A fast and highly enantioselective brominative dearomatization of naphthols catalyzed by diphenylamine‐linked bis(oxazoline)‐Cu(OTf)2 complexes has been developed. The corresponding products of chiral naphthalenones bearing a Br‐containing tetra...
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https://www.riss.kr/link?id=O113291357
2018년
-
1615-4150
1615-4169
SCI;SCIE;SCOPUS
학술저널
2285-2290 [※수록면이 p5 이하이면, Review, Columns, Editor's Note, Abstract 등일 경우가 있습니다.]
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
A fast and highly enantioselective brominative dearomatization of naphthols catalyzed by diphenylamine‐linked bis(oxazoline)‐Cu(OTf)2 complexes has been developed. The corresponding products of chiral naphthalenones bearing a Br‐containing tetra...
A fast and highly enantioselective brominative dearomatization of naphthols catalyzed by diphenylamine‐linked bis(oxazoline)‐Cu(OTf)2 complexes has been developed. The corresponding products of chiral naphthalenones bearing a Br‐containing tetrasubstituted stereogenic center could be obtained with good to excellent enantioselectivities (up to 95% ee) in excellent yields (up to 97% yield) within short reaction times.
Water‐Soluble Sulfo‐Fluorous Affinity (SOFA) Tag‐Assisted Enzymatic Synthesis of Oligosaccharides