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(Eta2-alkyne)methyl(dioxo)rhenium complexes as aldehyde-olefination catalysts.

Journal of the American Chemical Society

Santos AM, Romão CC, Kühn FE.
PMID: 12603128
J Am Chem Soc. 2003 Mar 05;125(9):2414-5. doi: 10.1021/ja021315c.

Complexes CH3ReO2L (L = 2-butyne, 3-hexyne, diphenylacetylene) are catalysts for the olefination of aldehydes, using 4-nitrobenzaldehyde (4-nba) as the standard aldehyde and ethyldiazoacetate (eda) as the diazo compound. Spectroscopic studies including in situ 31P, 17O, 13C, and 1H NMR...

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Santos AM, Romão CC, Kühn FE. (Eta2-alkyne)methyl(dioxo)rhenium complexes as aldehyde-olefination catalysts. J Am Chem Soc. 2003;125(9):2414-5doi: 10.1021/ja021315c.
Santos, A. M., Romão, C. C., & Kühn, F. E. (2003). (Eta2-alkyne)methyl(dioxo)rhenium complexes as aldehyde-olefination catalysts. Journal of the American Chemical Society, 125(9), 2414-5. https://doi.org/10.1021/ja021315c
Santos, Ana M, et al. "(Eta2-alkyne)methyl(dioxo)rhenium complexes as aldehyde-olefination catalysts." Journal of the American Chemical Society vol. 125,9 (2003): 2414-5. doi: https://doi.org/10.1021/ja021315c
Santos AM, Romão CC, Kühn FE. (Eta2-alkyne)methyl(dioxo)rhenium complexes as aldehyde-olefination catalysts. J Am Chem Soc. 2003 Mar 05;125(9):2414-5. doi: 10.1021/ja021315c. PMID: 12603128.
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A Polymer-Supported Phosphazine as a Stable and Practical Reagent in the Three-Component Synthesis of Substituted (Cyclopentadienyl)tricarbonylrhenium Complexes.

Angewandte Chemie (International ed. in English)

Minutolo F, Katzenellenbogen JA.
PMID: 29710984
Angew Chem Int Ed Engl. 1999 Jun 01;38(11):1617-1620. doi: 10.1002/(SICI)1521-3773(19990601)38:11<1617::AID-ANIE1617>3.0.CO;2-Z.

A very stable heterogenized difunctional cyclopentadienyl-ring precursor, storable under ambient conditions, readily participates in the simultaneous formation of a η

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Minutolo F, Katzenellenbogen JA. A Polymer-Supported Phosphazine as a Stable and Practical Reagent in the Three-Component Synthesis of Substituted (Cyclopentadienyl)tricarbonylrhenium Complexes. Angew Chem Int Ed Engl. 1999;38(11):1617-1620doi: 10.1002/(SICI)1521-3773(19990601)38:11<1617::AID-ANIE1617>3.0.CO;2-Z.
Minutolo, F., & Katzenellenbogen, J. A. (1999). A Polymer-Supported Phosphazine as a Stable and Practical Reagent in the Three-Component Synthesis of Substituted (Cyclopentadienyl)tricarbonylrhenium Complexes. Angewandte Chemie (International ed. in English), 38(11), 1617-1620. https://doi.org/10.1002/(SICI)1521-3773(19990601)38:11<1617::AID-ANIE1617>3.0.CO;2-Z
Minutolo, Filippo, and Katzenellenbogen, John A. "A Polymer-Supported Phosphazine as a Stable and Practical Reagent in the Three-Component Synthesis of Substituted (Cyclopentadienyl)tricarbonylrhenium Complexes." Angewandte Chemie (International ed. in English) vol. 38,11 (1999): 1617-1620. doi: https://doi.org/10.1002/(SICI)1521-3773(19990601)38:11<1617::AID-ANIE1617>3.0.CO;2-Z
Minutolo F, Katzenellenbogen JA. A Polymer-Supported Phosphazine as a Stable and Practical Reagent in the Three-Component Synthesis of Substituted (Cyclopentadienyl)tricarbonylrhenium Complexes. Angew Chem Int Ed Engl. 1999 Jun 01;38(11):1617-1620. doi: 10.1002/(SICI)1521-3773(19990601)38:11<1617::AID-ANIE1617>3.0.CO;2-Z. PMID: 29710984.
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Oxorhenium complexes as aldehyde-olefination catalysts.

Chemistry (Weinheim an der Bergstrasse, Germany)

Santos AM, Pedro FM, Yogalekar AA, Lucas IS, Romão CC, Kühn FE.
PMID: 15526317
Chemistry. 2004 Dec 03;10(24):6313-21. doi: 10.1002/chem.200400296.

