FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2146885184> ?p ?o ?g. }

• W2146885184 endingPage "13595" @default.
• W2146885184 startingPage "13592" @default.
• W2146885184 abstract "An organocatalytic asymmetric synthesis of δ-amino-β-ketoester derivatives has been developed. A chiral disulfonimide (DSI) serves as a highly efficient precatalyst for a vinylogous Mukaiyama-Mannich reaction of readily available dioxinone-derived silyloxydienes with N-Boc-protected imines, delivering products in excellent yields and enantioselectivities. The synthetic utility of this reaction is illustrated in various transformations, including a new CC bond-forming reaction, which provide useful enantioenriched building blocks. The methodology is applied in a formal synthesis of (-)-lasubin." @default.
• W2146885184 created "2016-06-24" @default.
• W2146885184 creator A5038925634 @default.
• W2146885184 creator A5040055598 @default.
• W2146885184 creator A5082979214 @default.
• W2146885184 date "2014-10-27" @default.
• W2146885184 modified "2023-10-12" @default.
• W2146885184 title "Asymmetric Disulfonimide-Catalyzed Synthesis of δ-Amino-β-Ketoester Derivatives by Vinylogous Mukaiyama-Mannich Reactions" @default.
• W2146885184 cites W1491388963 @default.
• W2146885184 cites W1964900972 @default.
• W2146885184 cites W1966490795 @default.
• W2146885184 cites W1968635147 @default.
• W2146885184 cites W1969641609 @default.
• W2146885184 cites W1975090409 @default.
• W2146885184 cites W1975199590 @default.
• W2146885184 cites W1975911527 @default.
• W2146885184 cites W1979278396 @default.
• W2146885184 cites W1979448452 @default.
• W2146885184 cites W1981504804 @default.
• W2146885184 cites W1997598559 @default.
• W2146885184 cites W1998740595 @default.
• W2146885184 cites W2008224435 @default.
• W2146885184 cites W2009951269 @default.
• W2146885184 cites W2012845712 @default.
• W2146885184 cites W2018993758 @default.
• W2146885184 cites W2022544128 @default.
• W2146885184 cites W2023703351 @default.
• W2146885184 cites W2026878838 @default.
• W2146885184 cites W2033605117 @default.
• W2146885184 cites W2039262224 @default.
• W2146885184 cites W2041754190 @default.
• W2146885184 cites W2042133606 @default.
• W2146885184 cites W2042211355 @default.
• W2146885184 cites W2044775413 @default.
• W2146885184 cites W2050419826 @default.
• W2146885184 cites W2051981379 @default.
• W2146885184 cites W2054030625 @default.
• W2146885184 cites W2054044327 @default.
• W2146885184 cites W2054551672 @default.
• W2146885184 cites W2056840844 @default.
• W2146885184 cites W2057996273 @default.
• W2146885184 cites W2059618595 @default.
• W2146885184 cites W2059869007 @default.
• W2146885184 cites W2062531971 @default.
• W2146885184 cites W2065236072 @default.
• W2146885184 cites W2074908177 @default.
• W2146885184 cites W2077427396 @default.
• W2146885184 cites W2080584760 @default.
• W2146885184 cites W2087538184 @default.
• W2146885184 cites W2090947896 @default.
• W2146885184 cites W2096993146 @default.
• W2146885184 cites W2097481499 @default.
• W2146885184 cites W2097718005 @default.
• W2146885184 cites W2103764485 @default.
• W2146885184 cites W2103808099 @default.
• W2146885184 cites W2114705091 @default.
• W2146885184 cites W2114745719 @default.
• W2146885184 cites W2121688286 @default.
• W2146885184 cites W2130136758 @default.
• W2146885184 cites W2130276904 @default.
• W2146885184 cites W2136343058 @default.
• W2146885184 cites W2141752019 @default.
• W2146885184 cites W2149110441 @default.
• W2146885184 cites W2149669555 @default.
• W2146885184 cites W2149831012 @default.
• W2146885184 cites W2153721661 @default.
• W2146885184 cites W2153961423 @default.
• W2146885184 cites W2156850248 @default.
• W2146885184 cites W2158974750 @default.
• W2146885184 cites W2163892628 @default.
• W2146885184 cites W2167619363 @default.
• W2146885184 cites W2168333473 @default.
• W2146885184 cites W2170070362 @default.
• W2146885184 cites W2170818643 @default.
• W2146885184 cites W2322165187 @default.
• W2146885184 cites W2325183145 @default.
• W2146885184 cites W2949575426 @default.
• W2146885184 cites W2949688130 @default.
• W2146885184 cites W2949905442 @default.
• W2146885184 cites W2951255856 @default.
• W2146885184 cites W2952074858 @default.
• W2146885184 cites W2952365084 @default.
• W2146885184 cites W2952895866 @default.
• W2146885184 cites W2952945800 @default.
• W2146885184 cites W2953092082 @default.
• W2146885184 cites W4206684155 @default.
• W2146885184 cites W4231604571 @default.
• W2146885184 cites W4235073603 @default.
• W2146885184 cites W4235569490 @default.
• W2146885184 cites W4241374560 @default.
• W2146885184 cites W4246647862 @default.
• W2146885184 cites W4323517676 @default.
• W2146885184 doi "https://doi.org/10.1002/anie.201407532" @default.
• W2146885184 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/25348924" @default.
• W2146885184 hasPublicationYear "2014" @default.
• W2146885184 type Work @default.
• W2146885184 sameAs 2146885184 @default.
• W2146885184 citedByCount "59" @default.

• next