Matches in SemOpenAlex for { <https://semopenalex.org/work/W2085524911> ?p ?o ?g. }
- W2085524911 endingPage "6152" @default.
- W2085524911 startingPage "6142" @default.
- W2085524911 abstract "An efficient one-pot synthesis of novel β-amino acid derivatives containing a thiadiazole moiety was developed using a chiral squaramide cinchona alkaloid as organocatalyst. The reactions afforded chiral β-amino acid derivatives in moderate yields and with moderate to excellent enantioselectivities. The present study demonstrated for the first time the use of a Mannich reaction catalyzed by a chiral bifunctional organocatalyst for the one-pot synthesis of novel β-amino acid derivatives bearing a 1,3,4-thiadiazole moiety on nitrogen." @default.
- W2085524911 created "2016-06-24" @default.
- W2085524911 creator A5001418213 @default.
- W2085524911 creator A5010310776 @default.
- W2085524911 creator A5021010784 @default.
- W2085524911 creator A5022635054 @default.
- W2085524911 creator A5026127442 @default.
- W2085524911 creator A5026810016 @default.
- W2085524911 creator A5056609542 @default.
- W2085524911 creator A5085853261 @default.
- W2085524911 creator A5088579856 @default.
- W2085524911 date "2013-05-23" @default.
- W2085524911 modified "2023-10-13" @default.
- W2085524911 title "One-Pot Synthesis of Novel Chiral β-Amino Acid Derivatives by Enantioselective Mannich Reactions Catalyzed by Squaramide Cinchona Alkaloids" @default.
- W2085524911 cites W1943025046 @default.
- W2085524911 cites W1977545284 @default.
- W2085524911 cites W2005148942 @default.
- W2085524911 cites W2012845137 @default.
- W2085524911 cites W2020481425 @default.
- W2085524911 cites W2021198082 @default.
- W2085524911 cites W2026334732 @default.
- W2085524911 cites W2029058298 @default.
- W2085524911 cites W2040390534 @default.
- W2085524911 cites W2042584758 @default.
- W2085524911 cites W2054786228 @default.
- W2085524911 cites W2062590568 @default.
- W2085524911 cites W2078910624 @default.
- W2085524911 cites W2086167852 @default.
- W2085524911 cites W2090600061 @default.
- W2085524911 cites W2096649736 @default.
- W2085524911 cites W2108722536 @default.
- W2085524911 cites W2120804041 @default.
- W2085524911 cites W2131510041 @default.
- W2085524911 cites W2147779414 @default.
- W2085524911 cites W2150377190 @default.
- W2085524911 cites W2313488206 @default.
- W2085524911 cites W2320002287 @default.
- W2085524911 cites W2949081548 @default.
- W2085524911 cites W2951318721 @default.
- W2085524911 cites W2951624905 @default.
- W2085524911 cites W2951927279 @default.
- W2085524911 cites W2952380363 @default.
- W2085524911 cites W2952397949 @default.
- W2085524911 cites W2953136102 @default.
- W2085524911 cites W2953173038 @default.
- W2085524911 cites W4292963219 @default.
- W2085524911 cites W4293587000 @default.
- W2085524911 doi "https://doi.org/10.3390/molecules18066142" @default.
- W2085524911 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6270396" @default.
- W2085524911 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23702920" @default.
- W2085524911 hasPublicationYear "2013" @default.
- W2085524911 type Work @default.
- W2085524911 sameAs 2085524911 @default.
- W2085524911 citedByCount "17" @default.
- W2085524911 countsByYear W20855249112013 @default.
- W2085524911 countsByYear W20855249112014 @default.
- W2085524911 countsByYear W20855249112015 @default.
- W2085524911 countsByYear W20855249112016 @default.
- W2085524911 countsByYear W20855249112017 @default.
- W2085524911 countsByYear W20855249112018 @default.
- W2085524911 countsByYear W20855249112019 @default.
- W2085524911 countsByYear W20855249112020 @default.
- W2085524911 countsByYear W20855249112021 @default.
- W2085524911 crossrefType "journal-article" @default.
- W2085524911 hasAuthorship W2085524911A5001418213 @default.
- W2085524911 hasAuthorship W2085524911A5010310776 @default.
- W2085524911 hasAuthorship W2085524911A5021010784 @default.
- W2085524911 hasAuthorship W2085524911A5022635054 @default.
- W2085524911 hasAuthorship W2085524911A5026127442 @default.
- W2085524911 hasAuthorship W2085524911A5026810016 @default.
- W2085524911 hasAuthorship W2085524911A5056609542 @default.
- W2085524911 hasAuthorship W2085524911A5085853261 @default.
- W2085524911 hasAuthorship W2085524911A5088579856 @default.
- W2085524911 hasBestOaLocation W20855249111 @default.
- W2085524911 hasConcept C146686406 @default.
- W2085524911 hasConcept C161790260 @default.
- W2085524911 hasConcept C178790620 @default.
- W2085524911 hasConcept C185592680 @default.
- W2085524911 hasConcept C21951064 @default.
- W2085524911 hasConcept C2776568683 @default.
- W2085524911 hasConcept C2776700668 @default.
- W2085524911 hasConcept C2777797831 @default.
- W2085524911 hasConcept C2780443040 @default.
- W2085524911 hasConcept C2780640045 @default.
- W2085524911 hasConcept C515207424 @default.
- W2085524911 hasConcept C55493867 @default.
- W2085524911 hasConcept C66972969 @default.
- W2085524911 hasConceptScore W2085524911C146686406 @default.
- W2085524911 hasConceptScore W2085524911C161790260 @default.
- W2085524911 hasConceptScore W2085524911C178790620 @default.
- W2085524911 hasConceptScore W2085524911C185592680 @default.
- W2085524911 hasConceptScore W2085524911C21951064 @default.
- W2085524911 hasConceptScore W2085524911C2776568683 @default.
- W2085524911 hasConceptScore W2085524911C2776700668 @default.
- W2085524911 hasConceptScore W2085524911C2777797831 @default.
- W2085524911 hasConceptScore W2085524911C2780443040 @default.
- W2085524911 hasConceptScore W2085524911C2780640045 @default.
- W2085524911 hasConceptScore W2085524911C515207424 @default.