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. Author manuscript; available in PMC: 2016 Aug 19.
Published in final edited form as: J Am Chem Soc. 2015 Aug 7;137(32):10336–10345. doi: 10.1021/jacs.5b06126

Table 2.

O - and C-Mannosylation with Donor 13.

Entry Nucleophile Equiv (M conc) β-gly/cycl α-gly/cycl

37/(28+29)c 38/(28+29)c
1a iPrOH 0.8 (0.014) 2.17 0.15
2a iPrOH 1.2 (0.020) 3.66 0.28
3a iPrOH 1.5 (0.026) 5.36 0.44
4a iPrOH 2.5 (0.043) 10.99 0.99
5a iPrOH 3 (0.051) 13.09 1.28
6a iPrOH 4 (0.068) 15.75 1.14
7a iPrOH 5 (0.085) 19.38 1.53
8a iPrOH 8 (0.136) 24.34 1.60
39/(28+29)c -
9b TMSCH2C(Me)=CH2 2 (0.034) 0.06 -
10b TMSCH2C(Me)=CH2 4 (0.068) 0.18 -
11b TMSCH2C(Me)=CH2 8 (0.136) 0.40 -
12b TMSCH2C(Me)=CH2 12 (0.204) 0.55 -
13b TMSCH2C(Me)=CH2 15 (0.255) 0.69 -
14b TMSCH2C(Me)=CH2 20 (0.34) 0.87 -
15b TMSCH2C(Me)=CH2 30 (0.51) 1.40 -
a

Experimental conditions: TTBP (4 equiv), 1-octene (10 equiv), molecular sieves 4 Å, Tf2O (1.2 equiv) at −72 °C;

b

Experimental conditions: TTBP (4 equiv), molecular sieves 4 Å, Tf2O (1.2 equiv) at − 72 °C;

c

Molar ratios were determined by UHPLC/UV/MS