-
1
-
-
79951793566
-
-
WO9967408
-
N. V. S. Ramakrishna, S. H. K. Swamy, M. M. S. Kushwaha, S. Kota, M. Raman, S. K. Deshmukh, D. Schummer, M. Kurz, H. Kogler, WO9967408, 1999.
-
(1999)
-
-
Ramakrishna, N.V.S.1
Swamy, S.H.K.2
Kushwaha, M.M.S.3
Kota, S.4
Raman, M.5
Deshmukh, S.K.6
Schummer, D.7
Kurz, M.8
Kogler, H.9
-
2
-
-
0035013045
-
-
L. Vértesy, M. Kurz, E. F. Paulus, D. Schummer, P. Hamann, J. Antibiot. 2001, 54, 354-363.
-
(2001)
J. Antibiot.
, vol.54
, pp. 354-363
-
-
Vértesy, L.1
Kurz, M.2
Paulus, E.F.3
Schummer, D.4
Hamann, P.5
-
3
-
-
84945041210
-
-
H. Lessmann, J. Krupa, H. Lackner, P. G. Jones, Z. Naturforsch. B 1989, 44, 353-363.
-
(1989)
Z. Naturforsch. B
, vol.44
, pp. 353-363
-
-
Lessmann, H.1
Krupa, J.2
Lackner, H.3
Jones, P.G.4
-
4
-
-
21144464589
-
-
H. Lessmann, J. Krupa, H. Lackner, K. Schmidt-Bräse, G. M. Sheldrick, Z. Naturforsch. B 1993, 48, 672-682.
-
(1993)
Z. Naturforsch. B
, vol.48
, pp. 672-682
-
-
Lessmann, H.1
Krupa, J.2
Lackner, H.3
Schmidt-Bräse, K.4
Sheldrick, G.M.5
-
5
-
-
79951802408
-
-
For reviews on G6Pase inhibitors, see
-
For reviews on G6Pase inhibitors, see
-
-
-
-
8
-
-
0034765181
-
-
for reviews on the pharmacologic inhibition of the hepatic glucose production see
-
J. C. Parker, Drugs Future 2001, 26, 687-693; for reviews on the pharmacologic inhibition of the hepatic glucose production see
-
(2001)
Drugs Future
, vol.26
, pp. 687-693
-
-
Parker, J.C.1
-
9
-
-
0037247641
-
-
R. Kurukulasuriya, J. T. Link, D. J. Madar, Z. Pei, J. J. Rhode, S. J. Richards, A. J. Souers, B. G. Szczepankiewic, Curr. Med. Chem. 2003, 10, 99-121
-
(2003)
Curr. Med. Chem.
, vol.10
, pp. 99-121
-
-
Kurukulasuriya, R.1
Link, J.T.2
Madar, D.J.3
Pei, Z.4
Rhode, J.J.5
Richards, S.J.6
Souers, A.J.7
Szczepankiewic, B.G.8
-
10
-
-
0037244781
-
-
R. Kurukulasuriya, J. T. Link, D. J. Madar, Z. Pei, S. J. Richards, J. J. Rhode, A. J. Souers, B. G. Szczepankiewic, Curr. Med. Chem. 2003, 10, 123-153.
-
(2003)
Curr. Med. Chem.
, vol.10
, pp. 123-153
-
-
Kurukulasuriya, R.1
Link, J.T.2
Madar, D.J.3
Pei, Z.4
Richards, S.J.5
Rhode, J.J.6
Souers, A.J.7
Szczepankiewic, B.G.8
-
11
-
-
77949921050
-
-
E. Tahanian, S. Lord-Dufour, A. Das, C. Khosla, R. Roy, B. Annabi, Chem. Biol. Drug Des. 2010, 75, 481-488
-
(2010)
Chem. Biol. Drug Des.
