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Biomimetic total synthesis of resorcylate natural products via a decarboxylative, allyl migration and aromatisation sequence

机译:通过脱羧,烯丙基迁移和芳构化序列仿生全合成resorcylate天然产物

摘要

Angelico in A (I), angelicoin B (II), cristatic acid ud(III) and grifolic acid (IV) (Figure A1) are members of the resorcylate family of natural products which contain a common 6-alkyl-2,4-dihydroxy benzoic acid core (β-resorcylate unit). The total syntheses of angelicoin A (I) and angelicoin B ud(II) from 2,2,6-trimethyl-4H-1,3-dioxin-4-one Vudare reported using late stage aromatisation reactions via diketo-dioxinones as advanced intermediates. In the case of angelicoin Aud(I), biomimetic aromatisation was coupled with a highly regioselective palladium(0)-catalysed uddecarboxylative prenyl migration as the key stepud(Scheme A1).(a)(b) The palladium(0)-catalysed decarboxylative, prenylation and aromatisation sequence furnished both linear VII and branched adducts VI. Extensive optimisation of conditions to improve the ratio of linear to branched adducts involved the screening of palladium catalysts, udligands, solvents, reactions times, temperature and organic and inorganic bases.(a)(c)udThe regioselectivity of this novel palladium(0)-udcatalysed decarboxylative prenyl migration was determined unambiguously through X-ray crystallographic studies.(a)(c) udFurthermore, an intermolecular mechanism is proposed after thorough mechanistic studies including cross over and variable concentration experiments, base studies and regioselectivity investigations. udTwo synthetic approaches towards the total synthesis of cristatic acid methyl ester are reported. The first approach investigated a one-pot reaction to install the furan moiety VIII (Scheme A2), via a Nef reaction, deprotection, decarboxylation and furan formation.udThe second approach attempted to perform a one-pot Pd(0)-decarboxylative allylation, TMSE deprotection and aromisation to provide the core of cristatic acid IX (Scheme A3).udFinally, studies towards the total synthesis of grifolic acid (IV) are reported utilising the palladium(0)-catalysed decarboxylative allyl migration and aromatisation sequence.
机译:A(I)中的Angelico,B(II)中的Angelicoin,丁香酸 ud(III)和草甘膦酸(IV)(图A1)是天然产物的间苯二酚家族的成员,它们含有常见的6-烷基-2,4 -二羟基苯甲酸核心(β-间苯二酸酯单元)。由二,二酮-二恶英通过后期芳构化反应报道了由2,2,6-三甲基-4H-1,3-二恶英-4-酮V由2,2,6-三甲基-4H-1,3-二恶英-4-酮V合成的当归A(I)和当归B(ud)作为高级中间体。在当归霉素A ud(I)的情况下,仿生芳构化与高度区域选择性的钯(0)催化的 udde羧化异戊二烯迁移是关键步骤 ud(方案A1)。(a)(b)钯( 0)-催化的脱羧,烯丙基化和芳构化顺序提供了线性VII和支链加合物VI。广泛优化条件以提高线性与支链加合物的比例涉及对钯催化剂,配体,溶剂,反应时间,温度以及有机碱和无机碱的筛选。(a)(c) ud这种新型钯的区域选择性(0通过X射线晶体学研究明确确定了催化脱羧异戊二烯的迁移。 ud报道了两种合成方法,可以合成全合成的月桂酸甲酯。第一种方法研究了一锅法,通过Nef反应,脱保护,脱羧和呋喃形成来安装呋喃部分VIII(方案A2)。 ud第二种方法尝试进行单锅Pd(0)-脱羧烯丙基化最后,报道了利用钯(0)催化的脱羧烯丙基迁移和芳构化顺序进行的对总草酸(IV)合成的研究。

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    Anderson Katie Elizabeth;

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  • 年度 2013
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