Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Lucas W. Erickson"'
Publikováno v:
J Am Chem Soc
We introduce a versatile strategy for the bioreversible modification of proteins. Our strategy is based on a tricomponent molecule, synthesized in three steps, that incorporates a diazo moiety for chemoselective esterification of carboxyl groups, a p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa2f7c64bbecb279bc96da6f781b630f
https://doi.org/10.1021/jacs.2c11325
https://doi.org/10.1021/jacs.2c11325
Autor:
Emily J. Tollefson, Lucas W. Erickson, Xin Hong, Erika L. Lucas, Pan-Pan Chen, Buck L. H. Taylor, Margaret A. Greene, Shuo-Qing Zhang, Elizabeth R. Jarvo
Publikováno v:
Journal of the American Chemical Society. 141:5835-5855
Ni-catalyzed C(sp(3))-O bond activation provides a useful approach to synthesize enantioenriched products from readily available enantioenriched benzylic alcohol derivatives. The control of stereospecificity is key to the success of these transformat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8733248a9385c9b8062275d441821f9b
https://doi.org/10.1021/jacs.9b00097
https://doi.org/10.1021/jacs.9b00097
Publikováno v:
Journal of the American Chemical Society. 138(42)
The stereospecific reductive cross-electrophile coupling reaction of 2-vinyl-4-halotetrahydropyrans for vinylcyclopropane synthesis is reported. The nickel-catalyzed reaction occurs with both alkyl fluorides and alkyl chlorides. To the best of our kn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::325c027060979cfd21eeb2cd17a537bd
https://pubmed.ncbi.nlm.nih.gov/27706939
https://pubmed.ncbi.nlm.nih.gov/27706939
Publikováno v:
ChemInform. 47
Stereospecific synthesis of di- and trisubstituted cyclopropanes is achieved via a Ni-catalyzed reductive cross-electrophile coupling of chlorotetrahydropyrans.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27ccc5642f5d72243dd6f32834e7ff72
https://doi.org/10.1002/chin.201602073
https://doi.org/10.1002/chin.201602073
Publikováno v:
Journal of the American Chemical Society. 137(31)
The stereospecific reductive cross-electrophile coupling reaction of 2-aryl-4-chlorotetrahydropyrans to afford disubstituted cyclopropanes is reported. This ring contraction presents surprises with respect to the stereochemical outcome of reaction of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60e09b4b70d7a525f4003d6c47136cea
https://pubmed.ncbi.nlm.nih.gov/26230365
https://pubmed.ncbi.nlm.nih.gov/26230365