亨利反应 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "亨利反应" in Chinese language version.

Last modified: 03:04:59, 19 July 2026 (UTC)

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1614doi.org

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archive.org (Global: 6^th place; Chinese: 2^nd place)

Kurti, L.; Czako, B. Strategic Applications of Named Reactions in Organic Synthesis. Burlington, MA: Elsevier Academic Press. 2005: 202–203. ISBN 978-0-12-369483-6.
Noboro, Ono. The Nitro Group in Organic Synthesis. New York, NY: Wiley-VCH. 2001: 30–69. ISBN 978-0-471-31611-4.
Sasai, Hiroaki; Suzuki, Takeyuki; Arai, Shigeru; Arai, Takayoshi; Shibasaki, Masakatsu. Basic character of rare earth metal alkoxides. Utilization in catalytic carbon-carbon bond-forming reactions and catalytic asymmetric nitroaldol reactions. Journal of the American Chemical Society. 1 May 1992, 114 (11): 4418–4420. doi:10.1021/ja00037a068.
Seayad, J., List, B. Asymmetric organocatalysis. Org. Biomol. Chem. 2005, 3 (5): 719–724. PMID 15731852. doi:10.1039/b415217b.
Gogoi, N., Boruwa, J., Barua, N.C. A total synthesis of (–)-bestatin using Shibasaki's asymmetric Henry reaction. Tetrahedron Letters. 2005, 46 (44): 7581–7582. doi:10.1016/j.tetlet.2005.08.153.

arkat-usa.org (Global: low place; Chinese: low place)

Alcaide, Benito; Almendros, Pedro; Luna, Amparo; Paz de Arriba, M.; Rosario Torresc, M. Organocatalyzed diastereoselective Henry reaction of enantiopure 4-oxoazetidine-2-carbaldehydes (PDF). Arkivoc. 2007, 2007 (iv): 285–296. doi:10.3998/ark.5550190.0008.425 .

bnf.fr (Global: 61^st place; Chinese: 533^rd place)

gallica.bnf.fr

Henry, Louis. Formation synthétique d'alcools nitrés [Synthetic formation of nitrated alcohols]. Comptes rendus. 1895, 120: 1265–1268 [2022-01-04]. （原始内容存档于2022-01-04）.
Wurtz, M.A. Sur un aldéhyde-alcool. Bull. Soc. Chim. Fr. 1872, 17: 436–442 [2022-01-04]. （原始内容存档于2017-04-07）.

doi.org (Global: 2^nd place; Chinese: 5^th place)

Matthews, Walter; et al. Equilibrium acidities of carbon acids. VI. Establishment of an absolute scale of acidities in dimethyl sulfoxide solution. Journal of the American Chemical Society. 1975, 97 (24): 7006. doi:10.1021/ja00857a010.
Bersohn, Malcolm. C versus O Alkylation in the Case of a Stable Cation. J. Am. Chem. Soc. 1961, 83 (9): 2136–2138. doi:10.1021/ja01470a022.
Begona, L., Arrieta, A., Morao, I., Cossio, F.P. Ab Initio Models for the Nitroaldol (Henry) Reaction. Chem. Eur. J. 1997, 3 (1): 20–28. doi:10.1002/chem.19970030105.
Sasai, Hiroaki; Suzuki, Takeyuki; Arai, Shigeru; Arai, Takayoshi; Shibasaki, Masakatsu. Basic character of rare earth metal alkoxides. Utilization in catalytic carbon-carbon bond-forming reactions and catalytic asymmetric nitroaldol reactions. Journal of the American Chemical Society. 1 May 1992, 114 (11): 4418–4420. doi:10.1021/ja00037a068.
Seayad, J., List, B. Asymmetric organocatalysis. Org. Biomol. Chem. 2005, 3 (5): 719–724. PMID 15731852. doi:10.1039/b415217b.
Westermann, B. Asymmetric catalytic aza-Henry reactions leading to 1,2-diamines and 1,2-diaminocarboxylic acids. Angew. Chem. Int. Ed. Engl. 2003, 42 (2): 151–153. PMID 12532343. doi:10.1002/anie.200390071.
Luzzio, F.A. The Henry Reaction: recent examples. Tetrahedron. 2001, 57 (22): 915–945. doi:10.1002/chin.200122233.
Menzel, A., Ohrlein, R., Griesser, H., Wehner, V., Jager, V. A Short Synthesis of L-Acosamine Based on Nitroaldol Addition (Henry Reaction). Analysis of the Key Step Concerning Solvent and Temperature Effects. Synthesis. 1999, 9 (45): 1691–1702. doi:10.1002/chin.199945325.
Palomo, Claudio; Oiarbide, Mikel; Laso, Antonio. Enantioselective Henry Reactions under Dual Lewis Acid/Amine Catalysis Using Chiral Amino Alcohol Ligands. Angewandte Chemie. 2005, 44 (25): 3881–3884. PMID 15892142. doi:10.1002/anie.200463075.
Alcaide, Benito; Almendros, Pedro; Luna, Amparo; Paz de Arriba, M.; Rosario Torresc, M. Organocatalyzed diastereoselective Henry reaction of enantiopure 4-oxoazetidine-2-carbaldehydes (PDF). Arkivoc. 2007, 2007 (iv): 285–296. doi:10.3998/ark.5550190.0008.425 .
Gogoi, N., Boruwa, J., Barua, N.C. A total synthesis of (–)-bestatin using Shibasaki's asymmetric Henry reaction. Tetrahedron Letters. 2005, 46 (44): 7581–7582. doi:10.1016/j.tetlet.2005.08.153.
Marcelli, T., van der Haas, R., van Maarseveen, J.H., Hiemstra, H. Asymmetric Organocatalytic Henry Reaction. Angew. Chem. Int. Ed. 2006, 45 (6): 929–931. PMID 16429453. doi:10.1002/anie.200503724.
Purkarthofer, T., Gruber, K., Gruber-Khadjawi, M., Waich, K., Skranc, W., Mink, D. and Griengl, H. A Biocatalytic Henry Reaction—The Hydroxynitrile Lyase from Hevea brasiliensis Also Catalyzes Nitroaldol Reactions.. Angewandte Chemie. 2006, 45 (21): 3454–3456. PMID 16634109. doi:10.1002/anie.200504230.
Fuhshuku K, Asano Y. Synthesis of (R)-β-nitro alcohols catalyzed by R-selective hydroxynitrile lyase from Arabidopsis thaliana in the aqueous-organic biphasic system.. J. Biotechnol. 2011, 153 (3–4): 153–159. PMID 21439333. doi:10.1016/j.jbiotec.2011.03.011.

