Zobrazeno 1 - 9
of 9
pro vyhledávání: '"A. W. M. Lefeber"'
Autor:
C. J. J. Elie, G. A. Van Der Marel, R. J. Tuinman, C. E. Dreef, J. H. Van Boom, A. W. M. Lefeber
Publikováno v:
ChemInform. 22
The partially benzyl protected myo -inositol derivatives 11a and 11b , the C-4 and C-1,4 hydroxyl function(s) of which are protected with temporary trans -prop-1-enyl protecting group(s), were readily converted into the respective title compounds 18a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7875db5db5f411d297b3fb7c7b45bef5
https://doi.org/10.1002/chin.199136258
https://doi.org/10.1002/chin.199136258
Publikováno v:
Synthesis. 1992:1269-1272
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad0a031d101d9513dff54dcdfa9f03c9
https://doi.org/10.1055/s-1992-26355
https://doi.org/10.1055/s-1992-26355
Autor:
J. H. Van Boom, R. J. Tuinman, C. E. Dreef, G. A. Van Der Marel, C. J. J. Elie, A. W. M. Lefeber
Publikováno v:
Tetrahedron. 47:4709-4722
The partially benzyl protected myo -inositol derivatives 11a and 11b , the C-4 and C-1,4 hydroxyl function(s) of which are protected with temporary trans -prop-1-enyl protecting group(s), were readily converted into the respective title compounds 18a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b654978a846ded3d00a2d346f4e72dd
https://doi.org/10.1016/s0040-4020(01)86476-0
https://doi.org/10.1016/s0040-4020(01)86476-0
Autor:
and Alfons W. M. Lefeber, Young Hae Choi, Cornelis Erkelens, Robert Verpoorte, Arno Hazekamp, Hye Kyong Kim
Publikováno v:
Journal of natural products. 67(6)
The metabolomic analysis of 12 Cannabis sativa cultivars was carried out by 1H NMR spectroscopy and multivariate analysis techniques. Principal component analysis (PCA) of the 1H NMR spectra showed a clear discrimination between those samples by prin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ad4bd5549d2bcaec0fc57dc5fbe47b3
https://pubmed.ncbi.nlm.nih.gov/15217272
https://pubmed.ncbi.nlm.nih.gov/15217272
Autor:
Hae Choi, Young, Kyong Kim, Hye, J. M. Linthorst, Huub, G. Hollander, Johan, W. M. Lefeber, Alfons, Erkelens, Cornelis, Nuzillard, Jean-Marc, Verpoorte, Robert
Publikováno v:
Journal of Natural Products; May 2006, Vol. 69 Issue: 5 p742-748, 7p
Publikováno v:
Tetrahedron. 44:6515-6523
The use of the 2-nitrophenylsulfenyl group for the protection of the N-terminus of peptides and the exocyclic-amino function of deoxyadenosine will be illustrated in the assemblage of the nucleopeptides H-Phe-Tyr (pATAT)-NH2 and H-Ala-Ser(pATAT)-Ala-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::231a422dbbcb1ccd4f517e7e201ea1d0
https://doi.org/10.1016/s0040-4020(01)89840-9
https://doi.org/10.1016/s0040-4020(01)89840-9
Autor:
Jan-Remt Mellema, P. Hoogerhout, Gerard N. Wagenaars, D. Evenberg, C. A. A. Van Boeckel, Jan Poolman, G. A. Van Der Marel, A. W. M. Lefeber, J. H. Van Booma, Carel W. Funke
Publikováno v:
Journal of Carbohydrate Chemistry. 7:399-416
The synthesis of spacer-containing fragments of the capsular poly-saccharide of H. influenzas, comprising two and three repeating units (9a and 9b, respectively), is presented. Ribosylribitol building blocks 1 and 2 were coupled with bis [1-benzotria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0a39bbc02783d0d89ca92068315d1ce
https://doi.org/10.1080/07328308808058933
https://doi.org/10.1080/07328308808058933
Publikováno v:
ChemInform. 20
The use of the 2-nitrophenylsulfenyl group for the protection of the N-terminus of peptides and the exocyclic-amino function of deoxyadenosine will be illustrated in the assemblage of the nucleopeptides H-Phe-Tyr (pATAT)-NH2 and H-Ala-Ser(pATAT)-Ala-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6847771959ebc35b13085fe874a933c
https://doi.org/10.1002/chin.198910340
https://doi.org/10.1002/chin.198910340