, vol.75
, pp. 481-488
-
-
Tahanian, E.1
Lord-Dufour, S.2
Das, A.3
Khosla, C.4
Roy, R.5
Annabi, B.6
-
12
-
-
65249185690
-
-
S. Lord-Dufour, I. B. Copland, L.-C. Levros Jr., M. Post, A. Das, C. Khosla, J. Galipeau, E. Rassart, B. Annabi, Stem Cells 2009, 27, 489-497
-
(2009)
Stem Cells
, vol.27
, pp. 489-497
-
-
Lord-Dufour, S.1
Copland, I.B.2
Levros Jr., L.-C.3
Post, M.4
Das, A.5
Khosla, C.6
Galipeau, J.7
Rassart, E.8
Annabi, B.9
-
13
-
-
34247242084
-
-
A. Belkaid, S. Fortier, J. Cao, B. Annabi, Neoplasia 2007, 9, 332-340
-
(2007)
Neoplasia
, vol.9
, pp. 332-340
-
-
Belkaid, A.1
Fortier, S.2
Cao, J.3
Annabi, B.4
-
14
-
-
33745167272
-
-
A. Belkaid, I. B. Copland, D. Massillon, B. Annabi, FEBS Lett. 2006, 580, 3746-3752.
-
(2006)
FEBS Lett.
, vol.580
, pp. 3746-3752
-
-
Belkaid, A.1
Copland, I.B.2
Massillon, D.3
Annabi, B.4
-
15
-
-
0347298578
-
-
F. Kaiser, L. Schwink, J. Velder, H.-G. Schmalz, J. Org. Chem. 2002, 67, 9248-9256
-
(2002)
J. Org. Chem.
, vol.67
, pp. 9248-9256
-
-
Kaiser, F.1
Schwink, L.2
Velder, J.3
Schmalz, H.-G.4
-
16
-
-
0345352744
-
-
F. Kaiser, L. Schwink, J. Velder, H.-G. Schmalz, Tetrahedron 2003, 59, 3201-3217.
-
(2003)
Tetrahedron
, vol.59
, pp. 3201-3217
-
-
Kaiser, F.1
Schwink, L.2
Velder, J.3
Schmalz, H.-G.4
-
17
-
-
29744446117
-
-
K. Krohn, J. Diederichs, M. Riaz, Tetrahedron 2006, 62, 1223-1230.
-
(2006)
Tetrahedron
, vol.62
, pp. 1223-1230
-
-
Krohn, K.1
Diederichs, J.2
Riaz, M.3
-
18
-
-
35348965789
-
-
D. Sucunza, D. Dembkowski, S. Neufeind, J. Velder, J. Lex, H.-G. Schmalz, Synlett 2007, 2569-2573.
-
(2007)
Synlett
, pp. 2569-2573
-
-
Sucunza, D.1
Dembkowski, D.2
Neufeind, S.3
Velder, J.4
Lex, J.5
Schmalz, H.-G.6
-
19
-
-
34249950925
-
-
T. S. Lee, A. Das, C. Khosla, Bioorg. Med. Chem. 2007, 15, 5207-5218.
-
(2007)
Bioorg. Med. Chem.
, vol.15
, pp. 5207-5218
-
-
Lee, T.S.1
Das, A.2
Khosla, C.3
-
20
-
-
79951798774
-
-
note
-
The anionic homo-Fries rearrangement has been successfully applied as a particular powerful method for the preparation of tetra-ortho-substituted benzophenones, such as the prominent PKC inhibitor balanol
-
-
-
-
21
-
-
0028124871
-
-
J. W. Lampe, P. F. Hughes, C. K. Biggers, S. H. Smith, H. Hu, J. Org. Chem. 1994, 59, 5147-5148
-
(1994)
J. Org. Chem.
, vol.59
, pp. 5147-5148
-
-
Lampe, J.W.1
Hughes, P.F.2
Biggers, C.K.3
Smith, S.H.4
Hu, H.5
-
22
-
-
0028090343
-
-
K. C. Nicolaou, M. E. Bunnage, K. Koide, J. Am. Chem. Soc. 1994, 116, 8402-8403; for other examples, see
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 8402-8403
-
-
Nicolaou, K.C.1
Bunnage, M.E.2
Koide, K.3
-
23
-
-
0037026451
-
-
A. Piettre, E. Chevenier, C. Massardier, Y. Gimbert, A. E. Greene, Org. Lett. 2002, 4, 3139-3142
-
(2002)
Org. Lett.
