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Synthesis, structure, and reactions of (acylimino)triaryl-lambda(5)-bismuthanes: first comparative study of the (acylimino)pnictorane series.

Journal of the American Chemical Society

Matano Y, Nomura H, Suzuki H, Shiro M, Nakano H.
PMID: 11686699
J Am Chem Soc. 2001 Nov 07;123(44):10954-65. doi: 10.1021/ja003623l.

The synthesis, structure, and reactions of (acylimino)triaryl-lambda(5)-bismuthanes and a comparative study of the structure and reactivity of a series of (acylimino)pnictoranes are reported. Treatment of ortho-substituted triarylbismuth dichlorides 1 (Ar(3)BiCl(2); Ar = 2-MeC(6)H(4), 2-MeOC(6)H(4), 2,4,6-Me(3)C(6)H(2)) with amides 2 (H(2)NCOR;...

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Matano Y, Nomura H, Suzuki H, et al. Synthesis, structure, and reactions of (acylimino)triaryl-lambda(5)-bismuthanes: first comparative study of the (acylimino)pnictorane series. J Am Chem Soc. 2001;123(44):10954-65doi: 10.1021/ja003623l.
Matano, Y., Nomura, H., Suzuki, H., Shiro, M., & Nakano, H. (2001). Synthesis, structure, and reactions of (acylimino)triaryl-lambda(5)-bismuthanes: first comparative study of the (acylimino)pnictorane series. Journal of the American Chemical Society, 123(44), 10954-65. https://doi.org/10.1021/ja003623l
Matano, Y, et al. "Synthesis, structure, and reactions of (acylimino)triaryl-lambda(5)-bismuthanes: first comparative study of the (acylimino)pnictorane series." Journal of the American Chemical Society vol. 123,44 (2001): 10954-65. doi: https://doi.org/10.1021/ja003623l
Matano Y, Nomura H, Suzuki H, Shiro M, Nakano H. Synthesis, structure, and reactions of (acylimino)triaryl-lambda(5)-bismuthanes: first comparative study of the (acylimino)pnictorane series. J Am Chem Soc. 2001 Nov 07;123(44):10954-65. doi: 10.1021/ja003623l. PMID: 11686699.
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Site of alkylation of N-methyl- and N-ethylaniline in the gas phase: a tandem mass spectrometric study.

Journal of mass spectrometry : JMS

Ackloo S, Harrison AG, Terlouw JK.
PMID: 15236303
J Mass Spectrom. 2004 Jun;39(6):647-54. doi: 10.1002/jms.632.

N-Methylaniline (NMA) was ethylated and N-ethylaniline (NEA) was methylated under chemical ionization conditions using C(2)H(5)I and CH(3)I, respectively, as reagent gases. The structures of the resulting m/z 136 adduct ions have been probed using metastable ion and collision-induced dissociation...

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Ackloo S, Harrison AG, Terlouw JK. Site of alkylation of N-methyl- and N-ethylaniline in the gas phase: a tandem mass spectrometric study. J Mass Spectrom. 2004;39(6):647-54doi: 10.1002/jms.632.
Ackloo, S., Harrison, A. G., & Terlouw, J. K. (2004). Site of alkylation of N-methyl- and N-ethylaniline in the gas phase: a tandem mass spectrometric study. Journal of mass spectrometry : JMS, 39(6), 647-54. https://doi.org/10.1002/jms.632
Ackloo, Suzanne, et al. "Site of alkylation of N-methyl- and N-ethylaniline in the gas phase: a tandem mass spectrometric study." Journal of mass spectrometry : JMS vol. 39,6 (2004): 647-54. doi: https://doi.org/10.1002/jms.632
Ackloo S, Harrison AG, Terlouw JK. Site of alkylation of N-methyl- and N-ethylaniline in the gas phase: a tandem mass spectrometric study. J Mass Spectrom. 2004 Jun;39(6):647-54. doi: 10.1002/jms.632. PMID: 15236303.
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Synthesis of 3-Amino-7-(N,N-Dimethylamino)-2-Substituted-5-Phenylphenazin-5-Ium Chlorides by Oxidative Cyclization.

