Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Vera M. Foley"'
Publikováno v:
Tetrahedron: Asymmetry. 27:1160-1167
(−)-Sparteine has proven itself to be a highly efficient and versatile ligand. However, in recent years it has become difficult to source. In addition the (+)-enantiomer is also not readily available. Here we report a suite of chiral diamines as po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::306f4f37c1375a76261aed4e9c769653
https://doi.org/10.1016/j.tetasy.2016.09.001
https://doi.org/10.1016/j.tetasy.2016.09.001
Publikováno v:
Organic Syntheses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f4fd4756ed3235523816d3b418726f82
https://doi.org/10.1002/0471264229.os094.19
https://doi.org/10.1002/0471264229.os094.19
Autor:
Simon E. Lawrence, Christina M. McSweeney, Kevin S. Eccles, Gerard P. McGlacken, Vera M. Foley
Publikováno v:
Organic Letters. 17:5642-5645
Methods for the preparation of 1,3-amino alcohols and their derivatives containing two stereogenic centers usually involve a two-step installation of the chiral centers. An aldol-Tishchenko reaction of chiral sulfinimines which involves the first rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78daed738104a9f07c99c0471473fd0b
https://doi.org/10.1021/acs.orglett.5b02919
https://doi.org/10.1021/acs.orglett.5b02919
Autor:
Kevin S. Eccles, Simon E. Lawrence, Gerard P. McGlacken, Christina M. McSweeney, Vera M. Foley
Publikováno v:
ChemInform. 47
Methods for the preparation of 1,3-amino alcohols and their derivatives containing two stereogenic centers usually involve a two-step installation of the chiral centers. An aldol-Tishchenko reaction of chiral sulfinimines which involves the first rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93e54d8e7a2b2757969798e07a8243fc
https://doi.org/10.1002/chin.201613061
https://doi.org/10.1002/chin.201613061
Publikováno v:
Chemical communications (Cambridge, England). 50(94)
The asymmetric alkylation of ketones represents a fundamental transformation in organic chemistry. Chiral auxiliaries have been used almost exclusively for this transformation. Herein we describe a strategy for the generation of enantiomerically enri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73bbcb64684df0a2a64070708c0505cb
https://pubmed.ncbi.nlm.nih.gov/25318599
https://pubmed.ncbi.nlm.nih.gov/25318599
Autor:
Vera M. Foley, Christina M. McSweeney, Kevin S. Eccles, SimonE. Lawrence, Gerard P. McGlacken
Publikováno v:
Organic Letters; Nov2015, Vol. 17 Issue 22, p5642-5645, 4p