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Beilstein J. Org. Chem. 2018, 14, 2340–2347, doi:10.3762/bjoc.14.209
Graphical Abstract
Scheme 1: Commercial process for the synthesis of 1.
Scheme 2: Previous work about asymmetric synthesis of I-13a.
Scheme 3: Asymmetric synthesis of 1.
Scheme 4: The second strategy for the asymmetric synthesis of 1.
Beilstein J. Org. Chem. 2018, 14, 1421–1427, doi:10.3762/bjoc.14.119
Scheme 1: Synthesis of dezocine by resolution.
Scheme 2: Synthesis of catalysts C1–C17.
Scheme 3: The proposed catalytic mechanism of stereoselective alkylation.
Beilstein J. Org. Chem. 2017, 13, 1064–1070, doi:10.3762/bjoc.13.105
Figure 1: Structure of ipragliflozin L-proline.
Scheme 1: Stereoselective synthesis of C-aryl glycoside by Lemarie.
Scheme 2: Stereoselective synthesis of β-C-arylglucoside 5.
Scheme 3: Synthesis of 1.
Scheme 4: Synthesis of diastereomer 6’ and 5’.