-
5
-
-
0026605647
-
-
doi:10.1080/07328319208021748
-
(e) C. Périgaud, G. Gosselin, J. L. Imbach, Nucleosides Nucleotides 1992, 11, 903. doi:10.1080/07328319208021748
-
(1992)
Nucleosides Nucleotides
, vol.11
, pp. 903
-
-
Périgaud, C.1
Gosselin, G.2
Imbach, J.L.3
-
6
-
-
0004011178
-
-
John Wiley & Sons, Inc: New York, NY
-
(a) H. Vorbrüggen, C. Ruh-Pohlenz, Handbook of Nucleoside Synthesis 2001, pp. 51-60 (John Wiley & Sons, Inc: New York, NY).
-
(2001)
Handbook of Nucleoside Synthesis
, pp. 51-60
-
-
Vorbrüggen, H.1
Ruh-Pohlenz, C.2
-
7
-
-
0000335222
-
-
doi:10.1021/CR00016A004
-
(b) D. M. Huryn, M. Okabe, Chem. Rev. 1992, 92, 1745. doi:10.1021/CR00016A004
-
(1992)
Chem. Rev
, vol.92
, pp. 1745
-
-
Huryn, D.M.1
Okabe, M.2
-
9
-
-
0020764119
-
-
doi:10.1021/JA00350A052
-
(b) M. J. Robins, J. S. Wilson, F. Hansske, J. Am. Chem. Soc. 1983, 105, 4059. doi:10.1021/JA00350A052
-
(1983)
J. Am. Chem. Soc
, vol.105
, pp. 4059
-
-
Robins, M.J.1
Wilson, J.S.2
Hansske, F.3
-
12
-
-
84982068675
-
-
doi:10.1002/CBER.19811140404
-
(c) H. Vorbrüggen, K. Krolikiewicz, B. Bennua, Chem. Ber. 1981, 114, 1234. doi:10.1002/CBER.19811140404
-
(1981)
Chem. Ber
, vol.114
, pp. 1234
-
-
Vorbrüggen, H.1
Krolikiewicz, K.2
Bennua, B.3
-
13
-
-
0029790593
-
-
doi:10.1021/JO960936J
-
(a) M. Park, C. J. Rizzo, J. Org. Chem. 1996, 61, 6092. doi:10.1021/JO960936J
-
(1996)
J. Org. Chem
, vol.61
, pp. 6092
-
-
Park, M.1
Rizzo, C.J.2
-
14
-
-
0030665608
-
-
doi:10.1016/S0040-4039(97)10251-9
-
(b) Z. W. Wang, C. J. Rizzo, Tetrahedron Lett. 1997, 38, 8177. doi:10.1016/S0040-4039(97)10251-9
-
(1997)
Tetrahedron Lett
, vol.38
, pp. 8177
-
-
Wang, Z.W.1
Rizzo, C.J.2
-
15
-
-
0000831182
-
-
doi:10.1021/JO971332Y
-
(c) D. R. Prudhomme, Z. W. Wang, C. J. Rizzo, J. Org. Chem. 1997, 62, 8257. doi:10.1021/JO971332Y
-
(1997)
J. Org. Chem
, vol.62
, pp. 8257
-
-
Prudhomme, D.R.1
Wang, Z.W.2
Rizzo, C.J.3
-
16
-
-
0034703343
-
-
doi:10.1021/JO0003652
-
(d) Z. W. Wang, D. R. Prudhomme, J. R. Buck, M. Park, C. J. Rizzo, J. Org. Chem. 2000, 65, 5969. doi:10.1021/JO0003652
-
(2000)
J. Org. Chem
, vol.65
, pp. 5969
-
-
Wang, Z.W.1
Prudhomme, D.R.2
Buck, J.R.3
Park, M.4
Rizzo, C.J.5
-
17
-
-
0000766373
-
-
doi:10.1021/JA00271A057
-
(a) I. Saito, H. Ikehira, R. Kasatani, M. Watanabe, T. Matsuura, J. Am. Chem. Soc. 1986, 108, 3115. doi:10.1021/JA00271A057
-
(1986)
J. Am. Chem. Soc
, vol.108
, pp. 3115
-
-
Saito, I.1
Ikehira, H.2
Kasatani, R.3
Watanabe, M.4
Matsuura, T.5
-
18
-
-
37049118068
-
-
doi:10.1039/C39750000439
-
(b) H. Deshayes, J. P. Pete, C. Portella, D. Scholler, J. Chem. Soc., Chem. Comm. 1975, 439. doi:10.1039/C39750000439
