Daniel Holmes

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2002-2004 Chemistry Michigan State University, East Lansing, MI 
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"Daniel Holmes"
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Yousefi R, Sarkar A, Ashtekar K, et al. (2020) Mechanistic Insights into the Origin of Stereoselectivity in an Asymmetric Chlorolactonization Catalyzed by (DHQD)PHAL. Journal of the American Chemical Society
Kakeshpour T, Bailey JP, Jenner MR, et al. (2017) High-Field NMR Spectroscopy Reveals Aromaticity-Modulated Hydrogen Bonding (AMHB) in Heterocycles. Angewandte Chemie (International Ed. in English)
Peyvandi A, Harsini I, Holmes D, et al. (2016) Characterization of ASR in concrete by 29Si MAS NMR spectroscopy Journal of Materials in Civil Engineering. 28
Ellsworth AA, Magyar CL, Hubbell GE, et al. (2016) One-pot triflic anhydride-mediated synthesis of 1,2-disubstituted 2-imidazolines from N-(2-haloethyl)amides and amines Tetrahedron. 72: 6380-6389
Ghaffari B, Vanchura BA, Chotana GA, et al. (2015) Reversible Borylene Formation from Ring Opening of Pinacolborane and Other Intermediates Generated from Five-Coordinate Tris-Boryl Complexes: Implications for Catalytic C-H Borylation. Organometallics. 34: 4732-4740
Peyvandi A, Holmes D, Soroushian P, et al. (2015) Fundamental assessment of graphite nanoplatelet effects on progress of alkali-silica reactions Aci Materials Journal. 112: 673-680
Ghaffari B, Vanchura BA, Chotana GA, et al. (2015) Reversible Borylene Formation from Ring Opening of Pinacolborane and Other Intermediates Generated from Five-Coordinate Tris-Boryl Complexes: Implications for Catalytic C-H Borylation Organometallics. 34: 4732-4740
Ghosh B, Amado-Sierra Mdel R, Holmes D, et al. (2014) A one-pot allylation-hydrostannation sequence with recycling of the intermediate tin waste. Organic Letters. 16: 2318-21
Schoen BW, Holmes D, Lee A. (2013) Identification and quantification of cis and trans isomers in aminophenyl double-decker silsesquioxanes using 1H-29Si gHMBC NMR. Magnetic Resonance in Chemistry : Mrc. 51: 490-6
Kulshrestha A, Schomaker JM, Holmes D, et al. (2011) Selectivity in the addition reactions of organometallic reagents to aziridine-2-carboxaldehydes: the effects of protecting groups and substitution patterns. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 12326-39
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