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A New and Simple Approach to Chemical Complexity. Application to the Synthesis of Natural Products
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inferred← citeshttps://doi.org/10.1002/9780470584170.ch1openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781118618110.ch10openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527335855.marprod004openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527645121.ch15openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527677016.ch7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/0-387-25871-x_1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-800874-4.00021-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-818349-6.00003-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmcl.2017.03.008openalex-snapshot
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inferred← citeshttps://doi.org/10.1039/b210844popenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c5ob00709gopenalex-snapshot
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inferred← citeshttps://doi.org/10.48550/arxiv.2111.03227openalex-snapshot
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inferred← citeshttps://doi.org/10.6084/m9.figshare.13551811openalex-snapshot
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inferred← citeshttps://doi.org/10.70675/75579381z6273z407fzb75ez414241fd24c2openalex-snapshot
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