About: Marsha R. Baar

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

academic, college faculty, Professor of Chemistry

Attributes	Values
rdf:type	Item
field of work	wds:Q100390653-0B766D95-B7A0-4627-BA40-2504B879E80A
field of work	chemistry
description	academic, college faculty, Professor of Chemistry (en)
rdfs:label	Marsha R. Baar (en) Marsha R. Baar (nl)
skos:prefLabel	Marsha R. Baar (en) Marsha R. Baar (nl)
name	Marsha R. Baar (en) Marsha R. Baar (nl)
affiliation	wds:Q100390653-2AFD1402-5B63-4F94-ADF8-26C8629D0A8D
affiliation	Muhlenberg College Department of Chemistry
given name	wds:Q100390653-14DFB1C4-0E11-457D-8A67-F6B26B828C74
given name	Marsha
instance of	wds:Q100390653-77B8AB5F-D7DA-442D-954E-C721F52B0B4C
instance of	Homo sapiens
award received	wds:Q100390653-01EA6387-968F-40A5-A648-E656871144A5
award received	Christian R. and Mary F. Lindback Foundation Award for Distinguished Teaching
skos:altLabel	Baar, M (en) Baar, M R (en) Baar, Marsha (en) M R Baar (en) Marsha Baar (en)
occupation	wds:Q100390653-B69DF93B-0AEB-4DB7-AF9E-05EFFA5F198B
employer	wds:Q100390653-2F42A5E9-4C92-47D0-AE1B-F5A8CFF9EE35
occupation	university teacher
employer	Muhlenberg College
ORCID iD	wds:Q100390653-f0778f4c-41be-e2a7-db21-6631002c9930
ORCID iD	https://orcid.org/0000-0001-8464-7757
ORCID iD	0000-0001-8464-7757
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q100390653
is author of	Comparable Educational Benefits in Half the Time: An Alternating Organic Chemistry Laboratory Sequence Targeting Prehealth Students Interception of [2+2] cycloadducts in the zinc bromide mediated reaction of di-tert-butyl methylenemalonate with simple enol ethers Microwave-Enhanced Organic Syntheses for the Undergraduate Laboratory: Diels-Alder Cycloaddition, Wittig Reaction, and Williamson Ether Synthesis Research Experience for the Organic Chemistry Laboratory: A Student-Centered Optimization of A Microwave-Enhanced Williamson Ether Synthesis and GC Analysis Diels-Alder Synthesis of endo-cis-N-phenylbicyclo[2.2.2]oct-5-en-2,3-dicarboximide Enantiomeric Resolution of (±)-Mandelic Acid by (1 R,2S)-(-)-Ephedrine. Nucleophilic addition to (methyl α-chloroacrylate)tetracarbonyliron. Activation of a vinyl halide The Ethylene Ketal Protecting Group Revisited: The Synthesis of 4-Hydroxy-4, 4-Diphenyl-2-Butanone
is author of	wds:Q108886621-DD2899E9-B6EC-4CF4-A359-3DB28D2F5718 wds:Q108886624-C340674A-7B6D-451C-BE4D-BFA81CAA687C wds:Q108886625-86D4A158-3B07-406E-81D5-649550F00B3C wds:Q108886629-369CBBB3-01EA-4DA1-9E84-4768E8D4FBA6 wds:Q108886622-E361788D-64FE-4A4F-BB4B-A7724201E9DB wds:Q108886623-A1A8DE98-83B6-49AB-A8F5-E33414023D18 wds:Q108886626-DF7BA58F-B666-45EA-8591-EC03C299574B wds:Q108886630-BE016AE2-8893-4A7D-B9C8-E1C043266A98

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