Synthesis of Fused B‐Containing Heterocyclic Compounds and Their Relevant Optical Properties
A series of fused 4,5‐borazaropyrrolo[1,2‐a]quinolines have been prepared from potassium organotrifluoroborates and substituted 1‐(2‐aminophenyl)pyrroles via direct formation of C–B and N–B bonds. The target products were obtained in moderate to high yields under mild conditions. The optical propert...
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Published in | European journal of organic chemistry Vol. 2018; no. 34; pp. 4812 - 4817 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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16.09.2018
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Abstract | A series of fused 4,5‐borazaropyrrolo[1,2‐a]quinolines have been prepared from potassium organotrifluoroborates and substituted 1‐(2‐aminophenyl)pyrroles via direct formation of C–B and N–B bonds. The target products were obtained in moderate to high yields under mild conditions. The optical properties of some products were investigated by UV/Vis spectroscopy and spectrofluorometry. Moreover, the influence of structural modification on the spectroscopic and electronic properties was studied by DFT calculations.
A new B‐containing heterocyclic compound! A series of azaborines were prepared through 1‐(2‐aminophenyl)pyrroles and organotrifluoroborates in a one‐pot reaction. The optical properties of these azaborines were investigated and the attractive photometrics could be applied in many scientific fields. |
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AbstractList | A series of fused 4,5‐borazaropyrrolo[1,2‐a]quinolines have been prepared from potassium organotrifluoroborates and substituted 1‐(2‐aminophenyl)pyrroles via direct formation of C–B and N–B bonds. The target products were obtained in moderate to high yields under mild conditions. The optical properties of some products were investigated by UV/Vis spectroscopy and spectrofluorometry. Moreover, the influence of structural modification on the spectroscopic and electronic properties was studied by DFT calculations. A series of fused 4,5‐borazaropyrrolo[1,2‐ a ]quinolines have been prepared from potassium organotrifluoroborates and substituted 1‐(2‐aminophenyl)pyrroles via direct formation of C–B and N–B bonds. The target products were obtained in moderate to high yields under mild conditions. The optical properties of some products were investigated by UV/Vis spectroscopy and spectrofluorometry. Moreover, the influence of structural modification on the spectroscopic and electronic properties was studied by DFT calculations. A series of fused 4,5‐borazaropyrrolo[1,2‐a]quinolines have been prepared from potassium organotrifluoroborates and substituted 1‐(2‐aminophenyl)pyrroles via direct formation of C–B and N–B bonds. The target products were obtained in moderate to high yields under mild conditions. The optical properties of some products were investigated by UV/Vis spectroscopy and spectrofluorometry. Moreover, the influence of structural modification on the spectroscopic and electronic properties was studied by DFT calculations. A new B‐containing heterocyclic compound! A series of azaborines were prepared through 1‐(2‐aminophenyl)pyrroles and organotrifluoroborates in a one‐pot reaction. The optical properties of these azaborines were investigated and the attractive photometrics could be applied in many scientific fields. |
Author | Yan, Rulong An, Zhenyu Qi, Zhenjie Yuan, Bingxiang Ni, Jixiang Kang, Jie Wu, Mingzhong |
