Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Cécile Glanzmann"'
Publikováno v:
Helvetica Chimica Acta. 85:417-430
Two novel, potentially antimicrobial erythronolide aglycon analogs ((-)-9 and (-)-30, respectively), which incorporate a large number of contiguous stereogenic centers, have been prepared by multistep synthesis from simple chirons. The chemistry pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fdf04b5343f63713f798814a169c780
https://doi.org/10.1002/1522-2675(200202)85:2<417::aid-hlca417>3.0.co
https://doi.org/10.1002/1522-2675(200202)85:2<417::aid-hlca417>3.0.co
Publikováno v:
Tetrahedron. 53:2835-2854
Electrophilic 5- exo-trig cyclizations of homoallylsilanes have been carried out leading to 2,4- and 2,4,5-substituted tetrahydrofurans with good yields and diastereoselectivities. With disubstituted homoallylsilanes, tetrahydrofurans having acyclic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71b0be12071270f4f17dd7d33ac766c7
https://doi.org/10.1016/s0040-4020(97)00003-3
https://doi.org/10.1016/s0040-4020(97)00003-3
Publikováno v:
ChemInform. 28
Electrophilic 5- exo-trig cyclizations of homoallylsilanes have been carried out leading to 2,4- and 2,4,5-substituted tetrahydrofurans with good yields and diastereoselectivities. With disubstituted homoallylsilanes, tetrahydrofurans having acyclic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f2a5da865f91173705e4507a0d54334
https://doi.org/10.1002/chin.199726139
https://doi.org/10.1002/chin.199726139
Publikováno v:
ChemInform. 33
Two novel, potentially antimicrobial erythronolide aglycon analogs ((-)-9 and (-)-30, respectively), which incorporate a large number of contiguous stereogenic centers, have been prepared by multistep synthesis from simple chirons. The chemistry pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4cfc237b6009687c92a59a2dcfc0e111
https://doi.org/10.1002/chin.200228207
https://doi.org/10.1002/chin.200228207
Starting from 2,2'-methylenedifuran, enantiomerically enriched (98%) (3R,5S,7R,9S,11R,13R)- and (3R,5S,7S,9R,11R,13R)-15-amino-5,7,9,11-tetrahydroxy-3,13-bis(4-methoxyb enzoyloxy)pentadec-1-yl) pivalate were prepared as well as (3R,5R,7R,9R,11S,13S)-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1532a8536f8d93c27fce92af1b9ca629
https://infoscience.epfl.ch/record/59378
https://infoscience.epfl.ch/record/59378
