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Highly stereoselective syntheses involving N-alkyl-4,4,7.alpha.-trimethyl-trans-octahydro-1,3-benzoxazine intermediates. 2.

https://doi.org/10.1021/jo00294a026
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inferred← citeshttps://doi.org/10.2139/ssrn.4765444openalex-extracted
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inferred← citeshttps://doi.org/10.1002/047084289x.re100openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adsc.200404361openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adsc.201000428openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adsc.201801454openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chin.199036225openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chir.10056openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/hc.21112openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11224-021-01735-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-417034-6.00011-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-824285-8.00004-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-008096518-5.00121-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-008096518-5.00252-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmc.2006.03.025openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jfluchem.2010.05.014openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jorganchem.2005.03.030openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molcata.2005.06.061openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molcata.2014.06.031openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molcatb.2007.12.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2014.06.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetasy.2005.02.015openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.01.124openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.03.013openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/10426507.2011.643435openalex-snapshot
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inferred← citeshttps://doi.org/10.1246/cl.2003.988openalex-snapshot
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