Author_xml | – sequence: 1 givenname: Zhenyu surname: An fullname: An, Zhenyu organization: Lanzhou University – sequence: 2 givenname: Mingzhong surname: Wu fullname: Wu, Mingzhong organization: Lanzhou University – sequence: 3 givenname: Jie surname: Kang fullname: Kang, Jie organization: Lanzhou University – sequence: 4 givenname: Jixiang surname: Ni fullname: Ni, Jixiang organization: Lanzhou University – sequence: 5 givenname: Zhenjie surname: Qi fullname: Qi, Zhenjie organization: Lanzhou University – sequence: 6 givenname: Bingxiang surname: Yuan fullname: Yuan, Bingxiang organization: Lanzhou University – sequence: 7 givenname: Rulong orcidid: 0000-0002-0450-3065 surname: Yan fullname: Yan, Rulong email: yanrl@lzu.edu.cn organization: Lanzhou University |
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Cites_doi | 10.1021/ja063519p 10.1021/ol502708z 10.1021/ol025973d 10.1002/anie.200903390 10.1021/jo402616w 10.1002/chem.200304793 10.1002/anie.201208351 10.1002/zaac.200400333 10.1021/ol501495d 10.1021/acs.jmedchem.5b01088 10.1021/jo5029437 10.1021/acs.orglett.6b00335 10.1021/jo900053b 10.1021/acs.joc.6b02291 10.1021/cr0101454 10.1021/ol502339h 10.1021/acs.orglett.6b00466 10.1021/ol070328y 10.1021/acs.joc.6b02574 10.1021/cr0783840 10.1021/ol5030508 10.1021/ja5063899 10.1016/j.jorganchem.2012.09.018 10.1021/acs.joc.6b00435 10.1021/ol501362w 10.1002/anie.201304443 10.1021/ja205779b 10.1021/jo5011894 10.1002/ejoc.201500622 10.1021/acs.joc.5b02548 10.1002/anie.201200063 10.1021/jacs.5b00822 10.1002/anie.200453690 10.1016/j.tet.2011.03.095 10.1021/acs.joc.5b00981 10.1007/BF00671228 10.1002/ange.19850970527 10.1016/S0143-7208(00)00100-5 10.1021/ol0001113 10.1002/ange.201200063 10.1021/cr950066q 10.1039/jr9590002728 10.1002/anie.200390320 10.1002/ange.201304443 10.1002/anie.198504161 10.1002/ange.200390291 10.1002/ange.200453690 10.1021/ja01465a022 10.1002/ange.200903390 10.1002/ange.201208351 10.1021/ja01468a046 10.1021/ja01520a024 |
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Keywords | CORES Boron Synthesis design CROSS-COUPLINGS ACID 2,1-BORAZARONAPHTHALENES Optical properties HETEROAROMATIC-COMPOUNDS Fused-ring systems Functional organic materials |
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References | 1990; 1 2013 2013 2015 1996 2009 2009; 52 125 58 96 48 121 2009; 74 2003 2003 2006 2011 2016 2014 2014 2014 2016; 42 115 128 133 81 136 16 16 18 2017; 82 2001 2002 2016 2016; 48 102 81 18 2012 2012 2014; 51 124 16 2014 2014 1985 1985 2015 1961; 16 16 24 97 80 83 2014 2016 2013 2011 2003 2003 2003 1959 2015 1961; 79 81 723 67 42 115 9 81 137 83 2009 2007; 9 2014; 79 2004 2004 2002; 43 116 4 2015 2004 2000 2006 2015; 630 2 128 80 2009; 109 1959 2013 2013; 52 125 Rudebusch, G. E. (000444540900020.47) 2013; 125 Molander, GA (WOS:000339367300021) 2014; 16 Rudebusch, GE (WOS:000323393100056) 2013; 52 GLASER, B (WOS:A1985ALY3200018) 1985; 24 Wisniewski, SR (WOS:000329472900033) 2014; 79 Brown, AN (WOS:000337869800043) 2014; 16 HAWTHORNE, M (WOS:A19613066B00033) 1961; 83 Jaska, CA (WOS:000239791100054) 2006; 128 Wang, J (WOS:000391248800071) 2016; 81 Campbell, P. G. (000444540900020.6) 2012; 124 Knack, D. H. (000444540900020.31) 2013; 125 Davies, GHM (WOS:000375890100034) 2016; 81 Paetzold, P (WOS:000226201400012) 2004; 630 Giambiagi, M (WOS:000208827100003) 1990; 1 Chrostowska, A (WOS:000340737900038) 2014; 136 DEWAR, MJ (WOS:A19613069B00019) 1961; 83 Jouffroy, M (WOS:000373519600028) 2016; 18 Abbey, ER (WOS:000293872800029) 2011; 133 Bosdet, MJD (WOS:000245084300056) 2007; 9 Liu, L. (000444540900020.34) 2009; 121 Liu, LJ (WOS:000269937200008) 2009; 48 Sameiro, M (WOS:000262482500006) 