Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 1226 entries
Sorted by: Best Match Show Resources per page
Correction to GPR103 Antagonists Demonstrating Anorexigenic Activity in Vivo: Design and Development of Pyrrolo[2,3-c]pyridines That Mimic the C-Terminal Arg-Phe Motif of QRFP26.

Journal of medicinal chemistry

Georgsson J, Bergström F, Nordqvist A, Watson MJ, Blundell CD, Johansson MJ, Petersson AU, Yuan ZQ, Zhou Y, Kristensson L, Kakol-Palm D, Tyrchan C, Wellner E, Bauer U, Brodin P, Svensson Henriksson A.
PMID: 25875054
J Med Chem. 2015 May 14;58(9):4086. doi: 10.1021/acs.jmedchem.5b00479. Epub 2015 Apr 15.

No abstract available.

Cite
Georgsson J, Bergström F, Nordqvist A, et al. Correction to GPR103 Antagonists Demonstrating Anorexigenic Activity in Vivo: Design and Development of Pyrrolo[2,3-c]pyridines That Mimic the C-Terminal Arg-Phe Motif of QRFP26. J Med Chem. 2015;58(9):4086doi: 10.1021/acs.jmedchem.5b00479.
Georgsson, J., Bergström, F., Nordqvist, A., Watson, M. J., Blundell, C. D., Johansson, M. J., Petersson, A. U., Yuan, Z. Q., Zhou, Y., Kristensson, L., Kakol-Palm, D., Tyrchan, C., Wellner, E., Bauer, U., Brodin, P., & Svensson Henriksson, A. (2015). Correction to GPR103 Antagonists Demonstrating Anorexigenic Activity in Vivo: Design and Development of Pyrrolo[2,3-c]pyridines That Mimic the C-Terminal Arg-Phe Motif of QRFP26. Journal of medicinal chemistry, 58(9), 4086. https://doi.org/10.1021/acs.jmedchem.5b00479
Georgsson, Jennie, et al. "Correction to GPR103 Antagonists Demonstrating Anorexigenic Activity in Vivo: Design and Development of Pyrrolo[2,3-c]pyridines That Mimic the C-Terminal Arg-Phe Motif of QRFP26." Journal of medicinal chemistry vol. 58,9 (2015): 4086. doi: https://doi.org/10.1021/acs.jmedchem.5b00479
Georgsson J, Bergström F, Nordqvist A, Watson MJ, Blundell CD, Johansson MJ, Petersson AU, Yuan ZQ, Zhou Y, Kristensson L, Kakol-Palm D, Tyrchan C, Wellner E, Bauer U, Brodin P, Svensson Henriksson A. Correction to GPR103 Antagonists Demonstrating Anorexigenic Activity in Vivo: Design and Development of Pyrrolo[2,3-c]pyridines That Mimic the C-Terminal Arg-Phe Motif of QRFP26. J Med Chem. 2015 May 14;58(9):4086. doi: 10.1021/acs.jmedchem.5b00479. Epub 2015 Apr 15. PMID: 25875054.
Copy Download .nbib Format: NLM
Synthesis of Indolizine Derivatives by Pd-Catalyzed Oxidative Carbonylation.

Organic letters

Xu T, Alper H.
PMID: 26331787
Org Lett. 2015 Sep 18;17(18):4526-9. doi: 10.1021/acs.orglett.5b02220. Epub 2015 Sep 02.

An efficient synthesis of indolizine derivatives by palladium-catalyzed oxidative carbonylation of propargylic pyridines has been developed. The reaction can be conducted at room temperature and under 3 bar of CO in the presence of Pd2(dba)3 or Pd/C. The catalyst...

