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0028151393
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[(±)-1]
-
Syntheses of bromoxone: (a) Gautier, E. C. L.; Lewis, N. J.; McKillop, A.; Taylor, R. J. K. Tetrahedron Lett. 1994, 55, 8759 [(±)-1].
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0033954172
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(c) Block, O.; Klein, G.; Altenbach, H.-J.; Brauer, D. J. J. Org. Chem. 2000, 65, 716 [(+)-1].
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19
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0345359348
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[(+)-1]
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(e) Barros, M. T.; Matias, P. M.; Maycock, C. D.; Ventura, M. R. Org. Lett. 2003, 5, 4321 [(+)-1].
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Barros, M.T.1
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85046528671
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[(+)-2]
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(b) Barros, M. T.; Maycock, C. D.; Ventura, M. R. Chem.-Eur. J. 2000, 6, 3991 [(+)-2].
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Barros, M.T.1
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0035802999
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[(+)-2]
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(c) Shimizu, H.; Okamura, H.; Yamashita, N.; Iwagawa, T.; Nakatani, M. Tetrahedron Lett. 2001, 42, 8649 [(+)-2].
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Shimizu, H.1
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23
-
-
70350194105
-
-
See ref 11d [(+)-2]
-
(d) See ref 11d [(+)-2].
-
-
-
-
24
-
-
33846615903
-
-
[(+)-2]
-
(e) Carreño, M. C.; Merino, E.; Ribagorda, M.; Somoza, Á.; Urbano, A. Chem.-Eur. J. 2007, 13, 1064 [(+)-2].
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Carreño, M.C.1
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Ribagorda, M.3
Somoza, Á.4
Urbano, A.5
-
25
-
-
0000646321
-
-
[(±)-3]
-
Syntheses of epiepoxydon: (a) Ichihara, A.; Kimura, R.; Oda, K.; Sakamura, S. Tetrahedron Lett. 1976, 17, 4741 [(±)-3].
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Tetrahedron Lett.
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Ichihara, A.1
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26
-
-
0030033034
-
-
[(+)-3]
-
(b) Kamikubo, T.; Hiroya, K.; Ogasawara, K. Tetrahedron Lett. 1996, 37, 499 [(+)-3]
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-
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Kamikubo, T.1
Hiroya, K.2
Ogasawara, K.3
-
27
-
-
70350172400
-
-
See ref 11d [(+)-3]
-
(c) See ref 11d [(+)-3].
-
-
-
-
29
-
-
0030573979
-
-
[(±)-4]
-
Syntheses of harveynone: (a) Graham, A. E.; McKerrecher, D.; Davies, D. H.; Taylor, R. J. K. Tetrahedron Lett. 1996, 37, 7445 [(±)-4].
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Tetrahedron Lett.
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Graham, A.E.1
McKerrecher, D.2
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32
-
-
70350206634
-
-
See ref 12b [(+)-4]
-
(d) See ref 12b [(+)-4].
-
-
-
-
33
-
-
60849121968
-
-
[(-)-4]
-
(e) Li, J.; Park, S.; Miller, R. L.; Lee, D. Org. Lett. 2009, 11, 571 [(-)-4].
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Org. Lett.
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Li, J.1
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-
34
-
-
70350172401
-
-
See ref 6a and 6c (±)-6 and (+)-6, respectively
-
Syntheses of panepophenanthrin: (a) See ref 6a and 6c [(±)-6 and (+)-6, respectively.
-
-
-
-
35
-
-
70350183218
-
-
See ref 6b [(+)-6]
-
(b) See ref 6b [(+)-6],
-
-
-
-
37
-
-
70350184882
-
-
See ref 13d [(-)-6]
-
(d) See ref 13d [(-)-6].
-
-
-
-
38
-
-
33845923179
-
-
[(+)-6]
-
(e) Matsuzawa, M.; Kakeya, H.; Yamaguchi, J.; Shoji, M.; Onose, R.; Osada, H.; Hayashi, Y. Chem. Asian J. 2006, 1, 845 [(+)-6].
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Shoji, M.4
Onose, R.5
Osada, H.6
Hayashi, Y.7
-
39
-
-
70350205066
-
-
See ref 8 [(+)-9]
-
Syntheses of hexacyclinol: (a) See ref 8 [(+)-9].
-
-
-
-
41
-
-
70350195850
-
-
See refs 12b, 14a,b, 15a,b,e, and 16a,b for examples of the use of these types of cross-coupling processes
-
See refs 12b, 14a,b, 15a,b,e, and 16a,b for examples of the use of these types of cross-coupling processes.
-
-
-
-
42
-
-
70350205065
-
-
See refs 11a-c, 12a,e, 13b,d, 14a,b, 15c and 16b for examples of this type of approach
-
See refs 11a-c, 12a,e, 13b,d, 14a,b, 15c and 16b for examples of this type of approach.
-
-
-
-
43
-
-
70350208290
-
-
See refs 11b-d, 12a, 13b,d, 14b, 15a,c, and 16b for examples of this type of approach
-
See refs 11b-d, 12a, 13b,d, 14b, 15a,c, and 16b for examples of this type of approach.
-
-
-
-
44
-
-
70350184881
-
-
Compounds 10-12 can be obtained from Questor, Queen's University of Belfast, Northern Ireland. Questor Centre Contact Page: (accessed July 21, 2009)
-
Compounds 10-12 can be obtained from Questor, Queen's University of Belfast, Northern Ireland. Questor Centre Contact Page: http://questor.qub.ac. uk/newsite/contact.htm (accessed July 21, 2009).
-
-
-
-
45
-
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0001846314
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-
For reviews on methods for generating cis-1,2-dihydrocatechols by microbial dihydroxylation of the corresponding aromatics, as well as the synthetic applications of these metabolites, see: (a) Hudlicky, T.; Gonzalez, D.; Gibson, D. T. Aldrichim. Acta 1999, 32, 35.
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49
-
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70350197490
-
-
Details of these analyses are presented in the Supporting Information
-
Details of these analyses are presented in the Supporting Information.
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50
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55
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70350186538
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These previously unreported compounds were prepared from (trimethylstannyl)methanol using standard methods
-
These previously unreported compounds were prepared from (trimethylstannyl)methanol using standard methods.
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