Relevant bibliographies by topics / Organoboron

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Organoboron'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 February 2022

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Journal articles on the topic "Organoboron"

1

Wang, Honggen, Yao-Fu Zeng, Wen-Xin Lv, and Dong-Hang Tan. "Synthetic Transformations of Alkenyl MIDA Boronates toward the Efficient Construction of Organoborons." Synlett 29, no. 11 (2018): 1415–20. http://dx.doi.org/10.1055/s-0036-1591958.

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The attachment of N-methyliminodiacetyl boron (MIDA boron) to alkenes leads to a new type of activated alkenes. Synthetic manipulation of the alkene double bond while retaining the boron moiety offers an unprecedented opportunity for the construction of organoborons. These reactions feature unique reactivity, good regioselectivity, and they can be used to access organoborons that are historically difficult to prepare. Herein, we give a brief summary of advances in the use of alkenyl MIDA boronates as starting materials for organoboron synthesis. Mechanisms are discussed where relevant.
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Maiti, Debabrata, Sumon Basak, and Jyoti Prasad Biswas. "Transition-Metal-Catalyzed C–H Arylation Using Organoboron Reagents." Synthesis 53, no. 18 (2021): 3151–79. http://dx.doi.org/10.1055/a-1485-4666.

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AbstractAryl rings are ubiquitous in the core of numerous natural product and industrially important molecules and thus their facile synthesis is of major interest in the scientific community and industry. Although multiple strategies enable access to these skeletons, metal-catalyzed C–H activation is promising due to its remarkable efficiency. Commercially available organoboron reagents, a prominent arylating partner in the cross-coupling domain, have also been utilized for direct arylation. Organoborons are bench-stable, inexpensive, and readily available coupling partners that promise regio
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Brown, Charles, R. Harry Cragg, Tim J. Miller, and David O'N Smith. "Organoboron compounds." Journal of Organometallic Chemistry 342, no. 2 (1988): 153–57. http://dx.doi.org/10.1016/s0022-328x(00)99452-x.

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Cragg, R. Harry, and Manije Nazery. "Organoboron compounds." Journal of Organometallic Chemistry 303, no. 3 (1986): 329–35. http://dx.doi.org/10.1016/0022-328x(86)82034-4.

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Bubnov, Yu N., A. I. Grandberg, M. Sh Grigorian, V. G. Kiselev, M. I. Struchkova, and B. M. Mikhailov. "Organoboron compounds." Journal of Organometallic Chemistry 292, no. 1-2 (1985): 93–104. http://dx.doi.org/10.1016/0022-328x(85)87325-3.

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Cragg, R. Harry, and Tim J. Miller. "Organoboron compounds." Journal of Organometallic Chemistry 294, no. 1 (1985): 1–6. http://dx.doi.org/10.1016/0022-328x(85)88048-7.

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Cragg, R. Harry, Tim J. Miller, and David O'N Smith. "Organoboron compounds." Journal of Organometallic Chemistry 302, no. 1 (1986): 19–21. http://dx.doi.org/10.1016/0022-328x(86)80058-4.

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Cragg, R. Harry, Tim J. Miller, and David O'N Smith. "Organoboron compounds." Journal of Organometallic Chemistry 291, no. 3 (1985): 273–75. http://dx.doi.org/10.1016/0022-328x(85)80179-0.

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Boldyreva, O. G., V. A. Dorokhov, and B. M. Mikhailov. "Organoboron compounds." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 34, no. 2 (1985): 390–92. http://dx.doi.org/10.1007/bf00951292.

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Dorokhov, V. A., O. G. Boldyreva, B. M. Mikhailov, Z. A. Starikova, and I. A. Teslya. "Organoboron compounds." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 34, no. 2 (1985): 393–97. http://dx.doi.org/10.1007/bf00951293.

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Dissertations / Theses on the topic "Organoboron"

1

La, Cascia Enrico. "Selective polyfunctional synthesis through organoboron compounds." Doctoral thesis, Universitat Rovira i Virgili, 2016. http://hdl.handle.net/10803/398028.