Cite
Xu T, Alper H. Synthesis of Indolizine Derivatives by Pd-Catalyzed Oxidative Carbonylation. Org Lett. 2015;17(18):4526-9doi: 10.1021/acs.orglett.5b02220.
Xu, T., & Alper, H. (2015). Synthesis of Indolizine Derivatives by Pd-Catalyzed Oxidative Carbonylation. Organic letters, 17(18), 4526-9. https://doi.org/10.1021/acs.orglett.5b02220
Xu, Tongyu, and Alper, Howard. "Synthesis of Indolizine Derivatives by Pd-Catalyzed Oxidative Carbonylation." Organic letters vol. 17,18 (2015): 4526-9. doi: https://doi.org/10.1021/acs.orglett.5b02220
Xu T, Alper H. Synthesis of Indolizine Derivatives by Pd-Catalyzed Oxidative Carbonylation. Org Lett. 2015 Sep 18;17(18):4526-9. doi: 10.1021/acs.orglett.5b02220. Epub 2015 Sep 02. PMID: 26331787.
Copy Download .nbib Format: NLM
Evidence that phospholipase C is involved in the antitumour action of NSC768313, a new thieno[2,3-b]pyridine derivative.

Cancer cell international

Reynisson J, Jaiswal JK, Barker D, D'mello SA, Denny WA, Baguley BC, Leung EY.
PMID: 26966420
Cancer Cell Int. 2016 Mar 10;16:18. doi: 10.1186/s12935-016-0293-6. eCollection 2016.

BACKGROUND: The thieno[2,3-b]pyridines were discovered by virtual high throughput screening as potential inhibitors of phospholipase C (PLC) isoforms and showed potent growth inhibitory effects in National Cancer Institute's human tumour cell line panel (NCI60). The mechanism of the anti-proliferative...

Cite
Reynisson J, Jaiswal JK, Barker D, et al. Evidence that phospholipase C is involved in the antitumour action of NSC768313, a new thieno[2,3-b]pyridine derivative. Cancer Cell Int. 2016;16:18doi: 10.1186/s12935-016-0293-6.
Reynisson, J., Jaiswal, J. K., Barker, D., D'mello, S. A., Denny, W. A., Baguley, B. C., & Leung, E. Y. (2016). Evidence that phospholipase C is involved in the antitumour action of NSC768313, a new thieno[2,3-b]pyridine derivative. Cancer cell international, 1618. https://doi.org/10.1186/s12935-016-0293-6
Reynisson, Jóhannes, et al. "Evidence that phospholipase C is involved in the antitumour action of NSC768313, a new thieno[2,3-b]pyridine derivative." Cancer cell international vol. 16 (2016): 18. doi: https://doi.org/10.1186/s12935-016-0293-6
Reynisson J, Jaiswal JK, Barker D, D'mello SA, Denny WA, Baguley BC, Leung EY. Evidence that phospholipase C is involved in the antitumour action of NSC768313, a new thieno[2,3-b]pyridine derivative. Cancer Cell Int. 2016 Mar 10;16:18. doi: 10.1186/s12935-016-0293-6. eCollection 2016. PMID: 26966420; PMCID: PMC4785615.
Copy Download .nbib Format: NLM
Regio- and Stereoselective Domino Synthesis of Oxazolo Fused Pyridoindoles and Benzofurooxazolo Pyridines from ortho-Alkynylarylaldehydes.

The Journal of organic chemistry

Pal S, Choudhary D, Jainth M, Kumar S, Tiwari RK, Verma AK.
PMID: 27626809
J Org Chem. 2016 Oct 07;81(19):9356-9371. doi: 10.1021/acs.joc.6b02062. Epub 2016 Sep 26.

An environmentally benign Au(III)-catalyzed regio- and stereoselective domino synthesis of oxazolo fused pyridoindoles 7a-v and benzofurooxazolo pyridines 8a-n by the reaction of o-alkynylaldehydes 4a-t and 5a-k with (S)-phenylglycinol 6a and (R)-phenylglycinol 6b under mild reaction conditions using water as...