Current organic synthesis

Liu Y, Jin L, Liu JF, Wang YQ, Zhou ZX.
PMID: 31975677
Curr Org Synth. 2019;16(2):283-287. doi: 10.2174/1570179416666181228122731.

AIM AND OBJECTIVE: Phenazines are substances with an extensive range of important applications. Recently, the synthesis of N-arylation has been made more feasible owing to the advent of a new methodology. But because the toxicity of the used oxidant...

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Liu Y, Jin L, Liu JF, et al. Synthesis of 3-Amino-7-(N,N-Dimethylamino)-2-Substituted-5-Phenylphenazin-5-Ium Chlorides by Oxidative Cyclization. Curr Org Synth. 2019;16(2):283-287doi: 10.2174/1570179416666181228122731.
Liu, Y., Jin, L., Liu, J. F., Wang, Y. Q., & Zhou, Z. X. (2019). Synthesis of 3-Amino-7-(N,N-Dimethylamino)-2-Substituted-5-Phenylphenazin-5-Ium Chlorides by Oxidative Cyclization. Current organic synthesis, 16(2), 283-287. https://doi.org/10.2174/1570179416666181228122731
Liu, Yuan, et al. "Synthesis of 3-Amino-7-(N,N-Dimethylamino)-2-Substituted-5-Phenylphenazin-5-Ium Chlorides by Oxidative Cyclization." Current organic synthesis vol. 16,2 (2019): 283-287. doi: https://doi.org/10.2174/1570179416666181228122731
Liu Y, Jin L, Liu JF, Wang YQ, Zhou ZX. Synthesis of 3-Amino-7-(N,N-Dimethylamino)-2-Substituted-5-Phenylphenazin-5-Ium Chlorides by Oxidative Cyclization. Curr Org Synth. 2019;16(2):283-287. doi: 10.2174/1570179416666181228122731. PMID: 31975677.
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Reduction and Acetylation of 2,4-Dinitrotoluene by a Pseudomonas aeruginosa Strain.

Applied and environmental microbiology

Noguera DR, Freedman DL.
PMID: 16535348
Appl Environ Microbiol. 1996 Jul;62(7):2257-63. doi: 10.1128/aem.62.7.2257-2263.1996.

Aerobic and anoxic biotransformation of 2,4-dinitrotoluene (DNT) was examined by using a Pseudomonas aeruginosa strain isolated from a plant treating propellant manufacturing wastewater. DNT biotransformation in the presence and absence of oxygen was mostly reductive and was representative of...

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Noguera DR, Freedman DL. Reduction and Acetylation of 2,4-Dinitrotoluene by a Pseudomonas aeruginosa Strain. Appl Environ Microbiol. 1996;62(7):2257-63doi: 10.1128/aem.62.7.2257-2263.1996.
Noguera, D. R., & Freedman, D. L. (1996). Reduction and Acetylation of 2,4-Dinitrotoluene by a Pseudomonas aeruginosa Strain. Applied and environmental microbiology, 62(7), 2257-63. https://doi.org/10.1128/aem.62.7.2257-2263.1996
Noguera, D R, and Freedman, D L. "Reduction and Acetylation of 2,4-Dinitrotoluene by a Pseudomonas aeruginosa Strain." Applied and environmental microbiology vol. 62,7 (1996): 2257-63. doi: https://doi.org/10.1128/aem.62.7.2257-2263.1996
Noguera DR, Freedman DL. Reduction and Acetylation of 2,4-Dinitrotoluene by a Pseudomonas aeruginosa Strain. Appl Environ Microbiol. 1996 Jul;62(7):2257-63. doi: 10.1128/aem.62.7.2257-2263.1996. PMID: 16535348; PMCID: PMC1388886.
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Showing 1 to 4 of 4 entries