-
1
-
-
59649114569
-
-
Ratnayake, R.; Covell, D.; Ransom, T. T.; Gustafson, K. R.; Beutler, J. A. Org. Lett. 2009, 11, 57
-
(2009)
Org. Lett.
, vol.11
, pp. 57
-
-
Ratnayake, R.1
Covell, D.2
Ransom, T.T.3
Gustafson, K.R.4
Beutler, J.A.5
-
3
-
-
84255169377
-
-
Pouwer, R. H.; Richard, J.-A.; Tseng, C.-C.; Chen, D. Y.-K. Chem.-Asian J. 2012, 7, 22
-
(2012)
Chem.-Asian J.
, vol.7
, pp. 22
-
-
Pouwer, R.H.1
Richard, J.-A.2
Tseng, C.-C.3
Chen, D.Y.-K.4
-
4
-
-
84860187174
-
-
Lu, Y.; Yao, H.-Q.; Sun, B.-F. Chin. J. Org. Chem. 2012, 32, 1
-
(2012)
Chin. J. Org. Chem.
, vol.32
, pp. 1
-
-
Lu, Y.1
Yao, H.-Q.2
Sun, B.-F.3
-
5
-
-
84855860684
-
-
Wang, C.-L.; Sun, B.-F.; Chen, S.-G.; Ding, R.; Lin, G.-Q.; Xu, J.-Y.; Shang, Y.-J. Synlett 2012, 23, 263
-
(2012)
Synlett
, vol.23
, pp. 263
-
-
Wang, C.-L.1
Sun, B.-F.2
Chen, S.-G.3
Ding, R.4
Lin, G.-Q.5
Xu, J.-Y.6
Shang, Y.-J.7
-
6
-
-
84859080425
-
-
Akee, R. K.; Ransom, T.; Ratnayake, R.; McMahon, J. B.; Beutler, J. A. J. Nat. Prod. 2012, 75, 459
-
(2012)
J. Nat. Prod.
, vol.75
, pp. 459
-
-
Akee, R.K.1
Ransom, T.2
Ratnayake, R.3
McMahon, J.B.4
Beutler, J.A.5
-
7
-
-
79955425788
-
-
Ushakov, D. B.; Navickas, V.; Strobele, M.; Maichle-Mossmer, C.; Sasse, F.; Maier, M. E. Org. Lett. 2011, 13, 2090
-
(2011)
Org. Lett.
, vol.13
, pp. 2090
-
-
Ushakov, D.B.1
Navickas, V.2
Strobele, M.3
Maichle-Mossmer, C.4
Sasse, F.5
Maier, M.E.6
-
9
-
-
84860476423
-
-
Xu, J.; Caro-Diaz, E. J. E.; Batova, A.; Sullivan, S. D. E.; Theodorakis, E. A. Chem.-Asian J 2012, 7, 1052
-
(2012)
Chem.-Asian J
, vol.7
, pp. 1052
-
-
Xu, J.1
Caro-Diaz, E.J.E.2
Batova, A.3
Sullivan, S.D.E.4
Theodorakis, E.A.5
-
10
-
-
79954576625
-
-
Radtke, L.; Willot, M.; Sun, H.; Ziegler, S.; Sauerland, S.; Strohmann, C.; Frohlich, R.; Habenberger, P.; Waldmann, H.; Christmann, M. Angew. Chem. Int. Ed. 2011, 50, 3998
-
(2011)
Angew. Chem. Int. Ed.
, vol.50
, pp. 3998
-
-
Radtke, L.1
Willot, M.2
Sun, H.3
Ziegler, S.4
Sauerland, S.5
Strohmann, C.6
Frohlich, R.7
Habenberger, P.8
Waldmann, H.9
Christmann, M.10
-
12
-
-
4143062538
-
-
Hoye, T. R.; Jeffrey, C. S.; Tennakoon, M. A.; Wang, J.; Zhao, H. J. Am. Chem. Soc. 2004, 126, 10210
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 10210
-
-
Hoye, T.R.1
Jeffrey, C.S.2
Tennakoon, M.A.3
Wang, J.4
Zhao, H.5
-
15
-
-
18844410382
-
-
Gao, Y.; Hanson, R. M.; Klunder, J. M.; Ko, S. Y.; Masamune, H.; Sharpless, K. B. J. Am. Chem. Soc. 1987, 109, 5765
-
(1987)
J. Am. Chem. Soc.
, vol.109
, pp. 5765
-
-
Gao, Y.1
Hanson, R.M.2
Klunder, J.M.3
Ko, S.Y.4
Masamune, H.5
Sharpless, K.B.6
-
16
-
-
58149316212
-
-
Ichige, T.; Okano, Y.; Kanoh, N.; Nakata, M. J. Org. Chem. 2009, 74, 230
-
(2009)
J. Org. Chem.
, vol.74
, pp. 230
-
-
Ichige, T.1
Okano, Y.2
Kanoh, N.3
Nakata, M.4
-
17
-
-
10044244964
-
-
Bravo, F.; McDonald, F. E.; Neiwert, W. A.; Hardcastle, K. I. Org. Lett. 2004, 6, 4487
-
(2004)
Org. Lett.
