Indexed keywords
2' DEOXY 4 METHOXY 3 O METHYL 2,6 DIOXOURIDINE;
3,4,5,6 TETRAHYDRO 4 METHOXY 3,6 EPOXY 2H,8H PYRIMIDO[6,1 B][1,3]OXAZOCIN 8,10(9H) DIONE;
3,4,5,6 TETRAHYDRO 4,10 DIMETHOXY 3,6 EPOXY 2H,8H PYRIMIDO[6,1 B][1,3]OXAZOCIN;
4 METHOXY 2,6 DIOXOPYRIMIDINE NUCLEOSIDE;
PYRIMIDINE NUCLEOSIDE;
UNCLASSIFIED DRUG;
ARTICLE;
CARBON NUCLEAR MAGNETIC RESONANCE;
CHEMICAL REACTION;
CONFORMATION;
CYCLIZATION;
GLYCOSYLATION;
HYDROGEN BOND;
PROTON NUCLEAR MAGNETIC RESONANCE;
SYNTHESIS;
THIN LAYER CHROMATOGRAPHY;
4
0028587019
Lipshutz, B. H.; Hayakawa, H.; Kato, K.; Lowe, R. F.; Stevens, K. L. Synthesis 1994, 1476-1484.
(1994)
Synthesis
, pp. 1476-1484
Lipshutz, B.H.1
Hayakawa, H.2
Kato, K.3
Lowe, R.F.4
Stevens, K.L.5
5
0028945431
Lipshutz, B. H.; Stevens, K. L.; Lowe, R. F. Tetrahedron Lett. 1995, 36, 2711-2712.
(1995)
Tetrahedron Lett.
, vol.36
, pp. 2711-2712
Lipshutz, B.H.1
Stevens, K.L.2
Lowe, R.F.3
6
0031575626
(e) Xia, X.Y.; Wang, J. W.; Hager, M. W.; Sisti, N.; Liotta, D. C. Tetrahedron Lett. 1997, 38, 1111-1114.
(1997)
Tetrahedron Lett.
, vol.38
, pp. 1111-1114
Xia, X.Y.1
Wang, J.W.2
Hager, M.W.3
Sisti, N.4
Liotta, D.C.5
7
0016137254
For a similar approaches using a thio bridge with a purine or pyrimidine base, see: (a) Mizuno, Y.; Kaneko, C.; Oikawa, Y. J. Org. Chem. 1974, 39, 1440-1444.
(1974)
J. Org. Chem.
, vol.39
, pp. 1440-1444
Mizuno, Y.1
Kaneko, C.2
Oikawa, Y.3
8
0026522187
(b) El Subbagh, H. I.; Ping, L.-J.; Abushanab, E. Nucleosides Nucleotides 1992, 11, 603-613.
(1992)
Nucleosides Nucleotides
, vol.11
, pp. 603-613
El Subbagh, H.I.1
Ping, L.-J.2
Abushanab, E.3
9
0003979082
Townsend, L. B., Ed.; Plenum Press: New York
Ueda, T. Chemistry of Nucleosides and Nucleotides, Vol. 1, Townsend, L. B., Ed.; Plenum Press: New York, 1988.
(1988)
Chemistry of Nucleosides and Nucleotides
, vol.1
Ueda, T.1
10
0026740888
Hsu, L.-Y.; Wise, D. S.; Kucera, L. S.; Drach, J. C.; Townsend, L. B. J. Org. Chem. 1992 57, 3354.
(1992)
J. Org. Chem.
, vol.57
, pp. 3354
Hsu, L.-Y.1
Wise, D.S.2
Kucera, L.S.3
Drach, J.C.4
Townsend, L.B.5
11
0031757644
We chose to protect the 3-hydroxyl as the sturdy methyl ether to minimize any possible side reactions due to a potentially labile protecting group
Jung, M. E.; Castro, C.; Khan, S. I. Nucleosides Nucleotides 1998, 17, 2383-2387. We chose to protect the 3-hydroxyl as the sturdy methyl ether to minimize any possible side reactions due to a potentially labile protecting group.
(1998)
Nucleosides Nucleotides
, vol.17
, pp. 2383-2387
Jung, M.E.1
Castro, C.2
Khan, S.I.3
12
0019955935
(a) Nicolaou, K. C.; Pavia, M. R.; Seitz, S. P. J. Am. Chem. Soc. 1982, 104, 2027-2029.
(1982)
J. Am. Chem. Soc.
, vol.104
, pp. 2027-2029
Nicolaou, K.C.1
Pavia, M.R.2
Seitz, S.P.3
13
33845551357
(b) Nicolaou, K. C.; Seitz, S. P.; Papahatjis, D. P. J. Am. Chem. Soc. 1983, 105, 2430-2434.
(1983)
J. Am. Chem. Soc.
, vol.105
, pp. 2430-2434
Nicolaou, K.C.1
Seitz, S.P.2
Papahatjis, D.P.3
14
1642631514
Ph.D. Dissertation, University of California, Los Angeles
Castro, C. Ph.D. Dissertation, University of California, Los Angeles, 1993.
(1993)
Castro, C.1
15
0026414082
Dyson, M. R.; Coe, P. L.; Walker, R. T. Carbohydr. Res. 1991, 216, 237-248.
(1991)
Carbohydr. Res.
, vol.216
, pp. 237-248
Dyson, M.R.1
Coe, P.L.2
Walker, R.T.3
16
1642631513
4) to remove the pyrimidyl methoxy group and/or cleave the tether cleaved the bond to the anomeric center
4) to remove the pyrimidyl methoxy group and/or cleave the tether cleaved the bond to the anomeric center.
18
0000791131
(b) Cadet, J.; Kan, L.-S.; Wang, S. Y. J. Am. Chem. Soc. 1978, 100, 6715-6720.
(1978)
J. Am. Chem. Soc.
, vol.100
, pp. 6715-6720
Cadet, J.1
Kan, L.-S.2
Wang, S.Y.3
19
0023277506
Sako, M.; Saito, K. K.; Hirota, K.; Maki, Y. Synthesis 1987, 829-831.
(1987)
Synthesis
, pp. 829-831
Sako, M.1
Saito, K.K.2
Hirota, K.3
Maki, Y.4
22
0002714675
Still, W. C.; Kahn, M.; Mitra, A J. Org. Chem. 1978, 43, 2923-2925.
(1978)
J. Org. Chem.
, vol.43
, pp. 2923-2925
Still, W.C.1
Kahn, M.2
Mitra, A.3