2009; 109 Kim, BJ (WOS:000222067400014) 2004; 43 Campbell, PG (WOS:000305180400006) 2012; 51 Molander, GA (WOS:000339368300027) 2014; 79 Emslie, D. J. H. (000444540900020.16) 2003; 115 Molander, GA (WOS:000344635200033) 2014; 16 Slabber, CA (WOS:000311680100018) 2013; 723 Chai, DI (WOS:000265073700017) 2009; 74 Goldberg, AR (WOS:000369771600023) 2016; 81 Kim, B. J. (000444540900020.28) 2004; 116 Claessens, CG (WOS:000174456500009) 2002; 102 NYILAS, E (WOS:A1959WB36200024) 1959; 81 Molander, GA (WOS:000345470000051) 2014; 16 Hadebe, SW (WOS:000291371900019) 2011; 67 Matteson, DS (WOS:000176354700010) 2002; 4 Sun, FY (WOS:000342719500015) 2014; 16 Kaupp, G (WOS:000185294800015) 2003; 9 Qiu, F (WOS:000372664600046) 2016; 18 Liu, XW (WOS:000353315000001) 2015; 80 Casado, MRS (WOS:000359295800021) 2015; 2015 Knack, DH (WOS:000315209900043) 2013; 52 DEWAR, MJS (WOS:A1959WK68900018) 1959 Noda, H (WOS:000351972000038) 2015; 137 Rombouts, FJR (WOS:000366340000015) 2015; 58 Ashe, AJ (WOS:000088039800028) 2000; 2 Glaser, B. (000444540900020.20) 1985; 97 Frisch, M. J. (000444540900020.18) 2009 Emslie, DJH (WOS:000181872300005) 2003; 42 Patani, GA (WOS:A1996VZ38400005) 1996; 96 Davies, GHM (WOS:000391781900052) 2017; 82 Chen, PL (WOS:000166846300002) 2001; 48 Molander, GA (WOS:000360103000001) 2015; 80 e_1_2_6_19_1 e_1_2_6_13_1 e_1_2_6_13_2 e_1_2_6_11_1 e_1_2_6_11_2 e_1_2_6_15_3 e_1_2_6_17_1 e_1_2_6_13_3 e_1_2_6_15_1 e_1_2_6_13_4 e_1_2_6_15_2 e_1_2_6_9_9 e_1_2_6_9_8 e_1_2_6_9_5 e_1_2_6_9_4 e_1_2_6_9_10 e_1_2_6_9_7 e_1_2_6_9_6 e_1_2_6_3_7 e_1_2_6_7_3 e_1_2_6_9_1 e_1_2_6_3_6 e_1_2_6_5_4 e_1_2_6_7_2 e_1_2_6_3_9 e_1_2_6_9_3 e_1_2_6_3_8 e_1_2_6_9_2 e_1_2_6_3_3 e_1_2_6_5_1 e_1_2_6_3_2 e_1_2_6_3_5 e_1_2_6_5_3 e_1_2_6_7_1 e_1_2_6_3_4 e_1_2_6_5_2 e_1_2_6_3_1 e_1_2_6_10_1 e_1_2_6_14_1 e_1_2_6_12_1 e_1_2_6_18_1 e_1_2_6_16_1 e_1_2_6_4_6 e_1_2_6_4_5 e_1_2_6_8_1 e_1_2_6_2_4 e_1_2_6_4_2 e_1_2_6_2_3 e_1_2_6_4_1 e_1_2_6_2_6 e_1_2_6_4_4 e_1_2_6_2_5 e_1_2_6_4_3 e_1_2_6_6_1 e_1_2_6_2_2 e_1_2_6_2_1 |
References_xml | – year: 2009 – volume: 1 start-page: 423 year: 1990 publication-title: Struct. Chem. – volume: 109 start-page: 190 year: 2009 publication-title: Chem. Rev. – volume: 48 102 81 18 start-page: 85 835 11316 1398 year: 2001 2002 2016 2016 publication-title: Dyes Pigm. Chem. Rev. J. Org. Chem. Org. Lett. – volume: 79 start-page: 365 year: 2014 publication-title: J. Org. Chem. – volume: 52 125 start-page: 9316 9486 year: 2013 2013 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 630 2 128 80 start-page: 2632 2089 10885 3737 year: 2004 2000 2006 2015 publication-title: Z. Anorg. Allg. Chem. Org. Lett. J. Am. Chem. Soc. J. Org. Chem. – volume: 16 16 24 97 80 83 start-page: 3692 5636 416 424 7837 1754 year: 2014 2014 1985 1985 2015 1961 publication-title: Org. Lett. Org. Lett. Angew. Chem. Int. Ed. Engl. Angew. Chem. J. Org. Chem. J. Am. Chem. Soc. – volume: 43 116 4 start-page: 3056 3118 2153 year: 2004 2004 2002 publication-title: Angew. Chem. Int. Ed. Angew. Chem. Org. Lett. – start-page: 2728 year: 1959 publication-title: J. Chem. Soc. – volume: 51 124 16 start-page: 6074 6178 5024 year: 2012 2012 2014 publication-title: Angew. Chem. Int. Ed. Angew. Chem. Org. Lett. – volume: 9 start-page: 1395 year: 2007 publication-title: Org. Lett. – volume: 82 start-page: 549 year: 2017 publication-title: J. Org. Chem. – volume: 79 81 723 67 42 115 9 81 137 83 start-page: 6663 969 122 4277 1252 1290 4156 2681 3958 831 year: 2014 2016 2013 2011 2003 2003 2003 1959 2015 1961 publication-title: J. Org. Chem. J. Org. Chem. J. Organomet. Chem. Tetrahedron