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Harusawa, S.1
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Yoneda, R.6
Kurihara, T.7
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7
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0023502864
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For reviews, see:
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For reviews, see: Caruthers M.H., Barone A.D., Beaucage S.L., Dodds D.R., Fisher E.F., Mc Bride L.J., Matteucci M., Stabinsky Z., Tang J.-.Y. Methods Enzymol. 154:1987;287-315.
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Caruthers, M.H.1
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Fisher, E.F.5
Mc Bride, L.J.6
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Stabinsky, Z.8
Tang -., J.Y.9
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9
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0029151591
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Wincott F., DiRenzo A., Shaffer C., Grimm S., Tracz D., Workman C., Sweedler D., Gonzalez C., Scaringe S., Usman N. Nucleic Acids Res. 23:1995;2677-2684.
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Sweedler, D.7
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Scaringe, S.9
Usman, N.10
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11
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0003463148
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Protective Groups in Organic Synthesis
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New York: John Wiley & Sons. pp 615-631 and references cited therein
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Greene T.W., Wuts P.G.M. Protective Groups in Organic Synthesis. Third Ed. 1999;John Wiley & Sons, New York. pp 615-631 and references cited therein.
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Third Ed.
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Greene, T.W.1
Wuts, P.G.M.2
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0002321576
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14
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0001037074
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-
N-POM group has been used in purine xanthine pyrrole indole systems and so on as a protecting group.
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N-POM group has been used in purine xanthine pyrrole indole systems and so on as a protecting group. Rasmussen M., Leonard N.J. J. Am. Chem. Soc. 89:1967;5439-5445.
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16
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0032509861
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Wutz, W.5
Schwabe, U.6
Unterlugauer, D.7
Olsson, R.A.8
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18
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37049076842
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Pieles U., Beijer B., Bohmann K., Weston S., O'Loughlin S., Adam V., Sproat B.S. J. Chem. Soc., Perkin Trans. 1. 1994;3423-3429.
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Pieles, U.1
Beijer, B.2
Bohmann, K.3
Weston, S.4
O'Loughlin, S.5
Adam, V.6
Sproat, B.S.7
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21
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1542373322
-
-
note
-
4OH (0.5 mL) was stirred for 3 h at rt to give 2 (15 mg, 92%) as a colorless oil.
-
-
-
-
22
-
-
1542343642
-
-
note
-
+ 315.1555, found, 315.1552.
-
-
-
-
24
-
-
1542373326
-
-
note
-
15N; δ s(ppm) relative to external DMF (103.2 ppm).
-
-
-
-
27
-
-
1542283390
-
-
note
-
+ calcd 953.46, found 953.52.
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-
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