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pro vyhledávání: '"Daniel C. Weinseimer"'
Publikováno v:
ChemInform. 31
A protocol for achieving stereoselective aldol reactions with cyclic ketones is presented. In terms of yield, the process is particularly effective when a quaternary center at the α-carbon of the β-hydroxy ketone product is created. The stereochemi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1dcaedef3a6ee43496824a2e3ef9fa22
https://doi.org/10.1002/chin.200032067
https://doi.org/10.1002/chin.200032067
Publikováno v:
Organic letters. 2(9)
[formula: see text] A protocol for achieving stereoselective aldol reactions with cyclic ketones is presented. In terms of yield, the process is particularly effective when a quaternary center at the alpha-carbon of the beta-hydroxy ketone product is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ed055f547e4e6c4c7b948db33723b49
https://pubmed.ncbi.nlm.nih.gov/10810705
https://pubmed.ncbi.nlm.nih.gov/10810705