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La primera part d’aquesta tesi aborda el tema de la b-boració d’iminas α,β-insaturades per la síntesi de γ-amino alcohols. Es descriu un nou mètode basat en la organocatàlisi, evitand la ultilizació de metalls de transició com catalizadors. En aquest cas el reactiu bis(pinacolat)diboron s’activa amb una base i MeOH generand in situ un bor nucleòfil que interacciona amb el doble enllaç d’imines α,β-insaturades, com sustrat acceptor. La ultilizació de fosfina és necessaria per activar el sustrat. En el cas de que la fosfina és (S)-MeBoPhoz la β-boración es produeix de forma enantioselectiva amb
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Hood, David Kent. "The Investigation of Organoboron Compounds and Organoboron/Nitrone Reactions." W&M ScholarWorks, 1991. https://scholarworks.wm.edu/etd/1539625664.

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Norbury, A. M. "Novel organoboron chemistry." Thesis, Swansea University, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.638337.

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The first part of the thesis deals with an investigation into some aspects of the chemistry of di-(2,4,6-triisopropylphenyl)boranes, a novel class of highly hindered organoborones. Chapter one investigates the synthesis of such compounds and discusses the formation of organoboranes in general. Chapter two discusses the chemistry of carbanions, especially those stabilized by an adjacent boron atom. The results of a study of the lithiation of ditripylboranes are reported. It is shown that the compounds are readily lithiated by unhindered bases. Chapters three, four and five report some of the re
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Molla, E. "Some sterically hindered organoboron complexes." Thesis, University of Sussex, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.381590.

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Molloy, John James. "Chemoselective reactions of organoboron compounds." Thesis, University of Strathclyde, 2018. http://digitool.lib.strath.ac.uk:80/R/?func=dbin-jump-full&object_id=29485.

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The Suzuki-Miyaura reaction is a landmark discovery which has revolutionised the field of palladium catalysis. Since its inception, reaction development has not only progressed the range of electrophiles which can be adopted in this transformation but has significantly enhanced the scope of organoboron reagents which can be used, cementing the reaction as the most favoured method for C-C bond formation. Despite these advances, investigation around this key transformation is continuous. A key highlight of this reaction, which is desirable to the synthetic community, is the chemoselectivity show
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Entwistle, Christopher Donald. "Conjugated organic and organoboron materials." Thesis, Durham University, 2005. http://etheses.dur.ac.uk/3932/.

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A series of compounds containing one or more dimesitylboryl groups (mesityl = 2,4,6-trimethylphenyl) has been synthesised. Triarylboranes were synthesised by reaction of dimesitylfluoroborane with an appropriate lithium reagent. Dimesitylvinyl boranes were synthesised by the hydroboration of an appropriate terminal alkyne with dimesitylborane. Compounds were characterised by standard analytical techniques, and investigated by single crystal X-ray diffraction, optical, thermal and electrochemical methods. The aim of the research was to determine whether such compounds might be useful in the fie
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Kim, Byeongmoon 1957. "Asymmetric organic synthesis using organoboron compounds." Thesis, Massachusetts Institute of Technology, 1987. http://hdl.handle.net/1721.1/14679.

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Nagata, Yuuya. "Synthesis of novel luminescent organoboron polymers." 京都大学 (Kyoto University), 2008. http://hdl.handle.net/2433/136307.

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Matsumoto, Fukashi. "Synthesis and functionalization of novel organoboron polymers." 京都大学 (Kyoto University), 2005. http://hdl.handle.net/2433/144938.

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Kyoto University (京都大学)<br>0048<br>新制・課程博士<br>博士(工学)<br>甲第11594号<br>工博第2540号<br>新制||工||1346(附属図書館)<br>23237<br>UT51-2005-D343<br>京都大学大学院工学研究科高分子化学専攻<br>(主査)教授 中條 善樹, 教授 増田 俊夫, 教授 檜山 爲次郎<br>学位規則第4条第1項該当
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Hou, D. "Functionalisation of polystyrene using organolithium and organoboron reagents." Thesis, Swansea University, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.637310.

