-
1
-
-
57449121750
-
-
4th edn., John Wiley & Sons, Hoboken, NJ
-
P. G. M. Wuts and T. W. Greene, Greene's Protective Groups in Organic Synthesis, 4th edn., John Wiley & Sons, Hoboken, NJ, 2007.
-
(2007)
Greene's Protective Groups in Organic Synthesis
-
-
Wuts, P.G.M.1
Greene, T.W.2
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4
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0042869554
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-
For a comprehensive review of TIPS in organic synthesis, see
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For a comprehensive review of TIPS in organic synthesis, see C. Rücker Chem. Rev. 1995 95 1009.
-
(1995)
Chem. Rev.
, vol.95
, pp. 1009
-
-
Rücker, C.1
-
13
-
-
18844440927
-
-
C. Visintin A. E. Aliev D. Riddall D. Baker M. Okuyama P. M. Hoi R. Hiley D. L. Selwood Org. Lett. 2005 7 1699.
-
(2005)
Org. Lett.
, vol.7
, pp. 1699
-
-
Visintin, C.1
Aliev, A.E.2
Riddall, D.3
Baker, D.4
Okuyama, M.5
Hoi, P.M.6
Hiley, R.7
Selwood, D.L.8
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16
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-
53849147230
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-
L. F. Tietze C. A. Vock I. K. Krimmelbein J. M. Wiegand L. Nacke T. Ramachandar K. M. D. Islam C. Gatz Chem.–Eur. J. 2008 14 3670.
-
(2008)
Chem.–Eur. J.
, vol.14
, pp. 3670
-
-
Tietze, L.F.1
Vock, C.A.2
Krimmelbein, I.K.3
Wiegand, J.M.4
Nacke, L.5
Ramachandar, T.6
Islam, K.M.D.7
Gatz, C.8
-
18
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-
0027370231
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-
P. Magnus M. Giles R. Bonnert G. Johnson L. McQuire M. Deluca A. Merritt C. S. Kim N. Vicker J. Am. Chem. Soc. 1993 115 8116.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 8116
-
-
Magnus, P.1
Giles, M.2
Bonnert, R.3
Johnson, G.4
McQuire, L.5
Deluca, M.6
Merritt, A.7
Kim, C.S.8
Vicker, N.9
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22
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85032774506
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A rough search for aryl TIPS ethers by SciFinder® in March 2009 returned 2683 hits, while aryl TBS ethers amounted to 14454 hits
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A rough search for aryl TIPS ethers by SciFinder® in March 2009 returned 2683 hits, while aryl TBS ethers amounted to 14454 hits.
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23
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85032778238
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Conventional glassware was reportedly detrimental to HF-mediated de-silylation, and teflon reaction vessel was required, see ref. 5e
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Conventional glassware was reportedly detrimental to HF-mediated de-silylation, and teflon reaction vessel was required, see ref. 5e.
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31
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37049068853
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3 = TBS, TBDPS and TIPS, respectively, see
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3 = TBS, TBDPS and TIPS, respectively, see: J. S. Davies C. L. Higginbotham E. J. Tremeer C. Brown R. C. Treadgold J. Chem. Soc., Perkin Trans. 1 1992 3043.
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(1992)
J. Chem. Soc., Perkin Trans. 1
, pp. 3043
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Davies, J.S.1
Higginbotham, C.L.2
Tremeer, E.J.3
Brown, C.4
Treadgold, R.C.5
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32
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0015217113
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3/MeOH/RT/45 min removes phenolic Ac protections, see
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3/MeOH/RT/45 min removes phenolic Ac protections, see: G. Büchi S. M. Weinreb J. Am. Chem. Soc. 1971 93 746.
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(1971)
J. Am. Chem. Soc.
, vol.93
, pp. 746
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Büchi, G.1
Weinreb, S.M.2
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36
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85032764083
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4) and concentrated under reduced pressure. The residue was purified by silica gel flash column chromatography. For details of a large-scale reaction, see ESI
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4) and concentrated under reduced pressure. The residue was purified by silica gel flash column chromatography. For details of a large-scale reaction, see ESI.
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