Henry reaksiyasi (Uzbek Wikipedia)

Analysis of information sources in references of the Wikipedia article "Henry reaksiyasi" in Uzbek language version.

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15doi.org

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6nih.gov

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2bnf.fr

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1archive.org

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1wisc.edu

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archive.org

Noboro, Ono. The Nitro Group in Organic Synthesis. New York, NY: Wiley-VCH, 2001 — 30–69-bet. ISBN 978-0-471-31611-4.

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-jild, № iv. 285–296-bet. doi:10.3998/ark.5550190.0008.425.

bnf.fr

gallica.bnf.fr

Henry, Louis (1895). „Formation synthétique d'alcools nitrés“. Comptes rendus. 120-jild. 1265–1268-bet. {{cite magazine}}: Unknown parameter |trans_title= ignored (|trans-title= suggested) (yordam)
Wurtz, M.A. (1872). „Sur un aldéhyde-alcool“. Bull. Soc. Chim. Fr. 17-jild. 436–442-bet.

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-jild, № 52. 855–858-bet. doi:10.1016/0040-4039(93)89031-K.{{cite magazine}}: CS1 maint: multiple names: authors list ()
Luzzio, F.A. (2001). „The Henry Reaction: recent examples“. Tetrahedron. 57-jild, № 22. 915–945-bet. 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-jild, № 24. 7006-bet. doi:10.1021/ja00857a010.
Bersohn, Malcolm (1961). „C versus O Alkylation in the Case of a Stable Cation“. J. Am. Chem. Soc. 83-jild, № 9. 2136–2138-bet. 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-jild, № 1. 20–28-bet. doi:10.1002/chem.19970030105.{{cite magazine}}: CS1 maint: multiple names: authors list ()
Sasai, Hiroaki; Suzuki, Takeyuki; Arai, Shigeru; Arai, Takayoshi; Shibasaki, Masakatsu (1-may 1992-yil). „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-jild, № 11. 4418–4420-bet. doi:10.1021/ja00037a068.{{cite magazine}}: CS1 maint: date format ()
Westermann, B. (2003). „Asymmetric catalytic aza-Henry reactions leading to 1,2-diamines and 1,2-diaminocarboxylic acids“. Angew. Chem. Int. Ed. Engl. 42-jild, № 2. 151–153-bet. doi:10.1002/anie.200390071. PMID 12532343.
Seayad, J., List, B. (2005). „Asymmetric organocatalysis“. Org. Biomol. Chem. 3-jild, № 5. 719–724-bet. doi:10.1039/b415217b. PMID 15731852.{{cite magazine}}: CS1 maint: multiple names: authors list ()
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-jild, № 45. 1691–1702-bet. doi:10.1002/chin.199945325.{{cite magazine}}: CS1 maint: multiple names: authors list ()
Palomo, Claudio; Oiarbide, Mikel; Laso, Antonio (2005). „Enantioselective Henry Reactions under Dual Lewis Acid/Amine Catalysis Using Chiral Amino Alcohol Ligands“. Angewandte Chemie. 44-jild, № 25. 3881–3884-bet. 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-jild, № iv. 285–296-bet. 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-jild, № 44. 7581–7582-bet. doi:10.1016/j.tetlet.2005.08.153.{{cite magazine}}: CS1 maint: multiple names: authors list ()
Marcelli, T., van der Haas, R., van Maarseveen, J.H., Hiemstra, H. (2006). „Asymmetric Organocatalytic Henry Reaction“. Angew. Chem. Int. Ed. 45-jild, № 6. 929–931-bet. doi:10.1002/anie.200503724. PMID 16429453.{{cite magazine}}: CS1 maint: multiple names: authors list ()
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-jild, № 21. 3454–3456-bet. doi:10.1002/anie.200504230. PMID 16634109.{{cite magazine}}: CS1 maint: multiple names: authors list ()
„Synthesis of (R)-β-nitro alcohols catalyzed by R-selective hydroxynitrile lyase from Arabidopsis thaliana in the aqueous-organic biphasic system“. J. Biotechnol. 153-jild, № 3–4. 2011. 153–159-bet. 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-jild, № 2. 151–153-bet. doi:10.1002/anie.200390071. PMID 12532343.
Seayad, J., List, B. (2005). „Asymmetric organocatalysis“. Org. Biomol. Chem. 3-jild, № 5. 719–724-bet. doi:10.1039/b415217b. PMID 15731852.{{cite magazine}}: CS1 maint: multiple names: authors list ()
Palomo, Claudio; Oiarbide, Mikel; Laso, Antonio (2005). „Enantioselective Henry Reactions under Dual Lewis Acid/Amine Catalysis Using Chiral Amino Alcohol Ligands“. Angewandte Chemie. 44-jild, № 25. 3881–3884-bet. 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-jild, № 6. 929–931-bet. doi:10.1002/anie.200503724. PMID 16429453.{{cite magazine}}: CS1 maint: multiple names: authors list ()
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-jild, № 21. 3454–3456-bet. doi:10.1002/anie.200504230. PMID 16634109.{{cite magazine}}: CS1 maint: multiple names: authors list ()
„Synthesis of (R)-β-nitro alcohols catalyzed by R-selective hydroxynitrile lyase from Arabidopsis thaliana in the aqueous-organic biphasic system“. J. Biotechnol. 153-jild, № 3–4. 2011. 153–159-bet. doi:10.1016/j.jbiotec.2011.03.011. PMID 21439333.

wisc.edu

chem.wisc.edu

Reich. „Bordwell pKa table: "Nitroalkanes"“. University of Wisconsin Chemistry Department. Qaraldi: 17-yanvar 2016-yil.