, vol.4
, pp. 3139-3142
-
-
Piettre, A.1
Chevenier, E.2
Massardier, C.3
Gimbert, Y.4
Greene, A.E.5
-
27
-
-
33748671861
-
-
P. Allevi, M. Anastasia, S. Bingham, P. Ciuffreda, A. Fiecchi, G. Cighetti, M. Muir, A. Scala, J. Tyman, J. Chem. Soc. Perkin Trans. 1 1998, 575-582
-
(1998)
J. Chem. Soc. Perkin Trans. 1
, pp. 575-582
-
-
Allevi, P.1
Anastasia, M.2
Bingham, S.3
Ciuffreda, P.4
Fiecchi, A.5
Cighetti, G.6
Muir, M.7
Scala, A.8
Tyman, J.9
-
32
-
-
84886340977
-
-
P. Avelli, M. Anastasia, P. Ciuffreda, A. Fecchi, A. Scala, S. Bingham, M. Muir, J. Tyman, J. Chem. Soc. Chem. Commun. 1991, 1319-1320
-
(1991)
J. Chem. Soc. Chem. Commun.
, pp. 1319-1320
-
-
Avelli, P.1
Anastasia, M.2
Ciuffreda, P.3
Fecchi, A.4
Scala, A.5
Bingham, S.6
Muir, M.7
Tyman, J.8
-
33
-
-
0001313281
-
-
D. W. Cameron, C. Conn, G. I. Feutrill, Aust. J. Chem. 1981, 34, 1945-1949
-
(1981)
Aust. J. Chem.
, vol.34
, pp. 1945-1949
-
-
Cameron, D.W.1
Conn, C.2
Feutrill, G.I.3
-
34
-
-
0000250385
-
-
D. W. Cameron, D. J. Deutscher, G. I. Feutrill, P. G. Griffiths, Aust. J. Chem. 1981, 34, 2401-2421
-
(1981)
Aust. J. Chem.
, vol.34
, pp. 2401-2421
-
-
Cameron, D.W.1
Deutscher, D.J.2
Feutrill, G.I.3
Griffiths, P.G.4
-
36
-
-
0141746906
-
-
(Ed.: L.A. Paquette), Wiley, New York, p..
-
Encyclopedia of Reagents for Organic Synthesis, Vol.6 (Ed.:, L.A. Paquette,), Wiley, New York, 1995, p. 4275.
-
(1995)
Encyclopedia of Reagents for Organic Synthesis, Vol.6
, pp. 4275
-
-
-
38
-
-
0000319914
-
-
H. Karaman, R. J. Barton, B. E. Robertson, D. G. Lee, J. Org. Chem. 1984, 49, 4509-4516.
-
(1984)
J. Org. Chem.
, vol.49
, pp. 4509-4516
-
-
Karaman, H.1
Barton, R.J.2
Robertson, B.E.3
Lee, D.G.4
-
39
-
-
0001076619
-
-
L. Friedman, D. L. Fishel, H. Shechter, J. Org. Chem. 1965, 30, 1453-1457.
-
(1965)
J. Org. Chem.
, vol.30
, pp. 1453-1457
-
-
Friedman, L.1
Fishel, D.L.2
Shechter, H.3
-
41
-
-
0043011084
-
-
N. Hirai, N. Sawatari, N. Nakamura, S. Sakaguchi, Y. Ishii, J. Org. Chem. 2003, 68, 6587-6590
-
(2003)