Angew. Chem. Int. Ed. Angew. Chem. Chem. Eur. J. J. Am. Chem. Soc. J. Am. Chem. Soc. J. Am. Chem. Soc. – volume: 74 start-page: 3054 year: 2009 publication-title: J. Org. Chem. – start-page: 5221 year: 2015 publication-title: Eur. J. Org. Chem. – volume: 42 115 128 133 81 136 16 16 18 start-page: 1252 1290 10885 11508 3771 11813 3340 6024 1606 year: 2003 2003 2006 2011 2016 2014 2014 2014 2016 publication-title: Angew. Chem. Int. Ed. Angew. Chem. J. Am. Chem. Soc. J. Am. Chem. Soc. J. Org. Chem. J. Am. Chem. Soc. Org. Lett. Org. Lett. Org. Lett. – volume: 52 125 58 96 48 121 start-page: 2599 2660 9287 3147 6817 6949 year: 2013 2013 2015 1996 2009 2009 publication-title: Angew. Chem. Int. Ed. Angew. Chem. J. Med. Chem. Chem. Rev. Angew. Chem. Int. Ed. Angew. Chem. – volume: 128 start-page: 10885 year: 2006 ident: WOS:000239791100054 article-title: Triphenylene analogues with B2N2C2 cores:: Synthesis, structure, redox behavior, and photophysical properties publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja063519p contributor: fullname: Jaska, CA – volume: 16 start-page: 5636 year: 2014 ident: WOS:000344635200033 article-title: Accessing an Azaborine Building Block: Synthesis and Substitution Reactions of 2-Chloromethy1-2,1-borazaronaphthalene publication-title: ORGANIC LETTERS doi: 10.1021/ol502708z contributor: fullname: Molander, GA – volume: 48 start-page: 85 year: 2001 ident: WOS:000166846300002 article-title: Synthesis and spectral properties of new soluble naphthalocyaninatometal derivatives publication-title: DYES AND PIGMENTS contributor: fullname: Chen, PL – volume: 4 start-page: 2153 year: 2002 ident: WOS:000176354700010 article-title: Asymmetric alkyldifluoroboranes and their use in secondary amine synthesis publication-title: ORGANIC LETTERS doi: 10.1021/ol025973d contributor: fullname: Matteson, DS – volume: 97 start-page: 424 year: 1985 ident: 000444540900020.20 publication-title: Angew. Chem. contributor: fullname: Glaser, B. – volume: 1 start-page: 423 year: 1990 ident: WOS:000208827100003 article-title: Definition of a Multicenter Bond Index publication-title: STRUCTURAL CHEMISTRY contributor: fullname: Giambiagi, M – volume: 48 start-page: 6817 year: 2009 ident: WOS:000269937200008 article-title: Boron Mimetics: 1,2-Dihydro-1,2-azaborines Bind inside a Nonpolar Cavity of T4 Lysozyme publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.200903390 contributor: fullname: Liu, LJ – volume: 79 start-page: 365 year: 2014 ident: WOS:000329472900033 article-title: A Convergent, Modular Approach to Functionalized 2,1-Borazaronaphthalenes from 2-Aminostyrenes and Potassium Organotrifluoroborates publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/jo402616w contributor: fullname: Wisniewski, SR – volume: 96 start-page: 3147 year: 1996 ident: WOS:A1996VZ38400005 article-title: Bioisosterism: A rational approach in drug design publication-title: CHEMICAL REVIEWS contributor: fullname: Patani, GA – volume: 121 start-page: 6949 year: 2009 ident: 000444540900020.34 publication-title: Angew. Chem. contributor: fullname: Liu, L. – volume: 9 start-page: 4156 year: 2003 ident: WOS:000185294800015 article-title: Waste-free and facile solid-state protection of diamines, anthranilic acid, diols, and polyols with phenylboronic acid publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.200304793 contributor: fullname: Kaupp, G – volume: 52 start-page: 2599 year: 2013 ident: WOS:000315209900043 article-title: BN/CC Isosteric Compounds as Enzyme Inhibitors: N- and B-Ethyl-1,2-azaborine Inhibit Ethylbenzene Hydroxylation as Nonconvertible Substrate Analogues publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201208351 contributor: fullname: Knack, DH – volume: 630 start-page: 2632 year: 2004 ident: WOS:000226201400012 article-title: 1-azonia-2-boratanaphthalenes publication-title: ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE doi: 10.1002/zaac.200400333 contributor: fullname: Paetzold, P – volume: 16 start-page: 3692 year: 2014 ident: WOS:000339367300021 article-title: Reductive Cross-Coupling of 3-Bromo-2,1-borazaronaphthalenes with Alkyl Iodides publication-title: ORGANIC LETTERS doi: 10.1021/ol501495d contributor: fullname: Molander, GA – volume: 58 start-page: 9287 year: 2015 ident: WOS:000366340000015 article-title: Benzazaborinines as Novel Bioisosteric Replacements of Naphthalene: Propranolol as an Example publication-title: JOURNAL OF MEDICINAL CHEMISTRY doi: 10.1021/acs.jmedchem.5b01088 contributor: fullname: Rombouts, FJR – volume: 80 start-page: 3737 year: 2015 ident: WOS:000353315000001 article-title: Synthesis of 1,2-Borazaronaphthalenes from Imines by Base-Promoted Borylation of C-H bond publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/jo5029437 contributor: fullname: Liu, XW – volume: 18 start-page: 1398 year: 2016 ident: WOS:000372664600046 article-title: Triple Boron-Cored Chromophores Bearing Discotic 5,11,17-Triazatrinaphthylene-Based Ligands publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.6b00335 contributor: fullname: Qiu, F – volume: 125 start-page: 2660 year: 2013 ident: 000444540900020.31 publication-title: Angew. Chem. contributor: fullname: Knack, D. H. – volume: 83 start-page: 831 year: 1961 ident: WOS:A19613066B00033 article-title: AMINE BORANES .5. PREPARATION OF TRIMETHYLAMINE ALKYLBORANES AND 2-ALKYLBOROBENZIMIDAZOLINES publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY contributor: fullname: HAWTHORNE, M – volume: 74 start-page: 3054 year: 2009 ident: WOS:000265073700017 article-title: Tandem Pd-Catalyzed Double C-C Bond Formation: Effect of Water publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/jo900053b contributor: fullname: Chai, DI – volume: 115 start-page: 1290 year: 2003 ident: 000444540900020.16 publication-title: Angew. Chem. contributor: fullname: Emslie, D. J. H. – volume: 81 start-page: 11316 year: 2016 ident: WOS:000391248800071 article-title: Aromatic Ring Fused BOPHYs as Stable Red Fluorescent Dyes publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/acs.joc.6b02291 contributor: fullname: Wang, J – volume: 116 start-page: 3118 year: 2004 ident: 000444540900020.28 article-title: Conversion of alkyltrifluoroborates into alkyldichloroboranes with tetrachlorosilane in coordinating solvents publication-title: Angew. Chem contributor: fullname: Kim, B. J. – volume: 102 start-page: 835 year: 2002 ident: WOS:000174456500009 article-title: Subphthalocyanines:: Singular nonplanar aromatic compounds-synthesis, reactivity, and physical properties publication-title: CHEMICAL REVIEWS doi: 10.1021/cr0101454 contributor: fullname: Claessens, CG – volume: 16 start-page: 5024 year: 2014 ident: WOS:000342719500015 article-title: Palladium-Catalyzed Cross-Coupling Reactions of 4a,8a-Azaboranaphthalene publication-title: ORGANIC LETTERS doi: 10.1021/ol502339h contributor: fullname: Sun, FY – volume: 18 start-page: 1606 year: 2016 ident: WOS:000373519600028 article-title: Accessing Elaborated 2,1-Borazaronaphthalene Cores Using Photoredox/Nickel Dual-Catalytic Functionalization publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.6b00466 contributor: fullname: Jouffroy, M – volume: 9 start-page: 1395 year: 2007 