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25
-
-
85030583596
-
-
Pentaerythrltol (1) Is commercially available (Tokyo Kasei Kogyo Co., Ltd)
-
Pentaerythrltol (1) Is commercially available (Tokyo Kasei Kogyo Co., Ltd).
-
-
-
-
26
-
-
43149122485
-
-
Tanaka, K.; Tanaka, T.; Hasegawa, T.; Shionoya, M. Chem. Lett. 2008, 37, 440.
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Tanaka, K.1
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27
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0345620976
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Campo, F.D.1
Lastécouères, D.2
Vincent, J.-M.3
Verlhac, J.-B.4
-
28
-
-
85030590790
-
-
+: 1722.6, found: 1723.5
-
+: 1722.6, found: 1723.5.
-
-
-
-
29
-
-
0017774822
-
-
Wang, S. S.; Grisin, B. F.; Winter, D. P.; Makofske, R.; Kulesha, D.; Tzougraki, C.; Meienhofer, J. J. Org. Chem. 1977, 42, 1286.
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Wang, S.S.1
Grisin, B.F.2
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Kulesha, D.5
Tzougraki, C.6
Meienhofer, J.7
-
30
-
-
85030585859
-
-
9OMe) isomers. It is called Novec™ HFE7100 and is miscible in common organic solvents and fluorous solvents
-
9OMe) isomers. It is called Novec™ HFE7100 and is miscible in common organic solvents and fluorous solvents.
-
-
-
-
31
-
-
4043099127
-
-
Kawakubo, M.; Ito, Y.; Okimura, Y.; Kobayashl, M.; Sakura, K.; Kasama, S.; Fukuda, M. N.; Fukuda, M.; Katsuyama, T.; Nakayama, J. Science 2004, 305, 1003.
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-
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Kawakubo, M.1
Ito, Y.2
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Kobayashl, M.4
Sakura, K.5
Kasama, S.6
Fukuda, M.N.7
Fukuda, M.8
Katsuyama, T.9
Nakayama, J.10
-
32
-
-
10844229062
-
-
Rele, S. M.; Iyer, S. S.; Baskaran, S.; Chaikof, E. L. J. Org. Chem. 2004, 69, 9159.
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J. Org. Chem.
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-
-
Rele, S.M.1
Iyer, S.S.2
Baskaran, S.3
Chaikof, E.L.4
-
34
-
-
85030586345
-
-
note
-
+ 2435.4, found: 2434.6.
-
-
-
-
35
-
-
85030574892
-
-
21 = 4:1) and 95% aq MeCN. None of the fluorous compounds was detected by TLC of the organic layer after three extractions with fluorous mixed solvent; this shows that these compounds were quantitatively extracted with the fluorous layer
-
21 = 4:1) and 95% aq MeCN. None of the fluorous compounds was detected by TLC of the organic layer after three extractions with fluorous mixed solvent; this shows that these compounds were quantitatively extracted with the fluorous layer.
-
-
-
-
36
-
-
85030587597
-
-
Compound 19 was partitioned between FC-72 and MeOH and extracted with the MeOH layer
-
Compound 19 was partitioned between FC-72 and MeOH and extracted with the MeOH layer.
-
-
-
-
37
-
-
85030574923
-
-
+ 490.1919, found: 490.1891. The correlation between anomeric protons of N-acetyl glucosamine residue and 4-position carbons of galactose residue was observed by HMQC and HMBC of NMR spectroscopic analysis
-
+ 490.1919, found: 490.1891. The correlation between anomeric protons of N-acetyl glucosamine residue and 4-position carbons of galactose residue was observed by HMQC and HMBC of NMR spectroscopic analysis.
-
-
-
-
38
-
-
85030585724
-
-
+: 1539.5, found: 1539.4.
-
+: 1539.5, found: 1539.4.
-
-
-
-
39
-
-
85030591696
-
-
14) isomers and is called Fluorinert™ FC-72
-
14) isomers and is called Fluorinert™ FC-72.
-
-
-
|