Cite
Pal S, Choudhary D, Jainth M, et al. Regio- and Stereoselective Domino Synthesis of Oxazolo Fused Pyridoindoles and Benzofurooxazolo Pyridines from ortho-Alkynylarylaldehydes. J Org Chem. 2016;81(19):9356-9371doi: 10.1021/acs.joc.6b02062.
Pal, S., Choudhary, D., Jainth, M., Kumar, S., Tiwari, R. K., & Verma, A. K. (2016). Regio- and Stereoselective Domino Synthesis of Oxazolo Fused Pyridoindoles and Benzofurooxazolo Pyridines from ortho-Alkynylarylaldehydes. The Journal of organic chemistry, 81(19), 9356-9371. https://doi.org/10.1021/acs.joc.6b02062
Pal, Shilpi, et al. "Regio- and Stereoselective Domino Synthesis of Oxazolo Fused Pyridoindoles and Benzofurooxazolo Pyridines from ortho-Alkynylarylaldehydes." The Journal of organic chemistry vol. 81,19 (2016): 9356-9371. doi: https://doi.org/10.1021/acs.joc.6b02062
Pal S, Choudhary D, Jainth M, Kumar S, Tiwari RK, Verma AK. Regio- and Stereoselective Domino Synthesis of Oxazolo Fused Pyridoindoles and Benzofurooxazolo Pyridines from ortho-Alkynylarylaldehydes. J Org Chem. 2016 Oct 07;81(19):9356-9371. doi: 10.1021/acs.joc.6b02062. Epub 2016 Sep 26. PMID: 27626809.
Copy Download .nbib Format: NLM
Access to Imidazo[1,2-a]pyridines via Annulation of α-Keto Vinyl Azides and 2-Aminopyridines.

Organic letters

Adiyala PR, Mani GS, Nanubolu JB, Shekar KC, Maurya RA.
PMID: 26308984
Org Lett. 2015 Sep 04;17(17):4308-11. doi: 10.1021/acs.orglett.5b02124. Epub 2015 Aug 26.

A novel strategy for the synthesis of imidazo[1,2-a]pyridines via efficient catalyst/metal-free annulations of α-keto vinyl azides and 2-aminopyridines is described. Several imidazo[1,2-a]pyridines were synthesized from readily available vinyl azides and 2-aminopyridines and obtained in highly pure form by simply...

Cite
Adiyala PR, Mani GS, Nanubolu JB, et al. Access to Imidazo[1,2-a]pyridines via Annulation of α-Keto Vinyl Azides and 2-Aminopyridines. Org Lett. 2015;17(17):4308-11doi: 10.1021/acs.orglett.5b02124.
Adiyala, P. R., Mani, G. S., Nanubolu, J. B., Shekar, K. C., & Maurya, R. A. (2015). Access to Imidazo[1,2-a]pyridines via Annulation of α-Keto Vinyl Azides and 2-Aminopyridines. Organic letters, 17(17), 4308-11. https://doi.org/10.1021/acs.orglett.5b02124
Adiyala, Praveen Reddy, et al. "Access to Imidazo[1,2-a]pyridines via Annulation of α-Keto Vinyl Azides and 2-Aminopyridines." Organic letters vol. 17,17 (2015): 4308-11. doi: https://doi.org/10.1021/acs.orglett.5b02124
Adiyala PR, Mani GS, Nanubolu JB, Shekar KC, Maurya RA. Access to Imidazo[1,2-a]pyridines via Annulation of α-Keto Vinyl Azides and 2-Aminopyridines. Org Lett. 2015 Sep 04;17(17):4308-11. doi: 10.1021/acs.orglett.5b02124. Epub 2015 Aug 26. PMID: 26308984.
Copy Download .nbib Format: NLM
High-Temperature Continuous-Flow Zincations of Functionalized Arenes and Heteroarenes Using (Cy2N)2Zn·2LiCl.

Organic letters

Becker MR, Knochel P.
PMID: 26942552
Org Lett. 2016 Mar 18;18(6):1462-5. doi: 10.1021/acs.orglett.6b00408. Epub 2016 Mar 04.

The treatment of sensitive arenes and heteroarenes with the zinc bis-amide (Cy2N)2Zn·2LiCl (0.55 equiv), prepared in quantitative yield by the reaction of Cy2NLi with ZnCl2, leads under flow conditions to a fast zincation within 10 min at temperatures between...

