-
15
-
-
0030949607
-
-
Posner G.H., Lee J.K., White C.M., Hutchings R.H., Dai H., Kachinski J.L., Dolan P., Kensler T.W. J. Org. Chem. 62:1997;3299
-
(1997)
J. Org. Chem.
, vol.62
, pp. 3299
-
-
Posner, G.H.1
Lee, J.K.2
White, C.M.3
Hutchings, R.H.4
Dai, H.5
Kachinski, J.L.6
Dolan, P.7
Kensler, T.W.8
-
16
-
-
0028203952
-
-
Evidente A., Conti L., Altomare C., Bottalico A., Sindona G., Segre A.L., Logrieco A. Nat. Toxins. 2:1994;4
-
(1994)
Nat. Toxins
, vol.2
, pp. 4
-
-
Evidente, A.1
Conti, L.2
Altomare, C.3
Bottalico, A.4
Sindona, G.5
Segre, A.L.6
Logrieco, A.7
-
17
-
-
0034874827
-
-
Watanadilok R., Sonchaeng P., Kijjoa A., Damas A.M., Gales L., Silva A.M.S., Herz W. J. Nat. Prod. 64:2001;1056
-
(2001)
J. Nat. Prod.
, vol.64
, pp. 1056
-
-
Watanadilok, R.1
Sonchaeng, P.2
Kijjoa, A.3
Damas, A.M.4
Gales, L.5
Silva, A.M.S.6
Herz, W.7
-
19
-
-
0000186209
-
-
The data provided from Tsuda does not unambiguously establish the regiochemistry of the pyrone product obtained from the cycloaddition of diyne
-
The data provided from Tsuda does not unambiguously establish the regiochemistry of the pyrone product obtained from the cycloaddition of diyne 14. See ref: Tsuda T., Morikawa S., Hasegawa N., Saegusa T. J. Org. Chem. 55:1990;2978
-
(1990)
J. Org. Chem.
, vol.55
, pp. 2978
-
-
Tsuda, T.1
Morikawa, S.2
Hasegawa, N.3
Saegusa, T.4
-
20
-
-
4043118703
-
-
A corrigendum has recently been submitted to J. Am. Chem. Soc.
-
A corrigendum has recently been submitted to J. Am. Chem. Soc.
-
-
-
-
21
-
-
33845279846
-
-
For an in-depth discussion of cyclotrimer side-product formation, see
-
For an in-depth discussion of cyclotrimer side-product formation, see Tsuda T., Morikawa S., Sumiya R., Saegusa T. J. Org. Chem. 53:1988;3140
-
(1988)
J. Org. Chem.
, vol.53
, pp. 3140
-
-
Tsuda, T.1
Morikawa, S.2
Sumiya, R.3
Saegusa, T.4
-
22
-
-
4043160955
-
-
note
-
In the cycloaddition reaction with substrate 3, a cyclotrimerized aromatic product was isolated in 18% yield. However, in reactions that typically afforded a mixture of products, the oligomers were not isolated
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-
-
-
24
-
-
0002542445
-
-
Hoberg H., Schaeffer D., Burkhardt G., Kruger C., Romao M. J. Organomet. Chem. 266:1984;203
-
(1984)
J. Organomet. Chem.
, vol.266
, pp. 203
-
-
Hoberg, H.1
Schaeffer, D.2
Burkhardt, G.3
Kruger, C.4
Romao, M.5
-
25
-
-
1842607439
-
-
This is a rare example where the formation of a carbon-carbon bond adjacent to the sterically more hindered side of an alkyne is favored. For other examples, see Ref. 7 and
-
This is a rare example where the formation of a carbon-carbon bond adjacent to the sterically more hindered side of an alkyne is favored. For other examples, see Ref. 7 and Miller K.M., Luanphaisarnnont T., Molinaro C., Jamison T.F. J. Am. Chem. Soc. 126:2004;4130
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 4130
-
-
Miller, K.M.1
Luanphaisarnnont, T.2
Molinaro, C.3
Jamison, T.F.4
-
26
-
-
5244370033
-
-
Pangborn A.B., Giardello M.A., Grubbs R.H., Rosen R.K., Timmers F. Organometallics. 15:1996;1518
-
(1996)
Organometallics
, vol.15
, pp. 1518
-
-
Pangborn, A.B.1
Giardello, M.A.2
Grubbs, R.H.3
Rosen, R.K.4
Timmers, F.5
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