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Allylic strain (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Allylic strain" in English language version.

refsWebsite
Global rank English rank
16doi.org
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2harvard.edu
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1nih.gov
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1semanticscholar.org
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doi.org

  • Johnson, F (1968). "Allylic Strain in Six-Membered Rings". Chem. Rev. 68 (4): 375–413. doi:10.1021/cr60254a001.
  • Johnson, F; Malhorta, S K (1965). "Steric Interference in Allylic and Pseudo-Allylic Systems. I. Two Stereochemical Theorems". J. Am. Chem. Soc. 87 (23): 5492–5493. doi:10.1021/ja00951a047.
  • Allinger, N. L.; Hirsch, Jerry A.; Miller, Mary Ann.; Tyminski, Irene J. (1968). "Conformational Analysis. LXIV. Calculation of the Structures and Energies of Unsaturated Hydrocarbons by the Westheimer Method". J. Am. Chem. Soc. 90 (21): 5773–5780. doi:10.1021/ja01023a021.
  • Brown, H.; Barbarahs, G. K.; Berneis, H. L.; Bonner, W. H.; Johannesen, M. G.; Grayson, M. (1953). "Strained Homomorphs. 14. General Summary". J. Am. Chem. Soc. 75 (1): 1–6. doi:10.1021/ja01097a001.
  • Hoffman, R (1989). "Allylic 1,3-strain as a controlling factor in stereoselective transformations". Chem. Rev. 89 (8): 1841–1860. doi:10.1021/cr00098a009.
  • Bach, T.; Jodicke K.; Kather, K.; Frohlich, R. (1997). "1,3-Allylic Strain as a Control Element in the Paterno-Buchi Reaction of Chiral Silyl Enol Ethers: Synthesis of Diastereomerically Pure Oxetanes Containing Four Contiguous Stereogenic Centers". J. Am. Chem. Soc. 119 (10): 5315–5316. doi:10.1021/ja963827v.
  • Ramey, B.; Gardner, P. (1967). "Mechanism of photochemical alcohol addition to alpha, beta-unsaturated ketones". J. Am. Chem. Soc. 89 (15): 3949–3950. doi:10.1021/ja00991a078.
  • McGarvey, G.; Williams, J. (1985). "Stereoelectronic controlling features of allylic asymmetry. Application to ester enolate alkylations". J. Am. Chem. Soc. 107 (5): 1435–1437. doi:10.1021/ja00291a067.
  • Harris, R. K.; Sheppard, N. (1967). "Comments on the ring inversion of cyclohexane studied by NMR". J. Mol. Spectrosc. 23 (2): 231–235. Bibcode:1967JMoSp..23..231H. doi:10.1016/0022-2852(67)90015-X.
  • Overton, K. H.; Renfrew, A. J. (1967). "The configuration at C-13 in labdanolic and eperuic acids". J. Chem. Soc. C: 931–935. doi:10.1039/J39670000931.
  • Vaughn, W R; Caple, R; Csapilla, J; Scheiner, P (1965). "β-Bromo Acids. II. Solvolysis of Cyclic β-Bromo Acids". J. Am. Chem. Soc. 87 (10): 2204. doi:10.1021/ja01088a020.
  • Houk K. N.; Paddon-Row, M.; Rondan, N.; Wu, Y.; Brown, F.; Spellmeyer, D.; Metz, J.; Li, Y; Loncharich, R.; et al. (1986). "Theory and Modeling of Stereoselective Organic Reactions". Science. 231 (4742): 1108–1117. Bibcode:1986Sci...231.1108H. doi:10.1126/science.3945819. PMID 3945819.
  • Fleming, I. (1988). "Stereocontrol in organic synthesis using silicon compounds". Pure Appl. Chem. 60: 71–78. doi:10.1351/pac198860010071.
  • Evans, D. A.; Takacs, J. M.; McGee, L. R.; Ennis, M. D.; Mathre, D. J.; Bartroli, J.; et al. (1981). "Chiral enolate design". Pure Appl. Chem. 53 (6): 1109. doi:10.1351/pac198153061109. S2CID 93637283.
  • Ichihara, A.; et al. (1986). "Stereoselective total synthesis and stereochemistry of diplodiatoxin, a mycotoxin from ?". Tetrahedron Lett. 27 (12): 1347–1350. doi:10.1016/S0040-4039(00)84255-0.
  • Roush, W. R.; Kageyama, Masanori; Riva, Renata; Brown, Bradley B.; Warmus, Joseph S.; Moriarty, Kevin J.; et al. (1991). "Enantioselective synthesis of the bottom half of chlorothricolide. 3. Studies of the steric directing group strategy for stereocontrol in intramolecular Diels-Alder reactions". J. Org. Chem. 56 (3): 1192. doi:10.1021/jo00003a049.

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