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1
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70449704849
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For a recent reviews of the use of electrochemistry in synthesis see
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For a recent reviews of the use of electrochemistry in synthesis see:
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4
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67649359769
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For a recent account see: For reviews of early work see:
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For a recent account see:. Moeller K.D. Synlett (2009) 1208 For reviews of early work see:
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(2009)
Synlett
, pp. 1208
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Moeller, K.D.1
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7
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53849147912
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For recent work with sulfonamide trapping groups see:
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For recent work with sulfonamide trapping groups see:. Xu H.-C., and Moeller K.D. J. Am. Chem. Soc. 130 (2008) 13542
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(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 13542
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Xu, H.-C.1
Moeller, K.D.2
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9
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35948984444
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For the synthesis of the arteannuin ring skeleton see
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For the synthesis of the arteannuin ring skeleton see. Wu H., and Moeller K.D. Org. Lett. 9 (2007) 4599
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(2007)
Org. Lett.
, vol.9
, pp. 4599
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Wu, H.1
Moeller, K.D.2
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10
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3242761398
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For the synthesis of alliacol a see:
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For the synthesis of alliacol a see:. Mihelcic J., and Moeller K.D. J. Am. Chem. Soc. 126 (2004) 9106
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(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 9106
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Mihelcic, J.1
Moeller, K.D.2
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11
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0033581760
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For a synthesis of the cyathin core skeleton see:
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For a synthesis of the cyathin core skeleton see:. Wright D.L., Whitehead C.R., Sessions E.H., Ghiviriga I., and Frey D.A. Org. Lett. 1 (1999) 1535
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(1999)
Org. Lett.
, vol.1
, pp. 1535
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Wright, D.L.1
Whitehead, C.R.2
Sessions, E.H.3
Ghiviriga, I.4
Frey, D.A.5
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12
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33845935517
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For the synthesis of guanacastepene see:
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For the synthesis of guanacastepene see:. Miller A.K., Hughes C.C., Kennedy-Smith J.J., Gradl S.N., and Trauner D. J. Am. Chem. Soc. 128 (2006) 17057
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(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 17057
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Miller, A.K.1
Hughes, C.C.2
Kennedy-Smith, J.J.3
Gradl, S.N.4
Trauner, D.5
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16
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70449702270
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Wavefunction, Inc, Irvine, CA, USA
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Wavefunction, Inc.: Irvine, CA, USA.
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17
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70449700458
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For the Michael, aldol sequence see
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For the Michael - aldol sequence see:
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18
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24044496540
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For the use of the Grignard reagent in the Michael reaction see:
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Li C.C., Liang S., Zhang X.H., Xie Z.X., Chen J.H., Wu Y.D., and Yang Z. Org. Lett. 7 (2005) 3709 For the use of the Grignard reagent in the Michael reaction see:
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(2005)
Org. Lett.
, vol.7
, pp. 3709
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Li, C.C.1
Liang, S.2
Zhang, X.H.3
Xie, Z.X.4
Chen, J.H.5
Wu, Y.D.6
Yang, Z.7
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21
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70449704848
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For the acid catalyzed cyclization see
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For the acid catalyzed cyclization see:
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23
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0001534917
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Smith III A.B., Liverton N.J., Hrib N.J., Sivaramakrishnan H., and Winzenbeg K.J. J. Am. Chem. Soc. 108 (1986) 3040
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(1986)
J. Am. Chem. Soc.
, vol.108
, pp. 3040
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Smith III, A.B.1
Liverton, N.J.2
Hrib, N.J.3
Sivaramakrishnan, H.4
Winzenbeg, K.J.5
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24
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0038681020
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Kulesza A., Ebetino F.H., Mishra R.K., Cross-Doersen D., and Mazur A.W. Org. Lett. 5 (2003) 1163
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(2003)
Org. Lett.
, vol.5
, pp. 1163
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Kulesza, A.1
Ebetino, F.H.2
Mishra, R.K.3
Cross-Doersen, D.4
Mazur, A.W.5
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26
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35348959410
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For a preliminary account of this work see:
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For a preliminary account of this work see:. Tang F., and Moeller K.D. J. Am. Chem. Soc. 129 (2007) 12414
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(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 12414
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Tang, F.1
Moeller, K.D.2
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27
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0001532754
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For examples see: Solvent trapping and elimination are the typical products generated from failed cyclizations
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For examples see: Solvent trapping and elimination are the typical products generated from failed cyclizations. New D.G., Tesfai Z., and Moeller K.D. J. Org. Chem. 61 (1996) 1578-1598
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(1996)
J. Org. Chem.
, vol.61
, pp. 1578-1598
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New, D.G.1
Tesfai, Z.2
Moeller, K.D.3
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29
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0001492157
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For the use of Na in toluene see:
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For the use of Na in toluene see:. Bode R.H., Bol J.E., Driessen W.L., Hulsbergen F.B., Reedijk J., and Spek A.L. Inorg. Chem. (1999) 1239
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(1999)
Inorg. Chem.
, pp. 1239
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Bode, R.H.1
Bol, J.E.2
Driessen, W.L.3
Hulsbergen, F.B.4
Reedijk, J.5
Spek, A.L.6
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32
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70449700457
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For evidence that ketene dithioacetal derived radical cations are less efficient at generating carbon-carbon bonds see Ref. 7b. For recent uses in synthesis see
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For evidence that ketene dithioacetal derived radical cations are less efficient at generating carbon-carbon bonds see Ref. 7b. For recent uses in synthesis see:
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38
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14844315917
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For a related study showing the relative abilities of S and N to stabilize radical cations see:
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For a related study showing the relative abilities of S and N to stabilize radical cations see:. Murphy J.A., Khan T.A., Zhou S., Thomson D.W., and Mahesh M. Angew. Chem. Int. Ed. Eng. 44 (2005) 1356
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(2005)
Angew. Chem. Int. Ed. Eng.
, vol.44
, pp. 1356
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Murphy, J.A.1
Khan, T.A.2
Zhou, S.3
Thomson, D.W.4
Mahesh, M.5
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39
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0009956633
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For examples see:
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For examples see:. Moeller K.D., Wang P.W., Tarazi S., Marzabadi M.R., and Wong P.L. J. Org. Chem. 56 (1991) 1058
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(1991)
J. Org. Chem.
, vol.56
, pp. 1058
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Moeller, K.D.1
Wang, P.W.2
Tarazi, S.3
Marzabadi, M.R.4
Wong, P.L.5
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40
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70449728353
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note
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4 in acetonitrile electrolyte solution, a substrate concentration of 0.025 M, and a sweep rate of 25 mV/s.
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41
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70449728354
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For examples see Ref. 7b as well as:
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For examples see Ref. 7b as well as:
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44
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70449725467
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For enol ether-furan couplings leading to seven-membered rings see Ref. 5d as well as:
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For enol ether-furan couplings leading to seven-membered rings see Ref. 5d as well as:
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