J. Org. Chem.
, vol.68
, pp. 6587-6590
-
-
Hirai, N.1
Sawatari, N.2
Nakamura, N.3
Sakaguchi, S.4
Ishii, Y.5
-
42
-
-
0000061116
-
-
Y. Yoshino, Y. Hayashi, T. Iwahma, S. Sakaguchi, A. Ishii, J. Org. Chem. 1997, 62, 6810-6813.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 6810-6813
-
-
Yoshino, Y.1
Hayashi, Y.2
Iwahma, T.3
Sakaguchi, S.4
Ishii, A.5
-
43
-
-
0000096029
-
-
Y. Sasson, G. D. Zappi, R. Naumann, J. Org. Chem. 1986, 51, 2880-2883.
-
(1986)
J. Org. Chem.
, vol.51
, pp. 2880-2883
-
-
Sasson, Y.1
Zappi, G.D.2
Naumann, R.3
-
44
-
-
33745462569
-
-
T. M. AliShaik, L. Emmanuvel, A. Sudalai, J. Org. Chem. 2006, 71, 5043-5046.
-
(2006)
J. Org. Chem.
, vol.71
, pp. 5043-5046
-
-
Alishaik, T.M.1
Emmanuvel, L.2
Sudalai, A.3
-
46
-
-
0026696415
-
-
W. P. Griffith, J. M. Jolliffe, S. V. Ley, K. F. Springhorn, P. D. Tiffin, Synth. Commun. 1992, 22, 1967-1971
-
(1992)
Synth. Commun.
, vol.22
, pp. 1967-1971
-
-
Griffith, W.P.1
Jolliffe, J.M.2
Ley, S.V.3
Springhorn, K.F.4
Tiffin, P.D.5
-
48
-
-
0030810208
-
-
K. Müller, H. Prinz, I. Gawlik, K. Ziereis, H.-S. Huang, J. Med. Chem. 1997, 40, 3773-3780
-
(1997)
J. Med. Chem.
, vol.40
, pp. 3773-3780
-
-
Müller, K.1
Prinz, H.2
Gawlik, I.3
Ziereis, K.4
Huang, H.-S.5
-
49
-
-
33947460144
-
-
N. Kornblum, W. J. Jones, G. J. Anderson, J. Am. Chem. Soc. 1959, 81, 4113-4114.
-
(1959)
J. Am. Chem. Soc.
, vol.81
, pp. 4113-4114
-
-
Kornblum, N.1
Jones, W.J.2
Anderson, G.J.3
-
50
-
-
32244447655
-
-
J. N. Moorthy, N. Singhal, K. Senapati, Tetrahedron Lett. 2006, 47, 1757-1761.
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 1757-1761
-
-
Moorthy, J.N.1
Singhal, N.2
Senapati, K.3
-
51
-
-
0037429063
-
-
S. Das, A. K. Panigrahi, G. C. Maikap, Tetrahedron Lett. 2003, 44, 1375-1377.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 1375-1377
-
-
Das, S.1
Panigrahi, A.K.2
Maikap, G.C.3
-
53
-
-
33748664603
-
-
B. S. Bal, W. E. Childers Jr., H. W. Pinnick, Tetrahedron 1981, 37, 2091-2096.
-
(1981)
Tetrahedron
, vol.37
, pp. 2091-2096
-
-
Bal, B.S.1
Childers Jr., W.E.2
Pinnick, H.W.3
-
54
-
-
38049089898
-
-
C. E. Anson, A. V. Malkov, C. Roe, E. J. Sandoe, G. R. Stephenson, Eur. J. Org. Chem. 2008, 196-213.
-
(2008)
Eur. J. Org. Chem.
, pp. 196-213
-
-
Anson, C.E.1
Malkov, A.V.2
Roe, C.3
Sandoe, E.J.4
Stephenson, G.R.5
-
55
-
-
0038263126
-
-
E. Piers, C. L. Harrison, C. Zetina-Rocha, Org. Lett. 2001, 3, 3245-3247
-
(2001)
Org. Lett.
