 Boranes
"Boranes" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The collective name for the boron hydrides, which are analogous to the alkanes and silanes. Numerous boranes are known. Some have high calorific values and are used in high-energy fuels. (From Grant & Hackh's Chemical Dictionary, 5th ed)
| Descriptor ID |
D001880
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| MeSH Number(s) |
D01.132.105 D02.203.087
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| Concept/Terms |
Boranes- Boranes
- Boron Hydrides
- Hydrides, Boron
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Below are MeSH descriptors whose meaning is more general than "Boranes".
Below are MeSH descriptors whose meaning is more specific than "Boranes".
This graph shows the total number of publications written about "Boranes" by people in this website by year, and whether "Boranes" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2006 | 1 | 0 | 1 | | 2011 | 0 | 1 | 1 | | 2013 | 1 | 0 | 1 | | 2015 | 1 | 0 | 1 | | 2017 | 1 | 0 | 1 | | 2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Boranes" by people in Profiles.
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Kumar P, Caruthers MH. DNA Analogues Modified at the Nonlinking Positions of Phosphorus. Acc Chem Res. 2020 10 20; 53(10):2152-2166.
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Niyonsaba E, Easton MW, Feng E, Yu Z, Zhang Z, Sheng H, Kong J, Easterling LF, Milton J, Chobanian HR, Deprez NR, Cancilla MT, Kilaz G, Kentt?maa HI. Differentiation of Deprotonated Acyl-, N-, and O-Glucuronide Drug Metabolites by Using Tandem Mass Spectrometry Based on Gas-Phase Ion-Molecule Reactions Followed by Collision-Activated Dissociation. Anal Chem. 2019 09 03; 91(17):11388-11396.
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Roy S, Paul S, Roy M, Kundu R, Monfregola L, Caruthers MH. Pyridinium Boranephosphonate Modified DNA Oligonucleotides. J Org Chem. 2017 02 03; 82(3):1420-1427.
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Jiang H, Bansal A, Pandey MK, Peng KW, Suksanpaisan L, Russell SJ, DeGrado TR. Synthesis of 18F-Tetrafluoroborate via Radiofluorination of Boron Trifluoride and Evaluation in a Murine C6-Glioma Tumor Model. J Nucl Med. 2016 09; 57(9):1454-9.
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Russell C, Roy S, Ganguly S, Qian X, Caruthers MH, Nilsson M. Formation of Silver Nanostructures by Rolling Circle Amplification Using Boranephosphonate-Modified Nucleotides. Anal Chem. 2015 Jul 07; 87(13):6660-6.
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Roy S, Olesiak M, Shang S, Caruthers MH. Silver nanoassemblies constructed from boranephosphonate DNA. J Am Chem Soc. 2013 Apr 24; 135(16):6234-41.
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Prokop A, Vacek J, Michl J. Friction in carborane-based molecular rotors driven by gas flow or electric field: classical molecular dynamics. ACS Nano. 2012 Mar 27; 6(3):1901-14.
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Krishna H, Caruthers MH. Solid-phase synthesis, thermal denaturation studies, nuclease resistance, and cellular uptake of (oligodeoxyribonucleoside)methylborane phosphine-DNA chimeras. J Am Chem Soc. 2011 Jun 29; 133(25):9844-54.
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Zimmerman PM, Zhang Z, Musgrave CB. Simultaneous two-hydrogen transfer as a mechanism for efficient CO(2) reduction. Inorg Chem. 2010 Oct 04; 49(19):8724-8.
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McCuen HB, No? MS, Sierzchala AB, Higson AP, Caruthers MH. Synthesis of mixed sequence borane phosphonate DNA. J Am Chem Soc. 2006 Jun 28; 128(25):8138-9.
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