Cite
Becker MR, Knochel P. High-Temperature Continuous-Flow Zincations of Functionalized Arenes and Heteroarenes Using (Cy2N)2Zn·2LiCl. Org Lett. 2016;18(6):1462-5doi: 10.1021/acs.orglett.6b00408.
Becker, M. R., & Knochel, P. (2016). High-Temperature Continuous-Flow Zincations of Functionalized Arenes and Heteroarenes Using (Cy2N)2Zn·2LiCl. Organic letters, 18(6), 1462-5. https://doi.org/10.1021/acs.orglett.6b00408
Becker, Matthias R, and Knochel, Paul. "High-Temperature Continuous-Flow Zincations of Functionalized Arenes and Heteroarenes Using (Cy2N)2Zn·2LiCl." Organic letters vol. 18,6 (2016): 1462-5. doi: https://doi.org/10.1021/acs.orglett.6b00408
Becker MR, Knochel P. High-Temperature Continuous-Flow Zincations of Functionalized Arenes and Heteroarenes Using (Cy2N)2Zn·2LiCl. Org Lett. 2016 Mar 18;18(6):1462-5. doi: 10.1021/acs.orglett.6b00408. Epub 2016 Mar 04. PMID: 26942552.
Copy Download .nbib Format: NLM
Corrigendum: Adjuvanted influenza-H1N1 vaccination reveals lymphoid signatures of age-dependent early responses and of clinical adverse events.

Nature immunology

Sobolev O, Binda E, O'Farrell S, Lorenc A, Pradines J, Huang Y, Duffner J, Schulz R, Cason J, Zambon M, Malim MH, Peakman M, Cope A, Capila I, Kaundinya GV, Hayday AC.
PMID: 27002849
Nat Immunol. 2016 Apr;17(4):469. doi: 10.1038/ni0416-469b.

No abstract available.

Cite
Sobolev O, Binda E, O'Farrell S, et al. Corrigendum: Adjuvanted influenza-H1N1 vaccination reveals lymphoid signatures of age-dependent early responses and of clinical adverse events. Nat Immunol. 2016;17(4):469doi: 10.1038/ni0416-469b.
Sobolev, O., Binda, E., O'Farrell, S., Lorenc, A., Pradines, J., Huang, Y., Duffner, J., Schulz, R., Cason, J., Zambon, M., Malim, M. H., Peakman, M., Cope, A., Capila, I., Kaundinya, G. V., & Hayday, A. C. (2016). Corrigendum: Adjuvanted influenza-H1N1 vaccination reveals lymphoid signatures of age-dependent early responses and of clinical adverse events. Nature immunology, 17(4), 469. https://doi.org/10.1038/ni0416-469b
Sobolev, Olga, et al. "Corrigendum: Adjuvanted influenza-H1N1 vaccination reveals lymphoid signatures of age-dependent early responses and of clinical adverse events." Nature immunology vol. 17,4 (2016): 469. doi: https://doi.org/10.1038/ni0416-469b
Sobolev O, Binda E, O'Farrell S, Lorenc A, Pradines J, Huang Y, Duffner J, Schulz R, Cason J, Zambon M, Malim MH, Peakman M, Cope A, Capila I, Kaundinya GV, Hayday AC. Corrigendum: Adjuvanted influenza-H1N1 vaccination reveals lymphoid signatures of age-dependent early responses and of clinical adverse events. Nat Immunol. 2016 Apr;17(4):469. doi: 10.1038/ni0416-469b. PMID: 27002849.
Copy Download .nbib Format: NLM
A novel symmetric TTF-pyridyl thiolato zinc complex: synthesis, characterization and crystal structure analysis.

Dalton transactions (Cambridge, England : 2003)

Okuno R, Yamaguchi M, Fujiwara H.
PMID: 28345714
Dalton Trans. 2017 Apr 11;46(15):4912-4916. doi: 10.1039/c7dt00468k.

We report the first preparation of a symmetric tetrathiafulvalene (TTF)-pyridyl thiolato zinc(ii) complex in which two TTF parts connect to the central zinc atom through pyridines and thiolates. We also discuss the crystal structure analysis and physical properties of...

Cite
Okuno R, Yamaguchi M, Fujiwara H. A novel symmetric TTF-pyridyl thiolato zinc complex: synthesis, characterization and crystal structure analysis. Dalton Trans. 2017;46(15):4912-4916doi: 10.1039/c7dt00468k.
Okuno, R., Yamaguchi, M., & Fujiwara, H. (2017). A novel symmetric TTF-pyridyl thiolato zinc complex: synthesis, characterization and crystal structure analysis. Dalton transactions (Cambridge, England : 2003), 46(15), 4912-4916. https://doi.org/10.1039/c7dt00468k
Okuno, Ryota, et al. "A novel symmetric TTF-pyridyl thiolato zinc complex: synthesis, characterization and crystal structure analysis." Dalton transactions (Cambridge, England : 2003) vol. 46,15 (2017): 4912-4916. doi: https://doi.org/10.1039/c7dt00468k
Okuno R, Yamaguchi M, Fujiwara H. A novel symmetric TTF-pyridyl thiolato zinc complex: synthesis, characterization and crystal structure analysis. Dalton Trans. 2017 Apr 11;46(15):4912-4916. doi: 10.1039/c7dt00468k. PMID: 28345714.
Copy Download .nbib Format: NLM
Calcium Hydride Catalyzed Highly 1,2-Selective Pyridine Hydrosilylation.

