Structure and Reactivity of Five‐ and Six‐Ring N, N‐, N, O‐, and O, O‐acetals: A lesson in allylic 1, 3‐strain (A1, 3strain)
- 6 May 1992
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 75 (3), 913-934
- https://doi.org/10.1002/hlca.19920750326
Abstract
No abstract availableKeywords
This publication has 127 references indexed in Scilit:
- Acyclic stereochemical control in free-radical reactionsAccounts of Chemical Research, 1991
- Synthese im Blickpunkt C2-Symmetrische Amine als chirale AuxiliareNachrichten aus Chemie, Technik und Laboratorium, 1991
- Acyclic tertiary and quaternary carbon stereocontrol via new aldol equivalent reactions of optically active (E)-enol ethersJournal of the American Chemical Society, 1989
- Pyrrolidine ring conformations in prolyl peptides from 13C spin‐lattice relaxation timesInternational Journal of Peptide and Protein Research, 1984
- Spezifikation des sterischen Verlaufs von asymmetrischen SynthesenAngewandte Chemie, 1982
- Amide group deformation in medium-ring lactamsActa Crystallographica Section B: Structural Science, Crystal Engineering and Materials, 1975
- Conformational structure, energy, and inversion rates of cyclohexane and some related oxanesJournal of the American Chemical Society, 1970
- Steric Interference in Allylic and Pseudo-Allylic Systems. II. Stereochemistry of Exocyclic Enolate Anion ProtonationJournal of the American Chemical Society, 1965
- Steric Interference in Allylic and Pseudo-Allylic Systems. I. Two Stereochemical TheoremsJournal of the American Chemical Society, 1965
- The Thermodynamics and Molecular Structure of Cyclopentane1Journal of the American Chemical Society, 1947