Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Caroline D. Evans"'
Publikováno v:
ChemInform. 43
Enolates of N-substituted amino esters (I) and (III) undergo intramolecular cyclization reactions to afford (syn)-aza-anions that undergo 4-exo-trig cyclization onto their ester carbonyl group to afford cyclic β-lactams (II) and (IV) in high diaster
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b053c2cd56b845fac365c65ec3013bf
https://doi.org/10.1002/chin.201214093
https://doi.org/10.1002/chin.201214093
Chirality plays a central role in the world around us, with nature and scientists producing an ever-increasing number of chiral molecules that have a wide range of different applications. The word chirality is used as a term to describe a molecule wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::faaed1e81a001830df1cc309a38fe97a
https://doi.org/10.1016/b978-0-08-095167-6.00845-4
https://doi.org/10.1016/b978-0-08-095167-6.00845-4
Publikováno v:
Organic letters. 13(23)
Enolates of chiral N-(α-methyl-p-methoxybenzyl)-ω-imino-esters undergo intramolecular cyclization reactions to afford (syn)-aza-anions of β-amino esters in high dr that cyclize to afford N-(α-methyl-p-methoxybenzyl)-β-lactams that can be readily
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86afc8684eb8b787448570975c9a4e6d
https://pubmed.ncbi.nlm.nih.gov/22050269
https://pubmed.ncbi.nlm.nih.gov/22050269
Publikováno v:
Organic Letters; Dec2011, Vol. 13 Issue 23, p6276-6279, 4p