Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Stefan Eissler"'
Publikováno v:
Organic Process Research & Development. 26:1450-1457
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::887ff7a4aaac3d2226a43c25bace0a31
https://doi.org/10.1021/acs.oprd.2c00052
https://doi.org/10.1021/acs.oprd.2c00052
Publikováno v:
Journal of Peptide Science. 23:757-762
In solid-phase peptide synthesis, the nominal batch size is calculated using the starting resin substitution and the mass of the starting resin. The starting resin substitution constitutes the basis for the calculation of a whole set of important pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7939220ef5ec3388a9d9ac943ac75d39
https://doi.org/10.1002/psc.3021
https://doi.org/10.1002/psc.3021
Publikováno v:
Journal of Peptide Science
In solid‐phase peptide synthesis, the nominal batch size is calculated using the starting resin substitution and the mass of the starting resin. The starting resin substitution constitutes the basis for the calculation of a whole set of important p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a0816acda8d8b6adc03238d026a11b31
https://pubmed.ncbi.nlm.nih.gov/28635051
https://pubmed.ncbi.nlm.nih.gov/28635051
Publikováno v:
Synlett. 2008:273-277
Unit A of cryptophycin 1 is a delta-hydroxy acid with four stereogenic centres. Our unit A synthesis introduces the first two stereogenic centres by a catalytic, asymmetric dihydroxylation, whereas the remaining two stereogenic centres are establishe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4f98c6bf00efeac75bd549afc9cb8d7
https://doi.org/10.1055/s-2007-1000868
https://doi.org/10.1055/s-2007-1000868
Publikováno v:
Synthesis. 2006:3747-3789
Nature provides a huge reservoir of highly diverse chemical compounds with interesting biological properties. Secondary metabolites continue to represent promising candidates for therapeutic applications and drugs are very often based on natural prod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fccc8fd1d4ebf7e8a7b045b4fb3a00d
https://doi.org/10.1055/s-2006-950332
https://doi.org/10.1055/s-2006-950332
Publikováno v:
Organic Letters. 9:817-819
[reaction: see text] Two short synthetic approaches toward cryptophycin unit A comprise a catalytic asymmetric dihydroxylation as the sole source of chirality, while all further stereogenic centers are introduced under substrate control. The key step
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98ff5b3390aa5c9c8c3a1eb9fce4b62d
https://doi.org/10.1021/ol063032l
https://doi.org/10.1021/ol063032l
Publikováno v:
Organic letters. 12(5)
An endocyclic trans-amide linkage within the macrocyclic antitumor agent cryptophycin-52 was replaced by a 1,4-disubstituted 1H-1,2,3-triazole ring. Macrocyclisation of the triazole analogue was accomplished by macrolactamization as well as by Cu(I)-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f219b6edccef5ecf674a708cab7b408e
https://pubmed.ncbi.nlm.nih.gov/20131817
https://pubmed.ncbi.nlm.nih.gov/20131817
Publikováno v:
ChemInform. 40
Many of today's most efficient anticancer chemotherapeutics interfere with microtubule dynamics. They prevent microtubules from forming correct mitotic spindles, therefore cause an arrest of the cell-division cycle and eventually trigger programmed c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7fe983f1aba8ab25bfcf46153155555
https://doi.org/10.1002/chin.200948244
https://doi.org/10.1002/chin.200948244
Cryptophycins are a family of highly cytotoxic, cyclic depsipeptides. They display antitumour activity that is largely maintained for multidrug-resistant tumour cells. Cryptophycins are composed of four building blocks (units A-D) that correspond to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5e8c4b7da64edd6b053b9a78f562cf2
https://doi.org/10.1002/chem.200901750
https://doi.org/10.1002/chem.200901750
Publikováno v:
Organic Letters; Mar2007, Vol. 9 Issue 5, p817-819, 3p