-
2
-
-
24644517245
-
-
Eds, H.-G. Schmalz, T. Wirth, Wiley-VCH, Weinheim
-
H. Hopf in Organic Synthesis Highlights V (Eds.: H.-G. Schmalz, T. Wirth), Wiley-VCH, Weinheim, 2003, pp. 419-427.
-
(2003)
Organic Synthesis Highlights V
, pp. 419-427
-
-
Hopf, H.1
-
3
-
-
0003989710
-
-
Wiley-VCH, Weinheim
-
H. Hopf, Classics in Hydrocarbon Chemistry: Syntheses, Concepts, Perspectives, Wiley-VCH, Weinheim, 2000.
-
(2000)
Classics in Hydrocarbon Chemistry: Syntheses, Concepts, Perspectives
-
-
Hopf, H.1
-
4
-
-
0001105257
-
-
H. Hopf, Angew. Chem. 2001, 113, 727-729;
-
(2001)
Angew. Chem
, vol.113
, pp. 727-729
-
-
Hopf, H.1
-
5
-
-
0035804403
-
-
Angew. Chem. Int. Ed. 2001, 40, 705-707.
-
(2001)
Angew. Chem. Int. Ed
, vol.40
, pp. 705-707
-
-
-
6
-
-
0000592651
-
-
H. Hopf, Angew. Chem. 1984, 96, 947-958;
-
(1984)
Angew. Chem
, vol.96
, pp. 947-958
-
-
Hopf, H.1
-
8
-
-
0001016532
-
-
S. Fielder, D. D. Rowan, M. S. Sherburn, Angew. Chem. 2000, 112, 4501-4503;
-
(2000)
Angew. Chem
, vol.112
, pp. 4501-4503
-
-
Fielder, S.1
Rowan, D.D.2
Sherburn, M.S.3
-
9
-
-
0034605940
-
-
Angew. Chem. Int. Ed. 2000, 39, 4331-4333.
-
(2000)
Angew. Chem. Int. Ed
, vol.39
, pp. 4331-4333
-
-
-
10
-
-
24644523544
-
-
A. D. Payne, A. C. Willis, M. S. Sherburn, J. Am. Chem. Soc. 2005, 127, 12188-12189.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 12188-12189
-
-
Payne, A.D.1
Willis, A.C.2
Sherburn, M.S.3
-
13
-
-
33947091124
-
-
b) K. Tamao, K. Sumitani, M. Kumada, J. Am. Chem. Soc. 1972, 94, 4374-4376.
-
(1972)
J. Am. Chem. Soc
, vol.94
, pp. 4374-4376
-
-
Tamao, K.1
Sumitani, K.2
Kumada, M.3
-
14
-
-
38549179207
-
-
2].
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2].
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-
-
-
15
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38549108306
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-
The crude product is contaminated with up to 10% [4]dendralene, which is the result of an oxidative dimerization process. This more volatile contaminant is easily removed by vacuum distillation.
-
The crude product is contaminated with up to 10% [4]dendralene, which is the result of an oxidative dimerization process. This more volatile contaminant is easily removed by vacuum distillation.
-
-
-
-
16
-
-
0000479137
-
-
For a review of diene-transmissive Diels-Alder reactions, see
-
For a review of diene-transmissive Diels-Alder reactions, see: J. D. Winkler, Chem. Rev. 1996, 96, 167-176.
-
(1996)
Chem. Rev
, vol.96
, pp. 167-176
-
-
Winkler, J.D.1
-
17
-
-
38549178789
-
-
All cycloadditions involving maleimide dienophiles were found to proceed exclusively through the endo mode.
-
All cycloadditions involving maleimide dienophiles were found to proceed exclusively through the endo mode.
-
-
-
-
18
-
-
38549151074
-
-
-1 is one-half that measured for the other three compounds.
-
-1 is one-half that measured for the other three compounds.
-
-
-
-
19
-
-
0000542953
-
-
a) P. T. Brain, B. A. Smart, H. E. Robertson, M. J. Davis, D. W. H. Rankin, W. J. Henry, I. Gosney, J. Org. Chem. 1997, 62, 2767-2773;
-
(1997)
J. Org. Chem
, vol.62
, pp. 2767-2773
-
-
Brain, P.T.1
Smart, B.A.2
Robertson, H.E.3
Davis, M.J.4
Rankin, D.W.H.5
Henry, W.J.6
Gosney, I.7
-
20
-
-
0030860095
-
-
b) M. H. Palmer, J. A. Blair-Fish, P. Sherwood, J. Mol. Struct. 1997, 412, 1-18.
-
(1997)
J. Mol. Struct
, vol.412
, pp. 1-18
-
-
Palmer, M.H.1
Blair-Fish, J.A.2
Sherwood, P.3
-
21
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38549136400
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-
See the Supporting Information for crystallographic details
-
See the Supporting Information for crystallographic details.
-
-
-
-
22
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27744512595
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-
R. von Essen, D. Frank, H. W. Sünnemann, D. Vidović, J. Magull, A. de Meijere, Chem. Eur. J. 2005, 11, 6583-6592.
-
(2005)
Chem. Eur. J
, vol.11
, pp. 6583-6592
-
-
von Essen, R.1
Frank, D.2
Sünnemann, H.W.3
Vidović, D.4
Magull, J.5
de Meijere, A.6
-
23
-
-
38549132802
-
-
The diene site selectivity witnessed during this cycloaddition is identical to that seen in the reaction of 1 with NMM (Scheme 3).
-
The diene site selectivity witnessed during this cycloaddition is identical to that seen in the reaction of 1 with NMM (Scheme 3).
-
-
-
-
24
-
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33846243792
-
-
a) R. Keese, Chem. Rev. 2006, 106, 4787-4808;
-
(2006)
Chem. Rev
, vol.106
, pp. 4787-4808
-
-
Keese, R.1
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