CAS: 34272-51-0; (-)-Histrionicotoxin

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    合成工艺路线路线简述

      📜Tert-Butyl-Pent-4-Ynyloxy-Diphenyl-Silane置于四(三苯基膦)钯 Chromium(Vi) Oxide,4-二甲氨基吡啶,Copper(L) Iodide,Lithium Aluminium Tetrahydride,正丁基锂,三氯化硼-甲硫醚,4 A Molecular Sieve,硫酸,1-芘乙酸,氢氟酸,Sodium Hexamethyldisilazane,双(三甲基硅烷基)氨基钾,Sodium Hydride,二异丁基氢化铝,Potassium Carbonate,溶剂黄146,二乙胺,三乙胺,对苯二酚,锌,2-碘酰基苯甲酸体系中,用 四氢呋喃,甲醇,正己烷,二氯甲烷,二甲基亚砜,丙酮,甲苯,乙腈 用作溶剂,化学反应 344.6H,反应生成(2S,6R,7S,8S)-7-[(E)-丁-1-烯-3-炔基]-2-[(E)-戊-2-烯-4-炔基]-1-氮杂螺[5.5]十一烷-8-醇
      参考文献:硝基偶极环加成途径为哌啶和吲哚并立兹.第9部分.(-)-吡啶的形式合成和(-)-组织毒素,(+)-组织毒素和(-)-组织毒素235A的总合成
      标题:硝基偶极环加成途径为哌啶和吲哚并立兹.第9部分.(-)-吡啶的形式合成和(-)-组织毒素,(+)-组织毒素和(-)-组织毒素235A的总合成
      摘要:分子内 羟胺--炔烃 环化用于环状硝酮36和44的对映选择性合成.我们已经证明了新的硝酮保护策略的使用环加成 的 苯乙烯环硫酮44的环硫毒素家族的螺环核心的合成中生物碱.偶极脱保护环回 的 苯乙烯 加合物(双环 异恶唑烷 39)和原位分子内偶极环加成(z)-α,β-不饱和侧链的腈与相应的(z)-烯炔36相比,中间体硝基50上的异恶唑烷51的收率高,区域选择性出人意料.该方法适合于合成三环核心结构的对映异构体51和62,它们可以分别通过常见的中间体(例如53和ent-53)转化为天然构型.生物碱(-)-Histrionicotoxin 1和(-)-Histrionicotoxin 235A 65以及非天然(+)-Histrionicotoxin 63.
      Doi:10.1039/b200328G

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      专利信息


      专利号:US-8008459-B2
      优先权日:2001-01-25
      标 题 :Concatemers of differentially expressed multiple genes
      发明人:GOLDSMITH NEIL; SORENSEN ALEXANDRA M P SANTANA; NIELSEN SOREN V S; NAESBY MICHAEL
      权利人:EVOLVA SA
      摘要:In the present invention are disclosed concatemers of concatenated expression cassettes and vectors that enable the synthesis of such concatemers. The concatemer comprises in the 5′→3′ direction a cassette of nucleotide sequence of the general formula [rs2-SP-PR-X-TR-SP-rs1]n wherein rs1 and rs2 together denote a functional restriction site, SP individually denotes a spacer of at least two nucleotide bases, PR denotes a promoter, capable of functioning in a cell, X denotes an expressible nucleotide sequence, TR denotes a terminator, and SP individually denotes a spacer of at least two nucleotide bases, and n>/=2, and wherein at least a first cassette is different from a second cassette. The main purpose of these concatemers is the controllable and co-ordinated expression of large numbers of heterologous genes in a single host. Furthermore, the invention relates to a concatemer of cassettes of nucleotide sequences and a method for preparing the concatemers. In a further aspect, the invention relates to transgenic host cells comprising at least one concatemer according to the invention, as well as to a method for preparing the transgenic host cells. Finally, the invention relates to a vector comprising a cassette of nucleotides, a method for preparing said vector, a nucleotide library comprising at least two primary vectors each comprising a cassette of nucleotides, a method for preparing the library.

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      ✅ COA系统入驻 | 共享模式

      主要参考文献

      参考标题:Total Synthesis Of (−)-Histrionicotoxin
      作者:Yohei Adachi,Noriyuki Kamei,Satoshi Yokoshima,Tohru Fukuyama |发布日期:2011.8.19
      摘要:A Total Synthesis Of (−)-Histrionicotoxin Was Achieved. Our Synthesis Features Preparation Of A Pseudosymmetrical Dienyne Through Chirality Transfer From An Allenylsilane, A Dienyne Metathesis To Produce The Bicyclo [5.4.0] System In Optically Active Form, Selective Functionalization Of A Diene Via A 5-Exo-Trig Iodoetherification, And An Asymmetric Propargylation.

      合成参考文献


      参考文献:10.1111/j.1476-5381.1980.tb10851.x
      摘要:ANWYL R, NARAHASHI T. INHIBITION OF THE ACETYLCHOLINE RECEPTOR BY HISTRIONICOTOXIN. British J Pharmacology. 1980 Apr;68(4):611–5. doi: 10.1111/j.1476-5381.1980.tb10851.x.
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