Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Shun-En Zhang"'
Publikováno v:
Organic Letters. 16:6472-6475
This work describes an efficient α-alkylation reaction of α-amino aldehydes with 3-indolylmethanols. In the promotion of catalyst 3f, the target products were obtained in high yields (up to 99%), good diastereoselectivities (up to 88:12), and excel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::625ee29439d7d7983307816fd7b25475
https://doi.org/10.1021/ol503318c
https://doi.org/10.1021/ol503318c
Publikováno v:
ChemInform. 46
This work describes an efficient α-alkylation reaction of α-amino aldehydes with 3-indolylmethanols. In the promotion of catalyst 3f, the target products were obtained in high yields (up to 99%), good diastereoselectivities (up to 88:12), and excel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f02e5f492d8a413c06322890be664f31
https://doi.org/10.1002/chin.201521136
https://doi.org/10.1002/chin.201521136
Publikováno v:
Tetrahedron Letters. 54:4653-4655
An efficient aldol reaction of indole-3-carbaldehydes with ketones is described. O-TBS-protected l -threonine promoted the aldol addition of ketones to indole-3-carbaldehydes affording 3-indolylmethanols with good to excellent yields and diastereosel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f4be6692360973db92a9c82e52553cb
https://doi.org/10.1016/j.tetlet.2013.06.056
https://doi.org/10.1016/j.tetlet.2013.06.056
Publikováno v:
ChemInform. 44
An efficient aldol reaction of indole-3-carbaldehydes with ketones is described. O-TBS-protected l -threonine promoted the aldol addition of ketones to indole-3-carbaldehydes affording 3-indolylmethanols with good to excellent yields and diastereosel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::252ec4eb0a42aa18ae01d75bd291f616
https://doi.org/10.1002/chin.201352113
https://doi.org/10.1002/chin.201352113