Enantioselective [4 + 1] cycloaddition of ortho-quinone methides and bromomalonates under phase-transfer catalysisElectronic supplementary information (ESI) available. CCDC 1531397. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7ob00484b
An enantioselective [4 + 1] cycloaddition reaction of ortho -quinone methides and bromomalonates using a quinine and BINOL derived phase-transfer catalyst is described. With high yields and enantioselectivities, the method provided a variety of optically active dihydrobenzofurans, which represent a...
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| creator | Lian, Xiao-Lei Adili, Alafate Liu, Bin Tao, Zhong-Lin Han, Zhi-Yong |
| description | An enantioselective [4 + 1] cycloaddition reaction of
ortho
-quinone methides and bromomalonates using a quinine and BINOL derived phase-transfer catalyst is described. With high yields and enantioselectivities, the method provided a variety of optically active dihydrobenzofurans, which represent a valuable structural motif present in numerous naturally occurring and biologically active molecules.
An enantioselective [4 + 1] cycloaddition reaction of
ortho
-quinone methides and bromomalonates using a quinine and BINOL derived phase-transfer catalyst is described. |
| doi_str_mv | 10.1039/c7ob00484b |
| format | Article |
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ortho
-quinone methides and bromomalonates using a quinine and BINOL derived phase-transfer catalyst is described. With high yields and enantioselectivities, the method provided a variety of optically active dihydrobenzofurans, which represent a valuable structural motif present in numerous naturally occurring and biologically active molecules.
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ortho
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ortho
-quinone methides and bromomalonates using a quinine and BINOL derived phase-transfer catalyst is described. With high yields and enantioselectivities, the method provided a variety of optically active dihydrobenzofurans, which represent a valuable structural motif present in numerous naturally occurring and biologically active molecules.
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ortho
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ortho
-quinone methides and bromomalonates using a quinine and BINOL derived phase-transfer catalyst is described. With high yields and enantioselectivities, the method provided a variety of optically active dihydrobenzofurans, which represent a valuable structural motif present in numerous naturally occurring and biologically active molecules.
An enantioselective [4 + 1] cycloaddition reaction of
ortho
-quinone methides and bromomalonates using a quinine and BINOL derived phase-transfer catalyst is described.</abstract><doi>10.1039/c7ob00484b</doi><tpages>4</tpages></addata></record> |
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| title | Enantioselective [4 + 1] cycloaddition of ortho-quinone methides and bromomalonates under phase-transfer catalysisElectronic supplementary information (ESI) available. CCDC 1531397. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7ob00484b |
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