Henry reaction (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Henry reaction" in English language version.

refsWebsite

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15doi.org

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6nih.gov

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2bnf.fr

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1wisc.edu

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1arkat-usa.org

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arkat-usa.org

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

bnf.fr

gallica.bnf.fr

Henry, Louis (1895). "Formation synthétique d'alcools nitrés" [Synthetic formation of nitrated alcohols]. Comptes rendus. 120: 1265–1268.
Wurtz, M.A. (1872). "Sur un aldéhyde-alcool". Bull. Soc. Chim. Fr. 17: 436–442.

doi.org

Sasai, H., Suzuki, T., Itoh, N., Arai, S., Shibasaki, M. (1993). "Catalytic Asymmetric Nitroaldol Reaction: an efficient synthesis of (s) propranolol using the lanthenum binaphthol complex". Tetrahedron Letters. 34 (52): 855–858. doi:10.1016/0040-4039(93)89031-K.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Luzzio, F.A. (2001). "The Henry Reaction: recent examples". Tetrahedron. 57 (22): 915–945. doi:10.1002/chin.200122233.
Matthews, Walter; et al. (1975). "Equilibrium acidities of carbon acids. VI. Establishment of an absolute scale of acidities in dimethyl sulfoxide solution". Journal of the American Chemical Society. 97 (24): 7006. doi:10.1021/ja00857a010.
Bersohn, Malcolm (1961). "C versus O Alkylation in the Case of a Stable Cation". J. Am. Chem. Soc. 83 (9): 2136–2138. doi:10.1021/ja01470a022.
Begona, L., Arrieta, A., Morao, I., Cossio, F.P. (1997). "Ab Initio Models for the Nitroaldol (Henry) Reaction". Chem. Eur. J. 3 (1): 20–28. doi:10.1002/chem.19970030105.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Sasai, Hiroaki; Suzuki, Takeyuki; Arai, Shigeru; Arai, Takayoshi; Shibasaki, Masakatsu (1 May 1992). "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. 114 (11): 4418–4420. doi:10.1021/ja00037a068.
Westermann, B. (2003). "Asymmetric catalytic aza-Henry reactions leading to 1,2-diamines and 1,2-diaminocarboxylic acids". Angew. Chem. Int. Ed. Engl. 42 (2): 151–153. doi:10.1002/anie.200390071. PMID 12532343.
Seayad, J., List, B. (2005). "Asymmetric organocatalysis". Org. Biomol. Chem. 3 (5): 719–724. doi:10.1039/b415217b. PMID 15731852.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Menzel, A., Ohrlein, R., Griesser, H., Wehner, V., Jager, V. (1999). "A Short Synthesis of L-Acosamine Based on Nitroaldol Addition (Henry Reaction). Analysis of the Key Step Concerning Solvent and Temperature Effects". Synthesis. 9 (45): 1691–1702. doi:10.1002/chin.199945325.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Palomo, Claudio; Oiarbide, Mikel; Laso, Antonio (2005). "Enantioselective Henry Reactions under Dual Lewis Acid/Amine Catalysis Using Chiral Amino Alcohol Ligands". Angewandte Chemie. 44 (25): 3881–3884. doi:10.1002/anie.200463075. PMID 15892142.
Alcaide, Benito; Almendros, Pedro; Luna, Amparo; Paz de Arriba, M.; Rosario Torresc, M. (2007). "Organocatalyzed diastereoselective Henry reaction of enantiopure 4-oxoazetidine-2-carbaldehydes" (PDF). Arkivoc. 2007 (iv): 285–296. doi:10.3998/ark.5550190.0008.425.
Gogoi, N., Boruwa, J., Barua, N.C. (2005). "A total synthesis of (–)-bestatin using Shibasaki's asymmetric Henry reaction". Tetrahedron Letters. 46 (44): 7581–7582. doi:10.1016/j.tetlet.2005.08.153.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Marcelli, T., van der Haas, R., van Maarseveen, J.H., Hiemstra, H. (2006). "Asymmetric Organocatalytic Henry Reaction". Angew. Chem. Int. Ed. 45 (6): 929–931. doi:10.1002/anie.200503724. PMID 16429453.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Purkarthofer, T., Gruber, K., Gruber-Khadjawi, M., Waich, K., Skranc, W., Mink, D. and Griengl, H. (2006). "A Biocatalytic Henry Reaction—The Hydroxynitrile Lyase from Hevea brasiliensis Also Catalyzes Nitroaldol Reactions". Angewandte Chemie. 45 (21): 3454–3456. doi:10.1002/anie.200504230. PMID 16634109.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Fuhshuku K, Asano Y (2011). "Synthesis of (R)-β-nitro alcohols catalyzed by R-selective hydroxynitrile lyase from Arabidopsis thaliana in the aqueous-organic biphasic system". J. Biotechnol. 153 (3–4): 153–159. doi:10.1016/j.jbiotec.2011.03.011. PMID 21439333.

nih.gov

pubmed.ncbi.nlm.nih.gov

Westermann, B. (2003). "Asymmetric catalytic aza-Henry reactions leading to 1,2-diamines and 1,2-diaminocarboxylic acids". Angew. Chem. Int. Ed. Engl. 42 (2): 151–153. doi:10.1002/anie.200390071. PMID 12532343.
Seayad, J., List, B. (2005). "Asymmetric organocatalysis". Org. Biomol. Chem. 3 (5): 719–724. doi:10.1039/b415217b. PMID 15731852.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Palomo, Claudio; Oiarbide, Mikel; Laso, Antonio (2005). "Enantioselective Henry Reactions under Dual Lewis Acid/Amine Catalysis Using Chiral Amino Alcohol Ligands". Angewandte Chemie. 44 (25): 3881–3884. doi:10.1002/anie.200463075. PMID 15892142.
Marcelli, T., van der Haas, R., van Maarseveen, J.H., Hiemstra, H. (2006). "Asymmetric Organocatalytic Henry Reaction". Angew. Chem. Int. Ed. 45 (6): 929–931. doi:10.1002/anie.200503724. PMID 16429453.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Purkarthofer, T., Gruber, K., Gruber-Khadjawi, M., Waich, K., Skranc, W., Mink, D. and Griengl, H. (2006). "A Biocatalytic Henry Reaction—The Hydroxynitrile Lyase from Hevea brasiliensis Also Catalyzes Nitroaldol Reactions". Angewandte Chemie. 45 (21): 3454–3456. doi:10.1002/anie.200504230. PMID 16634109.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Fuhshuku K, Asano Y (2011). "Synthesis of (R)-β-nitro alcohols catalyzed by R-selective hydroxynitrile lyase from Arabidopsis thaliana in the aqueous-organic biphasic system". J. Biotechnol. 153 (3–4): 153–159. doi:10.1016/j.jbiotec.2011.03.011. PMID 21439333.

wisc.edu

chem.wisc.edu

Reich, Hans. "Bordwell pKa table: "Nitroalkanes"". University of Wisconsin Chemistry Department. Retrieved 17 January 2016.