Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Anh Diep-Vohuule"'
Autor:
Vitomir Šunjić, Anh Diep-Vohuule, Thomas Isarno, Marin Roje, Arlette Solladié-Cavallo, V. Vinkovic
Publikováno v:
Tetrahedron. 54:9123-9128
Stereoselective catalytic and stoichiometric cyclopropanation of styrenes 3a,3b was studied; the stoichiometric method turned out superior in the terms of enantioselectivity. The intermediate carboxymethyl cyclopropane 11a,11b, obtained on reduction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0d152b63455f169d09dfb19e830959c
https://doi.org/10.1016/s0040-4020(98)00549-3
https://doi.org/10.1016/s0040-4020(98)00549-3
Publikováno v:
The Journal of Organic Chemistry. 60:3494-3498
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f709e2815e0f437622fa9fbb29a3e14
https://doi.org/10.1021/jo00116a041
https://doi.org/10.1021/jo00116a041
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb6067408529a195bc52a648b65039c5
https://doi.org/10.1002/chin.199845116
https://doi.org/10.1002/chin.199845116
Autor:
Marin Roje, Thomas Isarno, Arlette Solladié-Cavallo, Vitomir Šunjić, V. Vinkovic, Anh Diep-Vohuule
Publikováno v:
ChemInform. 29
Stereoselective catalytic and stoichiometric cyclopropanation of styrenes 3a,3b was studied; the stoichiometric method turned out superior in the terms of enantioselectivity. The intermediate carboxymethyl cyclopropane 11a,11b, obtained on reduction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::330a18b4744297e8e377c522c9acbd33
https://doi.org/10.1002/chin.199846099
https://doi.org/10.1002/chin.199846099
Pure trans -( R , R )-diaryl-epoxides are obtained in two steps and under aprotic conditions using Eliel's oxathiane as the chiral auxiliary. The enantiomeric excesses, determined by chiral HPLC, are 97.9% to 99.9% and the oxathiane is recovered in 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::480d9d609d6728bfbbb8df2165acd0f7
https://doi.org/10.1016/0957-4166(96)00213-3
https://doi.org/10.1016/0957-4166(96)00213-3