-
(1975)
J. Chem. Soc. Chem. Comm
, vol.439
-
-
Deshayes, H.1
Pete, J.P.2
Portella, C.3
Scholler, D.4
-
19
-
-
49549127558
-
-
doi:10.1016/S0040-4039(00)93806-1
-
(c) H. Deshayes, J. P. Pete, C. Portella, Tetrahedron Lett. 1976, 17, 2019. doi:10.1016/S0040-4039(00)93806-1
-
(1976)
Tetrahedron Lett
, vol.17
, pp. 2019
-
-
Deshayes, H.1
Pete, J.P.2
Portella, C.3
-
20
-
-
79957993858
-
-
doi:10.1039/C1CC00089F
-
(a) C. Wiles, P. Watts, Chem. Commun. 2011, 47, 6512. doi:10.1039/C1CC00089F
-
(2011)
Chem. Commun
, vol.47
, pp. 6512
-
-
Wiles, C.1
Watts, P.2
-
21
-
-
79953702549
-
-
doi:10.1039/C0CC05060A
-
(b) J. Wegner, S. Ceylan, A. Kirschning, Chem. Commun. 2011, 47, 4583. doi:10.1039/C0CC05060A
-
(2011)
Chem. Commun
, vol.47
, pp. 4583
-
-
Wegner, J.1
Ceylan, S.2
Kirschning, A.3
-
22
-
-
79961218749
-
-
doi:10.1002/ANIE.201004637
-
(c) R. L. Hartman, J. P. McMullen, K. F. Jensen, Angew. Chem. Int. Ed. 2011, 50, 7502. doi:10.1002/ANIE.201004637
-
(2011)
Angew. Chem. Int. Ed
, vol.50
, pp. 7502
-
-
Hartman, R.L.1
McMullen, J.P.2
Jensen, K.F.3
-
23
-
-
79955623916
-
-
doi:10.1002/CSSC.201000271
-
(d) J. I. Yoshida, H. Kim, A. Nagaki, ChemSusChem 2011, 4, 331. doi:10.1002/CSSC.201000271
-
(2011)
ChemSusChem
, vol.4
, pp. 331
-
-
Yoshida, J.I.1
Kim, H.2
Nagaki, A.3
-
24
-
-
77953138778
-
-
doi:10.1016/J.BMC.2010.03.073
-
(e) T. Illg, P. Lob, V. Hessel, Bioorg. Med. Chem. 2010, 18, 3707. doi:10.1016/J.BMC.2010.03.073
-
(2010)
Bioorg. Med. Chem
, vol.18
, pp. 3707
-
-
Illg, T.1
Lob, P.2
Hessel, V.3
-
28
-
-
34447109277
-
-
doi:10.1021/CR050944C
-
(i) B. P. Mason, K. E. Price, J. L. Steinbacher, A. R. Bogdan, D. T. McQuade, Chem. Rev. 2007, 107, 2300. doi:10.1021/CR050944C
-
(2007)
Chem. Rev
, vol.107
, pp. 2300
-
-
Mason, B.P.1
Price, K.E.2
Steinbacher, J.L.3
Bogdan, A.R.4
McQuade, D.T.5
-
30
-
-
33747189999
-
-
doi:10.1002/CHEM.200600236
-
(k) A. Kirschning, W. Solodenko, K. Mennecke, Chem.-Eur. J. 2006, 12, 5972. doi:10.1002/CHEM.200600236
-
(2006)
Chem.-Eur. J
, vol.12
, pp. 5972
-
-
Kirschning, A.1
Solodenko, W.2
Mennecke, K.3
-
31
-
-
17344391357
-
-
doi:10.1002/ANIE.200300577
-
(l) K. Jähnisch, V. Hessel, H. Lowe, M. Baerns, Angew. Chem. Int. Ed. 2004, 43, 406. doi:10.1002/ANIE.200300577
-
(2004)
Angew. Chem. Int. Ed
, vol.43
, pp. 406
-
-
Jähnisch, K.1
Hessel, V.2
Lowe, H.3
Baerns, M.4
-
32
-
-
80053246708
-
-
doi:10.3390/MOLE CULES16097522
-
(a) M. Oelgemoller, O. Shvydkiv, Molecules 2011, 16, 7522. doi:10.3390/MOLE CULES16097522
-
(2011)
Molecules
, vol.16
, pp. 7522
-
-
Oelgemoller, M.1
Shvydkiv, O.2
-
34
-
