-
1
-
-
0016809739
-
L-β-(5-Hydroxy-2-pyridyl)alanine and L-β-(3- hydroxyureido) alanine from streptomyces
-
Inouye, S.; Shomura, T.; Tsuruoka, T.; Ogawa, Y.; Watanabe, H.; Yoshida, J.; Niida, T. L-β-(5-Hydroxy-2-pyridyl)alanine and L-β-(3- hydroxyureido) alanine from streptomyces. Chem. Pharm. Bull. 1975, 23, 2669-2677.
-
(1975)
Chem. Pharm. Bull
, vol.23
, pp. 2669-2677
-
-
Inouye, S.1
Shomura, T.2
Tsuruoka, T.3
Ogawa, Y.4
Watanabe, H.5
Yoshida, J.6
Niida, T.7
-
2
-
-
0026573761
-
Inhibition of chemical carcinogenesis in vivo by azatyrosine
-
Izawa, M.; Takayama, S.; Shindo-Okada, N.; Doi, S.; Kimura, M.; Katsuki, M.; Nishimura, S. Inhibition of chemical carcinogenesis in vivo by azatyrosine. Cancer Res. 1992, 52, 1628-1630.
-
(1992)
Cancer Res
, vol.52
, pp. 1628-1630
-
-
Izawa, M.1
Takayama, S.2
Shindo-Okada, N.3
Doi, S.4
Kimura, M.5
Katsuki, M.6
Nishimura, S.7
-
3
-
-
0030023641
-
A practical synthesis of L-azatyrosine
-
Myers, A. G.; Gleason, J. L. A practical synthesis of L-azatyrosine. J. Org. Chem. 1996, 61, 813-815.
-
(1996)
J. Org. Chem
, vol.61
, pp. 813-815
-
-
Myers, A.G.1
Gleason, J.L.2
-
4
-
-
0030571302
-
A concise synthesis of either enantiomer of azatyrosine
-
Cooper, M. S.; Seton, A. W.; Stevens, M. F. G.; Westwell, A. D. A concise synthesis of either enantiomer of azatyrosine. Bioorg. Med. Chem. Lett. 1996, 21, 2613-2616.
-
(1996)
Bioorg. Med. Chem. Lett
, vol.21
, pp. 2613-2616
-
-
Cooper, M.S.1
Seton, A.W.2
Stevens, M.F.G.3
Westwell, A.D.4
-
5
-
-
0035807552
-
Enantioselective synthesis of (2-pyridyl)alanines via catalytic hydrogenation and application to the synthesis of L-azatyrosine
-
Adamczyk, M.; Akireddy, S. R.; Reddy, R. E. Enantioselective synthesis of (2-pyridyl)alanines via catalytic hydrogenation and application to the synthesis of L-azatyrosine. Org. Lett. 2001, 20, 3157-3159.
-
(2001)
Org. Lett
, vol.20
, pp. 3157-3159
-
-
Adamczyk, M.1
Akireddy, S.R.2
Reddy, R.E.3
-
6
-
-
0010527612
-
Preparation of Nα-Boc 4-O-diethylphospho-L-azatyrosine, a reagent potentially useful for the synthesis of signal transduction related peptides
-
Ye, B.; Otaka, B.; Burke Jr., T. R. Preparation of Nα-Boc 4-O-diethylphospho-L-azatyrosine, a reagent potentially useful for the synthesis of signal transduction related peptides. Synlett 1996, 459-460.
-
(1996)
Synlett
, pp. 459-460
-
-
Ye, B.1
Otaka, B.2
Burke Jr., T.R.3
-
7
-
-
36849051865
-
-
For a recent review covering all the recent advances in the area of catalytic α amino acid synthesis, see Nàjera, C, Sansano, J. M. Catalytic asymmetric synthesis of α-amino acids. Chem. Rev. 2007, 117, 4584-4671
-
For a recent review covering all the recent advances in the area of catalytic α amino acid synthesis, see Nàjera, C.; Sansano, J. M. Catalytic asymmetric synthesis of α-amino acids. Chem. Rev. 2007, 117, 4584-4671.
-
-
-
-
8
-
-
0026708781
-
Preparation of enantiomerically pure protected 4-oxo α-amino acids and 3-aryl α-amino acids from serine
-
Jackson, R. F. W.; Wishart, N.; Wood, A.; James, K.; Wythes, M. J. Preparation of enantiomerically pure protected 4-oxo α-amino acids and 3-aryl α-amino acids from serine. J. Org. Chem. 1992, 57, 3397-3404.
-
(1992)
J. Org. Chem
, vol.57
, pp. 3397-3404
-
-
Jackson, R.F.W.1
Wishart, N.2
Wood, A.3
James, K.4
Wythes, M.J.5
-
9
-
-
0348252422
-
Preparation of enantiomerically pure pyridyl amino acids from serine
-
Tabanella, S.; Valancogne, I.; Jackson, R. F. W. Preparation of enantiomerically pure pyridyl amino acids from serine. Org. Biomol. Chem. 2003, 1, 4254-4261.
-
(2003)
Org. Biomol. Chem
, vol.1
, pp. 4254-4261
-
-
Tabanella, S.1
Valancogne, I.2
Jackson, R.F.W.3
-
10
-
-
12344249722
-
Efficient synthesis of halohydroxypyridines by hydroxydeboronation
-
Voisin, A. S.; Bouillon, A.; Lancelot, J. C.; Rault, S. Efficient synthesis of halohydroxypyridines by hydroxydeboronation. Tetrahedron 2005, 61, 1417-1421.
-
(2005)
Tetrahedron
, vol.61
, pp. 1417-1421
-
-
Voisin, A.S.1
Bouillon, A.2
Lancelot, J.C.3
Rault, S.4
-
11
-
-
0348041999
-
-
Boc-β-iodo-Ala-OMe can be readily obtained as a stable white solid from Boc-Ser-OMe in just one-step following the procedure described by Trost, B. M, Rudd, M. T. Chemoselectivity of the ruthenium-catalyzed hydrative diyne cyclization: Total synthesis of, -cylindricine C, D, and E. Org. Lett. 2003, 5, 4599-4602
-
Boc-β-iodo-Ala-OMe can be readily obtained as a stable white solid from Boc-Ser-OMe in just one-step following the procedure described by Trost, B. M.; Rudd, M. T. Chemoselectivity of the ruthenium-catalyzed hydrative diyne cyclization: Total synthesis of (+)-cylindricine C, D, and E. Org. Lett. 2003, 5, 4599-4602.
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