Aldol reaction (English Wikipedia)

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

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Mahrwald, R. (2004). Modern Aldol Reactions, Volumes 1 and 2. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA. pp. 1218–23. ISBN 978-3-527-30714-2.

bnf.fr

gallica.bnf.fr

Wurtz, C. A. (1872). "Sur un aldéhyde-alcool" [On an aldehyde alcohol]. Comptes rendus de l'Académie des sciences (in French). 74: 1361.

books.google.com

Garner, Susan Amy (2007) "Hydrogen-mediated carbon-carbon bond formations: Applied to reductive aldol and Mannich reactions," Ph.D. dissertation, University of Texas (Austin), pp. 4 and 51.

caltech.edu

authors.library.caltech.edu

Northrup, Alan B.; MacMillan David W. C. (2002). "The First Direct and Enantioselective Cross-Aldol Reaction of Aldehydes" (PDF). Journal of the American Chemical Society. 124 (24): 6798–6799. Bibcode:2002JAChS.124.6798N. doi:10.1021/ja0262378. PMID 12059180.

doi.org

Wurtz, C. A. (1872). "Ueber einen Aldehyd-Alkohol" [About an aldehyde alcohol]. Journal für Praktische Chemie (in German). 5 (1): 457–464. doi:10.1002/prac.18720050148.
Smith, Michael B.; March, Jerry (2006). March's Advanced Organic Chemistry: Reactions, Mechanisms, and Structure. doi:10.1002/0470084960. ISBN 9780470084960.
Heathcock, C. H. (1991). "The Aldol Reaction: Acid and General Base Catalysis". In Trost, B. M.; Fleming, I. (eds.). Comprehensive Organic Synthesis. Vol. 2. Elsevier Science. pp. 133–179. doi:10.1016/B978-0-08-052349-1.00027-5. ISBN 978-0-08-052349-1.
Mestres R. (2004). "A green look at the aldol reaction". Green Chemistry. 6 (12): 583–603. doi:10.1039/b409143b.
Molander, G. A., ed. (2011). "Enzymatic Direct Aldol Additions". Stereoselective Synthesis 2: Stereoselective Reactions of Carbonyl and Imino Groups (1 ed.). Stuttgart: Georg Thieme Verlag. doi:10.1055/sos-sd-202-00331. ISBN 978-3-13-154121-5.
Guthrie, J.P.; Cooper, K.J.; Cossar, J.; Dawson, B.A.; Taylor, K.F. (1984). "The retroaldol reaction of cinnamaldehyde". Can. J. Chem. 62 (8): 1441–1445. doi:10.1139/v84-243.
Molander, ed. (2011). Stereoselective Synthesis 2: Stereoselective Reactions of Carbonyl and Imino Groups (1 ed.). Stuttgart: Georg Thieme Verlag. doi:10.1055/sos-sd-202-00331. ISBN 978-3-13-154121-5.
Evans, D. A.; Nelson J. V.; Vogel E.; Taber T. R. (1981). "Stereoselective aldol condensations via boron enolates". Journal of the American Chemical Society. 103 (11): 3099–3111. Bibcode:1981JAChS.103.3099E. doi:10.1021/ja00401a031.
Cowden, C. J.; Paterson, I. (2004). Asymmetric Aldol Reactions Using Boron Enolates. Organic Reactions. pp. 1–200. doi:10.1002/0471264180.or051.01. ISBN 978-0471264187.
Brown, H. C.; Dhar, R. K.; Bakshi, R. K.; Pandiarajan, P. K.; Singaram, B. (1989). "Major effect of the leaving group in dialkylboron chlorides and triflates in controlling the stereospecific conversion of ketones into either E- or Z-enol borinates". Journal of the American Chemical Society. 111 (9): 3441–3442. Bibcode:1989JAChS.111.3441B. doi:10.1021/ja00191a058.
Zimmerman, H. E.; Traxler, M. D. (1957). "The Stereochemistry of the Ivanov and Reformatsky Reactions. I". Journal of the American Chemical Society. 79 (8): 1920–1923. Bibcode:1957JAChS..79.1920Z. doi:10.1021/ja01565a041.
Evans, D. A.; Rieger D. L.; Bilodeau M. T.; Urpi F. (1991). "Stereoselective aldol reactions of chlorotitanium enolates. An efficient method for the assemblage of polypropionate-related synthons". Journal of the American Chemical Society. 113 (3): 1047–1049. Bibcode:1991JAChS.113.1047E. doi:10.1021/ja00003a051.
Heathcock, C. H.; Buse, C. T.; Kleschnick, W. A.; Pirrung, M. C.; Sohn, J. E.; Lampe, J. (1980). "Acyclic stereoselection. 7. Stereoselective synthesis of 2-alkyl-3-hydroxy carbonyl compounds by aldol condensation". Journal of Organic Chemistry. 45 (6): 1066–1081. doi:10.1021/jo01294a030.
Roush W. R. (1991). "Concerning the diastereofacial selectivity of the aldol reactions of .alpha.-methyl chiral aldehydes and lithium and boron propionate enolates". Journal of Organic Chemistry. 56 (13): 4151–4157. doi:10.1021/jo00013a015.
Masamune S.; Ellingboe J. W.; Choy W. (1982). "Aldol strategy: coordination of the lithium cation with an alkoxy substituent". Journal of the American Chemical Society. 104 (20): 1047–1049. Bibcode:1982JAChS.104.5526M. doi:10.1021/ja00384a062.
