About: James Stephen Clark

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organic chemist

Attributes	Values
rdf:type	Item
description	wetenschapper (nl) дослідник (uk) organic chemist (en)
rdfs:label	James Stephen Clark (en) James Stephen Clark (es) James Stephen Clark (nl) James Stephen Clark (sq) James Stephen Clark (tr) James Stephen Clark (ast)
skos:prefLabel	James Stephen Clark (en) James Stephen Clark (es) James Stephen Clark (nl) James Stephen Clark (sq) James Stephen Clark (tr) James Stephen Clark (ast)
name	James Stephen Clark (en) James Stephen Clark (es) James Stephen Clark (nl) James Stephen Clark (sq) James Stephen Clark (tr) James Stephen Clark (ast)
Scopus author ID	wds:Q56600029-46dc6aa3-4573-1acb-af73-bc37017fd104
Scopus author ID	23991652200
given name	wds:Q56600029-7397FCAA-5962-40B1-9BEC-AF23E838C449
given name	James
instance of	wds:Q56600029-1c045da5-4bce-0755-ebfc-70a39527367c
instance of	Homo sapiens
award received	wds:Q56600029-6fb5c1c4-4fad-3830-1e35-35ccf7cfd10b
award received	Bader Prize
doctoral advisor	wds:Q56600029-c565eef6-47ef-fb14-02af-178417eed686
doctoral advisor	Andrew Bruce Holmes
skos:altLabel	J. S. Clark (en) J. Stephen Clark (en) Stephen Clark (en)
occupation	wds:Q56600029-05075b61-44bd-7b59-dc9a-32dffa944078 wds:Q56600029-8c4d66ca-49a5-2f87-5a21-ba613e82d816
employer	wds:Q56600029-220fb8ac-4b1b-5aee-59db-983ba30e1f3e wds:Q56600029-C0767500-5A18-416C-A777-5BF4CC9D2DE3 wds:Q56600029-b919430b-4b54-6fde-21c3-53d39795a42e
sex or gender	wds:Q56600029-b91747de-4dd6-b44a-feaa-249f13c34b4b
member of	wds:Q56600029-48b45277-41a6-7419-03a9-65cf6098d933 wds:Q56600029-a8dec2c9-44b5-b4ef-c2bd-c95e413bd294
educated at	wds:Q56600029-8ed8364c-48e1-fabb-7e48-7bbe367f3800
official website	wds:Q56600029-2ef06479-4493-1df2-fc9b-98eeb2321863
occupation	professor organic chemist
employer	Harvard University University of Nottingham University of Glasgow
sex or gender	male
member of	Royal Society of Edinburgh Royal Society of Chemistry
educated at	John Ffowcs Williams
official website	https://www.gla.ac.uk/schools/chemistry/staff/stephenclark/
ORCID iD	wds:Q56600029-9d58e9a6-48df-18a2-36d3-f47586d63984
ORCID iD	https://orcid.org/0000-0003-3935-0377
ORCID iD	0000-0003-3935-0377
Gateway to Research person ID	wds:Q56600029-062F41C4-F40A-4F8C-9CBD-E67E557077F7
Gateway to Research person ID	49DE1F20-E67B-496A-B3D9-B003E2725FAC
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56600029
is author of	Synthesis of Polycyclic Ethers by Two-Directional Double Ring-Closing Metathesis Tuneable asymmetric copper-catalysed allylic amination and oxidation reactions. Total synthesis of the purported structure of sclerophytin F. Stereoselective Synthesis of Medium-Sized Cyclic Ethers by Sequential Ring-Closing Metathesis and Tsuji-Trost Allylation. Rapid synthesis of medium-ring fused polycarbocyclic systems by rearrangement of carbenoid-derived oxonium ylides Intramolecular Reactions of Metal Carbenoids with Allylic Ethers: Is a Free Ylide Involved in Every Case? Enantioselective Total Syntheses of Three Cladiellins (Eunicellins): A General Approach to the Entire Family of Natural Products Synthetic studies on the cornexistins: synthesis of (+/-)-5-epi-hydroxycornexistin. Synthesis of the Carbocyclic Core of the Cornexistins by Ring-Closing Metathesis Synthesis of the Core Framework of the Cornexistins by Intramolecular Nozaki-Hiyama-Kishi Coupling Synthesis of the Tricyclic Core of Labiatin A and Australin A A Concise Total Synthesis of (±)-Vigulariol Synthesis of the C-1–C-17 Fragment of Amphidinolides C, C2, C3, and F Synthesis of the C-18–C-34 Fragment of Amphidinolides C, C2, and C3 Synthesis of four diastereomers of sclerophytin F and structural reassignment of several sclerophytin natural products Rapid Synthesis of the A−E Fragment of Ciguatoxin CTX3C Rapid Two-Directional Synthesis of the F-J Fragment of the Gambieric Acids by Iterative Double Ring-Closing Metathesis A Concise and Stereoselective Synthesis of the A-Ring Fragment of the Gambieric Acids Concise synthesis of the C-1–C-12 fragment of amphidinolides T1–T5 Synthesis of the Fused Polyether Core of Hemibrevetoxin B by Two-Directional Ring-Closing Metathesis Stereoselective Synthesis of the I-L Fragment of the Pacific Ciguatoxins Stereoselective construction of the tricyclic core of neoliacinic acid. Synthesis of fused tricyclic systems by thermal Cope rearrangement of furan-substituted vinyl cyclopropanes Trialkylphosphine-Mediated Synthesis of 2-Acyl Furans from Ynenones. β-Turn Mimics by Chemical Ligation Synthesis of cyclopropyl-substituted furans by brønsted Acid promoted cascade reactions. Synthesis of the A-D Ring System of the Gambieric Acids. Total Synthesis of 7-epi-Pukalide and 7-Acetylsinumaximol B. Bidirectional Synthesis of the IJK Fragment of Ciguatoxin CTX3C by Sequential Double Ring-Closing Metathesis and Tsuji-Trost Allylation Total Syntheses of 11-Acetoxy-4-deoxyasbestinin D, 4-Deoxyasbestinin C, Asbestinin-10, -20, -21 and -23 Total Synthesis of (−)-Nakadomarin A Total Syntheses of Amphidinolides T1, T3, and T4 Organocatalytic Synthesis of Highly Substituted Furfuryl Alcohols and Amines Diels-Alder adducts of medium-ring carbocyclic dienes prepared by rearrangement of catalytically generated cyclic oxonium ylides. Construction of building-blocks for polyether synthesis using sequential catalytic ring-closing enyne and cross metathesis
is author of	wds:Q51065978-61633351-6CFA-4D5B-B856-1A6746A36070 wds:Q52314341-7570F374-1A93-4544-AD5E-51F1C6D666AD wds:Q60509288-432EBD94-58FF-40C7-81F3-BA160C31670D wds:Q60509316-1B83B4F2-CCA7-4F59-855E-F887A968FCE5

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