共查询到20条相似文献,搜索用时 31 毫秒
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D. J. Harris E. R. Lee C. S. Siegel I. R. Davison C. B. Jackson R. D. Brown 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-4)
Abstract Two routes are described for the synthesis of pharmaceutical grade phospholipids at the multi-kilogram scale. 相似文献
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Mohamed E. Khalifa 《合成通讯》2020,50(17):2590-2616
Abstract Thiophenes are a highly important group of heterocycles and have been of great interest to researchers due to their various reactivities. Many synthetic strategies are used to generate functionalized thiophene derivatives. Several reactions are described, depending on the reactivity of the substituents attached to the thiophene nucleus toward different nucleophiles to yield the versatile thiophene products. Many diverse applications have been utilized for thiophenes from medicinal chemistry to material science. 相似文献
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Divergent strategy in natural product synthesis allows the comprehensive synthesis of family natural products. Efficient formulation of this idea requires the biosynthetic/biosynthesis-inspired insight toward the well-orchestrated design of a pluripotent late-stage intermediate, in concomitant with the applicability of the intermediates for versatile transformations. This digest focuses on the actual applications of those strategies in natural product synthesis with an emphasis on the recipes for the choice of the common intermediates. 相似文献
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Jakob Ewald Rasmussen Marcello Massimo Boccia John Nielsen Claude Taillefumier Sophie Faure Thomas Hjelmgaard 《Tetrahedron letters》2014
A facile and expedient route to the synthesis of arylopeptoid oligomers (N-alkylated aminomethyl benz-amides) using semi-automated microwave-assisted solid-phase synthesis is presented. The synthesis was optimized for the incorporation of side chains derived from sterically hindered or unreactive amines and both ortho- and para-substituted arylo-backbones. By utilizing this optimized protocol a complex nonameric arylopeptoid was synthesized in less than 11 h, featuring a novel alternating ortho-, meta-, and para-substituted backbone pattern and a variety of chemically diverse and challenging side chains. 相似文献
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Takaaki Matsubara Dr. Keisuke Takahashi Dr. Jun Ishihara Prof. Dr. Susumi Hatakeyama 《Angewandte Chemie (International ed. in English)》2014,53(3):757-760
The first asymmetric total synthesis of (?)‐ophiodilactone A and (?)‐ophiodilactone B, isolated from the ophiuroid (Ophiocoma scolopendrina), is reported. The key features of the synthesis include the highly stereocontrolled construction of the structurally congested γ‐lactone/δ‐lactone skeleton through an asymmetric epoxidation, diastereoselective iodolactonization, and intramolecular epoxide‐opening with a carboxylic acid, and biomimetic radical cyclization of ophiodilactone A to ophiodilactone B. 相似文献
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Donglin Fu Xuemin Rao Jinyi Xu Genzoh Tanabe Osamu Muraoka Xiaoming Wu Weijia Xie 《Tetrahedron letters》2018,59(30):2876-2879
The first total syntheses of naturally occurring cyclodepsipeptides Hikiamides A–C are described. The key linear pentapeptide precursors, prepared efficiently via Fmoc-solid-phase synthesis, were cyclized in dilute solution to provide the target Hikiamides A–C. The structures of the synthetic Hikiamides A–C were characterized by NMR and HRMS spectroscopy which were in agreement with those of natural products. 相似文献
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Preparation of Optically Enriched Secondary Alkyllithium and Alkylcopper Reagents—Synthesis of (−)‐Lardolure and Siphonarienal 下载免费PDF全文
Varvara Morozova Juri Skotnitzki Dr. Kohei Moriya Prof. Dr. Konstantin Karaghiosoff Prof. Dr. Paul Knochel 《Angewandte Chemie (International ed. in English)》2018,57(19):5516-5519
Optically enriched secondary alkyl iodides were converted into secondary alkyllithium and secondary alkylcopper compounds with very high retention of configuration. Quenching with various electrophiles, including chiral epoxides, provided a range of chiral molecules with high enantiomeric purity (>90 % ee). This method has been applied in an iterative fashion in the total synthesis of (?)‐lardolure in 13 steps and 5.4 % overall yield (>99 % ee, dr>99:1) and siphonarienal in 15 steps and 5.6 % overall yield (>99 % ee, dr>99:1) starting from commercially available ethyl (R)‐3‐hydroxybutyrate (>99 % ee). 相似文献
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Solid-phase organic synthesis is a rapidly expanding area of synthetic chemistry that is being widely exploited in the search for new medicinally important compounds using combinatorial techniques. In recent decades, a large number of reports related to solid-phase synthesis of heterocycles have appeared because of the wide variety of their biological activity. In this review, we report the important role of solid-phase synthesis in the synthesis of nitrogen containing six-membered ring heterocycles. 相似文献
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Gregory L. Hamilton 《Tetrahedron letters》2006,47(6):967-968
A simple one-pot, solution phase method for the parallel synthesis of carbamates from amines and alcohols is described. The high-yielding method does not require support-bound reagents, extractions or resin washing steps and should be broadly applicable to the manual or automated generation of carbamate libraries. 相似文献
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Artemisinin, existing in the Chinese medicinal plant Artemisia annua L., is a kind of sesquiterpenoid lactone endoperoxide. It has received extensive attention from all over the world owing to its unusual trioxane structure and potent antimalarial properties. Here we demonstrate the complete chemical synthetic pathway of artemisinin, investigated the past three decades, including the total and partial syntheses. 相似文献
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A synthetic approach to the C1–C19 polyketide fragment of the phorboxazoles is disclosed here. While an initial two-directional approach was efficient, it did not proceed in a high enough yield to justify moving forward. A subsequent successful strategy for the generation of the C11–C15 pyrans of both of the phorboxazoles was achieved, and the installation of the C9 stereocenter was able to be demonstrated. Furthermore, an efficient route for the preparation of the C1–C8 fragment with suitable functionality to allow for elaboration into the complete C1–C19 fragment, with the capricious C2–C3 Z-geometry installed, was also achieved. 相似文献
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A new synthetic method for the preparation of allyl amines has been developed. The key steps of this method are enantioselective addition of diethylzinc and [1,3]-chirality transfer through the [3.3] sigmatropic rearrangement of allyl cyanates. Stereocontrolled syntheses of lentiginosine (1) and polyoxamic acid derivative 2 from a common intermediate 7 derived from D-tartaric acid (8), have been accomplished. 相似文献
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Aicha Mhamdi 《Green Chemistry Letters and Reviews》2018,11(1):12-17
A green and versatile method for the preparation of γ-hydroxyphosphonate and phosphine oxide derivatives in 5?min, is accomplished through the reduction of γ-phosphonylketones with sodium borohydride supported on alumina, at room temperature, under solvent free conditions. 相似文献
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Divergent Total Syntheses of Enmein‐Type Natural Products: (−)‐Enmein, (−)‐Isodocarpin,and (−)‐Sculponin R 下载免费PDF全文
Saiyong Pan Sicong Chen Guangbin Dong 《Angewandte Chemie (International ed. in English)》2018,57(21):6333-6336
Divergent total syntheses of the enmein‐type natural products (?)‐enmein, (?)‐isodocarpin, and (?)‐sculponin R have been achieved in a concise fashion. Key features of the strategy include 1) an efficient early‐stage cage formation to control succeeding diastereoselectivity, 2) a one‐pot acylation/akylation/lactonization to construct the C‐ring and C8 quarternary center, 3) a reductive alkenylation approach to construct the enmain D/E rings and 4) a flexible route to allow divergent syntheses of three natural products. 相似文献