, vol.3
, pp. 3245-3247
-
-
Piers, E.1
Harrison, C.L.2
Zetina-Rocha, C.3
-
56
-
-
70349644859
-
-
A. Putey, F. Popawycz, Q.-T. Do, P. Bernard, S. K. Talapatra, F. Kozielski, C. M. Galmrini, B. Joseph, J. Med. Chem. 2009, 52, 5916-5925
-
(2009)
J. Med. Chem.
, vol.52
, pp. 5916-5925
-
-
Putey, A.1
Popawycz, F.2
Do, Q.-T.3
Bernard, P.4
Talapatra, S.K.5
Kozielski, F.6
Galmrini, C.M.7
Joseph, B.8
-
57
-
-
67449116637
-
-
E. Fillion, V. E. Trépanier, J. J. Heikkinen, A. A. Remorova, R. J. Carson, J. M. Goll, A. Seed, Organometallics 2009, 28, 3518-3531.
-
(2009)
Organometallics
, vol.28
, pp. 3518-3531
-
-
Fillion, E.1
Trépanier, V.E.2
Heikkinen, J.J.3
Remorova, A.A.4
Carson, R.J.5
Goll, J.M.6
Seed, A.7
-
59
-
-
0001033833
-
-
O. Mitsunobu, M. Yamada, M. Mukaiyama, Bull. Chem. Soc. Jpn. 1967, 40, 935-939.
-
(1967)
Bull. Chem. Soc. Jpn.
, vol.40
, pp. 935-939
-
-
Mitsunobu, O.1
Yamada, M.2
Mukaiyama, M.3
-
60
-
-
79951804181
-
-
For examples of halogen-lithium or halogen-magnesium exchange reactions on molecules bearing carbonyl groups see
-
For examples of halogen-lithium or halogen-magnesium exchange reactions on molecules bearing carbonyl groups see
-
-
-
-
61
-
-
79951796795
-
-
N. Slavov, J. CvengroÅ, J.-M. Neudörfl, H.-G. Schmalz, Angew. Chem. 2010, 122, 7751-7754
-
(2010)
Angew. Chem.
, vol.122
, pp. 7751-7754
-
-
Slavov, N.1
Cvengroå, J.2
Neudörfl, J.-M.3
Schmalz, H.-G.4
-
62
-
-
77957598358
-
-
Angew. Chem. Int. Ed. 2010, 49, 7588-7591
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 7588-7591
-
-
-
63
-
-
79951777365
-
-
see also refs. [28a], [33] and [34].
-
see also refs. [28a], [33] and [34].
-
-
-
-
64
-
-
79951801867
-
-
For examples of halogen-metal exchange in the presence of carbonyl electrophiles (in situ quench conditions) see
-
For examples of halogen-metal exchange in the presence of carbonyl electrophiles (in situ quench conditions) see
-
-
-
-
65
-
-
45849094782
-
-
S. Goto, J. Velder, S. ElSheikh, Y. Sakamoto, M. Mitani, S. Elmas, A. Adler, A. Becker, J.-M. Neudörfl, J. Lex, H.-G. Schmalz, Synlett 2008, 1361-1365
-
(2008)
Synlett
, pp. 1361-1365
-
-
Goto, S.1
Velder, J.2
Elsheikh, S.3
Sakamoto, Y.4
Mitani, M.5
Elmas, S.6
Adler, A.7
Becker, A.8
Neudörfl, J.-M.9
Lex, J.10
Schmalz, H.-G.11
-
66
-
-
3042713093
-
-
F. D. Therkelsen, M. Rottländer, N. Throup, E. B. Pedersen, Org. Lett. 2004, 6, 1991-1994.
-
(2004)
Org. Lett.