Several oxorhenium compounds in the formal oxidation states V and VII are examined as catalysts for the aldehyde-olefination starting from diazo compounds, phosphines, and aldehydes. Of these, [ReMeO2(eta2-alkyne)] complexes provide the simplest catalysts to study, although [ReOCl3(PPh3)2] still remains...

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Santos AM, Pedro FM, Yogalekar AA, et al. Oxorhenium complexes as aldehyde-olefination catalysts. Chemistry. 2004;10(24):6313-21doi: 10.1002/chem.200400296.
Santos, A. M., Pedro, F. M., Yogalekar, A. A., Lucas, I. S., Romão, C. C., & Kühn, F. E. (2004). Oxorhenium complexes as aldehyde-olefination catalysts. Chemistry (Weinheim an der Bergstrasse, Germany), 10(24), 6313-21. https://doi.org/10.1002/chem.200400296
Santos, Ana M, et al. "Oxorhenium complexes as aldehyde-olefination catalysts." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 10,24 (2004): 6313-21. doi: https://doi.org/10.1002/chem.200400296
Santos AM, Pedro FM, Yogalekar AA, Lucas IS, Romão CC, Kühn FE. Oxorhenium complexes as aldehyde-olefination catalysts. Chemistry. 2004 Dec 03;10(24):6313-21. doi: 10.1002/chem.200400296. PMID: 15526317.
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Ultramark 1621 as a reference compound for positive and negative ion fast-atom bombardment high-resolution mass spectrometry.

Journal of the American Society for Mass Spectrometry

Jiang L, Moini M.
PMID: 24234707
J Am Soc Mass Spectrom. 1992 Nov;3(8):842-6. doi: 10.1016/1044-0305(92)80007-8.

Ultramark 1621, a commercially available mixture of fluorinated phosphazines, was found to be a useful calibration compound for negative and positive ion fast-atom bombardment (FAB) high-resolution mass spectrometry. Ultramark 1621 worked very well with the most widely used matrices...

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Jiang L, Moini M. Ultramark 1621 as a reference compound for positive and negative ion fast-atom bombardment high-resolution mass spectrometry. J Am Soc Mass Spectrom. 1992;3(8):842-6doi: 10.1016/1044-0305(92)80007-8.
Jiang, L., & Moini, M. (1992). Ultramark 1621 as a reference compound for positive and negative ion fast-atom bombardment high-resolution mass spectrometry. Journal of the American Society for Mass Spectrometry, 3(8), 842-6. https://doi.org/10.1016/1044-0305(92)80007-8
Jiang, L, and Moini, M. "Ultramark 1621 as a reference compound for positive and negative ion fast-atom bombardment high-resolution mass spectrometry." Journal of the American Society for Mass Spectrometry vol. 3,8 (1992): 842-6. doi: https://doi.org/10.1016/1044-0305(92)80007-8
Jiang L, Moini M. Ultramark 1621 as a reference compound for positive and negative ion fast-atom bombardment high-resolution mass spectrometry. J Am Soc Mass Spectrom. 1992 Nov;3(8):842-6. doi: 10.1016/1044-0305(92)80007-8. PMID: 24234707.
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N-Phosphino- and N-Phosphonionitrilimines: From Nucleophilic to Electrophilic 1,3-Dipoles.

The Journal of organic chemistry

Palacios F, Pagalday J, Piquet V, Dahan F, Baceiredo A, Bertrand G.
PMID: 11671401
J Org Chem. 1997 Jan 24;62(2):292-296. doi: 10.1021/jo961443h.

N-[Bis(diisopropylamino)phosphino]-C-[bis(diisopropylamino)thioxophosphoranyl]nitrilimine (1) reacts with electron-poor dipolarophiles such as maleimide, methyl vinyl ketone, and 1,4-naphthoquinone via HOMO(dipole)-controlled [2+3] cycloadditions, while N-[bis(diisopropylamino)(methyl)phosphonio]-C-[bis(diisopropylamino)thioxophosphoranyl]nitrilimine (2a) reacts with electron-rich dipolarophiles such as norbornadiene and ethyl trans-pyrrolineacrylate via LUMO(dipole)-controlled [2+3] cycloadditions. Carbon disulfide reacts with...