-
36048985775
-
-
doi:10.1351/PAC200779111959
-
(c) Y. Matsushita, T. Ichimura, N. Ohba, S. Kumada, K. Sakeda, T. Suzuki, H. Tanibata, T. Murata, Pure Appl. Chem. 2007, 79, 1959. doi:10.1351/ PAC200779111959
-
(2007)
Pure Appl. Chem
, vol.79
, pp. 1959
-
-
Matsushita, Y.1
Ichimura, T.2
Ohba, N.3
Kumada, S.4
Sakeda, K.5
Suzuki, T.6
Tanibata, H.7
Murata, T.8
-
35
-
-
24944575233
-
-
For a seminal design of a flow photochemical set-up doi:10.1021/JO050705P
-
(d) For a seminal design of a flow photochemical set-up, see: B. D. A. Hook, W. Dohle, P. R. Hirst, M. Pickworth, M. B. Berry, K. I. Booker-Milburn, J. Org. Chem. 2005, 70, 7558. doi:10.1021/JO050705P
-
(2005)
J. Org. Chem
, vol.70
, pp. 7558
-
-
Hook, B.D.A.1
Dohle, W.2
Hirst, P.R.3
Pickworth, M.4
Berry, M.B.5
Booker-Milburn, K.I.6
-
36
-
-
84857029523
-
-
For a recent eminent example of utilizing photochemistry in flow for the synthesis of a drug doi:10.1002/ANIE.201107446
-
(e) For a recent eminent example of utilizing photochemistry in flow for the synthesis of a drug, see: F. Lévesque, P. H. Seeberger, Angew. Chem. Int. Ed. 2012, 51, 1706. doi:10.1002/ANIE.201107446
-
(2012)
Angew. Chem. Int. Ed
, vol.51
, pp. 1706
-
-
Lévesque, F.1
Seeberger, P.H.2
-
37
-
-
84863644759
-
-
doi:10.1039/C2CC33356B
-
B. Shen, M. W. Bedore, A. Sniady, T. F. Jamison, Chem. Commun. 2012, 48, 7444. doi:10.1039/C2CC33356B
-
(2012)
Chem. Commun
, vol.48
, pp. 7444
-
-
Shen, B.1
Bedore, M.W.2
Sniady, A.3
Jamison, T.F.4
-
38
-
-
84964976684
-
-
Aluminium is best for UV reflection (80) CRC Press: Bristol
-
Aluminium is best for UV reflection (.80 %). H. A. Macleod, Thinfilm Optical Filters, 3rd Edn 2001, pp. 158-159 (CRC Press: Bristol).
-
(2001)
Thinfilm Optical Filters, 3rd Edn
, pp. 158-159
-
-
MacLeod, H.A.1
-
39
-
-
0016534489
-
-
doi:10.1149/1.2134365
-
J. F. Ambrose, L. L. Carpenter, R. F. Nelson, J. Electrochem. Soc. 1975, 122, 876. doi:10.1149/1.2134365
-
(1975)
J. Electrochem. Soc
, vol.122
, pp. 876
-
-
Ambrose, J.F.1
Carpenter, L.L.2
Nelson, R.F.3
-
40
-
-
0025815749
-
-
Described as capricious by Rizzo, [5d] the cytidine derivative failed in the deoxygenation reaction, which is consistent with previous studies by Benner doi:10.1021/JO00012A018
-
Described as capricious by Rizzo, [5d] the cytidine derivative failed in the deoxygenation reaction, which is consistent with previous studies by Benner: Z. Huang, K. C. Schneider, S. A. Benner, J. Org. Chem. 1991, 56, 3869. doi:10.1021/JO00012A018
-
(1991)
J. Org. Chem
, vol.56
, pp. 3869
-
-
Huang, Z.1
Schneider, K.C.2
Benner, S.A.3
-
41
-
-
79551614063
-
-
