2 Mechanistic Aspects of Carbon—Boron Bond Formation
Buch
Herausgeber: Fernández, E.
Titel: Advances in Organoboron Chemistry towards Organic Synthesis
Print ISBN: 9783132429710; Online ISBN: 9783132429758; Buch-DOI: 10.1055/b-006-164898
1st edition © 2020. Thieme. All rights reserved.
Georg Thieme Verlag KG, Stuttgart
Fachgebiete: Organische Chemie;Chemische Reaktionen, Katalyse;Organometallchemie;Chemische Labormethoden, Stöchiometrie
Science of Synthesis Reference Libraries
Übergeordnete Publikation
Titel: Science of Synthesis
DOI: 10.1055/b-00000101
Reihenherausgeber: Fürstner, A. (Editor-in-Chief); Carreira, E. M.; Faul, M.; Kobayashi, S.; Koch, G.; Molander, G. A.; Nevado, C.; Trost, B. M.; You, S.-L.
Typ: Mehrbändiges Werk
Abstract
Mechanisms for the selective formation of carbon–boron bonds under mild reaction conditions can be better understood with the help of computational studies, either alone or in collaboration with experimental research. There is a diversity of reaction mechanisms, many of which can be effectively characterized with currently available techniques.
Schlüsselwörter
carbon–boron bonds - hydroboration - borylation - nucleophilic substitution - electrophilic substitution - Lewis base catalysts - computational studies- 6 Pietsch S, Neeve EC, Apperley DC, Bertermann R, Mo F, Qiu D, Cheung MS, Dang L, Wang J, Radius U, Lin Z, Kleeberg C, Marder TB. Chem.–Eur. J. 2015; 21: 7082
- 8 Huang X, Lin Z, In: Computational Modeling of Homogeneous Catalysis Maseras F, Lledós A. Springer Boston 2002; 189
- 25 Verma A, Snead RF, Dai Y, Slebodnick C, Yang Y, Yu H, Yao F, Santos WL. Angew. Chem. Int. Ed. 2017; 56: 5111
- 27 García-López D, Civit MG, Vogels CM, Ricart JM, Westcott SA, Fernández E, Carbó JJ. Catal. Sci. Technol. 2018; 8: 3617
- 30 Hata T, Kitagawa H, Masai H, Kurahashi T, Shimizu M, Hiyama T. Angew. Chem. Int. Ed. 2001; 40: 790
- 35 García L, Sendra J, Miralles N, Reyes E, Carbó JJ, Vicario JL, Fernández E. Chem.–Eur. J. 2018; 24: 14059
- 37 Wu H, Garcia JM, Haeffner F, Radomkit S, Zhugralin AR, Hoveyda AH. J. Am. Chem. Soc. 2015; 137: 10585
- 48 Geier SJ, LaFortune JHW, Zhu D, Kosnik SC, Macdonald CLB, Stephan DW, Westcott SA. Dalton Trans. 2017; 46: 10876
- 50 Daley EN, Vogels CM, Geier SJ, Decken A, Doherty S, Westcott SA. Angew. Chem. Int. Ed. 2015; 54: 2121
- 52 Civit MG, Sanz X, Vogels CM, Webb JD, Geier SJ, Decken A, Bo C, Westcott SA, Fernández E. J. Org. Chem. 2015; 80: 2148
- 53 Sanz X, Vogels CM, Decken A, Bo C, Westcott SA, Fernández E. Chem. Commun. (Cambridge) 2014; 50: 8420
- 60 Royes J, Ni S, Farré A, La Cascia E, Carbó JJ, Cuenca AB, Maseras F, Fernández E. ACS Catal. 2018; 8: 2833
- 67 Isegawa M, Sameera WMC, Sharma AK, Kitanosono T, Kato M, Kobayashi S, Morokuma K. ACS Catal. 2017; 7: 5370
- 77 Ansell MB, Menezes da Silva VH, Heerdt G, Braga AAC, Spencer J, Navarro O. Catal. Sci. Technol. 2016; 6: 7461
- 78 Lillo V, Mas-Marzá E, Segarra AM, Carbó JJ, Bo C, Peris E, Fernández E. Chem. Commun. (Cambridge) 2007; 3380
- 81 Lillo V, Fructos MR, Ramírez J, Braga AAC, Maseras F, Díaz-Requejo MM, Pérez PJ, Fernández E. Chem.–Eur. J. 2007; 13: 2614
- 88 Vanchura II BA, Preshlock SM, Roosen PC, Kallepalli VA, Staples RJ, Maleczka Jr RE, Singleton DA, Smith III MR. Chem. Commun. (Cambridge) 2010; 46: 7724
- 89 Roosen PC, Kallepalli VA, Chattopadhyay B, Singleton DA, Maleczka Jr RE, Smith III MR. J. Am. Chem. Soc. 2012; 134: 11350
- 92 Bai H, Xu H, Zhang H, Guo Y, Shan J, Wei D, Zhu Y, Zhang S, Zhang W. Catal. Sci. Technol. 2018; 8: 5165
- 96 Hartwig JF, Cook KS, Hapke M, Incarvito CD, Fan Y, Webster CE, Hall MB. J. Am. Chem. Soc. 2005; 127: 2538