, vol.6
, pp. 4487
-
-
Bravo, F.1
McDonald, F.E.2
Neiwert, W.A.3
Hardcastle, K.I.4
-
18
-
-
1542759075
-
-
See, however, the regiospecific ring opening of vinyl substituted examples
-
See, however, the regiospecific ring opening of vinyl substituted examples: Narjes, F.; Schaumann, E. Liebigs Ann. Chem 1993, 841
-
(1993)
Liebigs Ann. Chem
, pp. 841
-
-
Narjes, F.1
Schaumann, E.2
-
19
-
-
0001025010
-
-
In addition, one might note the successful addition of acetylide to the 3-position of 2-substituted 2,3-epoxy esters
-
In addition, one might note the successful addition of acetylide to the 3-position of 2-substituted 2,3-epoxy esters: Bartlett, P. A.; Tanzella, D. J.; Barstow, J. F. J. Org. Chem. 1982, 47, 3941
-
(1982)
J. Org. Chem.
, vol.47
, pp. 3941
-
-
Bartlett, P.A.1
Tanzella, D.J.2
Barstow, J.F.3
-
21
-
-
0010253112
-
-
Inanaga, J.; Kawanami, Y.; Yamaguchi, M. Bull. Chem. Soc. Jpn. 1986, 59, 1521
-
(1986)
Bull. Chem. Soc. Jpn.
, vol.59
, pp. 1521
-
-
Inanaga, J.1
Kawanami, Y.2
Yamaguchi, M.3
-
23
-
-
0009569697
-
-
Petrier, C.; Einhorn, J.; Luche, J. L. Tetraheron Lett 1985, 26, 1449
-
(1985)
Tetraheron Lett
, vol.26
, pp. 1449
-
-
Petrier, C.1
Einhorn, J.2
Luche, J.L.3
-
24
-
-
37049137254
-
-
The known bromide 12 was prepared from the corresponding alcohol (see the Supporting Information) by the method of
-
The known bromide 12 was prepared from the corresponding alcohol (see the Supporting Information) by the method of Barton, D. H.; Shioiri, T.; Widdowson, D. A. J. Chem. Soc. C 1971, 1968
-
(1971)
J. Chem. Soc. C
, pp. 1968
-
-
Barton, D.H.1
Shioiri, T.2
Widdowson, D.A.3
-
25
-
-
34247487884
-
-
Stewart, I. C.; Ung, T.; Pletnev, A. A.; Berlin, J. M.; Grubbs, R. H.; Schrodi, Y. Org. Lett. 2007, 9, 1589
-
(2007)
Org. Lett.
, vol.9
, pp. 1589
-
-
Stewart, I.C.1
Ung, T.2
Pletnev, A.A.3
Berlin, J.M.4
Grubbs, R.H.5
Schrodi, Y.6
-
26
-
-
78249268215
-
-
This result may be compared with the nonspecific, nonrelay ene-yne-ene metathesis of a similar, highly substituted system in which reaction, carried out under ethylene, is presumably initiated at the acetylene; see
-
This result may be compared with the nonspecific, nonrelay ene-yne-ene metathesis of a similar, highly substituted system in which reaction, carried out under ethylene, is presumably initiated at the acetylene; see: Knueppel, S.; Rogachev, V. O.; Metz, P. Eur. J. Org. Chem. 2010, 6145
-
(2010)
Eur. J. Org. Chem.
, pp. 6145
-
-
Knueppel, S.1
Rogachev, V.O.2
Metz, P.3
-
28
-
-
10044269693
-
-
Kang, S. H.; Kim, M.; Kang, S. Y. Angew. Chem., Int. Ed. 2004, 43, 6177
-
(2004)
Angew. Chem., Int. Ed.
, vol.43
, pp. 6177
-
-
Kang, S.H.1
Kim, M.2
Kang, S.Y.3
-
29
-
-
37049102895
-
-
One should note that this result is not inconsistent with regiochemistry observed in the oxymercuration of simple conjugated dienes; see
-
One should note that this result is not inconsistent with regiochemistry observed in the oxymercuration of simple conjugated dienes; see: Barluenga, J.; Perez-Prieto, J.; Asensio, G. J. Chem. Soc., Perkin Trans. 1 1984, 629
-
(1984)
Chem. Soc., Perkin Trans. 1
, pp. 629
-
-
Barluenga, J.1
Perez-Prieto, J.2
Asensio, G.J.3
-
31
-
-
77952397509
-
-
This alcohol is a known compound, prepared from alcohol 17 in two steps and 60% yield as described in
-
This alcohol is a known compound, prepared from alcohol 17 in two steps and 60% yield as described in Molawi, K.; Delpont, N; Echavarren, A. M. Angew. Chem., Int. Ed. 2010, 49, 3517
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 3517
-
-
Molawi, K.1
Delpont, N.2
Echavarren, A.M.3
|