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Titlebook: Selectivity in the Synthesis of Cyclic Sulfonamides; Application in the S Kimberly Geoghegan Book 2014 Springer International Publishing Sw

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发表于 2025-3-21 19:55:18 | 显示全部楼层 |阅读模式
书目名称Selectivity in the Synthesis of Cyclic Sulfonamides
副标题Application in the S
编辑Kimberly Geoghegan
视频video
概述Nominated as an Outstanding Ph.D. thesis by the University College Dublin, Ireland.Development of new methodology combined with target synthesis.Experimental details provided for all transformations-i
丛书名称Springer Theses
图书封面Titlebook: Selectivity in the Synthesis of Cyclic Sulfonamides; Application in the S Kimberly Geoghegan Book 2014 Springer International Publishing Sw
描述In the area of organic chemistry one major challenge we are currently faced with is how to assemble potentially useful molecules in new ways that generate molecular complexity and in sequences that are as efficient as possible. Our efforts in this regard, specifically for the preparation of amino containing compounds incorporating an aromatic ring, are described in this doctoral thesis. We discovered an interesting regioselectivity in an intramolecular Heck reaction, which we studied for a series of substrates that are unbiased in terms of the size of the newly formed ring, where very high levels of selectivity in relation to the new carbon-carbon bond are typically observed. DFT calculations were performed to attempt to shed light on the reaction sequence. This regioselective Heck reaction, combined with the reductive removal of the temporary amino-protecting group, allowed us to synthesize the Sceletium alkaloids: mesembrane, mesembranol and mesembrine.
出版日期Book 2014
关键词Cyclic Sulfonamides; Generation of All-Carbon Quaternary Centres; Intramolecular Heck Reaction; Multi-T
版次1
doihttps://doi.org/10.1007/978-3-319-10338-9
isbn_softcover978-3-319-36431-5
isbn_ebook978-3-319-10338-9Series ISSN 2190-5053 Series E-ISSN 2190-5061
issn_series 2190-5053
copyrightSpringer International Publishing Switzerland 2014
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发表于 2025-3-21 22:14:56 | 显示全部楼层
2190-5053 esis.Experimental details provided for all transformations-iIn the area of organic chemistry one major challenge we are currently faced with is how to assemble potentially useful molecules in new ways that generate molecular complexity and in sequences that are as efficient as possible. Our efforts
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Introduction,dance in the natural world they find uses as pharmaceuticals and are used for inspiration for structural targets. Naturally occurring alkaloids can often be isolated from natural sources relatively easily via simple acid-base extraction. However, the quantities obtained are often minute. These compo
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An Investigation into the One-Pot Heck Olefination-Hydrogenation Reaction, molecules. Taking inspiration from nature, where multi-enzymatic systems carry out two or more transformations to access structurally intricate molecules, one-pot procedures involving multiple catalytic events, i.e. multi-task, or cascade/tandem/domino processes, are being sought by synthetic chemi
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Double Reduction of Cyclic Aromatic Sulfonamides,tantly, the basicity/nucleophilicity of the nitrogen atom is reduced dramatically due to the presence of the electron-withdrawing sulfonyl moiety. Unlike their carbamate or amide analogues, there are no spectroscopic problems associated with rotamers when employing sulfonamides as protecting group.
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Experimental,ssembled hot and cooled to room temperature under a stream of N.. Anhydrous THF was freshly distilled from sodium-benzophenone prior to use, anhydrous CH.Cl. was freshly distilled from CaH., anhydrous DMF, Toluene (PhMe) and MeCN were purchased from Sigma Aldrich. Reagents from Acros, Fluka or Sigma
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re presented with clear explanation of all the steps involved from problem formulation to finding the solution. Thevenin’s and Norton’s theorems, maximum power transfer theorem and source transformation are the additional topics covered. Supplementary programs for verifying the analytically obtained
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