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64
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0029906967
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Since this route was developed, McWhorter and Savall have published a route to 45 which is shorter and higher yielding, but the applicability of their synthesis on a large scale has not yet been demonstrated. Savall, B. M.; McWhorter, W. W. J. Org. Chem. 1996, 61, 8696-8697.
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(1996)
J. Org. Chem.
, vol.61
, pp. 8696-8697
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Savall, B.M.1
McWhorter, W.W.2
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65
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0032125820
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He, F.; Foxman, B. M.; Snider, B. B. J. Am. Chem. Soc. 1998, 120, 6417-6418.
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(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 6417-6418
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He, F.1
Foxman, B.M.2
Snider, B.B.3
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66
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0000052926
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(a) Somei, M.; Karasawa, Y.; Kaneko, C. Heterocycles 1981, 16, 941-949.
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(1981)
Heterocycles
, vol.16
, pp. 941-949
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Somei, M.1
Karasawa, Y.2
Kaneko, C.3
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67
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0342927518
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(b) Kametani, T.; Kanaya, N.; Ihara, M. J. Chem. Soc., Perkin Trans. 1 1981, 959-963.
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(1981)
J. Chem. Soc., Perkin Trans. 1
, pp. 959-963
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Kametani, T.1
Kanaya, N.2
Ihara, M.3
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68
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0141905418
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note
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1H NMR data. In compounds where the indole substituent is on the same face of the diketopiperazine as the MOM ether, the signal for the methoxy group is at significantly higher field than in the situation where these two substituents are on opposite faces. This is due to the proximity of the methoxy group to the shielding effects of the aromatic system.
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69
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0001136978
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Corey, E. J.; Kim, C. U.; Takeda, M. Tetrahedron Lett. 1972, 13, 4339-4342.
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(1972)
Tetrahedron Lett.
, vol.13
, pp. 4339-4342
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Corey, E.J.1
Kim, C.U.2
Takeda, M.3
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70
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0142009147
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note
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The synlanti relationship in this case refers to the relative stereochemistry between the C-20 stereogenic center (see paraherquamide numbering) and the proline residue. Equation Presented
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