N.M.R. Spectra and Conformational Analysis of 4-Alkylcyclohexanols

This article is cited by 36 publications.

1. Harlan. Foster. Magnetic Resonance Spectrometry. Analytical Chemistry 1964, 36 (5) , 266-278. https://doi.org/10.1021/ac60211a022
2. . Fundamentals in Organic Fluorine Chemistry. 2007,,, 1-100. https://doi.org/10.1002/9780470988589.ch1
3. . Saul Winstein: Contributions to Physical Organic Chemistry and Bibliography. 2007,,, 1-24. https://doi.org/10.1002/9780470171882.ch1
4. Jerry A. Hirsch. Table of Conformational Energies-1967. 2007,,, 199-222. https://doi.org/10.1002/9780470147108.ch4
5. G. W. Buchanan, A. B. Driega, R. C. Laister, K. Bourque. Conformational analysis of crown ether analogs in solution:cis-cyclohexano-8-crown-3 as studied via low-temperature13C and1H NMR spectroscopy and molecular mechanics calculations. Magnetic Resonance in Chemistry 1999, 37 (6) , 401-4O6. https://doi.org/10.1002/(SICI)1097-458X(199906)37:6<401::AID-MRC469>3.0.CO;2-Z
6. G.W. Buchanan. Nuclear magnetic resonance studies of crown ethers. Progress in Nuclear Magnetic Resonance Spectroscopy 1999, 34 (3-4) , 327-377. https://doi.org/10.1016/S0079-6565(99)00006-0
7. Manfred Schlosser, Dominique Michel. About the “physiological size” of fluorine substituents: Comparison of sensorially active compounds with fluorine and methyl substituted analogues. Tetrahedron 1996, 52 (1) , 99-108. https://doi.org/10.1016/0040-4020(95)00886-D
8. Z. I. Safarova, V. I. Larionov, I. G. Bresler, R. S. Musavirov, T. F. Akhunov, D. L. Rakhmankulov. Conformational behavior of methyldialkoxysilanes by the MNDO method and IR spectroscopy. Journal of Structural Chemistry 1988, 28 (4) , 513-518. https://doi.org/10.1007/BF00749584
9. R. Saliba, XuÂn-Hoa Bui, R. Devis, P. Genard. Sur les ligands stéroïdoïdes de l'androgen binding protein. les énantiomères des Trans-trans etCis-trans perhydrohexestrols et Trans-trans perhydrodicétones. Journal of Steroid Biochemistry 1982, 17 (1) , 101-112. https://doi.org/10.1016/0022-4731(82)90599-4
10. O. A. Subbotin, N. M. Sergeyev, V. N. Chlopkov, N. G. Nikishova, Yu. G. Bundel. Conformational equilibria in isomeric methylcyclohexanols studied by13C NMR spectroscopy. Organic Magnetic Resonance 1980, 13 (4) , 259-262. https://doi.org/10.1002/mrc.1270130407
11. Yoko Kobayashi, Hirofumi Takahara, Hiroaki Takahashi, Keniti Higasi. Infiiared and raman studies of the structure of crystalline glygolaldehyde. Journal of Molecular Structure 1976, 32 (2) , 235-246. https://doi.org/10.1016/0022-2860(76)85002-8
12. J. C. van Ravenswaay Claasen, A. C. van der Linden. Substrate specificity of the paraffin hydroxylase ofPseudomonas aeruginosa. Antonie van Leeuwenhoek 1971, 37 (1) , 339-352. https://doi.org/10.1007/BF02218504
13. Edouard Demole. Synthèses stéréospécifiques et étude organoleptique comparée de onze triméthyl-2,2,3- exo -norbornyl-5- exo -cyclohexanols racémiques. Helvetica Chimica Acta 1969, 52 (7) , 2065-2085. https://doi.org/10.1002/hlca.19690520730
14. H. van Bekkum, H. M. A. Buurmans, G. van Minnen-Pathuis, B. M. Wepster. Hydrogenation of 1,3,5-tri-t-butylbenzene over platinum and palladium: Synthesis of cis,cis- and cis,trans-1,3,5-tri-t-butylcyclohexane. Recueil des Travaux Chimiques des Pays-Bas 1969, 88 (7) , 779-794. https://doi.org/10.1002/recl.19690880703
15. Harold Booth. Chapter 3 Applications of 1H nuclear magnetic resonance spectroscopy to the conformational analysis of cyclic compounds. Progress in Nuclear Magnetic Resonance Spectroscopy 1969, 5 , 149-381. https://doi.org/10.1016/0079-6565(69)80013-0
16. . REFERENCES. 1969,,, 385-440. https://doi.org/10.1016/B978-0-08-012542-8.50032-3
17. . REFERENCES. 1969,,, 385-440. https://doi.org/10.1016/B978-0-08-022953-9.50033-8
18. F.A.L. Anet, P.M. Henrichs. Conformational data from the chemical shifts of methine protons in deuterated cyclohexyl derivatives. Tetrahedron Letters 1969, 10 (9) , 741-744. https://doi.org/10.1016/S0040-4039(01)87797-2
