Diastereoselective Synthesis of 2,8-Dioxabicyclo[3.3.1]Nonane Derivatives via I

IF 0.8 4区 化学 Q4 CHEMISTRY, ORGANIC Heterocycles Pub Date : 2023-11-01 DOI:10.3987/com-23-14891
-Mediated Cascade Reactions
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Abstract

The highly diastereoselective one-pot synthesis generating a variety of 9,9-dimethyl-2,8-dioxabicyclo[3.3.1]nonane derivatives up to dr >19:1 has been established by the reaction of a 2’-methoxylchalcone with isobutyraldehyde via a spontaneous sequential one-pot Michael addition/aldol reaction/demethylative bicyclization in the presence of molecular iodine.

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1,2 -二氧杂环[3.3.1]壬烷衍生物的非对映选择性合成
在碘分子存在下,2 ' -甲氧基查尔酮与异丁醛通过自发的连续一锅迈克尔加成反应/醛醇反应/去甲基双环化反应,建立了高度非对映选择性的一锅合成方法,生成了多种达dr >19:1的9,9-二甲基-2,8-二氧杂环[3.3.1]壬烷衍生物。
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来源期刊
Heterocycles
Heterocycles 化学-有机化学
CiteScore
1.50
自引率
0.00%
发文量
108
审稿时长
1 months
期刊介绍: Since its inception in 1973 HETEROCYCLES has provided a platform for the rapid exchange of research in the areas of organic, pharmaceutical, analytical, and medicinal chemistry of heterocyclic compounds in addition to communications, papers, reviews, a special section of the journal presents newly-discovered natural products whose structure has recently been established. Another section is devoted to the total synthesis of previously documented natural products with heterocyclic ring systems. Due to the fact that the journal is able to publish articles within two months of receipt of the manuscripts, researchers in this field can obtain up-to-date information on heterocyclic research by reading Heterocycles regularly. Audience: Organic and Physical Organic Chemists, Biochemists, Pharmacologists and Scientists studying heterocyclic compounds
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