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Structures 28a-c and 28aTS-cTS were reoptimized with electron correlation included at the MP2/6-31G* level. The MP2/6-31G*//6-31G*-optimized structures are not dramatically different from those obtained at the HF/6-31G*//6-31G* level, in particular conformer 28a-Z does persist as minimum at this computational level.
-
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Moss, R. A.; Ho, G.-J.; Shen, S.; Krogh-Jesperson, K. J. Am. Chem. Soc. 1990, 112, 1638. Ho, G.-J.; Krogh-Jespersen, K.; Moss, R. A.; Shen, S.; Sheridan, R. S.; Subramanian, R. Ibid. 1989, 111, 6875.
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For example, the additions of ArCCl to various alkenes are accelerated by electron-withdrawing groups, with ρ ≈ 1.4-1.6: Moss, R. A.; Perez, L. A.; Turro, N. J.; Gould, I. R.; Hacker, N. P. Tetrahedron Lett. 1983, 24, 685.
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J. Phys. Org. Chem.
, vol.5
, pp. 104
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Moss, R.A.1
Jang, E.G.2
Fan, H.3
Wlostowski, M.4
Krogh-Jespersen, K.5
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63
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1542601132
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Moss, R. A.; Fan, H.; Hadel, L. M.; Shen, S.; Wlostowska, J.; Wlostowski, M.; Krogh-Jespersen, K. Tetrahedron Lett. 1987, 28, 4779.
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(1987)
Tetrahedron Lett.
, vol.28
, pp. 4779
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Moss, R.A.1
Fan, H.2
Hadel, L.M.3
Shen, S.4
Wlostowska, J.5
Wlostowski, M.6
Krogh-Jespersen, K.7
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64
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0011828418
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Platz, M. S., Ed.; Plenum Press: New York, and references therein
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Moss, R. A.; Turro, N. J. In Kinetics and Spectroscopy of Carbenes and Biradicals; Platz, M. S., Ed.; Plenum Press: New York, 1990; pp 213ff and references therein.
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(1990)
Kinetics and Spectroscopy of Carbenes and Biradicals
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Moss, R.A.1
Turro, N.J.2
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65
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0000955563
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Moss, R. A.; Lawrynowicz, W.; Hadel, L. M. Tetrahedron Lett. 1986, 27, 4125.
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(1986)
Tetrahedron Lett.
, vol.27
, pp. 4125
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Moss, R.A.1
Lawrynowicz, W.2
Hadel, L.M.3
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66
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12644316007
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note
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50
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67
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0005618983
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Brandstrom, A.; Berntsson, P.; Carlsson, S.; Djurhuus, A.; Gustavii, K.; Junggren, U.; Lamm, B.; Samuelsson, B. Acta Chem. Scand. 1969, 23, 2202.
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(1969)
Acta Chem. Scand.
, vol.23
, pp. 2202
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Brandstrom, A.1
Berntsson, P.2
Carlsson, S.3
Djurhuus, A.4
Gustavii, K.5
Junggren, U.6
Lamm, B.7
Samuelsson, B.8
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68
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12644252770
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note
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All diazirine yields were determined by NMR and are based on consumed bromodiazirine.
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69
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12644280670
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note
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max of 9 is erroneously given as 336 instead of 364 nm.
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70
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85083011615
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Armesto, D.; Horspool, W. M.; Ortiz, M. J.; Perez-Ossorio, R. Synthesis 1988, 799.
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(1988)
Synthesis
, pp. 799
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Armesto, D.1
Horspool, W.M.2
Ortiz, M.J.3
Perez-Ossorio, R.4
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73
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33947482230
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In view of the higher field appearance of the OOCMe singlet and lower field appearance of the upfield cyclopropyl Me singlet of the major isomer, this isomer is likely to be of the syn-OAc configuration. For NMR shielding effects in phenylcyclopropanes, see: Closs, G. L.; Moss, R. A. J. Am. Chem. Soc. 1964, 86, 4042.
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(1964)
J. Am. Chem. Soc.
, vol.86
, pp. 4042
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Closs, G.L.1
Moss, R.A.2
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