-
2
-
-
84972910099
-
-
Grob, C. A.; Schiess, P. W. Angew. Chem., Int. Ed. Engl. 1967, 6, 1.
-
(1967)
Angew. Chem., Int. Ed. Engl
, vol.6
, pp. 1
-
-
Grob, C.A.1
Schiess, P.W.2
-
4
-
-
0000814530
-
-
Trost, B. M, Fleming, I, Eds, Pergamon: Oxford
-
Shing, T. K. M. In Comprehensive Organic Synthesis Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 7, p 703.
-
(1991)
Comprehensive Organic Synthesis
, vol.7
, pp. 703
-
-
Shing, T.K.M.1
-
5
-
-
0000036757
-
-
Trost, B. M, Fleming, I, Eds, Pergamon: Oxford
-
Lee, D. G.; Chen, T. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 7, p 541.
-
(1991)
Comprehensive Organic Synthesis
, vol.7
, pp. 541
-
-
Lee, D.G.1
Chen, T.2
-
7
-
-
84972910099
-
-
Grob, C. A.; Schiess, P. W. Angew. Chem., Int. Ed. Engl. 1967, 6, 1.
-
(1967)
Angew. Chem., Int. Ed. Engl
, vol.6
, pp. 1
-
-
Grob, C.A.1
Schiess, P.W.2
-
10
-
-
84982078321
-
-
Eschenmoser, A.; Felix, D.; Ohloff, G. Helv. Chim. Acta 1967, 50, 708.
-
(1967)
Helv. Chim. Acta
, vol.50
, pp. 708
-
-
Eschenmoser, A.1
Felix, D.2
Ohloff, G.3
-
11
-
-
84985634005
-
-
Felix, D.; Shreiber, J.; Ohloff, G.; Eschenmoser, A. Helv. Chim. Acta 1971, 54, 2896.
-
(1971)
Helv. Chim. Acta
, vol.54
, pp. 2896
-
-
Felix, D.1
Shreiber, J.2
Ohloff, G.3
Eschenmoser, A.4
-
13
-
-
0005744324
-
-
Tanabe, M.; Crowe, D. F.; Dehn, R. L.; Detre, G. Tetrahedron Lett. 1967, 3739.
-
(1967)
Tetrahedron Lett
, pp. 3739
-
-
Tanabe, M.1
Crowe, D.F.2
Dehn, R.L.3
Detre, G.4
-
20
-
-
75349086884
-
-
Draghici, C. Discovery of a novel ring fragmentation reaction; Efficient preparation of tethered aldehyde ynoates and N-containing heterocycles; Radical addition approach to asymmetric amine synthesis. Ph.D., University of Vermont, Burlington, VT, February 2009.
-
Draghici, C. Discovery of a novel ring fragmentation reaction; Efficient preparation of tethered aldehyde ynoates and N-containing heterocycles; Radical addition approach to asymmetric amine synthesis. Ph.D., University of Vermont, Burlington, VT, February 2009.
-
-
-
-
21
-
-
66149156863
-
-
Javed, M. I.; Wyman, J. M.; Brewer, M. Org. Lett. 2009, 11, 2189.
-
(2009)
Org. Lett
, vol.11
, pp. 2189
-
-
Javed, M.I.1
Wyman, J.M.2
Brewer, M.3
-
22
-
-
70350719267
-
-
Draghici, C.; Huang, Q.; Brewer, M. J. Org. Chem. 2009, 74, 8410.
-
(2009)
J. Org. Chem
, vol.74
, pp. 8410
-
-
Draghici, C.1
Huang, Q.2
Brewer, M.3
-
23
-
-
84981881954
-
-
Schöllkopf, U.; Frasnelli, H. Angew. Chem., Int. Ed. Engl. 1970, 9, 301.
-
(1970)
Angew. Chem., Int. Ed. Engl
, vol.9
, pp. 301
-
-
Schöllkopf, U.1
Frasnelli, H.2
-
28
-
-
0001992687
-
-
Pellicciari, R.; Natalini, B.; Sadeghpour, B. M.; Marinozzi, M.; Snyder, J. P.; Williamson, B. L.; Kuethe, J. T.; Padwa, A. J. Am. Chem. Soc. 1996, 118, 1.
-
(1996)
J. Am. Chem. Soc
, vol.118
, pp. 1
-
-
Pellicciari, R.1
Natalini, B.2
Sadeghpour, B.M.3
Marinozzi, M.4
Snyder, J.P.5
Williamson, B.L.6
Kuethe, J.T.7
Padwa, A.8
-
29
-
-
0035831231
-
-
Zhu, Y.; Shu, L.; Tu, Y.; Shi, Y. J. Org. Chem. 2001, 66, 1818.
-
(2001)
J. Org. Chem
, vol.66
, pp. 1818
-
-
Zhu, Y.1
Shu, L.2
Tu, Y.3
Shi, Y.4
-
31
-
-
0042354575
-
-
Sneddon, H. F.; Gaunt, M. J.; Ley, S. V. Org. Lett. 2003, 5, 1147.
-
(2003)
Org. Lett
, vol.5
, pp. 1147
-
-
Sneddon, H.F.1
Gaunt, M.J.2
Ley, S.V.3
-
32
-
-
33845237100
-
-
Silva, F.; Sawicki, M.; Gouverneur, V. Org. Lett. 2006, 8, 5417.
-
(2006)
Org. Lett
, vol.8
, pp. 5417
-
-
Silva, F.1
Sawicki, M.2
Gouverneur, V.3
-
33
-
-
0034867881
-
-
Lu, X.; Zhang, C.; Xu, Z. Acc. Chem. Res. 2001, 34, 535.
-
(2001)
Acc. Chem. Res
, vol.34
, pp. 535
-
-
Lu, X.1
Zhang, C.2
Xu, Z.3
-
37
-
-
75349106658
-
-
The results shown in Tables 3 and 4 are for the fragmentation of the isolated major diastereomer. In several cases, the minor diastereomer was also subjected to fragmentation and provided comparable yields of product. The results shown in Table 5 are for mixtures of diastereomers.
-
The results shown in Tables 3 and 4 are for the fragmentation of the isolated major diastereomer. In several cases, the minor diastereomer was also subjected to fragmentation and provided comparable yields of product. The results shown in Table 5 are for mixtures of diastereomers.
-
-
-
-
38
-
-
68049091005
-
-
Gouault, N.; Le Roch, M.; Cornée, C.; David, M. l.; Uriac, P. J. Org. Chem. 2009, 74, 5614.
-
(2009)
J. Org. Chem
, vol.74
, pp. 5614
-
-
Gouault, N.1
Le Roch, M.2
Cornée, C.3
David, M.L.4
Uriac, P.5
-
39
-
-
75349083143
-
-
In some cases the aldehyde product was susceptible to oxidation and during purification, or upon standing, would convert to the corresponding tethered ynone carboxylic acid
-
In some cases the aldehyde product was susceptible to oxidation and during purification, or upon standing, would convert to the corresponding tethered ynone carboxylic acid.
-
-
-
|