Chemistry (Weinheim an der Bergstrasse, Germany)

Intemann J, Bauer H, Pahl J, Maron L, Harder S.
PMID: 26120024
Chemistry. 2015 Aug 03;21(32):11452-61. doi: 10.1002/chem.201501072. Epub 2015 Jun 26.

Reaction of the calcium hydride complex (DIPPnacnac-CaH⋅THF)2 with pyridine is much faster and selective than that of the corresponding magnesium hydride complex (DIPPnacnac = [(2,6-iPr2 C6 H3 )NC(Me)]2 CH). With a range of pyridine, picoline and quinoline substrates, exclusive...

Cite
Intemann J, Bauer H, Pahl J, et al. Calcium Hydride Catalyzed Highly 1,2-Selective Pyridine Hydrosilylation. Chemistry. 2015;21(32):11452-61doi: 10.1002/chem.201501072.
Intemann, J., Bauer, H., Pahl, J., Maron, L., & Harder, S. (2015). Calcium Hydride Catalyzed Highly 1,2-Selective Pyridine Hydrosilylation. Chemistry (Weinheim an der Bergstrasse, Germany), 21(32), 11452-61. https://doi.org/10.1002/chem.201501072
Intemann, Julia, et al. "Calcium Hydride Catalyzed Highly 1,2-Selective Pyridine Hydrosilylation." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,32 (2015): 11452-61. doi: https://doi.org/10.1002/chem.201501072
Intemann J, Bauer H, Pahl J, Maron L, Harder S. Calcium Hydride Catalyzed Highly 1,2-Selective Pyridine Hydrosilylation. Chemistry. 2015 Aug 03;21(32):11452-61. doi: 10.1002/chem.201501072. Epub 2015 Jun 26. PMID: 26120024.
Copy Download .nbib Format: NLM
Three closely related 4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridines: synthesis, molecular conformations and hydrogen bonding in zero, one and two dimensions.

Acta crystallographica. Section C, Structural chemistry

Sagar BK, Harsha KB, Yathirajan HS, Rangappa KS, Rathore RS, Glidewell C.
PMID: 28257028
Acta Crystallogr C Struct Chem. 2017 Mar 01;73:298-304. doi: 10.1107/S205322961700273X. Epub 2017 Feb 23.

In each of 1-(4-fluorophenyl)-5-methylsulfonyl-3-[4-(trifluoromethyl)phenyl]-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine, C

Cite
Sagar BK, Harsha KB, Yathirajan HS, et al. Three closely related 4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridines: synthesis, molecular conformations and hydrogen bonding in zero, one and two dimensions. Acta Crystallogr C Struct Chem. 2017;73:298-304doi: 10.1107/S205322961700273X.
Sagar, B. K., Harsha, K. B., Yathirajan, H. S., Rangappa, K. S., Rathore, R. S., & Glidewell, C. (2017). Three closely related 4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridines: synthesis, molecular conformations and hydrogen bonding in zero, one and two dimensions. Acta crystallographica. Section C, Structural chemistry, 73298-304. https://doi.org/10.1107/S205322961700273X
Sagar, Belakavadi K, et al. "Three closely related 4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridines: synthesis, molecular conformations and hydrogen bonding in zero, one and two dimensions." Acta crystallographica. Section C, Structural chemistry vol. 73 (2017): 298-304. doi: https://doi.org/10.1107/S205322961700273X
Sagar BK, Harsha KB, Yathirajan HS, Rangappa KS, Rathore RS, Glidewell C. Three closely related 4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridines: synthesis, molecular conformations and hydrogen bonding in zero, one and two dimensions. Acta Crystallogr C Struct Chem. 2017 Mar 01;73:298-304. doi: 10.1107/S205322961700273X. Epub 2017 Feb 23. PMID: 28257028.
Copy Download .nbib Format: NLM
Electrocatalytic intramolecular oxidative annulation of N-aryl enamines into substituted indoles mediated by iodides.

