Qualitative evaluation of regioselectivity in the formation of di- and tri-6-O-tritylates of α-cyclodextrin

Keisuke Yoshikiyo, Yoshihisa Matsui and Tatsuyuki Yamamoto
Beilstein J. Org. Chem. 2015, 11, 1530–1540. https://doi.org/10.3762/bjoc.11.168

Supporting Information

Supporting Information File 1: 1H NMR spectra of mono-, di-, and tri-O-trityl-α-CD, together 2D COSY and TOCSY spectra of the AD-isomer.
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Qualitative evaluation of regioselectivity in the formation of di- and tri-6-O-tritylates of α-cyclodextrin
Keisuke Yoshikiyo, Yoshihisa Matsui and Tatsuyuki Yamamoto
Beilstein J. Org. Chem. 2015, 11, 1530–1540. https://doi.org/10.3762/bjoc.11.168

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Yoshikiyo, K.; Matsui, Y.; Yamamoto, T. Beilstein J. Org. Chem. 2015, 11, 1530–1540. doi:10.3762/bjoc.11.168

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