-
1
-
-
43449108881
-
-
For examples of biologically active compounds bearing a hydropyran unit, see:
-
For examples of biologically active compounds bearing a hydropyran unit, see:. MacMillan J.B., Zhou G.X.-., Skepper C.K., and Molinski T.F. J. Org. Chem. 73 (2008) 3699
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(2008)
J. Org. Chem.
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MacMillan, J.B.1
Zhou, G.X.-.2
Skepper, C.K.3
Molinski, T.F.4
-
2
-
-
34247142390
-
-
Wright A.E., Botelho J.C., Guzman E., Harmody D., Linley P., McCarthy P.J., Pitts T.P., Pomponi S.A., and Reed J.K. J. Nat. Prod. 70 (2007) 412
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(2007)
J. Nat. Prod.
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Wright, A.E.1
Botelho, J.C.2
Guzman, E.3
Harmody, D.4
Linley, P.5
McCarthy, P.J.6
Pitts, T.P.7
Pomponi, S.A.8
Reed, J.K.9
-
5
-
-
0016212606
-
-
Ménard M., Rivest P., Morris L., Meunier J., and Perron Y.G. Can. J. Chem. 52 (1974) 2316
-
(1974)
Can. J. Chem.
, vol.52
, pp. 2316
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-
Ménard, M.1
Rivest, P.2
Morris, L.3
Meunier, J.4
Perron, Y.G.5
-
6
-
-
62749096972
-
-
Wu X., Chen J., Ji M., Levant B., and Wang S. Bioorg. Med. Chem. 14 (2000) 5813
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(2000)
Bioorg. Med. Chem.
, vol.14
, pp. 5813
-
-
Wu, X.1
Chen, J.2
Ji, M.3
Levant, B.4
Wang, S.5
-
7
-
-
35348836592
-
-
For reviews regarding Prins reaction and Prins cyclization, see:
-
For reviews regarding Prins reaction and Prins cyclization, see:. Pastor I.M., and Yus M. Curr. Org. Chem. 11 (2007) 925
-
(2007)
Curr. Org. Chem.
, vol.11
, pp. 925
-
-
Pastor, I.M.1
Yus, M.2
-
12
-
-
57149124789
-
-
For examples, see:
-
For examples, see:. Vintonyak V.V., Kunze B., Sasse F., and Maier M.E. Chem. Eur. J. 14 (2008) 11132
-
(2008)
Chem. Eur. J.
, vol.14
, pp. 11132
-
-
Vintonyak, V.V.1
Kunze, B.2
Sasse, F.3
Maier, M.E.4
-
24
-
-
34547938472
-
-
Few examples were reported using ketones: and references therein
-
Few examples were reported using ketones:. Yadav J.S., Reddy B.V.S., Krishna V.H., Swamy T., and Kumar G.G.K.S. Can. J. Chem. 85 (2007) 412 and references therein
-
(2007)
Can. J. Chem.
, vol.85
, pp. 412
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Krishna, V.H.3
Swamy, T.4
Kumar, G.G.K.S.5
-
26
-
-
44949148096
-
-
For recent reviews concerning iodine, see:
-
For recent reviews concerning iodine, see:. Stavber S., Jereb M., and Zupan M. Synthesis (2008) 1487
-
(2008)
Synthesis
, pp. 1487
-
-
Stavber, S.1
Jereb, M.2
Zupan, M.3
-
31
-
-
10044267850
-
-
For some reactions using iodine as Lewis acid, see:
-
For some reactions using iodine as Lewis acid, see:. Sun J., Dong Y., Cao L., Wang X., Wang S., and Hu Y. J. Org. Chem. 69 (2004) 8932
-
(2004)
J. Org. Chem.
, vol.69
, pp. 8932
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-
Sun, J.1
Dong, Y.2
Cao, L.3
Wang, X.4
Wang, S.5
Hu, Y.6
-
34
-
-
50249125912
-
-
For selected recent examples, see:
-
For selected recent examples, see:. Kishi Y., Nagura H., Inagi S., and Fushigami T. Chem. Commun. (2008) 3876
-
(2008)
Chem. Commun.