ident: WOS:000245084300056 article-title: Blue fluorescent 4a-aza-4b-boraphenanthrenes publication-title: ORGANIC LETTERS doi: 10.1021/ol070328y contributor: fullname: Bosdet, MJD – volume: 82 start-page: 549 year: 2017 ident: WOS:000391781900052 article-title: Method for Accessing Nitrogen-Containing, B-Heteroaryl-Substituted 2,1-Borazaronaphthalenes publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/acs.joc.6b02574 contributor: fullname: Davies, GHM – volume: 124 start-page: 6178 year: 2012 ident: 000444540900020.6 publication-title: Angew. Chem. contributor: fullname: Campbell, P. G. – volume: 109 start-page: 190 year: 2009 ident: WOS:000262482500006 article-title: Fluorescent Labeling of Biomolecules with Organic Probes publication-title: CHEMICAL REVIEWS doi: 10.1021/cr0783840 contributor: fullname: Sameiro, M – volume: 16 start-page: 6024 year: 2014 ident: WOS:000345470000051 article-title: Accessing 2-(Hetero)arylmethyl-, -allyl-, and -propargyl-2,1-borazaronaphthalenes: Palladium-Catalyzed Cross-Couplings of 2-(Chloromethyl)-2,1-borazaronaphthalenes publication-title: ORGANIC LETTERS doi: 10.1021/ol5030508 contributor: fullname: Molander, GA – volume: 136 start-page: 11813 year: 2014 ident: WOS:000340737900038 article-title: UV-Photoelectron Spectroscopy of BN lndoles: Experimental and Computational Electronic Structure Analysis publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja5063899 contributor: fullname: Chrostowska, A – volume: 723 start-page: 122 year: 2013 ident: WOS:000311680100018 article-title: Solution-state 15N NMR and solid-state single-crystal XRD study of heterosubstituted diazaboroles and borinines prepared via an effective and simple microwave-assisted solvent-free synthesis publication-title: JOURNAL OF ORGANOMETALLIC CHEMISTRY doi: 10.1016/j.jorganchem.2012.09.018 contributor: fullname: Slabber, CA – volume: 81 start-page: 3771 year: 2016 ident: WOS:000375890100034 article-title: Synthesis of Functionalized 1,3,2-Benzodiazaborole Cores Using Bench-Stable Components publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/acs.joc.6b00435 contributor: fullname: Davies, GHM – year: 2009 ident: 000444540900020.18 publication-title: Gaussian 09, Revision A.02 contributor: fullname: Frisch, M. J. – volume: 81 start-page: 2681 year: 1959 ident: WOS:A1959WB36200024 article-title: BORON-CONTAINING HETEROCYCLES .1. SYNTHESIS OF SEVERAL BORIMIDAZOLINES publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY contributor: fullname: NYILAS, E – volume: 16 start-page: 3340 year: 2014 ident: WOS:000337869800043 article-title: Rhodium-Catalyzed B-H Activation of 1,2-Azaborines: Synthesis and Characterization of BN Isosteres of Stilbenes publication-title: ORGANIC LETTERS doi: 10.1021/ol501362w contributor: fullname: Brown, AN – volume: 52 start-page: 9316 year: 2013 ident: WOS:000323393100056 article-title: Rhodium-Catalyzed Boron Arylation of 1,2-Azaborines publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201304443 contributor: fullname: Rudebusch, GE – volume: 125 start-page: 9486 year: 2013 ident: 000444540900020.47 publication-title: Angew. Chem. contributor: fullname: Rudebusch, G. E. – start-page: 2728 year: 1959 ident: WOS:A1959WK68900018 article-title: NEW HETEROAROMATIC COMPOUNDS .3. 