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Syntheses of Tetrahydrofurobenzofurans and Dihydromethanobenzodioxepines from 5-Hydroxy-3-methyl-3H-benzofuran-2-one. Rearrangement and Ring Expansion under Reductive Conditions on Treatment with Hydrides

机译：来自5-羟基-3-甲基-3H-苯并呋喃-2-一体的四氢呋喃脲和二氢甲基苯并二氧化肟的合成。氢化物处理的还原条件下重排和环形扩展

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1. Syntheses of tetrahydrofurobenzofurans and dihydromethanobenzodioxepines from 5-hydroxy-3-methyl-3H-benzofuran-2-one. Rearrangement and ring expansion under reductive conditions on treatment with hydrides [J] . Luo WM, Yu QS, Holloway HW, The Journal of Organic Chemistry . 2005,第16期

机译：由5-羟基-3-甲基-3H-苯并呋喃-2-酮合成四氢呋喃苯并呋喃和二氢甲基苯并二氧杂环丁烷。在氢化物处理下还原条件下的重排和扩环
2. Regioselective Synthesis of Heterocycles Containing Nitrogen Neighboring an Aromatic Ring by Reductive Ring Expansion Using Diisobutylaluminum Hydride and Studies on the Reaction Mechanism [J] . Hidetsura Cho, Yusuke Iwama, Kenji Sugimoto, The Journal of Organic Chemistry . 2010,第3期

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机译：通过使用二异丁基铝氢化物的还原环扩环反应，合成含氮杂原子的杂原子的杂环的未取代基本骨架的区域比合成
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机译：I.炭中镍和炭中铜催化的非均相交叉偶联反应。二。氢化铜催化的不对称1,2 / 1,4-还原反应。三，利用内部束缚的非外消旋配体进行万古霉素联芳基A-B环系统的选择性催化合成。
6. Selective Syntheses of Δαβ and Δβγ Butenolides from Allylic Cyclopropenecarboxylates via Tandem Ring Expansion/33-Sigmatropic Rearrangements [O] . Xiaocong Xie, Yi Li, Joseph M. Fox -1

机译：Δαβ和Δβ的选择性合成γ丁烯羟酸内酯从烯丙基Cyclopropenecarboxylates经由串联环扩展/ 33 -sigmatropic重排
7. Selective Syntheses of Δα,β and Δβ,γ Butenolides from Allylic Cyclopropenecarboxylates via Tandem Ring Expansion/3,3-Sigmatropic Rearrangements [O] . Xiaocong Xie, Yi Li, Joseph M. Fox 2013

机译：通过串联环形膨胀/ 3,3从烯丙基环烯烃羧酸盐的选择性合成Δα，β和δβ，γ丁烯醇酯/ 3,3 - 具有胶质重排

Syntheses of Tetrahydrofurobenzofurans and Dihydromethanobenzodioxepines from 5-Hydroxy-3-methyl-3H-benzofuran-2-one. Rearrangement and Ring Expansion under Reductive Conditions on Treatment with Hydrides

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