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2
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51049107532
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-
Karstedt, B. U.S. Patent, 3 775 452 1973; Chem. Abstr. 1974, 80, 135655. DVDS = 1,3-divinyl-1,1,3,3-tetramethyldisiloxane.
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Karstedt, B. U.S. Patent, 3 775 452 1973; Chem. Abstr. 1974, 80, 135655. DVDS = 1,3-divinyl-1,1,3,3-tetramethyldisiloxane.
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-
-
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8
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0003907945
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Chem. Abstr. 1969, 53, 6995g
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Petrov A.D., and Sadykh-Zade S.I. Izv. Akad. Nauk SSSR, Ser. Khim. Nauk (1968) 513 Chem. Abstr. 1969, 53, 6995g
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(1968)
Izv. Akad. Nauk SSSR, Ser. Khim. Nauk
, pp. 513
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-
Petrov, A.D.1
Sadykh-Zade, S.I.2
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12
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51049091929
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The systematical name of the triisobutyl proazaphosphatrane ligand 1 is 2,8,9-triisobutyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane and it is commercially available from Sigma-Aldrich (CAS No. 331465-71-5).
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The systematical name of the triisobutyl proazaphosphatrane ligand 1 is 2,8,9-triisobutyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane and it is commercially available from Sigma-Aldrich (CAS No. 331465-71-5).
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21
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0035351150
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Tallarico J.A., Depew K.M., Pelish H.E., Westwood N.J., Lindsley C.W., Shair M.D., Schreiber S.L., and Foley M.A. J. Comb. Chem. 3 (2001) 312-318
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(2001)
J. Comb. Chem.
, vol.3
, pp. 312-318
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-
Tallarico, J.A.1
Depew, K.M.2
Pelish, H.E.3
Westwood, N.J.4
Lindsley, C.W.5
Shair, M.D.6
Schreiber, S.L.7
Foley, M.A.8
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22
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51049112530
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1H NMR. The vinylic protons in the α-isomer appear at 5.72 and 6.11 ppm with a characteristic geminal coupling of 2.9 Hz.
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1H NMR. The vinylic protons in the α-isomer appear at 5.72 and 6.11 ppm with a characteristic geminal coupling of 2.9 Hz.
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24
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0002108435
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Keifer P.A., Baltusis L., Rice D.M., Tymiak A.A., and Shoolery J.N. J. Magn. Reson. 119 (1996) 65-75
-
(1996)
J. Magn. Reson.
, vol.119
, pp. 65-75
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-
Keifer, P.A.1
Baltusis, L.2
Rice, D.M.3
Tymiak, A.A.4
Shoolery, J.N.5
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25
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0032974703
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Lippens G., Bourdonneau M., Dhalluin C., Warrass R., Richert T., Seetharaman C., Boutillon C., and Piotto M. Curr. Org. Chem. 3 (1999) 147-169
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(1999)
Curr. Org. Chem.
, vol.3
, pp. 147-169
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-
Lippens, G.1
Bourdonneau, M.2
Dhalluin, C.3
Warrass, R.4
Richert, T.5
Seetharaman, C.6
Boutillon, C.7
Piotto, M.8
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26
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0000847671
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Grøtli M., Gotfredsen C.H., Rademann J., Buchardt J., Clark A.J., Duus J.Ø., and Meldal M. J. Comb. Chem. 2 (2000) 108-119
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(2000)
J. Comb. Chem.
, vol.2
, pp. 108-119
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-
Grøtli, M.1
Gotfredsen, C.H.2
Rademann, J.3
Buchardt, J.4
Clark, A.J.5
Duus, J.Ø.6
Meldal, M.7
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32
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0001155919
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Miranda L.P., Lubell W.D., Halkes K.M., Groth T., Grøtli M., Rademann J., Gotfredsen C.H., and Meldal M. J. Comb. Chem. 4 (2002) 523-529
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(2002)
J. Comb. Chem.
, vol.4
, pp. 523-529
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-
Miranda, L.P.1
Lubell, W.D.2
Halkes, K.M.3
Groth, T.4
Grøtli, M.5
Rademann, J.6
Gotfredsen, C.H.7
Meldal, M.8
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33
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51049119685
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SPOCC = Superpermeable organic combinatorial chemistry.
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SPOCC = Superpermeable organic combinatorial chemistry.
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34
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51049104332
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TM VO 2000 (6) resins is 0.94 mmol/g.
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TM VO 2000 (6) resins is 0.94 mmol/g.
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35
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51049088894
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Available in one step from the corresponding alcohol. See the Supplementary data for the experimental procedure.
-
Available in one step from the corresponding alcohol. See the Supplementary data for the experimental procedure.
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37
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51049124557
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note
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13C NMR.
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-
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38
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51049103035
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note
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The silyl ethers 10-12 are available in one step from the alcohol and chlorodiisopropylsilane. See the Supplementary data for the experimental procedure.
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-
-
-
42
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51049089797
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-
note
-
Detailed experimental procedures, characterization data and copies of NMR spectra are available in the Supplementary data.
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