Matches in SemOpenAlex for { <https://semopenalex.org/work/W1909722318> ?p ?o ?g. }
- W1909722318 endingPage "1226" @default.
- W1909722318 startingPage "1220" @default.
- W1909722318 abstract "1-Benzyl-2-(bromomethyl)aziridine was successfully substituted with protected glycine esters to afford alkyl 3-(N-benzylaziridin-2-yl)-2-aminopropanoates, as constrained heterocyclic diamino acid derivatives, in good isolated yields. These new aziridines proved to be excellent building blocks for ring transformation to the corresponding stereochemically defined 2-(aminomethyl)-1-aminocyclopropanecarboxylic acid derivatives, including methyl esters, piperidyl amides, and free carboxylic acids." @default.
- W1909722318 created "2016-06-24" @default.
- W1909722318 creator A5007697761 @default.
- W1909722318 creator A5010124138 @default.
- W1909722318 creator A5013840465 @default.
- W1909722318 creator A5037254778 @default.
- W1909722318 creator A5037582954 @default.
- W1909722318 creator A5042134160 @default.
- W1909722318 creator A5047127829 @default.
- W1909722318 creator A5085164806 @default.
- W1909722318 date "2013-12-16" @default.
- W1909722318 modified "2023-09-26" @default.
- W1909722318 title "Synthesis of γ,δ-Aziridino α-Amino Acid Derivatives and their Stereoselective Ring Transformation to 2-(Aminomethyl)-1-aminocyclopropanecarboxylic Acid Derivatives" @default.
- W1909722318 cites W1969935124 @default.
- W1909722318 cites W1974992903 @default.
- W1909722318 cites W1983014227 @default.
- W1909722318 cites W1984513388 @default.
- W1909722318 cites W1988531810 @default.
- W1909722318 cites W1989716545 @default.
- W1909722318 cites W1997883323 @default.
- W1909722318 cites W2003870591 @default.
- W1909722318 cites W2006083014 @default.
- W1909722318 cites W2006569337 @default.
- W1909722318 cites W2010163597 @default.
- W1909722318 cites W2019024371 @default.
- W1909722318 cites W2019897247 @default.
- W1909722318 cites W2020064546 @default.
- W1909722318 cites W2029514910 @default.
- W1909722318 cites W2034870271 @default.
- W1909722318 cites W2035732212 @default.
- W1909722318 cites W2036878215 @default.
- W1909722318 cites W2044632153 @default.
- W1909722318 cites W2047649130 @default.
- W1909722318 cites W2049256895 @default.
- W1909722318 cites W2054026208 @default.
- W1909722318 cites W2057534911 @default.
- W1909722318 cites W2067070913 @default.
- W1909722318 cites W2067368663 @default.
- W1909722318 cites W2072823150 @default.
- W1909722318 cites W2075783792 @default.
- W1909722318 cites W2075959014 @default.
- W1909722318 cites W2078021048 @default.
- W1909722318 cites W2084519147 @default.
- W1909722318 cites W2088266704 @default.
- W1909722318 cites W2109967743 @default.
- W1909722318 cites W2111812217 @default.
- W1909722318 cites W2112788266 @default.
- W1909722318 cites W2116320854 @default.
- W1909722318 cites W2123221735 @default.
- W1909722318 cites W2125621895 @default.
- W1909722318 cites W2146416161 @default.
- W1909722318 cites W2163373100 @default.
- W1909722318 cites W2949748842 @default.
- W1909722318 cites W2950349801 @default.
- W1909722318 cites W2951124328 @default.
- W1909722318 cites W2951131708 @default.
- W1909722318 cites W2951584881 @default.
- W1909722318 cites W2951705806 @default.
- W1909722318 cites W2952817814 @default.
- W1909722318 cites W2996982618 @default.
- W1909722318 cites W334918 @default.
- W1909722318 doi "https://doi.org/10.1002/ejoc.201301030" @default.
- W1909722318 hasPublicationYear "2013" @default.
- W1909722318 type Work @default.
- W1909722318 sameAs 1909722318 @default.
- W1909722318 citedByCount "7" @default.
- W1909722318 countsByYear W19097223182014 @default.
- W1909722318 countsByYear W19097223182015 @default.
- W1909722318 countsByYear W19097223182017 @default.
- W1909722318 countsByYear W19097223182018 @default.
- W1909722318 countsByYear W19097223182021 @default.
- W1909722318 crossrefType "journal-article" @default.
- W1909722318 hasAuthorship W1909722318A5007697761 @default.
- W1909722318 hasAuthorship W1909722318A5010124138 @default.
- W1909722318 hasAuthorship W1909722318A5013840465 @default.
- W1909722318 hasAuthorship W1909722318A5037254778 @default.
- W1909722318 hasAuthorship W1909722318A5037582954 @default.
- W1909722318 hasAuthorship W1909722318A5042134160 @default.
- W1909722318 hasAuthorship W1909722318A5047127829 @default.
- W1909722318 hasAuthorship W1909722318A5085164806 @default.
- W1909722318 hasConcept C155647269 @default.
- W1909722318 hasConcept C161790260 @default.
- W1909722318 hasConcept C178790620 @default.
- W1909722318 hasConcept C181647583 @default.
- W1909722318 hasConcept C185592680 @default.
- W1909722318 hasConcept C2777756961 @default.
- W1909722318 hasConcept C2778544067 @default.
- W1909722318 hasConcept C2779074116 @default.
- W1909722318 hasConcept C2780263894 @default.
- W1909722318 hasConcept C2780378348 @default.
- W1909722318 hasConcept C515207424 @default.
- W1909722318 hasConcept C55493867 @default.
- W1909722318 hasConcept C71240020 @default.
- W1909722318 hasConceptScore W1909722318C155647269 @default.
- W1909722318 hasConceptScore W1909722318C161790260 @default.
- W1909722318 hasConceptScore W1909722318C178790620 @default.
- W1909722318 hasConceptScore W1909722318C181647583 @default.
- W1909722318 hasConceptScore W1909722318C185592680 @default.