Matches in SemOpenAlex for { <https://semopenalex.org/work/W3026142576> ?p ?o ?g. }
- W3026142576 endingPage "10597" @default.
- W3026142576 startingPage "10591" @default.
- W3026142576 abstract "The need for alternative, complementary approaches to enable C−C bond formation within organic chemistry is an on-going challenge in the area. Of particular relevance are transformations that proceed in the absence of transition-metal reagents. In the current study, we report a comprehensive investigation of the coupling of nitrile imines and aryl boronic acids as an approach towards sustainable C−C bond formation. In situ generation of the highly reactive 1,3-dipole facilitates a Petasis–Mannich-type coupling via a nucleophilic boronate complex. The introduction of hydrazonyl chlorides as a complementary nitrile imine source to the 2,5-tetrazoles previously reported by our laboratory further broadens the scope of the approach. Additionally, we exemplify for the first time the extension of this protocol into another 1,3-dipole, through the synthesis of aryl ketone oximes from aryl boronic acids and nitrile N-oxides." @default.
- W3026142576 created "2020-05-29" @default.
- W3026142576 creator A5004400491 @default.
- W3026142576 creator A5041199149 @default.
- W3026142576 creator A5055231644 @default.
- W3026142576 creator A5066959055 @default.
- W3026142576 date "2020-07-21" @default.
- W3026142576 modified "2023-10-17" @default.
- W3026142576 title "Transition‐Metal‐Free Coupling of 1,3‐Dipoles and Boronic Acids as a Sustainable Approach to C−C Bond Formation" @default.
- W3026142576 cites W1484574620 @default.
- W3026142576 cites W1568434617 @default.
- W3026142576 cites W1927660426 @default.
- W3026142576 cites W1968845526 @default.
- W3026142576 cites W1979813209 @default.
- W3026142576 cites W1989743179 @default.
- W3026142576 cites W1990293308 @default.
- W3026142576 cites W1993041693 @default.
- W3026142576 cites W2002319811 @default.
- W3026142576 cites W2008047664 @default.
- W3026142576 cites W2010621614 @default.
- W3026142576 cites W2010642173 @default.
- W3026142576 cites W2020314347 @default.
- W3026142576 cites W2021118061 @default.
- W3026142576 cites W2023668057 @default.
- W3026142576 cites W2029620120 @default.
- W3026142576 cites W2033798446 @default.
- W3026142576 cites W2035856006 @default.
- W3026142576 cites W2040329937 @default.
- W3026142576 cites W2046203654 @default.
- W3026142576 cites W2049611192 @default.
- W3026142576 cites W2052362331 @default.
- W3026142576 cites W2056658992 @default.
- W3026142576 cites W2062773033 @default.
- W3026142576 cites W2063397125 @default.
- W3026142576 cites W2066284690 @default.
- W3026142576 cites W2088871267 @default.
- W3026142576 cites W2096060622 @default.
- W3026142576 cites W2096540568 @default.
- W3026142576 cites W2100711758 @default.
- W3026142576 cites W2101460690 @default.
- W3026142576 cites W2109661842 @default.
- W3026142576 cites W2111608896 @default.
- W3026142576 cites W211382461 @default.
- W3026142576 cites W2117452103 @default.
- W3026142576 cites W2177326785 @default.
- W3026142576 cites W2285732370 @default.
- W3026142576 cites W2286998574 @default.
- W3026142576 cites W2326639051 @default.
- W3026142576 cites W2327370237 @default.
- W3026142576 cites W2331294264 @default.
- W3026142576 cites W2444638664 @default.
- W3026142576 cites W2471778414 @default.
- W3026142576 cites W2530127401 @default.
- W3026142576 cites W2558839892 @default.
- W3026142576 cites W2564893019 @default.
- W3026142576 cites W2593674320 @default.
- W3026142576 cites W2761643084 @default.
- W3026142576 cites W2784111191 @default.
- W3026142576 cites W2791681086 @default.
- W3026142576 cites W2802021564 @default.
- W3026142576 cites W2805571380 @default.
- W3026142576 cites W2885015322 @default.
- W3026142576 cites W2897104364 @default.
- W3026142576 cites W2942989113 @default.
- W3026142576 cites W2950731738 @default.
- W3026142576 cites W2950784434 @default.
- W3026142576 cites W2952616218 @default.
- W3026142576 cites W2970902789 @default.
- W3026142576 cites W2973474617 @default.
- W3026142576 cites W4238398773 @default.
- W3026142576 cites W4242773223 @default.
- W3026142576 cites W4248801111 @default.
- W3026142576 doi "https://doi.org/10.1002/chem.202001590" @default.
- W3026142576 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7496359" @default.
- W3026142576 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/32428258" @default.
- W3026142576 hasPublicationYear "2020" @default.
- W3026142576 type Work @default.
- W3026142576 sameAs 3026142576 @default.
- W3026142576 citedByCount "12" @default.
- W3026142576 countsByYear W30261425762020 @default.
- W3026142576 countsByYear W30261425762021 @default.
- W3026142576 countsByYear W30261425762022 @default.
- W3026142576 countsByYear W30261425762023 @default.
- W3026142576 crossrefType "journal-article" @default.
- W3026142576 hasAuthorship W3026142576A5004400491 @default.
- W3026142576 hasAuthorship W3026142576A5041199149 @default.
- W3026142576 hasAuthorship W3026142576A5055231644 @default.
- W3026142576 hasAuthorship W3026142576A5066959055 @default.
- W3026142576 hasBestOaLocation W30261425761 @default.
- W3026142576 hasConcept C106773901 @default.
- W3026142576 hasConcept C161790260 @default.
- W3026142576 hasConcept C178790620 @default.
- W3026142576 hasConcept C185592680 @default.
- W3026142576 hasConcept C20774148 @default.
- W3026142576 hasConcept C21951064 @default.
- W3026142576 hasConcept C2776573223 @default.
- W3026142576 hasConcept C2777864310 @default.
- W3026142576 hasConcept C2779240715 @default.