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Volumn 62, Issue 22, 1997, Pages 7548-7549

Asymmetric Aldol-Ring-Closing Metathesis Strategy for the Enantioselective Construction of Six- To Nine-Membered Oxygen Heterocycles

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Indexed keywords


EID: 0000081509     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9716688     Document Type: Article
Times cited : (132)

References (31)
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    • Meng, D.1    Su, D.-S.2    Balog, A.3    Bertinato, P.4    Sorensen, E.J.5    Danishefsky, S.J.6    Zheng, Y.-H.7    Chou, T.-C.8    He, L.9    Horwitz, S.B.10
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    • A single example of an N-tosylamide in the formation of an eight-membered ring from an acyclic diene has been reported. See: Visser, M. S.; Heron, N. M.; Didiuk, M. T.; Sagal, J. F.; Hoveyda, A. H. J. Am. Chem. Soc. 1996, 118, 4291-4298. Immediately prior to the submission of our manuscript, a similar approach to the metathetic construction of medium ring cyclic ethers was reported. Linderman, R. J.; Siedlecki, J.; O'Neill, S. A.; Sun, H. J. Am. Chem. Soc. 1997, 119, 6919-6920.
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    • A single example of an N-tosylamide in the formation of an eight-membered ring from an acyclic diene has been reported. See: Visser, M. S.; Heron, N. M.; Didiuk, M. T.; Sagal, J. F.; Hoveyda, A. H. J. Am. Chem. Soc. 1996, 118, 4291-4298. Immediately prior to the submission of our manuscript, a similar approach to the metathetic construction of medium ring cyclic ethers was reported. Linderman, R. J.; Siedlecki, J.; O'Neill, S. A.; Sun, H. J. Am. Chem. Soc. 1997, 119, 6919-6920.
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    • Yields are for isolated, chromatographically purified products. Yields for the aldol reactions are based on recovered acyl oxazolidinone
    • Yields are for isolated, chromatographically purified products. Yields for the aldol reactions are based on recovered acyl oxazolidinone.
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    • Molecular mechanics calculations were made using the MM2 force field
    • Molecular mechanics calculations were made using the MM2 force field.


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