19. G. N. Zhizhin, Kh. E. Sterin. A spectroscopic investigation of the conformational equilibrium of methyl cyclohexane. Journal of Applied Spectroscopy 1966, 5 (4) , 377-383. https://doi.org/10.1007/BF01132717
20. J.C. Celotti, J. Reisse, G. Chiurdoglu. Analyse conformationnelle par resonance nucleaire magnetique—III. Tetrahedron 1966, 22 (7) , 2249-2269. https://doi.org/10.1016/S0040-4020(01)82145-1
21. Walter Hückel, Peter Heinzelmann. Beiträge zur Konstellationsanalyse, XII. (Solvolyse von Toluolsulfonsäureestern, XXII). Die Carvomenthole. Justus Liebigs Annalen der Chemie 1965, 687 (1) , 82-102. https://doi.org/10.1002/jlac.19656870107
22. E. L. Eliel. Konformationsanalyse beweglicher Cyclohexan-Systeme. Angewandte Chemie 1965, 77 (17-18) , 784-797. https://doi.org/10.1002/ange.19650771708
23. H. Feltkamp, N. C. Franklin. Kernresonanzspektroskopische Konformationsanalyse an Cyclohexanderivaten. Angewandte Chemie 1965, 77 (17-18) , 798-807. https://doi.org/10.1002/ange.19650771709
24. N. Baggett, J.M. Duxbury, A.B. Foster, J.M. Webber. Diastereoisomeric forms of methyl 4,6-O-benzylidene-2,3-di-O-methyl-α-d-gluco- and α- and β-d-galactopyranoside. Carbohydrate Research 1965, 1 (1) , 22-30. https://doi.org/10.1016/S0008-6215(00)80209-8
25. G.E. McCasland. Chemical and Physical Studies of Cyclitols Containing Four or Five Hydroxyl Groups. 1965,,, 11-65. https://doi.org/10.1016/S0096-5332(08)60296-9
26. Yves-René Naves. Etudes sur les matières végétales volatiles. CXCIV [1] Stéréochimie conformationnelle des carvomenthols d'après leurs spectres d'absorption infrarouge et leyrs spectres de résonance magnétique nucléaire (2 e communication). Helvetica Chimica Acta 1964, 47 (6) , 1617-1621. https://doi.org/10.1002/hlca.19640470625
27. Edouard Demole, M. Stoll. Synthèses et relations entre constitution chimique et odeur dans la série des terpényl-3-cyclohexanols. Helvetica Chimica Acta 1964, 47 (7) , 1766-1774. https://doi.org/10.1002/hlca.19640470713
28. B.J. Armitage, G.W. Kenner, M.J.T. Robinson. Conformational effects in compounds with six-membered rings—II. Tetrahedron 1964, 20 (4) , 747-764. https://doi.org/10.1016/S0040-4020(01)98409-1
29. W.D. Cotterill, M.J.T. Robinson. Conformational effects in compounds with six-membered rings—III. Tetrahedron 1964, 20 (4) , 765-775. https://doi.org/10.1016/S0040-4020(01)98410-8
30. B.J. Armitage, G.W. Kenner, M.J.T. Robinson. Conformational effects in compounds with six-membered rings—I. Tetrahedron 1964, 20 (3) , 723-739. https://doi.org/10.1016/S0040-4020(01)98632-6
31. M. Anteunis, D. Tavernier. New models for conformational analysis by N.M.R.. Tetrahedron Letters 1964, 5 (52) , 3949-3951. https://doi.org/10.1016/S0040-4039(01)89346-1
32. J. Reisse, J.C. Celotti, D. Zimmermann, G. Chiurdoglu. Analyse conformationnelle par resonance nucleaire magnetique I. Difference d'enthalpie et d'enthalpie libre entre conformers du cyclohexanol.. Tetrahedron Letters 1964, 5 (31) , 2145-2150. https://doi.org/10.1016/S0040-4039(01)89470-3
33. Nobuo Mori, Satoshi Omura, Osamu Yamamoto, Teruo Suzuki, Yojiro Tsuzuki. Intramolecular Hydrogen Bonding in Some Aliphatic α- and β- Hydroxy-carboxylates. Bulletin of the Chemical Society of Japan 1963, 36 (11) , 1401-1407. https://doi.org/10.1246/bcsj.36.1401
34. Nobuo Mori, Fumie Suda. The Difference in Free Energy between Equatorial and Axial Isopropyl Groups. Bulletin of the Chemical Society of Japan 1963, 36 (2) , 227-228. https://doi.org/10.1246/bcsj.36.227
35. J. Sicher, J. Jonáš, M. Tichý. The a-values of the amino acid and dimethylamino groups. Tetrahedron Letters 1963, 4 (13) , 825-830. https://doi.org/10.1016/S0040-4039(01)90723-3
36. E.L. Eliel, M.H. Gianni, Th.H. Williams, J.B. Stothers. Chemical shifts in the nmr spectra of substituted cyclohexanols. Tetrahedron Letters 1962, 3 (17) , 741-747. https://doi.org/10.1016/S0040-4039(00)70511-9