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Photochemical Functionalization of Cubanes

https://doi.org/10.1021/jo00108a037
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inferred← citeshttps://doi.org/10.2139/ssrn.4837417openalex-extracted
Synthesis and Characterization of a New Cage-Like Energetic Compound 9-Nitro-3,7-Dinitrato-9-Azanoradamantane
inferred← citeshttps://doi.org/10.1002/(sici)1097-461x(2000)76:3<434::aid-qua12>3.0.co;2-wopenalex-snapshot
Cubic fuels?
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(20000117)112:2<422::aid-ange422>3.0.co;2-2openalex-snapshot
Hepta- und Octanitrocubane
inferred← citeshttps://doi.org/10.1002/1521-4087(200203)27:1<1::aid-prep1>3.0.co;2-6openalex-snapshot
Octanitrocubane: A New Nitrocarbon
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0333openalex-snapshot
Chemistry of Cubane and Other Prismanes
inferred← citeshttps://doi.org/10.1002/9781118662083.cot09-003openalex-snapshot
Formation of Nitriles, Carboxylic Acids, and Derivatives by Carbonylation, Carboxylation, and Related Reactions
inferred← citeshttps://doi.org/10.1002/ejoc.202401055openalex-snapshot
Strategy for C−H Functionalization of Cubanes: From Stoichiometric Reaction to Catalytic Methodology
inferred← citeshttps://doi.org/10.1002/hlca.202300200openalex-snapshot
Functionalization of Cubane Formation of C−C and C−Heteroatom Bonds
inferred← citeshttps://doi.org/10.1002/poc.404openalex-snapshot
Theoretical studies on heats of formation for polynitrocubanes using the density functional theory B3LYP method and semiempirical MO methods
inferred← citeshttps://doi.org/10.1002/tcr.201500234openalex-snapshot
Systematic Enumeration and Symmetries of Cubane Derivatives
inferred← citeshttps://doi.org/10.1007/bf01665815openalex-snapshot
Distortions in nitramine substituted cubanes: The structures of N,N′-dinitro-1,4-diaminocubane, N,N′-dinitro-N,N′-(2-pyridyl)-1,4-diaminocubane, and 1,2,4,7-tetrakis(N-methoxycarbonylnitramino)cubane
inferred← citeshttps://doi.org/10.1007/s10573-005-0031-1openalex-snapshot
Novel Ultrahigh-Energy Materials
inferred← citeshttps://doi.org/10.1016/j.enmf.2024.06.005openalex-snapshot
Synthesis and characterization of a new cage-like energetic compound 3,7-dinitrato-9-nitro-9-azanoradamantane
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.01.037openalex-snapshot
Preparation of ‘cage molecule’ based polyazido core units for dendrimer synthesis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.02.161openalex-snapshot
Thermo-cage opening of 4-iodo-1-vinylcubane to a novel styrene derivative
inferred← citeshttps://doi.org/10.1016/s0040-4039(97)10185-xopenalex-snapshot
Norcubanes from cubanes novel reaction of amidocubanes with oxalyl chloride
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.8b00888openalex-snapshot
Cubanes in Medicinal Chemistry
inferred← citeshttps://doi.org/10.1021/acs.oprd.5c00479openalex-snapshot
Convenient Access to Trisubstituted Cubanes and Nitrated Derivatives
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01702openalex-snapshot
Synthesis of Ortho-Functionalized 1,4-Cubanedicarboxylate Derivatives through Photochemical Chlorocarbonylation
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03144openalex-snapshot
ortho-C–H Acetoxylation of Cubane Enabling Access to Cubane Analogues of Pharmaceutically Relevant Scaffolds
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c04019openalex-snapshot
C–H Alkylation of Cubanes via Catalytic Generation of Cubyl Radicals
inferred← citeshttps://doi.org/10.1021/cr300246popenalex-snapshot
Surface Chemoselective Phototransformation of C–H Bonds on Organic Polymeric Materials and Related High-Tech Applications
inferred← citeshttps://doi.org/10.1021/ja970552qopenalex-snapshot
