VIAF

Virtual International Authority File

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Leader     00000nz a2200037n 45 0
001     WKP|Q61005546  (VIAF cluster)  (Authority/Source Record)
003     WKP
005     20241120235809.0
008     241120nneanz||abbn n and d
035 ‎‡a  (WKP)Q61005546‏
024 ‎‡a  0000-0001-8653-0843‏ ‎‡2  orcid‏
024 ‎‡a  55323941600‏ ‎‡2  scopus‏
035 ‎‡a  (OCoLC)Q61005546‏
100 0 ‎‡a  Michael R Harris‏ ‎‡9  es‏ ‎‡9  ast‏
375 ‎‡a  1‏ ‎‡2  iso5218‏
400 0 ‎‡a  মাইকেল আর হ্যারিস‏ ‎‡9  bn‏
400 0 ‎‡a  Michael R Harris‏ ‎‡c  researcher ORCID ID = 0000-0001-8653-0843‏ ‎‡9  en‏
400 0 ‎‡a  Michael R Harris‏ ‎‡c  wetenschapper‏ ‎‡9  nl‏
670 ‎‡a  Author's A Modular Approach to the Synthesis of gem-Disubstituted Cyclopropanes‏
670 ‎‡a  Author's Construction of 1-Heteroaryl-3-azabicyclo[3.1.0]hexanes by sp3-sp2 Suzuki-Miyaura and Chan-Evans-Lam Coupling Reactions of Tertiary Trifluoroborates.‏
670 ‎‡a  Author's Enantiospecific intramolecular Heck reactions of secondary benzylic ethers‏
670 ‎‡a  Author's Nickel-Catalyzed Hydrogenolysis and Conjugate Addition of 2-‏
670 ‎‡a  Author's Nickel-Catalyzed Hydrogenolysis and Conjugate Addition of 2-(Hydroxymethyl)pyridines via Organozinc Intermediates.‏
670 ‎‡a  Author's Selective synthesis of either enantiomer of an anti-breast cancer agent via a common enantioenriched intermediate.‏
670 ‎‡a  Author's Synthesis of enantioenriched triarylmethanes by stereospecific cross-coupling reactions.‏
909 ‎‡a  (scopus) 55323941600‏ ‎‡9  1‏
909 ‎‡a  (orcid) 0000000186530843‏ ‎‡9  1‏
919 ‎‡a  modularapproachtothesynthesisofgemdisubstitutedcyclopropanes‏ ‎‡A  A Modular Approach to the Synthesis of gem-Disubstituted Cyclopropanes‏ ‎‡9  1‏
919 ‎‡a  constructionof1heteroaryl3azabicyclohexanesbysp3sp2suzukimiyauraandchanevanslamcouplingreactionsoftertiarytrifluoroborates‏ ‎‡A  Construction of 1-Heteroaryl-3-azabicyclo[3.1.0]hexanes by sp3-sp2 Suzuki-Miyaura and Chan-Evans-Lam Coupling Reactions of Tertiary Trifluoroborates.‏ ‎‡9  1‏
919 ‎‡a  enantiospecificintramolecularheckreactionsofsecondarybenzylicethers‏ ‎‡A  Enantiospecific intramolecular Heck reactions of secondary benzylic ethers‏ ‎‡9  1‏
919 ‎‡a  nickelcatalyzedhydrogenolysisandconjugateadditionof2‏ ‎‡A  Nickel-Catalyzed Hydrogenolysis and Conjugate Addition of 2-‏ ‎‡9  1‏
919 ‎‡a  nickelcatalyzedhydrogenolysisandconjugateadditionof2hydroxymethylpyridinesviaorganozincintermediates‏ ‎‡A  Nickel-Catalyzed Hydrogenolysis and Conjugate Addition of 2-(Hydroxymethyl)pyridines via Organozinc Intermediates.‏ ‎‡9  1‏
919 ‎‡a  selectivesynthesisofeitherenantiomerofanantibreastcanceragentviaacommonenantioenrichedintermediate‏ ‎‡A  Selective synthesis of either enantiomer of an anti-breast cancer agent via a common enantioenriched intermediate.‏ ‎‡9  1‏
919 ‎‡a  synthesisofenantioenrichedtriarylmethanesbystereospecificcrosscouplingreactions‏ ‎‡A  Synthesis of enantioenriched triarylmethanes by stereospecific cross-coupling reactions.‏ ‎‡9  1‏
946 ‎‡a  b‏ ‎‡9  1‏
996 ‎‡2  DNB|1160414599
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996 ‎‡2  LC|n 97120131
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996 ‎‡2  BNF|17152680
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996 ‎‡2  NTA|381238172
996 ‎‡2  J9U|987007403904305171
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996 ‎‡2  BNC|981058612371906706
996 ‎‡2  LNB|LNC10-000217900
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997 ‎‡a  0 0 lived 0 0‏ ‎‡9  1‏