Chemical communications (Cambridge, England)

Tang S, Gao X, Lei A.
PMID: 28261710
Chem Commun (Camb). 2017 Mar 16;53(23):3354-3356. doi: 10.1039/c7cc00410a.

An electrocatalytic reaction protocol is developed for achieving intramolecular dehydrogenative annulation of N-aryl enamines. It offers a simple and efficient way for the synthesis of indoles in an undivided cell. Good to excellent yields are obtained under oxidant-free and...

Cite
Tang S, Gao X, Lei A. Electrocatalytic intramolecular oxidative annulation of N-aryl enamines into substituted indoles mediated by iodides. Chem Commun (Camb). 2017;53(23):3354-3356doi: 10.1039/c7cc00410a.
Tang, S., Gao, X., & Lei, A. (2017). Electrocatalytic intramolecular oxidative annulation of N-aryl enamines into substituted indoles mediated by iodides. Chemical communications (Cambridge, England), 53(23), 3354-3356. https://doi.org/10.1039/c7cc00410a
Tang, Shan, et al. "Electrocatalytic intramolecular oxidative annulation of N-aryl enamines into substituted indoles mediated by iodides." Chemical communications (Cambridge, England) vol. 53,23 (2017): 3354-3356. doi: https://doi.org/10.1039/c7cc00410a
Tang S, Gao X, Lei A. Electrocatalytic intramolecular oxidative annulation of N-aryl enamines into substituted indoles mediated by iodides. Chem Commun (Camb). 2017 Mar 16;53(23):3354-3356. doi: 10.1039/c7cc00410a. PMID: 28261710.
Copy Download .nbib Format: NLM
Why vertically π-expanded imidazo[1,2-a]pyridines are weak fluorescence emitters: experimental and computational studies.

Physical chemistry chemical physics : PCCP

Banasiewicz M, Deperasińska I, Makarewicz A, Firmansyah D, Gryko DT, Kozankiewicz B.
PMID: 25746202
Phys Chem Chem Phys. 2015 Apr 14;17(14):8945-50. doi: 10.1039/c5cp00216h. Epub 2015 Mar 09.

Photophysics of π-expanded analogs of imidazo[1,2-a]pyridine, a well-known heterocyclic compound, has been experimentally and theoretically studied. Two regioisomeric systems differing only in the arrangement of the benzene ring have shown different optical properties (electronic transition energies, fluorescence quantum yields...

Cite
Banasiewicz M, Deperasińska I, Makarewicz A, et al. Why vertically π-expanded imidazo[1,2-a]pyridines are weak fluorescence emitters: experimental and computational studies. Phys Chem Chem Phys. 2015;17(14):8945-50doi: 10.1039/c5cp00216h.
Banasiewicz, M., Deperasińska, I., Makarewicz, A., Firmansyah, D., Gryko, D. T., & Kozankiewicz, B. (2015). Why vertically π-expanded imidazo[1,2-a]pyridines are weak fluorescence emitters: experimental and computational studies. Physical chemistry chemical physics : PCCP, 17(14), 8945-50. https://doi.org/10.1039/c5cp00216h
Banasiewicz, Marzena, et al. "Why vertically π-expanded imidazo[1,2-a]pyridines are weak fluorescence emitters: experimental and computational studies." Physical chemistry chemical physics : PCCP vol. 17,14 (2015): 8945-50. doi: https://doi.org/10.1039/c5cp00216h
Banasiewicz M, Deperasińska I, Makarewicz A, Firmansyah D, Gryko DT, Kozankiewicz B. Why vertically π-expanded imidazo[1,2-a]pyridines are weak fluorescence emitters: experimental and computational studies. Phys Chem Chem Phys. 2015 Apr 14;17(14):8945-50. doi: 10.1039/c5cp00216h. Epub 2015 Mar 09. PMID: 25746202.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 1226 entries