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The thesis deals with the synthesis and applications of two different types of polystyrene-supported sulfonic acids and bis-(2,4,6, -triisopropylphenyl)boranes (abbreviated to ditripylboranes). Some new methods have been developed by using organolithium reagents. <B>Chapter 1</B> outlines the research project. <B>Chapter 2</B> introduces the synthesis and applications of polymer-supported catalysts and reagents. <B>Chapter 3</B> gives a brief review of the preparation of organolithium reagents and intermediates. <B>Chapter 4</B> discusses the preparation of benzyllithiums in general and report
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Books on the topic "Organoboron"

1

Fernández, Elena, and Andrew Whiting, eds. Synthesis and Application of Organoboron Compounds. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-13054-5.

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Grimes, Russell N. Carboranes. 2nd ed. Academic Press, 2011.

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Kubota, Koji. Synthesis of Functionalized Organoboron Compounds Through Copper(I) Catalysis. Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-4935-4.

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Mennekes, Theodor. Zur Reduktion von Dihalogenorganylboranen mit Alkalimetallen. Verlag Shaker, 1992.

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Otrzymywanie i niektóre reakcje chemiczne tetraalkilodiboroksanów. Wydawnictwa Politechniki Warszawskiej, 1989.

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Sporzyński, Andrzej. Właściwości i niektóre reakcje chemiczne trialkilo- i triaryloboroksynów. Wydawnictwa Politechniki Warszawskiej, 1993.

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Weinig, Peter. Chirale Organoborreagenzien als Katalysatoren für enantioselektive C-C-Verknüpfungen. Intemann, 1989.

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Grenʹ, A. I. Khimii͡a︡ t͡s︡iklicheskikh ėfirov bornykh kislot. Nauk. dumka, 1988.

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Organic synthesis: The roles of boron and silicon. Oxford University Press, 1991.

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Pelter, Andrew. Borane reagents. Academic Press, 1988.

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Book chapters on the topic "Organoboron"

1

Nagata, Yuuya, and Yoshiki Chujo. "Organoboron Polymers." In Macromolecules Containing Metal and Metal-Like Elements. John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/9780470139653.ch4.

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Tanaka, Kazuo. "Organoboron Polymers." In Encyclopedia of Polymeric Nanomaterials. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-29648-2_142.

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Miyaura, Norio. "Organoboron Compounds." In Topics in Current Chemistry. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-45313-x_2.

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Tanaka, Kazuo. "Organoboron Polymers." In Encyclopedia of Polymeric Nanomaterials. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-36199-9_142-1.

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Smith, Keith. "Organoboron Chemistry." In Organometallics in Synthesis. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118750407.ch6.

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Smith, Keith. "Organoboron Chemistry." In Organometallics in Synthesis: A Manual. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118750421.ch3.

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Mellerup, Soren K., and Suning Wang. "Photoresponsive Organoboron Systems." In Main Group Strategies towards Functional Hybrid Materials. John Wiley & Sons, Ltd, 2018. http://dx.doi.org/10.1002/9781119235941.ch3.

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Nagai, Atsushi, and Yoshiki Chujo. "Organoboron Conjugated Polymers." In Conjugated Polymer Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527632664.ch7.

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Petasis, Nicos A. "Multicomponent Reactions with Organoboron Compounds." In Multicomponent Reactions. Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527605118.ch7.

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Marqués-López, Eugenia, and Raquel P. Herrera. "Multicomponent Reactions with Organoboron Compounds." In Multicomponent Reactions. John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118863992.ch4.

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Conference papers on the topic "Organoboron"

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Jaekle, Frieder, and Yang Qin. "Tuning of the Emission of Organoboron Quinolate Polymers." In Organic Photonics and Electronics. OSA, 2006. http://dx.doi.org/10.1364/ope.2006.optua5.

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Brondani, Patrícia B., Gonzalo de Gonzalo, Marco W. Fraaije, and Leandro H. Andrade. "Selective oxidations of organoboron compounds catalyzed by Baeyer-Villiger monooxygenases." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0097-2.

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Janczyk, Martyna, Wojciech Wróblewski, Agnieszka Adamczyk-Wózniak, and Andrzej Sporzynski. "P2.1.11 Fluoride sensing by polymeric membranes based on organoboron Lewis acid receptors." In 14th International Meeting on Chemical Sensors - IMCS 2012. AMA Service GmbH, Von-Münchhausen-Str. 49, 31515 Wunstorf, Germany, 2012. http://dx.doi.org/10.5162/imcs2012/p2.1.11.

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