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. Author manuscript; available in PMC: 2017 Nov 29.
Published in final edited form as: Carbohydr Res. 2016 Oct 24;435:195–207. doi: 10.1016/j.carres.2016.10.008

Table 3.

Coupling of various glycosyl acceptors to C(2)-N-benzylidene substituted glucosamine donor 5.

graphic file with name nihms-827590-t0015.jpg

Entry Acceptors Products Yieldd (α:βe)
1a graphic file with name nihms-827590-t0016.jpg graphic file with name nihms-827590-t0017.jpg 85%, 15:1
2b graphic file with name nihms-827590-t0018.jpg graphic file with name nihms-827590-t0019.jpg 93%, α-only
3a graphic file with name nihms-827590-t0020.jpg graphic file with name nihms-827590-t0021.jpg 90%, 11:1
4a graphic file with name nihms-827590-t0022.jpg graphic file with name nihms-827590-t0023.jpg 76%, α-only
71%, α-onlyf
5c graphic file with name nihms-827590-t0024.jpg graphic file with name nihms-827590-t0025.jpg 58%, α-only
a

Donor/Acceptor = 1:1.2.

b

Donor/Acceptor = 1:2.

c

Donor/Acceptor = 2:1.

d

Isolated by chromatography.

e

Calculated based on 1H NMR.

f

Conducted with 15 mol % commercially available Ni(OTf)2 for 16 h.