2,1-BORAZARONAPHTHALENE (1,2-DIHYDRO-1-AZA-2-BORANAPHTHALENE) publication-title: JOURNAL OF THE CHEMICAL SOCIETY contributor: fullname: DEWAR, MJS – volume: 133 start-page: 11508 year: 2011 ident: WOS:000293872800029 article-title: Boron in Disguise: The Parent "Fused" BN Indole publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja205779b contributor: fullname: Abbey, ER – volume: 42 start-page: 1252 year: 2003 ident: WOS:000181872300005 article-title: 2,2′-diborabiphenyl:: A Lewis acid analogue of 2,2′-bipyridine publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION contributor: fullname: Emslie, DJH – volume: 24 start-page: 416 year: 1985 ident: WOS:A1985ALY3200018 article-title: 9-FLUORENYLIDENE-2,2,6,6-TETRAMETHYLPIPERIDINOBORANE - AN ALLENE ISOESTER WITH 2-COORDINATED BORON AND B=C DOUBLE-BOND publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH contributor: fullname: GLASER, B – volume: 79 start-page: 6663 year: 2014 ident: WOS:000339368300027 article-title: Accessing Molecularly Complex Azaborines: Palladium-Catalyzed Suzuki-Miyaura Cross-Couplings of Brominated 2,1-Borazaronaphthalenes and Potassium Organotrifluoroborates publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/jo5011894 contributor: fullname: Molander, GA – volume: 2 start-page: 2089 year: 2000 ident: WOS:000088039800028 article-title: A synthesis of aromatic five- and six-membered B-N heterocycles via ring closing metathesis publication-title: ORGANIC LETTERS contributor: fullname: Ashe, AJ – volume: 2015 start-page: 5221 year: 2015 ident: WOS:000359295800021 article-title: Synthesis of 2,1-Borazaroquinolines and 2,1-Borazaroisoquinolines from Vinylaminopyridines and Potassium Organotrifluoroborates by Microwave-Assisted Heating publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY doi: 10.1002/ejoc.201500622 contributor: fullname: Casado, MRS – volume: 81 start-page: 969 year: 2016 ident: WOS:000369771600023 article-title: Spectroscopic and Computational Investigations of The Thermodynamics of Boronate Ester and Diazaborole Self-Assembly publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/acs.joc.5b02548 contributor: fullname: Goldberg, AR – volume: 51 start-page: 6074 year: 2012 ident: WOS:000305180400006 article-title: Recent Advances in Azaborine Chemistry publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201200063 contributor: fullname: Campbell, PG – volume: 137 start-page: 3958 year: 2015 ident: WOS:000351972000038 article-title: Synthesis of Chemically and Configurationally Stable Monofluoro Acylboronates: Effect of Ligand Structure on their Formation, Properties, and Reactivities publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.5b00822 contributor: fullname: Noda, H – volume: 43 start-page: 3056 year: 2004 ident: WOS:000222067400014 article-title: Conversion of alkyltrifluoroborates into alkyldichloroboranes with tetrachlorosilane in coordinating solvents publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.200453690 contributor: fullname: Kim, BJ – volume: 83 start-page: 1754 year: 1961 ident: WOS:A19613069B00019 article-title: NEW HETEROAROMATIC COMPOUNDS .10. GRIGNARD REACTIONS AND HYDRIDE REDUCTIONS OF B-OXIDES DERIVED FROM 10,9-BORAZAROPHENANTHRENE AND 2,1-BORAZARONAPHTHALENE publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY contributor: fullname: DEWAR, MJ – volume: 67 start-page: 4277 year: 2011 ident: WOS:000291371900019 article-title: Microwave-assisted Suzuki-Miyaura cross-coupling of 2-alkyl and 2-alkenyl-benzo-1,3,2-diazaborolanes publication-title: TETRAHEDRON doi: 10.1016/j.tet.2011.03.095 contributor: fullname: Hadebe, SW – volume: 80 start-page: 7837 year: 2015 ident: WOS:000360103000001 article-title: Organotrifluoroborates: Another Branch of the Mighty Oak publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/acs.joc.5b00981 contributor: fullname: Molander, GA – ident: e_1_2_6_3_8 doi: 10.1021/ol5030508 – ident: e_1_2_6_17_1 doi: 10.1021/jo900053b – ident: e_1_2_6_19_1 doi: 10.1007/BF00671228 – ident: e_1_2_6_7_3 doi: 10.1021/ol502339h – ident: e_1_2_6_2_4 doi: 10.1002/ange.19850970527 – ident: e_1_2_6_5_1 doi: 10.1016/S0143-7208(00)00100-5 – ident: e_1_2_6_13_2 doi: 10.1021/ol0001113 – ident: e_1_2_6_7_2 doi: 10.1002/ange.201200063 – ident: e_1_2_6_16_1 doi: 10.1021/jo402616w – ident: e_1_2_6_13_4 doi: 10.1021/jo5029437 – ident: e_1_2_6_4_3 doi: 10.1021/acs.jmedchem.5b01088 – ident: e_1_2_6_4_4 doi: 10.1021/cr950066q – ident: e_1_2_6_3_3 doi: 10.1021/ja063519p – ident: e_1_2_6_10_1 doi: 10.1039/jr9590002728 – ident: e_1_2_6_13_1 doi: 10.1002/zaac.200400333 – ident: e_1_2_6_15_1 doi: 10.1002/anie.200453690 – ident: e_1_2_6_9_4 doi: 10.1016/j.tet.2011.03.095 – ident: e_1_2_6_9_1 doi: 10.1021/jo5011894 – ident: e_1_2_6_9_7 doi: 10.1002/chem.200304793 – ident: e_1_2_6_14_1 doi: 10.1021/acs.joc.6b02574 – ident: e_1_2_6_3_1 doi: 10.1002/anie.200390320 – ident: e_1_2_6_13_3 doi: 10.1021/ja063519p – ident: e_1_2_6_3_7 doi: 10.1021/ol501362w – ident: e_1_2_6_5_2 doi: 10.1021/cr0101454 – ident: e_1_2_6_11_2 doi: 10.1002/ange.201304443 – ident: e_1_2_6_2_3 doi: 10.1002/anie.198504161 – ident: e_1_2_6_5_4 doi: 10.1021/acs.orglett.6b00335 – ident: e_1_2_6_9_6 doi: 10.1002/ange.200390291 – ident: e_1_2_6_15_2 doi: 10.1002/ange.200453690 – ident: e_1_2_6_9_5 doi: 10.1002/anie.200390320 – ident: e_1_2_6_9_3 doi: 10.1016/j.jorganchem.2012.09.018 – ident: e_1_2_6_18_1 – ident: e_1_2_6_3_6 doi: 10.1021/ja5063899 – ident: e_1_2_6_3_4 doi: 10.1021/ja205779b – ident: e_1_2_6_2_1 doi: 10.1021/ol501495d – ident: e_1_2_6_3_5 doi: 10.1021/acs.joc.6b00435 – ident: e_1_2_6_9_10 doi: 10.1021/ja01465a022 – ident: e_1_2_6_4_6 doi: 10.1002/ange.200903390 – ident: e_1_2_6_4_2 doi: 10.1002/ange.201208351 – ident: e_1_2_6_2_6 doi: 10.1021/ja01468a046 – ident: e_1_2_6_11_1 doi: 10.1002/anie.201304443 – ident: e_1_2_6_3_2 doi: 10.1002/ange.200390291 – ident: e_1_2_6_3_9 doi: 10.1021/acs.orglett.6b00466 – ident: e_1_2_6_2_5 doi: 10.1021/acs.joc.5b00981 – ident: e_1_2_6_2_2 doi: 10.1021/ol502708z – ident: e_1_2_6_12_1 doi: 10.1002/ejoc.201500622 – ident: e_1_2_6_9_8 doi: 10.1021/ja01520a024 – ident: e_1_2_6_5_3 doi: 10.1021/acs.joc.6b02291 – ident: e_1_2_6_9_2 doi: 10.1021/acs.joc.5b02548 – ident: e_1_2_6_7_1 doi: 10.1002/anie.201200063 – ident: e_1_2_6_4_5 doi: 10.1002/anie.200903390 – ident: e_1_2_6_4_1 doi: 10.1002/anie.201208351 – ident: e_1_2_6_6_1 doi: 10.1021/cr0783840 – ident: e_1_2_6_15_3 doi: 10.1021/ol025973d – ident: e_1_2_6_8_1 doi: 10.1021/ol070328y – ident: e_1_2_6_9_9 doi: 10.1021/jacs.5b00822 |
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Snippet | A series of fused 4,5‐borazaropyrrolo[1,2‐a]quinolines have been prepared from potassium organotrifluoroborates and substituted 1‐(2‐aminophenyl)pyrroles via... A series of fused 4,5-borazaropyrrolo[1,2-a]quinolines have been prepared from potassium organotrifluoroborates and substituted 1-(2-aminophenyl)pyrroles via... A series of fused 4,5‐borazaropyrrolo[1,2‐ a ]quinolines have been prepared from potassium organotrifluoroborates and substituted 1‐(2‐aminophenyl)pyrroles via... |
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SubjectTerms | Boron Chemistry Chemistry, Organic Functional organic materials Fused‐ring systems Heterocyclic compounds Optical properties Organic compounds Physical Sciences Pyrroles Science & Technology Synthesis design |
Title | Synthesis of Fused B‐Containing Heterocyclic Compounds and Their Relevant Optical Properties |
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