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For malonic acid half-thioesters, see: Magdziak D., Lalic G., Lee H. M., Fortner K. C., Aloise A. D., Shair M. D., J. Am. Chem. Soc., 127, 7284-7285 (2005).
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For N-acyl pyrroles, see: Harada S., Handa S., Matsunaga S., Shibasaki M., Angew. Chem., Int. Ed., 44, 4365-4368 (2005).
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For trichloromethyl ketones, see: Morimoto H., Wiedemann S. H., Yamaguchi A., Harada S., Chen Z., Matsunaga S., Shibasaki M., Angew. Chem., Int. Ed., 45, 3146-3150 (2006).
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For N-acyl Boc-amides, see
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For N-acyl Boc-amides, see: Saito S., Kobayashi S., J. Am. Chem. Soc., 128, 8704-8705 (2006).
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For an example of catalytic chemoselective nucleophilic activation of alkylnitrile, see: Kumagai N., Matsunaga M., Shibasaki M., J. Am. Chem. Soc., 126, 13632-13633 (2004).
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24044486627
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34447513871
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46749152555
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78650825964
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Calculated at the B3LYP/6-31G+(d,p) level in ref. 142
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Calculated at the B3LYP/6-31G+(d,p) level in ref. 142.
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33847713336
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51049122384
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67650657513
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Adachi, S.1
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31444453628
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For an example of catalytic asymmetric addition to ketones coupled with hydrogenation, see: Kong J.-R., Ngai M.-Y., Krische M. J., J. Am. Chem. Soc., 128, 718-719 (2006).
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33744913650
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For an example of catalytic asymmetric addition to ketones coupled with hydrogenation, see: Deschamp J., Chuzel O., Hannedouche J., Riant O., Angew. Chem., Int. Ed., 45, 1292-1297 (2006).
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For an example of catalytic asymmetric addition to ketones coupled with hydrogenation, see: Komanduri V., Krische M. J., J. Am. Chem. Soc., 128, 16448-16449 (2006).
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For an example of catalytic asymmetric addition to ketones coupled with hydrogenation, see: Bower J. F., Kim I. S., Patman R. L., Krische M. J., Angew. Chem., Int. Ed., 48, 34-46 (2009).
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33748250873
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For an example of catalytic asymmetric addition to ketones coupled with hydrogenation, see
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For an example of catalytic asymmetric addition to ketones coupled with hydrogenation, see: Chmura A., van der Kraan G. M., van Langen L. M., van Rantwijk F., Sheldon R. A., Adv. Synth. Catal., 348, 1655-1661 (2006).
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Enhanced Lewis basicity of LiOPh was observed by using bidentate phosphine oxide 25 in Mukaiyama aldol reactions. X-ray crystallographic analysis confirmed the coordination of 25 to Li cation in a bidentate fashion, Hatano M., Takagi E., Ishihara K., Org. Lett., 9, 4527-4530 (2007).
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For an asymmetric aldol reaction mediated by a stoichiometric amount of a strong base and a chiral ligand, see
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For a recent review of direct catalytic asymmetric aldol reactions, see refs. 111-118.
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176
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For a pioneering example of a direct catalytic asymmetric aldol reaction promoted by a metal-based catalyst, see: Yamada Y. M. A., Yoshikawa N., Sasai H., Shibasaki M., Angew. Chem., Int. Ed., 36, 1871-1873 (1997).
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For an early example of a direct aldol-type reaction using α-isocyanoacetate as an active methylene type aldol donor, see
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For an early example of a direct aldol-type reaction using α-isocyanoacetate as an active methylene type aldol donor, see: Ito Y., Sawamura M., Hayashi T., J. Am. Chem. Soc., 108, 6405-6406 (1986).
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For a pioneering example of a direct catalytic asymmetric aldol reaction promoted by a metal-based catalyst, see: Yoshikawa N., Yamada Y. M. A., Das J., Sasai H., Shibasaki M., J. Am. Chem. Soc., 121, 4168-4178 (1999).
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For a pioneering example of a direct catalytic asymmetric aldol reaction promoted by a metal-based catalyst, see: Trost B. M., Ito H., J. Am. Chem. Soc., 122, 12003-12004 (2000).
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For a pioneering example of a direct catalytic asymmetric aldol reaction promoted by a metal-based catalyst, see: Mahrwald R., Ziemer B., Tetrahedron Lett., 43, 4459-4461 (2002).
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For a pioneering example of a direct catalytic asymmetric intermolecular aldol reaction promoted by organocatalysts, see: List B., Lerner R. A., Barbas C. F. III, J. Am. Chem. Soc., 122, 2395-2396 (2000).
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For a pioneering example of a direct catalytic asymmetric intermolecular aldol reaction promoted by organocatalysts, see: Sakthivel K., Notz W., Bui T., Barbas C. F. III, J. Am. Chem. Soc., 123, 5260-5267 (2001).
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For a pioneering example of a direct catalytic asymmetric intermolecular aldol reaction promoted by organocatalysts, see: Saito S., Nakadai M., Yamamoto H., Synlett, 2001, 1245-1248 (2001).
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For direct catalytic asymmetric aldol (-type) reactions using aldol donors in the carboxylic acid oxidation state without electron-withdrawing α-substituents: alkylnitriles (up to 77% ee), see
-
For direct catalytic asymmetric aldol (-type) reactions using aldol donors in the carboxylic acid oxidation state without electron-withdrawing α-substituents: alkylnitriles (up to 77% ee), see: Suto Y., Tsuji R., Kanai M., Shibasaki M., Org. Lett., 7, 3757-3760 (2005).
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-
For direct catalytic asymmetric aldol (-type) reactions using aldol donors in the carboxylic acid oxidation state without electron-withdrawing α-substituents: activated amides (up to 33% ee), see: Saito S., Kobayashi S., J. Am. Chem. Soc., 128, 8704-8705 (2006).
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-
For direct catalytic asymmetric aldol (-type) reactions using aldol donors in the carboxylic acid oxidation state without electron-withdrawing α-substituents: β,γ-unsaturated esters, see: Yamaguchi A., Matsunaga S., Shibasaki M., J. Am. Chem. Soc., 131, 10842-10843 (2009).
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