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A Maitland-Japp inspired synthesis of dihydropyran-4-ones and their stereoselective conversion to functionalised tetrahydropyran-4-ones.
Org Biomol Chem. 2015 Apr 28;13(16):4743-50. doi: 10.1039/c5ob00292c.
Org Biomol Chem. 2015.
PMID: 25804802
Free article.
Synthesis of 2,6-trans- and 3,3,6-trisubstituted tetrahydropyran-4-ones from Maitland-Japp derived 2H-dihydropyran-4-ones: a total synthesis of diospongin B.
Clarke PA, Nasir NM, Sellars PB, Peter AM, Lawson CA, Burroughs JL.
Clarke PA, et al. Among authors: sellars pb.
Org Biomol Chem. 2016 Jul 12;14(28):6840-52. doi: 10.1039/c6ob01182a.
Org Biomol Chem. 2016.
PMID: 27340028
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Axially Chiral Enamides: Substituent Effects, Rotation Barriers, and Implications for their Cyclization Reactions.
Clark AJ, Curran DP, Fox DJ, Ghelfi F, Guy CS, Hay B, James N, Phillips JM, Roncaglia F, Sellars PB, Wilson P, Zhang H.
Clark AJ, et al. Among authors: sellars pb.
J Org Chem. 2016 Jul 1;81(13):5547-65. doi: 10.1021/acs.joc.6b00889. Epub 2016 Jun 21.
J Org Chem. 2016.
PMID: 27267662
Free article.
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