-
1
-
-
84914020355
-
-
New Synth. Methodol. Bio. Act. Subst.
-
(a) Johnson, W. S. Stud. Org, Chem. (Amsterdam) 1981, 6 (New Synth. Methodol. Bio. Act. Subst.), 1. (b) Johnson, W. S. Bioorg. Chem. 1976, 5, 51 and references therein.
-
(1981)
Stud. Org, Chem. (Amsterdam)
, vol.6
, pp. 1
-
-
Johnson, W.S.1
-
2
-
-
0017122726
-
-
and references therein
-
(a) Johnson, W. S. Stud. Org, Chem. (Amsterdam) 1981, 6 (New Synth. Methodol. Bio. Act. Subst.), 1. (b) Johnson, W. S. Bioorg. Chem. 1976, 5, 51 and references therein.
-
(1976)
Bioorg. Chem.
, vol.5
, pp. 51
-
-
Johnson, W.S.1
-
3
-
-
0029902231
-
-
and references therein
-
Several noteworthy accounts involving highly stereoselective polyene cyclizations have recently appeared, (a) Corey, E. J.; Wood, H. B., Jr. J. Am. Chem. Soc. 1996, 118, 11982 and references therein. (b) Johnson, W. S.; Fletcher, V. R.; Chenera, B.; Bartlett, W. R.; Tham, F. S.; Kullnig, R. K. J. Am. Chem. Soc. 1993, 115, 497. Johnson, W. S.; Plummer, M. S.; Reddy, S. P.; Bartlett, W. R. J. Am. Chem. Soc. 1993, 115, 515.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 11982
-
-
Corey, E.J.1
Wood Jr., H.B.2
-
4
-
-
0027509297
-
-
Several noteworthy accounts involving highly stereoselective polyene cyclizations have recently appeared, (a) Corey, E. J.; Wood, H. B., Jr. J. Am. Chem. Soc. 1996, 118, 11982 and references therein. (b) Johnson, W. S.; Fletcher, V. R.; Chenera, B.; Bartlett, W. R.; Tham, F. S.; Kullnig, R. K. J. Am. Chem. Soc. 1993, 115, 497. Johnson, W. S.; Plummer, M. S.; Reddy, S. P.; Bartlett, W. R. J. Am. Chem. Soc. 1993, 115, 515.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 497
-
-
Johnson, W.S.1
Fletcher, V.R.2
Chenera, B.3
Bartlett, W.R.4
Tham, F.S.5
Kullnig, R.K.6
-
5
-
-
0027476042
-
-
Several noteworthy accounts involving highly stereoselective polyene cyclizations have recently appeared, (a) Corey, E. J.; Wood, H. B., Jr. J. Am. Chem. Soc. 1996, 118, 11982 and references therein. (b) Johnson, W. S.; Fletcher, V. R.; Chenera, B.; Bartlett, W. R.; Tham, F. S.; Kullnig, R. K. J. Am. Chem. Soc. 1993, 115, 497. Johnson, W. S.; Plummer, M. S.; Reddy, S. P.; Bartlett, W. R. J. Am. Chem. Soc. 1993, 115, 515.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 515
-
-
Johnson, W.S.1
Plummer, M.S.2
Reddy, S.P.3
Bartlett, W.R.4
-
6
-
-
0000719822
-
-
(a) Harring, S. R.; Edstrom, E. D.; Livinghouse, T. Adv. Heterocycl. Nat. Prod. Synth. 1992, 2, 299-376.
-
(1992)
Adv. Heterocycl. Nat. Prod. Synth.
, vol.2
, pp. 299-376
-
-
Harring, S.R.1
Edstrom, E.D.2
Livinghouse, T.3
-
8
-
-
0019962962
-
-
White, J. D.; Avery, M. A.; Carter, J. P. J. Am. Chem. Soc. 1982, 104, 3923.
-
(1982)
J. Am. Chem. Soc.
, vol.104
, pp. 3923
-
-
White, J.D.1
Avery, M.A.2
Carter, J.P.3
-
9
-
-
0020361157
-
-
Hoye, T. R.; Caruso, A. J.; Dellaria, J. F.; Kurth, M. J. Am. Chem. Soc. 1982, 104, 6704.
-
(1982)
J. Am. Chem. Soc.
, vol.104
, pp. 6704
-
-
Hoye, T.R.1
Caruso, A.J.2
Dellaria, J.F.3
Kurth, M.4
-
10
-
-
1542414112
-
-
(e) Nishizawa, M.; Yamada, H.; Hayashi, Y. Tetrahedron Lett. 1987, 28, 3255.
-
(1987)
Tetrahedron Lett.
, vol.28
, pp. 3255
-
-
Nishizawa, M.1
Yamada, H.2
Hayashi, Y.3
-
15
-
-
85086290044
-
-
7b,c may be serving as the electrophile
-
7b,c may be serving as the electrophile
-
-
-
-
16
-
-
33845561243
-
-
and references therein
-
(b) Smit, W. A.; Zefirov, N. S.; Bodrikov, I. V.; Krimer, M. Z. Acc Chem. Res. 1979, 12, 282 and references therein,
-
(1979)
Acc Chem. Res.
, vol.12
, pp. 282
-
-
Smit, W.A.1
Zefirov, N.S.2
Bodrikov, I.V.3
Krimer, M.Z.4
-
17
-
-
1542623516
-
-
Smit, W. S.; Zefirov, N. S.; Bodrikov, I. V. Org. Sulfur Chem. Invited Lect. Int. Symp., 9th, 1980 1981, 159.
-
(1980)
Org. Sulfur Chem. Invited Lect. Int. Symp., 9th
, vol.1981
, pp. 159
-
-
Smit, W.S.1
Zefirov, N.S.2
Bodrikov, I.V.3
-
19
-
-
0009345236
-
-
3, see: Chang, L. L.; Denney, D. B.; Denney, D. Z.; Kazior, R. J. J. Am. Chem. Soc. 1977, 99, 2293.
-
(1977)
J. Am. Chem. Soc.
, vol.99
, pp. 2293
-
-
Chang, L.L.1
Denney, D.B.2
Denney, D.Z.3
Kazior, R.J.4
-
20
-
-
85086290664
-
-
3 in quantities exceeding 3.15 equiv resulted in no observable increase in yield
-
3 in quantities exceeding 3.15 equiv resulted in no observable increase in yield.
-
-
-
-
21
-
-
0003132679
-
-
Axtell, D. D.; Cambell, A. C.; Keller, P. C.; Rund, J. V. J. Coord. Chem. 1976, 5, 129.
-
(1976)
J. Coord. Chem.
, vol.5
, pp. 129
-
-
Axtell, D.D.1
Cambell, A.C.2
Keller, P.C.3
Rund, J.V.4
-
23
-
-
85086289736
-
-
3 and 9b is not stable after 30 min at -20°C, as evidenced by the failure to observe (by GC and TLC) or isolate cyclized products from reactions in which the Lewis acid and sulfenate ester were allowed to age for 30 min at -20°C before introducing the substrate
-
3 and 9b is not stable after 30 min at -20°C, as evidenced by the failure to observe (by GC and TLC) or isolate cyclized products from reactions in which the Lewis acid and sulfenate ester were allowed to age for 30 min at -20°C before introducing the substrate.
-
-
-
-
24
-
-
33947092680
-
-
Vedejs, E.; Engler, D. A.; Telschow, J. E. J. Org. Chem. 1978, 43, 188.
-
(1978)
Org. Chem.
, vol.43
, pp. 188
-
-
Vedejs, E.1
Engler, D.A.2
Telschow, J.E.J.3
|