Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Honoré Monti"'
Publikováno v:
Synthesis. 2009:290-296
Starting from ethyl (1 S,4 R)-4-hydroxy-2-methylcyclopent-2-ene-1-carboxylate,as a common enantiopure building block readily obtained by enzymatickinetic resolution of the corresponding racemic derivative, 3′-methylcarbovir,3′-methylabacavir, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1e6dd93aabff9df15f2df1d7bd6b4f1
https://doi.org/10.1055/s-0028-1083213
https://doi.org/10.1055/s-0028-1083213
Publikováno v:
Synthesis. 2008:3253-3260
A series of 3'-methyl-branched and purine-modified analogues of aristeromycin were synthesized via the SN 2 displacement of a key triflate, which was prepared from a readily available enantiopure building block in eight steps. The synthesized compoun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0acb39de9d6115c25215e02d589354a
https://doi.org/10.1055/s-0028-1083146
https://doi.org/10.1055/s-0028-1083146
Publikováno v:
The Journal of Organic Chemistry. 73:6033-6036
Danishefsky's taxol CD ring key intermediate is synthesized in 15 steps and 11.4% overall yield from a readily available starting material. Absolute stereochemistry of the starting material and stereocontrolled steps determine the absolute configurat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a11b2d664d93c20378827484346ed429
https://doi.org/10.1021/jo800913x
https://doi.org/10.1021/jo800913x
Publikováno v:
European Journal of Organic Chemistry. 2007:2802-2807
The first enantioselective synthesis of two new monoterpene aldehyde-esters from Bupleurum gibraltaricum, starting from an enantiopure building block, is described. The key step is a strictly controlled esterification to afford the somewhat unstable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a18040e8bdf79e4ccfbb589150de632f
https://doi.org/10.1002/ejoc.200601080
https://doi.org/10.1002/ejoc.200601080
Publikováno v:
Tetrahedron. 63:5050-5055
Starting from a readily available enantiopure building block, a straightforward enantioselective approach to 3′-methyl-2′,3′-β-oxirane-fused carbanucleosides bearing adenosine analogues is detailed. The key steps in the syntheses involved a li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::081fc4bf7aff340d6890a6a7efc5c4da
https://doi.org/10.1016/j.tet.2007.03.122
https://doi.org/10.1016/j.tet.2007.03.122
Publikováno v:
Synlett. 2006:2215-2218
This paper describes the racemic and stereoselective synthesis of novel conformationally locked 3'-methyl-2',3'-oxiranefused carbocyclic nucleosides (nucleosides numbering). The key step is the direct coupling of an alcohol bearing the 1-methyl-6-oxa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e95cb0b6d14cb92b1b026822cb7e662
https://doi.org/10.1055/s-2006-949635
https://doi.org/10.1055/s-2006-949635
Publikováno v:
Synlett. 2006:0403-0406
A convenient chemoenzymatic enantioconvergent access to enantiomerically pure (+)- or (-)-4-hydroxy-3-methyl-2-cyclohexenone is described using a one-pot two-step kinetic resolution-stereoinversion protocol followed by hydrolysis. The key step of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ddf0439a4f32c81ba3cb5e21302a1fe
https://doi.org/10.1055/s-2006-926258
https://doi.org/10.1055/s-2006-926258
Publikováno v:
Tetrahedron. 61:9545-9549
This paper reports the straightforward enantioselective synthesis of (+)-ancistrofuran starting from a readily available enantiopure building block. A stereofacial directed diastereoselective addition of an organocerate for the installation of the re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c681eb4c8b37561023587984952737e
https://doi.org/10.1016/j.tet.2005.07.087
https://doi.org/10.1016/j.tet.2005.07.087
Publikováno v:
European Journal of Organic Chemistry. 2004:5092-5099
An enantioselective synthesis of (+)-1,14-herbertenediol, and a formal enantioselective synthesis of (−)-α-herbertenol and (−)-herbertenediol, employing a lipase-promoted and a key stereoselective alkylation of a cyclopentane unit based methodol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4656efdc8e8c0e219beed6e9e8c1ba21
https://doi.org/10.1002/ejoc.200400395
https://doi.org/10.1002/ejoc.200400395
Publikováno v:
Tetrahedron. 60:5907-5912
The first enantioselective synthesis of tochuinyl acetate and dihydrotochuinyl acetate, two natural marine products isolated from Tochuina tetraquetra and Gersemia rubiformis, has been achieved starting from an enantiopure building block. The key fea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12a8721cb738659de23ae445222c758d
https://doi.org/10.1016/j.tet.2004.05.037
https://doi.org/10.1016/j.tet.2004.05.037