, vol.6
, pp. 1991-1994
-
-
Therkelsen, F.D.1
Rottländer, M.2
Throup, N.3
Pedersen, E.B.4
-
68
-
-
0035843330
-
-
Y. Kondo, M. Asai, T. Miura, M. Uchiyama, T. Sakamoto, Org. Lett. 2001, 3, 13-15.
-
(2001)
Org. Lett.
, vol.3
, pp. 13-15
-
-
Kondo, Y.1
Asai, M.2
Miura, T.3
Uchiyama, M.4
Sakamoto, T.5
-
72
-
-
4544311534
-
-
Angew. Chem. Int. Ed. 2004, 43, 3333-3336
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 3333-3336
-
-
-
73
-
-
33644946046
-
-
A. Krasovskiy, B. F. Straub, P. Knochel, Angew. Chem. 2006, 118, 165-169
-
(2006)
Angew. Chem.
, vol.118
, pp. 165-169
-
-
Krasovskiy, A.1
Straub, B.F.2
Knochel, P.3
-
76
-
-
9444224983
-
-
H. Ren, A. Krasovskiy, P. Knochel, Org. Lett. 2004, 6, 4215-4217
-
(2004)
Org. Lett.
, vol.6
, pp. 4215-4217
-
-
Ren, H.1
Krasovskiy, A.2
Knochel, P.3
-
80
-
-
84970623512
-
-
M. R. Anderson, R. F. C. Brown, K. J. Coulston, F. W. Eastwood, A. Ward, Aust. J. Chem. 1990, 43, 1137-1150
-
(1990)
Aust. J. Chem.
, vol.43
, pp. 1137-1150
-
-
Anderson, M.R.1
Brown, R.F.C.2
Coulston, K.J.3
Eastwood, F.W.4
Ward, A.5
-
81
-
-
33847086855
-
-
B. M. Trost, T. Rivers, J. M. Gold, J. Org. Chem. 1980, 45, 1835-1838.
-
(1980)
J. Org. Chem.
, vol.45
, pp. 1835-1838
-
-
Trost, B.M.1
Rivers, T.2
Gold, J.M.3
-
83
-
-
33646564507
-
-
E. H. Vickery, L. F. Pahler, E. J. Eisenbraun, J. Org. Chem. 1979, 44, 4444-4446
-
(1979)
J. Org. Chem.
, vol.44
, pp. 4444-4446
-
-
Vickery, E.H.1
Pahler, L.F.2
Eisenbraun, E.J.3
-
84
-
-
33845559035
-
-
for an example of deprotection of a phenolic hydroxyl group at an anthraquinone, see ref. [12c].
-
M. Demuynck, P. DeClercq, M. Vandewalle, J. Org. Chem. 1979, 44, 4863-4866; for an example of deprotection of a phenolic hydroxyl group at an anthraquinone, see ref. [12c].
-
(1979)
J. Org. Chem.
, vol.44
, pp. 4863-4866
-
-
Demuynck, M.1
Declercq, P.2
Vandewalle, M.3
-
87
-
-
49749105279
-
-
J. CvengroÅ, S. Neufeind, A. Becker, H.-G. Schmalz, Synlett 2008, 1993-1998.
-
(2008)
Synlett
, pp. 1993-1998
-
-
Cvengroå, J.1
Neufeind, S.2
Becker, A.3
Schmalz, H.-G.4
-
89
-
-
34047232186
-
-
L. F. Tietze, K. M. Gericke, R. R. Singidi, I. Schuberth, Org. Biomol. Chem. 2007, 5, 1191-1200
-
(2007)
Org. Biomol. Chem.
, vol.5
, pp. 1191-1200
-
-
Tietze, L.F.1
Gericke, K.M.2
Singidi, R.R.3
Schuberth, I.4
-
90
-
-
37249011908
-
-
L. F. Tietze, K. M. Gericke, R. R. Singidi, I. Schuberth, Chem. Eur. J. 2007, 13, 9939-9947
-
(2007)
Chem. Eur. J.
