VIAF

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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
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997 ‎‡a 0 0 lived 0 0‏ ‎‡9 1‏