About: Michael Shipman

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British organic chemistry professor and academic administrator

Attributes	Values
rdf:type	Item
description	forskare (sv) 연구원 (ko) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) British organic chemistry professor and academic administrator (en)
rdfs:label	Michael Shipman (en) Michael Shipman (es) Michael Shipman (nl) Michael Shipman (sl) Michael Shipman (ast)
skos:prefLabel	Michael Shipman (en) Michael Shipman (es) Michael Shipman (nl) Michael Shipman (sl) Michael Shipman (ast)
name	Michael Shipman (en) Michael Shipman (es) Michael Shipman (nl) Michael Shipman (sl) Michael Shipman (ast)
LinkedIn personal profile ID	wds:Q53709796-bd207931-4621-b9a5-fb6b-8e08d7e1beae
LinkedIn personal profile ID	mike-shipman-5589b65
Scopus author ID	wds:Q53709796-6F487A6B-BAD5-4666-93DF-459FF26355B8
Scopus author ID	7005526197
given name	wds:Q53709796-3A47C94E-DD3D-4D26-8CEF-3B733EA93ABE
given name	Michael
instance of	wds:Q53709796-9DD268D9-A8EB-451B-861A-155CF952FAD7
instance of	Homo sapiens
skos:altLabel	Mike Shipman (en)
occupation	wds:Q53709796-8ED560DE-D574-4BA1-9114-80D630E38C20 wds:Q53709796-a79add42-475f-1f1e-55cd-73b58c223b65
sex or gender	wds:Q53709796-D5C2CF88-6572-4648-8362-F5B5A6902CE7
country of citizenship	wds:Q53709796-cf7e2509-49f8-217e-a461-1a23c1c11ff9
date of birth	wds:Q53709796-7940d821-40aa-f914-796d-3d770a175861
educated at	wds:Q53709796-d1e75932-4f97-043e-ffd3-3b9f03889f9c wds:Q53709796-f0d80c52-44ac-c35a-0d2e-1fa74470dc03
family name	wds:Q53709796-5F5472FD-EE07-4AD8-AD96-906FB61D725B
occupation	researcher organic chemist
sex or gender	male
country of citizenship	United Kingdom
date of birth	1967-01-01 00:00:00Z (xsd:dateTime)
educated at	Imperial College London
family name	Shipman
ORCID iD	wds:Q53709796-AB5630B1-2148-462F-89F2-39238CEE92FA
ORCID iD	https://orcid.org/0000-0002-3349-5594
ORCID iD	0000-0002-3349-5594
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q53709796
is author of	Palladium-catalyzed multicomponent synthesis of 2-aryl-2-imidazolines from aryl halides and diamines Tetrahydroxanthones by Sequential Pd-Catalyzed C−O and C−C Bond Construction and Use in the Identification of the “Antiausterity” Pharmacophore of the Kigamicins Multicomponent reactions involving 2-methyleneaziridines: rapid synthesis of 1,3-disubstituted propanones. Increased hyphal branching and growth of ectomycorrhizal fungus Lactarius rufus by the helper bacterium Paenibacillus sp Synthesis and structure of oxetane containing tripeptide motifs Study of boron–nitrogen dative bonds using azetidine inversion dynamics Synthesis of optically active arylaziridines by regio- and stereospecific lithiation of N-bus-phenylaziridine Stereocontrolled lithiation/trapping of chiral 2-alkylideneaziridines: investigation into the role of the aziridine nitrogen stereodynamics Delineating noncovalent interactions between the azinomycins and double-stranded DNA: importance of the naphthalene substitution pattern on interstrand cross-linking efficiency Divergent approach to imino sugar C-glycosides using imino glycals: application to the stereocontrolled synthesis of (+)-deoxoprosophylline Solid-Phase Synthesis of Oxetane Modified Peptides. Control of Pyramidal Inversion Rates by Redox Switching Asymmetric synthesis of 2-substituted oxetan-3-ones via metalated SAMP/RAMP hydrazones Synthesis and functionalization of 3-alkylidene-1,2-diazetidines using transition metal catalysis Enzymatically-stable oxetane-based dipeptide hydrogels. Chemical synthesis and cytotoxicity of some azinomycin analogues devoid of the 1-azabicyclo[3.1.0]hexane subunit Rapid synthesis of 1,3,4,4-tetrasubstituted beta-lactams from methyleneaziridines using a four-component reaction Four-component reaction for the preparation of alpha-amino phosphonates from methyleneaziridines Functionalization of Alkenes through Telescoped Continuous Flow Aziridination Processes Nitrogen Stereodynamics and Complexation Phenomena as Key Factors in the Deprotonative Dynamic Resolution of Alkylideneaziridines: A Spectroscopic and Computational Study. Development of oxetane modified building blocks for peptide synthesis Ring closing metathesis reactions of α-methylene-β-lactams: application to the synthesis of a simplified phyllostictine analogue with herbicidal activity A Lewis acid catalyzed intramolecular [4+3] cycloaddition route to polycyclic systems that contain a seven-membered ring Lewis acid promoted intramolecular (3 + 2) 'cycloadditions' of methyleneaziridines with alkene and alkyne acceptors Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes Azinomycin inspired bisepoxides: influence of linker structure on in vitro cytotoxicity and DNA interstrand cross-linking. Impact of oxetane incorporation on the structure and stability of alpha-helical peptides Rare example of nucleophilic substitution at vinylic carbon with inversion: mechanism of methyleneaziridine formation by sodium amide induced ring closure revisited. Absolute Differential Positronium-Formation Cross Sections Macrocyclisation of small peptides enabled by oxetane incorporation Solid-phase, multicomponent reactions of methyleneaziridines: synthesis of 1,3-disubstituted propanones Synthesis of 4,5-Diazaspiro[2.3]hexanes and 1,2-Diazaspiro[3.3]heptanes as Hexahydropyridazine Analogues. Intramolecular radical rearrangement reactions of 2-methyleneaziridines: application to the synthesis of substituted piperidines, decahydroquinolines, and octahydroindolizines Chemo- and enantioselective Rh-catalysed hydrogenation of 3-methylene-1,2-diazetidines: application to vicinal diamine synthesis Asymmetric Synthesis of 2-Substituted Azetidin-3-ones via Metalated SAMP/RAMP Hydrazones Iterative Arylation of Itaconimides with Diazonium Salts through Electrophilic Palladium Catalysis: Divergent β-H-Elimination Pathways in Repetitive Matsuda-Heck Reactions Studies Toward the Synthesis of Luminacin D: Assembly of Simplified Analogues Devoid of the Epoxide Displaying Antiangiogenic Activity Regio- and Stereocontrolled Synthesis of 3-Substituted 1,2-Diazetidines by Asymmetric Allylic Amination of Vinyl Epoxide. Readily accessible sp3-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality Rapid generation of molecular complexity using "hybrid" multi-component reactions (MCRs): application to the synthesis of alpha-amino nitriles and 1,2-diamines. Aziridine Scaffolds for the Detection and Quantification of Hydrogen-Bonding Interactions through Transition-State Stabilization
is author of	wds:Q57948680-67710E7F-B9F6-4786-B154-F8638AA30D2A wds:Q61823284-FF7D3060-4A1E-405C-ACFF-D2A2BF45AD74 wds:Q82989154-99909AC7-85EF-4BF6-899E-458E0BF601F0

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