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  On the Origin of π-Facial Diastereoselectivity in Nucleophilic Additions to Chiral Carbonyl Compounds 3. Rotational Profiles of 2-Methoxypropanal and 2-N,N-Dimethylaminopropanal.

Frenking, G., Köhler, K., & Reetz, M. T. (1993). On the Origin of π-Facial Diastereoselectivity in Nucleophilic Additions to Chiral Carbonyl Compounds 3. Rotational Profiles of 2-Methoxypropanal and 2-N,N-Dimethylaminopropanal. Tetrahedron, 49(19), 3971-3982. doi:10.1016/S0040-4020(01)89911-7.

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 Creators:
Frenking, G.1, 2, Author
Köhler, K.F.1, 2, Author
Reetz, Manfred T.1, 2, Author           
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1Research Department Reetz, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445588              
2Fachbereich Chemie, Philipps-Universität Marburg, Hans-Meerwein-Straße, D-W-3550 Marburg, Germany, ou_persistent22              

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 Abstract: The rotational profiles of 2-methoxypropanal and 2-N,N-dimethylaminopropanal are theoretically predicted using ab initio methods at the MP2/6-31G(d)//3-21G level of theory. The conformational energies show a strong dependence on the torsion angle not only around the CπC bond but also around the CπR (R=OMe, NMe2) bond.

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 Dates: 2001-04-231993-05-07
 Publication Status: Issued
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1016/S0040-4020(01)89911-7
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Title: Tetrahedron
  Other : Tetrahedron
Source Genre: Journal
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Publ. Info: Oxford : Pergamon
Pages: - Volume / Issue: 49 (19) Sequence Number: - Start / End Page: 3971 - 3982 Identifier: ISSN: 0040-4020
CoNE: https://pure.mpg.de/cone/journals/resource/954925448773