, pp. 3876
-
-
Kishi, Y.1
Nagura, H.2
Inagi, S.3
Fushigami, T.4
-
36
-
-
33748625993
-
-
Carballo R.M., Ramírez M.A., Rodríguez M.L., Martín V.S., and Padrón J.I. Org. Lett. 8 (2006) 3837
-
(2006)
Org. Lett.
, vol.8
, pp. 3837
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-
Carballo, R.M.1
Ramírez, M.A.2
Rodríguez, M.L.3
Martín, V.S.4
Padrón, J.I.5
-
38
-
-
41949093836
-
-
Yadav J.S., Reddy B.V.S., Chaya D.N., Kumar G.G.K.S.N., Aravind S., Kunwar A.C., and Madavi C. Tetrahedron Lett. 49 (2008) 3330
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(2008)
Tetrahedron Lett.
, vol.49
, pp. 3330
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-
Yadav, J.S.1
Reddy, B.V.S.2
Chaya, D.N.3
Kumar, G.G.K.S.N.4
Aravind, S.5
Kunwar, A.C.6
Madavi, C.7
-
39
-
-
33947522545
-
-
Silva Jr. L.F., Quintiliano S.A.P., Craveiro M.V., Vieira F.Y.M., and Ferraz H.M.C. Synthesis (2007) 355
-
(2007)
Synthesis
, pp. 355
-
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Silva Jr., L.F.1
Quintiliano, S.A.P.2
Craveiro, M.V.3
Vieira, F.Y.M.4
Ferraz, H.M.C.5
-
40
-
-
33749556058
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-
Silva Jr. L.F., Quintiliano S.A.P., Ferraz H.M.C., Santos L.S., and Eberlin M.N. J. Braz. Chem. Soc. 17 (2006) 981
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(2006)
J. Braz. Chem. Soc.
, vol.17
, pp. 981
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-
Silva Jr., L.F.1
Quintiliano, S.A.P.2
Ferraz, H.M.C.3
Santos, L.S.4
Eberlin, M.N.5
-
43
-
-
85034356760
-
-
For examples of 5-endo-trig iodocyclization, see:
-
For examples of 5-endo-trig iodocyclization, see:. Barks J.M., Weingarten G.G., and Knight D.W. J. Chem. Soc., Perkin Trans. 1 (2000) 3469
-
(2000)
J. Chem. Soc., Perkin Trans. 1
, pp. 3469
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Barks, J.M.1
Weingarten, G.G.2
Knight, D.W.3
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44
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0001544820
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Bedford S.B., Bell K.E., Bennett F., Hayes C.J., Knight D.W., and Shaw D.E. J. Chem. Soc., Perkin Trans. 1 (1999) 2143
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(1999)
J. Chem. Soc., Perkin Trans. 1
, pp. 2143
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Bedford, S.B.1
Bell, K.E.2
Bennett, F.3
Hayes, C.J.4
Knight, D.W.5
Shaw, D.E.6
-
47
-
-
0027956693
-
-
Terminal olefins and endocyclic olefins afforded 4-exo-tet iodocyclization products:
-
Terminal olefins and endocyclic olefins afforded 4-exo-tet iodocyclization products:. Galatsis P., and Parks D.J. Tetrahedron Lett. 35 (1994) 6611
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(1994)
Tetrahedron Lett.
, vol.35
, pp. 6611
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-
Galatsis, P.1
Parks, D.J.2
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52
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0343013131
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-
Yadav J.S., Patil D.G., Krishna R.R., Chawla H.P.S., and Dev S. Tetrahedron 38 (1982) 1003
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(1982)
Tetrahedron
, vol.38
, pp. 1003
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Yadav, J.S.1
Patil, D.G.2
Krishna, R.R.3
Chawla, H.P.S.4
Dev, S.5
-
54
-
-
33644696397
-
-
The relative configuration of 23 and 24 was assigned by comparison to the NMR data of other 4-hydroxy-tetrahydropyrans.
-
The relative configuration of 23 and 24 was assigned by comparison to the NMR data of other 4-hydroxy-tetrahydropyrans. Abate A., Allievi M., Brenna E., Fuganti C., Gatti F.G., and Serra S. Helv. Chim. Acta 89 (2006) 177
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(2006)
Helv. Chim. Acta
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Abate, A.1
Allievi, M.2
Brenna, E.3
Fuganti, C.4
Gatti, F.G.5
Serra, S.6
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