doi:10.1039/C0SC00381F
-
(a) D. Webb, T. F. Jamison, Chem. Sci. 2010, 1, 675. doi:10.1039/ C0SC00381F
-
(2010)
Chem. Sci
, vol.1
, pp. 675
-
-
Webb, D.1
Jamison, T.F.2
-
42
-
-
84856840761
-
-
doi:10.1002/ADSC.201100584
-
(b) J. Wegner, S. Ceylan, A. Kirschning, Adv. Synth. Catal. 2012, 354, 17. doi:10.1002/ADSC.201100584
-
(2012)
Adv. Synth. Catal
, vol.354
, pp. 17
-
-
Wegner, J.1
Ceylan, S.2
Kirschning, A.3
-
43
-
-
79951923094
-
-
doi:10.1002/ANIE.201006440
-
(a) A. Sniady, M. W. Bedore, T. F. Jamison, Angew. Chem. Int. Ed. 2011, 50, 2155. doi:10.1002/ANIE.201006440
-
(2011)
Angew. Chem. Int. Ed
, vol.50
, pp. 2155
-
-
Sniady, A.1
Bedore, M.W.2
Jamison, T.F.3
-
44
-
-
84862100890
-
-
doi:10.1021/OP200349F
-
(b) K. D. Nagy, B. Shen, T. F. Jamison, K. F. Jensen, Org. Process Res. Dev. 2012, 16, 976. doi:10.1021/OP200349F
-
(2012)
Org. Process Res. Dev
, vol.16
, pp. 976
-
-
Nagy, K.D.1
Shen, B.2
Jamison, T.F.3
Jensen, K.F.4
-
45
-
-
84863614587
-
-
doi:10.1021/OL301324G
-
(c) B. Shen, T. F. Jamison, Org. Lett. 2012, 14, 3348. doi:10.1021/OL301324G
-
(2012)
Org. Lett
, vol.14
, pp. 3348
-
-
Shen, B.1
Jamison, T.F.2
-
47
-
-
0035132466
-
-
doi:10.1023/A:1008354603366
-
(b) C. Kojima, E. Kawashima, T. Sekine, Y. Ishido, A. Ono, M. Kainosho, Y. Kyogoku, J. Biomol. NMR 2001, 19, 19. doi:10.1023/A:1008354603366
-
(2001)
J. Biomol. NMR
, vol.19
, pp. 19
-
-
Kojima, C.1
Kawashima, E.2
Sekine, T.3
Ishido, Y.4
Ono, A.5
Kainosho, M.6
Kyogoku, Y.7
-
48
-
-
0027475496
-
-
doi:10.1016/S0040-4039(00)91784-2
-
(a) E. Kawashima, Y. Aoyama, T. Sekine, E. Nakamura, M. Kainosho, Y. Kyogoku, Y. Ishido, Tetrahedron Lett. 1993, 34, 1317. doi:10.1016/S0040-4039(00) 91784-2
-
(1993)
Tetrahedron Lett
, vol.34
, pp. 1317
-
-
Kawashima, E.1
Aoyama, Y.2
Sekine, T.3
Nakamura, E.4
Kainosho, M.5
Kyogoku, Y.6
Ishido, Y.7
-
49
-
-
0001515873
-
-
doi:10.1021/JO00126A058
-
(b) E. Kawashima, Y. Aoyama, T. Sekine, M. Miyahara, M. F. Radwan, E. Nakamura, M. Kainosho, Y. Kyogoku, Y. Ishido, J. Org. Chem. 1995, 60, 6980. doi:10.1021/JO00126A058
-
(1995)
J. Org. Chem
, vol.60
, pp. 6980
-
-
Kawashima, E.1
Aoyama, Y.2
Sekine, T.3
Miyahara, M.4
Radwan, M.F.5
Nakamura, E.6
Kainosho, M.7
Kyogoku, Y.8
Ishido, Y.9
-
50
-
-
0029073245
-
-
doi:10.1080/15257779508012375
-
E. Kawashima, Y. Aoyama, M. F. Radwan, M. Miyahara, T. Sekine, M. Kainosho, Y. Kyogoku, Y. Ishido, Nucleosides Nucleotides 1995, 14, 333. doi:10.1080/15257779508012375
-
(1995)
Nucleosides Nucleotides
, vol.14
, pp. 333
-
-
Kawashima, E.1
Aoyama, Y.2
Radwan, M.F.3
Miyahara, M.4
Sekine, T.5
Kainosho, M.6
Kyogoku, Y.7
Ishido, Y.8
|