Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Qi-Wen Shen"'
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-11 (2022)
The catalytic asymmetric benzylations of prochiral nucleophiles are very limited. Here, the authors disclose an asymmetric α−benzylation of N-unprotected amino acids with benzyl alcohol derivatives by a chiral aldehyde-involved catalytic system.
Externí odkaz:
https://doaj.org/article/7c065e82cf004c54b2f42c01db8f0970
Publikováno v:
Structures. 53:1267-1282
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1f12cfa386fbdba8b1dc89e9cd92635
https://doi.org/10.1016/j.istruc.2023.05.012
https://doi.org/10.1016/j.istruc.2023.05.012
Publikováno v:
Organic Letters. 25:3163-3167
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::276cd95f3bd7ee6f8affbf19f3ac1244
https://doi.org/10.1021/acs.orglett.3c01119
https://doi.org/10.1021/acs.orglett.3c01119
Publikováno v:
Journal of Constructional Steel Research. 206:107914
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::179e03ab91cbddce9292c0b908c88828
https://doi.org/10.1016/j.jcsr.2023.107914
https://doi.org/10.1016/j.jcsr.2023.107914
Publikováno v:
Nature communications. 13(1)
Catalytic asymmetric Tsuji–Trost benzylation is a promising strategy for the preparation of chiral benzylic compounds. However, only a few such transformations with both good yields and enantioselectivities have been achieved since this reaction wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::374c9cb07999223ab483dd6e4400fb92
https://pubmed.ncbi.nlm.nih.gov/35523802
https://pubmed.ncbi.nlm.nih.gov/35523802
Publikováno v:
Organic letters. 23(4)
A ternary catalytic system comprising a chiral aldehyde, a transition metal, and a Lewis acid is rationally designed for the asymmetric α-allylic alkylation reaction of aza-aryl methylamines and π-allylmetal electrophiles. Structural diversity chir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5ed8996873d42b2ddca7ee1e65ba440
https://pubmed.ncbi.nlm.nih.gov/33544606
https://pubmed.ncbi.nlm.nih.gov/33544606
Publikováno v:
Sheng li xue bao : [Acta physiologica Sinica]. 67(5)
Transient receptor potential vanilloid 4 (TRPV4) channel is a member of transient receptor potential superfamily. TRPV4 is selectively permeable to calcium. Activation of the TRPV4 channel induces an increase in intracellular calcium concentration an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f70bd4a80555bbdbe4a865bd67477ba7
https://pubmed.ncbi.nlm.nih.gov/26490071
https://pubmed.ncbi.nlm.nih.gov/26490071