nih.gov (Global: 5^th place; Chinese: 3^rd place)

ncbi.nlm.nih.gov

Seayad, J., List, B. Asymmetric organocatalysis. Org. Biomol. Chem. 2005, 3 (5): 719–724. PMID 15731852. doi:10.1039/b415217b.
Westermann, B. Asymmetric catalytic aza-Henry reactions leading to 1,2-diamines and 1,2-diaminocarboxylic acids. Angew. Chem. Int. Ed. Engl. 2003, 42 (2): 151–153. PMID 12532343. doi:10.1002/anie.200390071.
Palomo, Claudio; Oiarbide, Mikel; Laso, Antonio. Enantioselective Henry Reactions under Dual Lewis Acid/Amine Catalysis Using Chiral Amino Alcohol Ligands. Angewandte Chemie. 2005, 44 (25): 3881–3884. PMID 15892142. doi:10.1002/anie.200463075.
Marcelli, T., van der Haas, R., van Maarseveen, J.H., Hiemstra, H. Asymmetric Organocatalytic Henry Reaction. Angew. Chem. Int. Ed. 2006, 45 (6): 929–931. PMID 16429453. doi:10.1002/anie.200503724.
Purkarthofer, T., Gruber, K., Gruber-Khadjawi, M., Waich, K., Skranc, W., Mink, D. and Griengl, H. A Biocatalytic Henry Reaction—The Hydroxynitrile Lyase from Hevea brasiliensis Also Catalyzes Nitroaldol Reactions.. Angewandte Chemie. 2006, 45 (21): 3454–3456. PMID 16634109. doi:10.1002/anie.200504230.
Fuhshuku K, Asano Y. Synthesis of (R)-β-nitro alcohols catalyzed by R-selective hydroxynitrile lyase from Arabidopsis thaliana in the aqueous-organic biphasic system.. J. Biotechnol. 2011, 153 (3–4): 153–159. PMID 21439333. doi:10.1016/j.jbiotec.2011.03.011.

web.archive.org (Global: 1^st place; Chinese: 1^st place)

Henry, Louis. Formation synthétique d'alcools nitrés [Synthetic formation of nitrated alcohols]. Comptes rendus. 1895, 120: 1265–1268 [2022-01-04]. （原始内容存档于2022-01-04）.
Wurtz, M.A. Sur un aldéhyde-alcool. Bull. Soc. Chim. Fr. 1872, 17: 436–442 [2022-01-04]. （原始内容存档于2017-04-07）.
Reich, Hans. Bordwell pKa table: "Nitroalkanes". University of Wisconsin Chemistry Department. [17 January 2016]. （原始内容存档于2008-10-09）.

wisc.edu (Global: 891^st place; Chinese: 1,070^th place)

chem.wisc.edu

Reich, Hans. Bordwell pKa table: "Nitroalkanes". University of Wisconsin Chemistry Department. [17 January 2016]. （原始内容存档于2008-10-09）.

亨利反应 (Chinese Wikipedia)

archive.org (Global: 6th place; Chinese: 2nd place)

arkat-usa.org (Global: low place; Chinese: low place)

bnf.fr (Global: 61st place; Chinese: 533rd place)

gallica.bnf.fr

doi.org (Global: 2nd place; Chinese: 5th place)

nih.gov (Global: 5th place; Chinese: 3rd place)