Pyrido1,2-αpyrimidinone Derivatives Containing a Neonicotinoid Moiety [O] . Jianke Pan, Lu Yu, Dengyue Liu, 2018

机译：含有Neonicotinoid部分的中硫酸吡啶的合成和杀虫活性1,2-α嘧啶酮衍生物

Synthesis of Novel Pyrido1,2-cpyrimidine Derivatives with 6-Fluoro-3-(4-piperidynyl)-1,2-benzisoxazole Moiety as Potential SSRI and 5-HT1A Receptor Ligands

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