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Palacios F, Pagalday J, Piquet V, et al. N-Phosphino- and N-Phosphonionitrilimines: From Nucleophilic to Electrophilic 1,3-Dipoles. J Org Chem. 1997;62(2):292-296doi: 10.1021/jo961443h.
Palacios, F., Pagalday, J., Piquet, V., Dahan, F., Baceiredo, A., & Bertrand, G. (1997). N-Phosphino- and N-Phosphonionitrilimines: From Nucleophilic to Electrophilic 1,3-Dipoles. The Journal of organic chemistry, 62(2), 292-296. https://doi.org/10.1021/jo961443h
Palacios, Francisco, et al. "N-Phosphino- and N-Phosphonionitrilimines: From Nucleophilic to Electrophilic 1,3-Dipoles." The Journal of organic chemistry vol. 62,2 (1997): 292-296. doi: https://doi.org/10.1021/jo961443h
Palacios F, Pagalday J, Piquet V, Dahan F, Baceiredo A, Bertrand G. N-Phosphino- and N-Phosphonionitrilimines: From Nucleophilic to Electrophilic 1,3-Dipoles. J Org Chem. 1997 Jan 24;62(2):292-296. doi: 10.1021/jo961443h. PMID: 11671401.
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Interaction between chemical mutagens with a delayed effect and metabolites of seeds : Communication 2: changes in mutagenic activity.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik

Shevchenko VV, Protopopova EM, Grigoriyeva GA, Bolotova TK.
PMID: 24430019
Theor Appl Genet. 1971 Jan;41(2):52-6. doi: 10.1007/BF00277045.

A study was made of chromosome aberrations in Crepis capillaris seedlings, induced by the reaction products of chemical mutagens with seed metabolites. Interaction between ethylenimine and seed metabolites of some plants of the family Compositae (C. capillaris, Taraxacum officinale,...

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Shevchenko VV, Protopopova EM, Grigoriyeva GA, et al. Interaction between chemical mutagens with a delayed effect and metabolites of seeds : Communication 2: changes in mutagenic activity. Theor Appl Genet. 1971;41(2):52-6doi: 10.1007/BF00277045.
Shevchenko, V. V., Protopopova, E. M., Grigoriyeva, G. A., & Bolotova, T. K. (1971). Interaction between chemical mutagens with a delayed effect and metabolites of seeds : Communication 2: changes in mutagenic activity. TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 41(2), 52-6. https://doi.org/10.1007/BF00277045
Shevchenko, V V, et al. "Interaction between chemical mutagens with a delayed effect and metabolites of seeds : Communication 2: changes in mutagenic activity." TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik vol. 41,2 (1971): 52-6. doi: https://doi.org/10.1007/BF00277045
Shevchenko VV, Protopopova EM, Grigoriyeva GA, Bolotova TK. Interaction between chemical mutagens with a delayed effect and metabolites of seeds : Communication 2: changes in mutagenic activity. Theor Appl Genet. 1971 Jan;41(2):52-6. doi: 10.1007/BF00277045. PMID: 24430019.
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Electrohydrodynamics of Gas-Assisted Electrospray Ionization Mass Spectrometry.

Journal of the American Society for Mass Spectrometry

Lee JY, Kottke PA, Fedorov AG.
PMID: 32869991
J Am Soc Mass Spectrom. 2020 Oct 07;31(10):2073-2085. doi: 10.1021/jasms.0c00197. Epub 2020 Sep 17.

Gas-flow assistance is commonly used in ESI-MS for improved transport and desolvation, and fundamental understanding of the underlying phenomena is essential for improvement of aerodynamic interfaces that couple ESI sources and MS. For this purpose, an electrohydrodynamic model is...

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Lee JY, Kottke PA, Fedorov AG. Electrohydrodynamics of Gas-Assisted Electrospray Ionization Mass Spectrometry. J Am Soc Mass Spectrom. 2020;31(10):2073-2085doi: 10.1021/jasms.0c00197.
Lee, J. Y., Kottke, P. A., & Fedorov, A. G. (2020). Electrohydrodynamics of Gas-Assisted Electrospray Ionization Mass Spectrometry. Journal of the American Society for Mass Spectrometry, 31(10), 2073-2085. https://doi.org/10.1021/jasms.0c00197
Lee, Jung Y, et al. "Electrohydrodynamics of Gas-Assisted Electrospray Ionization Mass Spectrometry." Journal of the American Society for Mass Spectrometry vol. 31,10 (2020): 2073-2085. doi: https://doi.org/10.1021/jasms.0c00197
Lee JY, Kottke PA, Fedorov AG. Electrohydrodynamics of Gas-Assisted Electrospray Ionization Mass Spectrometry. J Am Soc Mass Spectrom. 2020 Oct 07;31(10):2073-2085. doi: 10.1021/jasms.0c00197. Epub 2020 Sep 17. PMID: 32869991.
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Showing 1 to 7 of 7 entries