Synthesis and Chemistry of 1,3,5,7-Tetranitrocubane Including Measurement of Its Acidity, Formation of o-Nitro Anions, and the First Preparations of Pentanitrocubane and Hexanitrocubane1
inferred← citeshttps://doi.org/10.1021/ja980514mopenalex-snapshot
Electron Density Distribution in a 1,2-Difluorinated Cubane Derivative
inferred← citeshttps://doi.org/10.1021/ja981967uopenalex-snapshot
Cubanecarboxylic Acids. Crystal Engineering Considerations and the Role of C−H···O Hydrogen Bonds in Determining O−H···O Networks
inferred← citeshttps://doi.org/10.1021/jacs.2c10878openalex-snapshot
Mechanochemistry of Cubane
inferred← citeshttps://doi.org/10.1021/jacs.6c15216openalex-snapshot
Leveraging Cubenes to Access Highly Functionalized Fused Cubes
inferred← citeshttps://doi.org/10.1021/jo800927topenalex-snapshot
Formation of Cubane-like Photodimers from 2-Naphthalenecarbonitrile
inferred← citeshttps://doi.org/10.1021/jo981299vopenalex-snapshot
Photochemical Chlorocarbonylation of HCTD by Oxalyl Chloride. Carbocation-Mediated Rearrangement of HCTD Derivatives to Novel, Substituted Heptacyclopentadecanes
inferred← citeshttps://doi.org/10.1021/la020896gopenalex-snapshot
Photochemical Lithography: Creation of Patterned, Acid Chloride Functionalized Surfaces Using UV Light and Gas-Phase Oxalyl Chloride
inferred← citeshttps://doi.org/10.1021/la063532nopenalex-snapshot
Photochemical Grafting and Activation of Organic Layers on Glassy Carbon and Pyrolyzed Photoresist Films
inferred← citeshttps://doi.org/10.1021/ma961115jopenalex-snapshot
Novel Glass-Forming Organic Materials. 3. Cubane with Pendant Nematogens, Carbazole, and Disperse Red 1
inferred← citeshttps://doi.org/10.1039/c8ra06275gopenalex-snapshot
Photoinduced nucleophilic substitution of iodocubanes with arylthiolate and diphenylphosphanide ions. Experimental and computational approaches
inferred← citeshttps://doi.org/10.1039/c9ob01238aopenalex-snapshot
The cubane paradigm in bioactive molecule discovery: further scope, limitations and the cyclooctatetraene complement
inferred← citeshttps://doi.org/10.1039/d5cc07169kopenalex-snapshot
Photochemical HAT-mediated site-selective C(sp 3 )–H aminoalkylation of cubanes catalyzed by TBADT
inferred← citeshttps://doi.org/10.1055/a-2124-3823openalex-snapshot
Decoration on Cubane with an Awareness of Chirality: Development of Substituted Cubane Syntheses
inferred← citeshttps://doi.org/10.1055/a-2360-8218openalex-snapshot
Recent Progress in Accessing Multi-functionalized Caged Hydrocarbons: En Route to Highly Functionalized Saturated (Bio)isosteres of Benzene Rings
inferred← citeshttps://doi.org/10.1080/02678299608032880openalex-snapshot
Novel glass-forming liquid crystals. IV. Effects of central core and pendant group on vitrification and morphological stability
inferred← citeshttps://doi.org/10.1080/104265091001281openalex-snapshot
Trifluoromethylthiocubanes and (Trifluoromethylthio)cubylcubanes
inferred← citeshttps://doi.org/10.1080/17415990701684701openalex-snapshot
Derivatization of dicubyl disulfide
inferred← citeshttps://doi.org/10.1107/s1600536802012448openalex-snapshot
4,7-Dichlorotricyclo[3.1.1.03,6]heptane-2-carboxylic acid
inferred← citeshttps://doi.org/10.1246/cl.230101openalex-snapshot
Directed Metalation of 1-Cuneanecarboxamide: Simple Route to 1,2-Disubstituted Cuneanes
inferred← citeshttps://doi.org/10.26434/chemrxiv-2023-s8fkropenalex-snapshot
C–H Alkylation of Cubanes via Polar Effect-Assisted Photocatalytic Generation of Cubyl Radicals
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.83.615openalex-snapshot
Precise Synthetic Organic Chemistry of Cubanes and Cuneanes Aspiring to Medicinal Application
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