, vol.13
, pp. 9939-9947
-
-
Tietze, L.F.1
Gericke, K.M.2
Singidi, R.R.3
Schuberth, I.4
-
91
-
-
33846321864
-
-
L. F. Tietze, R. Ramakrishna, K. M. Gericke, Org. Lett. 2006, 8, 5873-5876
-
(2006)
Org. Lett.
, vol.8
, pp. 5873-5876
-
-
Tietze, L.F.1
Ramakrishna, R.2
Gericke, K.M.3
-
92
-
-
20744455214
-
-
L. F. Tietze, C. Günther, K. M. Gericke, I. Schuberth, G. Bunkoczi, Eur. J. Org. Chem. 2005, 2459-2467.
-
(2005)
Eur. J. Org. Chem.
, pp. 2459-2467
-
-
Tietze, L.F.1
Günther, C.2
Gericke, K.M.3
Schuberth, I.4
Bunkoczi, G.5
-
95
-
-
70349200706
-
-
T. Nol, K. Robeyns, L. VanMeervelt, E. VanderEyken, J. VanderEyken, Tertrahedron: Asymmetry 2009, 20, 1962-1968
-
(2009)
Tertrahedron: Asymmetry
, vol.20
, pp. 1962-1968
-
-
Nol, T.1
Robeyns, K.2
Vanmeervelt, L.3
Vandereyken, E.4
Vandereyken, J.5
-
96
-
-
1642272391
-
-
R. G. Harvey. Q. Dai, C. Ran, T. M. Penning, J. Org. Chem. 2004, 69, 2024-2032.
-
(2004)
J. Org. Chem.
, vol.69
, pp. 2024-2032
-
-
Dai, R.G.Harvey.Q.1
Ran, C.2
Penning, T.M.3
-
97
-
-
0345761233
-
-
W. Li, J. Li, D. DeVincentis, T. S. Mansour, Tetrahedron Lett. 2004, 45, 1071-1074.
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 1071-1074
-
-
Li, W.1
Li, J.2
Devincentis, D.3
Mansour, T.S.4
-
98
-
-
79951790292
-
-
For preparative purposes the photolysis of 1-alkylanthraquinones has found miscellaneous application in their benzylic oxidation. For examples see
-
For preparative purposes the photolysis of 1-alkylanthraquinones has found miscellaneous application in their benzylic oxidation. For examples see
-
-
-
-
101
-
-
1042275586
-
-
K. Krohn, Md. H. Sohrab, U. Flörke, Tetrahedron: Asymmetry 2004, 15, 713-718
-
(2004)
Tetrahedron: Asymmetry
, vol.15
, pp. 713-718
-
-
Krohn, K.1
Sohrab, Md.H.2
Flörke, U.3
-
104
-
-
79951795580
-
-
see also ref. [8].
-
see also ref. [8].
-
-
-
-
105
-
-
79951788965
-
-
For insights into the mechanism of the photolysis of 1-alkyl-9,10- anthraquninones and 1-alkylquinones in general, see
-
For insights into the mechanism of the photolysis of 1-alkyl-9,10- anthraquninones and 1-alkylquinones in general, see
-
-
-
-
107
-
-
17044399740
-
-
A. Konosonoks, J. Wright, M.-L. Tsao, J. Pika, K. Novak, S. M. Mandel, J. A. Krause Bauer, C. Bohne, A. D. Gudmundsdottir, J. Org. Chem. 2005, 70, 2763-2770
-
(2005)
J. Org. Chem.
, vol.70
, pp. 2763-2770
-
-
Konosonoks, A.1
Wright, J.2
Tsao, M.-L.3
Pika, J.4
Novak, K.5
Mandel, S.M.6
Bauer, J.A.K.7
Bohne, C.8
Gudmundsdottir, A.D.9
-
108
-
-
0031789010
-
-
M. Saito, Y. Kamei, K. Kuribara, J. Org. Chem. 1998, 63, 9013-9018
-
(1998)
