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Andrew B. Holmes
Researcher at University of Melbourne
Publications - 547
Citations - 43432
Andrew B. Holmes is an academic researcher from University of Melbourne. The author has contributed to research in topics: Polymer & Supercritical carbon dioxide. The author has an hindex of 75, co-authored 524 publications receiving 42062 citations. Previous affiliations of Andrew B. Holmes include University of Washington & Clare College.
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Biological clues to an enigmatic treatment for traumatic stress
TL;DR: A study in mice offers potential clues into the biological basis of a treatment called eye-movement desensitization and reprocessing that alleviates post-traumatic stress disorder through enigmatic mechanisms.
Cyano-derivatives of poly(p-phenylene vinylene) for use in thin-film light-emitting-diodes
Neil C. Greenham,Franco Cacialli,Donal D. C. Bradley,Richard H. Friend,Stephen C. Moratti,Andrew B. Holmes +5 more
TL;DR: In this paper, a conjugated polymer with high electron affinity, a cyano derivative of poly (p-phenylene vinylene), was proposed for use as the electron transporting layer in heterostructure LEDs.
Journal ArticleDOI
Spirocyclic synthesis by [4+2]-cycloaddition: the preparation of 11,13-dioxa-1,4-dithia-12, 12,18-trimethyl-10, 14, 17-trioxotrispiro[4.2.0.5.4.2]eicosane
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Synthesis of 4,4-disubstituted cyclohexenones by the Baeyer–Villiger fragmentation of 1-methoxybicyclo[2.2.2]oct-5-enones
Nigel C. Madge,Andrew B. Holmes +1 more
TL;DR: The peracetic acid oxidation of various 1-methoxybicyclo[2.2]oct-5-enones, prepared by hydrolysis of the adducts derived from dihydroanisole derivatives and α-chloroacrylonitrile, leads to 4-substituted cyclohex-2-en-1-one 4-ACetic acid derivatives as discussed by the authors.
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Synthesis of 4,4-disubstituted cyclohexenones. Part 2. Cycloaddition of 2-chloroacrylonitrile to 5-substituted 1,3-dimethoxycyclohexa-1,4-dienes
TL;DR: The cycloaddition of 2-chloroacrylonitrile to 1,3-dimethoxycyclohexadienes (3; R1= OMe, R2= H), derived by in situ conjugation of the Birch reduction products (12) produced from aromatic precursors (11) gave after acid work-up mainly bicyclo[2.2]octanone derivatives (5) and rearranged products(13).