Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jannine M. Haberman"'
Publikováno v:
Synthetic Communications. 36:2129-2133
An improved, two‐step synthesis of efaproxiral, used in breast cancer therapy, is described, utilizing inexpensive commodity chemicals for starting materials. Selective amide formation and O‐alkylation in the presence of multireactive functional
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f65138056590fbed766bd21c666f0856
https://doi.org/10.1080/00397910600636527
https://doi.org/10.1080/00397910600636527
Autor:
Jannine M. Haberman, David Y. Gin
Publikováno v:
Organic Letters. 3:1665-1668
The installation of the novel N,N-dimethylglycolamide ester auxiliary onto the C(1)-position of protected neuraminic acid donors allows for the exploitation of C(1)-neighboring group participation to generate sialoside conjugates with good to excelle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0be546382ea37982a2b3422308dc3551
https://doi.org/10.1021/ol015854i
https://doi.org/10.1021/ol015854i
Autor:
David Y. Gin, Jannine M. Haberman
Publikováno v:
Organic Letters. 5:2539-2541
[reaction: see text] A new method for sialylation involving the dehydrative coupling of sialyl donors with the reagent combination of (p-nitrophenyl)(phenyl) sulfoxide and triflic anhydride is reported. This process establishes sialyl C2-hemiketals a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6e9b8ff3b6a80f123a30857f588f545
https://doi.org/10.1021/ol034815z
https://doi.org/10.1021/ol034815z
Autor:
Jannine M. Haberman, David Y. Gin
Publikováno v:
ChemInform. 32
The installation of the novel N,N-dimethylglycolamide ester auxiliary onto the C(1)-position of protected neuraminic acid donors allows for the exploitation of C(1)-neighboring group participation to generate sialoside conjugates with good to excelle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e294ea915b2ea3878a58d63b5e114b3
https://doi.org/10.1002/chin.200140199
https://doi.org/10.1002/chin.200140199