J. Org. Chem.
, vol.63
, pp. 9013-9018
-
-
Saito, M.1
Kamei, Y.2
Kuribara, K.3
-
109
-
-
37049070141
-
-
M. Yoshioka, K. Nishizawa, J. Suzuki, Y. Iwata, S. Kumakura, T. Hasegawa, J. Chem. Soc. Perkin Trans. 1 1995, 3097-3101
-
(1995)
J. Chem. Soc. Perkin Trans. 1
, pp. 3097-3101
-
-
Yoshioka, M.1
Nishizawa, K.2
Suzuki, J.3
Iwata, Y.4
Kumakura, S.5
Hasegawa, T.6
-
111
-
-
64349107036
-
-
M. Chaumontet, P. Retailleau, O. Baudoin, J. Org. Chem. 2009, 74, 1774-1776
-
(2009)
J. Org. Chem.
, vol.74
, pp. 1774-1776
-
-
Chaumontet, M.1
Retailleau, P.2
Baudoin, O.3
-
112
-
-
0033537953
-
-
H. Ishiyama, T. Takemura, M. Tsuda, J. Kobayashi, Tetrahedron 1999, 55, 4583-4594.
-
(1999)
Tetrahedron
, vol.55
, pp. 4583-4594
-
-
Ishiyama, H.1
Takemura, T.2
Tsuda, M.3
Kobayashi, J.4
-
113
-
-
79951797516
-
-
note
-
The TIPS-protecting group has been proved to be the most base-resistant silyl protecting group. Therefore, we anticipated a triisopropylsilylalkyl ether to stay untouched under the strong basic conditions (pH ⥠12) of the planned reductive methylation of rac-44.
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-
-
-
115
-
-
79951792521
-
-
For reviews on the use of organocerium reagents, see
-
For reviews on the use of organocerium reagents, see
-
-
-
-
116
-
-
0033605830
-
-
H.-J. Liu, K.-S. Shia, X. Shang, B.-Y. Zhu, Tetrahedron 1999, 55, 3803-3830
-
(1999)
Tetrahedron
, vol.55
, pp. 3803-3830
-
-
Liu, H.-J.1
Shia, K.-S.2
Shang, X.3
Zhu, B.-Y.4
-
118
-
-
33845471319
-
-
T. Imamoto, T. Kusumoto, Y. Tawarayama, Y. Sugiura, T. Mita, Y. Hatanaka, M. Yokoyama, J. Org. Chem. 1984, 49, 3904-3911
-
(1984)
J. Org. Chem.
, vol.49
, pp. 3904-3911
-
-
Imamoto, T.1
Kusumoto, T.2
Tawarayama, Y.3
Sugiura, Y.4
Mita, T.5
Hatanaka, Y.6
Yokoyama, M.7
-
119
-
-
0000889671
-
-
T. Imamoto, Y. Sugiura, N. Takiyama, Tetrahedron Lett. 1984, 25, 4233-4236.
-
(1984)
Tetrahedron Lett.
, vol.25
, pp. 4233-4236
-
-
Imamoto, T.1
Sugiura, Y.2
Takiyama, N.3
-
120
-
-
79951779565
-
-
note
-
8]toluene, supported by the calculation of selected spin systems with DNMR.
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-
-
-
121
-
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0023272463
-
-
For the conversion of TIPS-protected alcohols into the corresponding carboxylic acids employing Jones reagent see.
-
For the conversion of TIPS-protected alcohols into the corresponding carboxylic acids employing Jones reagent see:, J. Cooper, D. W. Knight, P. T. Gallagher, J. Chem. Soc. Chem. Commun. 1987, 1220-1222.
-
(1987)
J. Chem. Soc. Chem. Commun.
, pp. 1220-1222
-
-
Cooper, J.1
Knight, D.W.2
Gallagher, P.T.3
-
122
-
-
79951805030
-
-
note
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CCDC799897 (11), 799901 (rac-22), 799898 (30), 799899 (31), and 799900 (35) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
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