Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Pierre Calinaud"'
Publikováno v:
European Journal of Organic Chemistry. 2006:3421-3433
The highly diastereoselective synthesis of five trifluoro-substituted analogues of mono-, di-, and trisubstituted piperidine alkaloids was accomplished in two to four steps from 2-trifluoromethyl keto-protected 4-piperidones, prepared by an intramole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23bd2751f1f802e515b8c72a9dc926ce
https://doi.org/10.1002/ejoc.200600157
https://doi.org/10.1002/ejoc.200600157
Publikováno v:
Synthesis. 1995:561-565
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd7ce10ebeab1fd39f337518dc2e60d4
https://doi.org/10.1055/s-1995-3955
https://doi.org/10.1055/s-1995-3955
Publikováno v:
Carbohydrate Research. 267:227-237
The reaction of ketene acetals with d -glucose, d -mannose, and their methyl glycosides is described as a new route to unusual cyclic orthoesters (at non anomeric positions). The reaction proceeds by preferential attack of the reagent on the primary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::035ec66ab73fa32e9ae72b986ad6d2fd
https://doi.org/10.1016/0008-6215(94)00306-z
https://doi.org/10.1016/0008-6215(94)00306-z
Publikováno v:
Carbohydrate Research. 264:33-44
d -Ribono-1,4-lactone, after acetalation, tritylation, and reduction, leads to a cyclization compound which gave with tosyl chloride 1,4-anhydro-2,3- O -isopropylidene-5- O -trityl- d -ribitol. The latter was transformed (acid hydrolysis, periodate o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3237abbf540dc5beae04dc6a21b63a5e
https://doi.org/10.1016/0008-6215(94)00190-1
https://doi.org/10.1016/0008-6215(94)00190-1
Publikováno v:
ChemInform. 26
d -Ribono-1,4-lactone, after acetalation, tritylation, and reduction, leads to a cyclization compound which gave with tosyl chloride 1,4-anhydro-2,3- O -isopropylidene-5- O -trityl- d -ribitol. The latter was transformed (acid hydrolysis, periodate o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94a51f1aebb139f890993262d6cf5db7
https://doi.org/10.1002/chin.199514181
https://doi.org/10.1002/chin.199514181
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4788f00695d26daa7916283f64d6d050
https://doi.org/10.1002/chin.199549241
https://doi.org/10.1002/chin.199549241
Publikováno v:
ChemInform. 31
An enantioselective preparation of both enantiomers of alkaloid 241D 1 and its C-4 epimer is reported. This simple and concise synthesis, seven steps from pent-3-en-2-one, involves a highly diastereoselective Mannich-type cyclisation as the key step.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::971dbb7a85dc851ae4ee0b2180da1935
https://doi.org/10.1002/chin.200022193
https://doi.org/10.1002/chin.200022193
Publikováno v:
ChemInform. 34
Synthesis of 4-substituted indolizidin-9-one amino acid by cyclization of pipecolic acid derivatives has been described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0658102e90ecc104fc284aa010bf96fa
https://doi.org/10.1002/chin.200339179
https://doi.org/10.1002/chin.200339179
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78a012dda4440184bb79948e0cb51c71
https://doi.org/10.1002/chin.199033343
https://doi.org/10.1002/chin.199033343
Publikováno v:
European Journal of Organic Chemistry; Aug2006, Vol. 2006 Issue 15, p3421-3433, 13p