Zobrazeno 1 - 10
of 78
pro vyhledávání: '"Bruce L. Currie"'
Autor:
Bruce L. Currie, Michael E. Johnson
Publikováno v:
Current Medicinal Chemistry. 1:418-422
Sickle cell anemia is a genetic disease that affects a large number of people throughout the world. This disease is very well understood at the molecular level, but for which there is still no effective treatment or cure. Phenylalanine, a natural ami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9df74ccc6f1334feadd35baed31b0864
https://doi.org/10.2174/092986730105220216104353
https://doi.org/10.2174/092986730105220216104353
Autor:
Zhao Lan Lin, Michelle del Rosario-Chow, Michael E. Johnson, John L. Krstenansky, Jiraporn Ungwitayatorn, Wen Sing Sheu, Yu Hwei Lee, Bruce L. Currie
Publikováno v:
Tetrahedron. 49:3489-3500
If the important functional groups of a biologically active peptide can be arrayed on a non-peptide framework in the “biologically active conformation” it may be possible to maximize the receptor interaction and eliminate or reduce the number of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc891067942c9a8d6231f02bcb7fbceb
https://doi.org/10.1016/s0040-4020(01)90209-1
https://doi.org/10.1016/s0040-4020(01)90209-1
Publikováno v:
Synthetic Communications. 23:531-534
A convenient method has been developed to selectivly form the monotriphenylmethyl derivatives of symmetric 1,n-diols, both straight chain and cyclic, in moderate to high yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ee71d7f79ebe85c4dba127a8af0fc9e
https://doi.org/10.1080/00397919308009809
https://doi.org/10.1080/00397919308009809
Publikováno v:
ChemInform. 22
A convenient synthesis of 5-bromotryptophan and protected intermediates for peptide synthesis is reported. Only three steps are required to convert ethyl pyruvate into 5-bromo-tryptophan ethyl ester.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::582b0f943a0c5d4daf74fd53fb1f16e9
https://doi.org/10.1002/chin.199130264
https://doi.org/10.1002/chin.199130264
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9035604f6bd41f083f902bca71fefb2f
https://doi.org/10.1002/chin.199151173
https://doi.org/10.1002/chin.199151173
Autor:
J. N. Patel, Noojaree Prasitpan, Michael E. Johnson, P. Manavalan, P. Z. De Croos, Bruce L. Currie, B. L. Stockwell, Leela Kar
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c63646090448320f22806c430a2f17fa
https://doi.org/10.1002/chin.199238237
https://doi.org/10.1002/chin.199238237
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c140e092a8657460ea7cb55f7095f15
https://doi.org/10.1002/chin.199248182
https://doi.org/10.1002/chin.199248182
Publikováno v:
ChemInform. 25
A convenient method has been developed to selectivly form the monotriphenylmethyl derivatives of symmetric 1,n-diols, both straight chain and cyclic, in moderate to high yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::054d6e744b191f49e9066c4f08ccf56b
https://doi.org/10.1002/chin.199414112
https://doi.org/10.1002/chin.199414112
Publikováno v:
Journal of Heterocyclic Chemistry. 29:707-711
The synthesis of the syn- 14 and anti- 13 isomers of 2(S)-phthalimidornethyl-2,3,4,4a,7,7a-hexahydro-6-oxo-5H-pyrano[2,3-b]pyrrole was accomplished starting from sodium 3,4-dihydro-2H-pyran-2-carboxylate. The isomers were separated by preparative hig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c84dda51a707dffb989a7c4824b521d6
https://doi.org/10.1002/jhet.5570290406
https://doi.org/10.1002/jhet.5570290406
Autor:
Parthasarathy Manavalan, Michael E. Johnson, Bruce L. Currie, Brenda L. Stockwell, Philomen Z. De Croos, Jayeshkumar N. Patel, Noojaree Prasitpan, Leela Kar
Publikováno v:
Journal of Heterocyclic Chemistry. 29:335-341
A series of N-1 or C-2 phenylalkyl substituted tryptophans and C-1 phenylalkyl substituted 3,4-dihydro-β-carbolines were prepared from the apropriate aniline, 1b or 1e, or tryptophan, 8 or 11, by ring closure methods. None of the compounds prepared
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f21ce83346731ec4bc6f476940574a4
https://doi.org/10.1002/jhet.5570290210
https://doi.org/10.1002/jhet.5570290210