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Data from: Readily Available Primary Aminoboranes as Powerful Reagents for Aldimine Synthesis

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Data from: Readily Available Primary Aminoboranes as Powerful Reagents for Aldimine Synthesis

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Extent

1 digital object.

Cite This Work

Junor, Glen P.; Romero, Erik A.; Chen, Xi; Jazzar, Rodolphe; Bertrand, Guy (2019). Data From: Readily Available Primary Aminoboranes as Powerful Reagents for Aldimine Synthesis. UC San Diego Library Digital Collections. https://doi.org/10.6075/J00Z71HW

Description

Abstract: Primary aminoboranes (RNHBR2), which are readily available by spontaneous dehydrocoupling of amines and boranes cleanly react at room temperature with aldehydes to give aldimines. The overall transformation from amines to aldimines can be conveniently performed by a sequential one-pot reaction. This synthetic strategy is especially useful for electron poor and bulky amines which are reluctant to react with aldehydes under dehydration conditions. Using a Glorius robustness screen, we show that this methodology is chemoselective, and functional group tolerant. Computational and experimental data support the irreversible formation of the aldimine product in marked contrast with traditional methods.

Scope And Content

Data pertaining to each computed pathway, for the reaction between aldehydes and aminoboranes, can be downloaded. Within each .zip file are a number of folders containing .log, .chk, and .fchk files for each species along the reaction coordinate. Some folders contain additional subfolders.

Creation Date
  • 2017 to 2018
Date Issued
  • 2019
Authors
Principal Investigator
Co Principal Investigator
Technical Details

Gaussian 09, Revision D.01,M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, G. Scalmani, V. Barone, B. Mennucci, G. A. Petersson, H. Nakatsuji, M. Caricato, X. Li, H. P. Hratchian, A. F. Izmaylov, J. Bloino, G. Zheng, J. L. Sonnenberg, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, T. Vreven, J. A. Montgomery, Jr., J. E. Peralta, F. Ogliaro, M. Bearpark, J. J. Heyd, E. Brothers, K. N. Kudin, V. N. Staroverov, T. Keith, R. Kobayashi, J. Normand, K. Raghavachari, A. Rendell, J. C. Burant, S. S. Iyengar, J. Tomasi, M. Cossi, N. Rega, J. M. Millam, M. Klene, J. E. Knox, J. B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R. E. Stratmann, O. Yazyev, A. J. Austin, R. Cammi, C. Pomelli, J. W. Ochterski, R. L. Martin, K. Morokuma, V. G. Zakrzewski, G. A. Voth, P. Salvador, J. J. Dannenberg, S. Dapprich, A. D. Daniels, O. Farkas, J. B. Foresman, J. V. Ortiz, J. Cioslowski, and D. J. Fox, Gaussian, Inc., Wallingford CT, 2013.

Funding

This work was supported by the U.S. Department of Energy, Office of Science, Basic Energy Sciences, Catalysis Science Program, under Award No. DE-SC0009376. Thanks are due to the U.S. Department of Education for a GAANN fellowship (E.A.R.), and to the Alfred P. Sloan Foundation’s University Centre for Exemplary Mentoring (G.P.J.). This material is based upon work supported by the National Science Foundation Graduate Research Fellowship Program under Grant No. (DGE-1650112; G.P.J.). Any opinions, findings, and conclusions or recommendations expressed in this material are those of the author(s) and do not necessarily reflect the views of the National Science Foundation. We also acknowledge the Keck Foundation as well as the Extreme Science and Engineering Discovery Environment (XSEDE), which is supported by National Science Foundation grant number ACI-1548562 for provided computational resources.

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Language
  • No linguistic content; Not applicable
Identifier

Identifier: Erik A Romero: https://orcid.org/0000-0002-5155-1684

Identifier: Glen P. Junor: https://orcid.org/0000-0002-6733-3577

Identifier: Guy Bertrand: https://orcid.org/0000-0003-2623-2363

Identifier: Rodolphe Jazzar: https://orcid.org/0000-0002-4156-7826

Identifier: Xi Chen: https://orcid.org/0000-0001-7086-5753

Related Resources
Data from: Readily Available Primary Aminoboranes as Powerful Reagents for Aldimine Synthesis
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