Evans, D. A.; Dart M. J.; Duffy J. L.; Rieger D. L. (1995). "Double Stereodifferentiating Aldol Reactions. The Documentation of "Partially Matched" Aldol Bond Constructions in the Assemblage of Polypropionate Systems". Journal of the American Chemical Society. 117 (35): 9073–9074. Bibcode:1995JAChS.117.9073E. doi:10.1021/ja00140a027.
Masamune S.; Choy W.; Petersen J. S.; Sita L. R. (1985). "Double Asymmetric Synthesis and a New Strategy for Stereochemical Control in Organic Synthesis". Angew. Chem. Int. Ed. Engl. 24: 1–30. doi:10.1002/anie.198500013.
Evans, D. A.; Bartroli J.; Shih T. L. (1981). "Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates". Journal of the American Chemical Society. 103 (8): 2127–2129. Bibcode:1981JAChS.103.2127E. doi:10.1021/ja00398a058.
Evans, D. A.; Bender S. L.; Morris J. (1988). "The total synthesis of the polyether antibiotic X-206". Journal of the American Chemical Society. 110 (8): 2506–2526. Bibcode:1988JAChS.110.2506E. doi:10.1021/ja00216a026.
Crimmins M. T.; King B. W.; Tabet A. E. (1997). "Asymmetric Aldol Additions with Titanium Enolates of Acyloxazolidinethiones: Dependence of Selectivity on Amine Base and Lewis Acid Stoichiometry". Journal of the American Chemical Society. 119 (33): 7883–7884. Bibcode:1997JAChS.119.7883C. doi:10.1021/ja9716721.
Crimmins M. T.; Chaudhary K. (2000). "Titanium enolates of thiazolidinethione chiral auxiliaries: Versatile tools for asymmetric aldol additions". Organic Letters. 2 (6): 775–777. doi:10.1021/ol9913901. PMID 10754681.
Crimmins, Michael T.; Shamszad, Mariam (2007). "Highly Selective Acetate Aldol Additions Using Mesityl-Substituted Chiral Auxiliaries". Org. Lett. 9 (1): 149–152. doi:10.1021/ol062688b. PMID 17192107.
S. B. Jennifer Kan; Kenneth K.-H. Ng; Ian Paterson (2013). "The Impact of the Mukaiyama Aldol Reaction in Total Synthesis". Angewandte Chemie International Edition. 52 (35): 9097–9108. doi:10.1002/anie.201303914. PMID 23893491.
Teruaki Mukaiyama; Kazuo Banno; Koichi Narasaka (1974). "Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachloride". Journal of the American Chemical Society. 96 (24): 7503–7509. doi:10.1021/ja00831a019.
Carreira, E. M.; Fettes, A.; Martl, C. (2006). Catalytic Enantioselective Aldol Addition Reactions. Org. React. Vol. 67. pp. 1–216. doi:10.1002/0471264180.or067.01. ISBN 978-0471264187.
Hajos, Zoltan G.; Parrish, David R. (1974). "Asymmetric synthesis of bicyclic intermediates of natural product chemistry". Journal of Organic Chemistry. 39 (12): 1615–1621. doi:10.1021/jo00925a003.
Eder, Ulrich; Sauer, Gerhard; Wiechert, Rudolf (1971). "New Type of Asymmetric Cyclization to Optically Active Steroid CD Partial Structures". Angewandte Chemie International Edition in English. 10 (7): 1615–1621. doi:10.1002/anie.197104961.
Northrup, Alan B.; MacMillan David W. C. (2002). "The First Direct and Enantioselective Cross-Aldol Reaction of Aldehydes" (PDF). Journal of the American Chemical Society. 124 (24): 6798–6799. Bibcode:2002JAChS.124.6798N. doi:10.1021/ja0262378. PMID 12059180.
Evans, D. A.; Tedrow, J. S.; Shaw, J. T.; Downey, C. W. (2002). "Diastereoselective Magnesium Halide-Catalyzed anti-Aldol Reactions of Chiral N-Acyloxazolidinones". Journal of the American Chemical Society. 124 (3): 392–393. Bibcode:2002JAChS.124..392E. doi:10.1021/ja0119548. PMID 11792206.
Evans, David A.; Downey, C. Wade; Shaw, Jared T.; Tedrow, Jason S. (2002). "Magnesium Halide-Catalyzed Anti-Aldol Reactions of Chiral N-Acylthiazolidinethiones". Organic Letters. 4 (7): 1127–1130. doi:10.1021/ol025553o. PMID 11922799.
Northrup A. B.; Mangion I. K.; Hettche F.; MacMillan D. W. C. (2004). "Enantioselective Organocatalytic Direct Aldol Reactions of -Oxyaldehydes: Step One in a Two-Step Synthesis of Carbohydrates". Angewandte Chemie International Edition in English. 43 (16): 2152–2154. doi:10.1002/anie.200453716. PMID 15083470.
Kane, Robert (1838). "Ueber den Essiggeist und einige davon abgeleitete Verbindungen". Journal für Praktische Chemie. 15: 129–155. doi:10.1002/prac.18380150112. Retrieved 14 March 2025.
Kane, Robert (1838). "Ueber den Essiggeist und einige davon abgeleitete Verbindungen". Journal für Praktische Chemie. 15: 129–155. doi:10.1002/prac.18380150112. Retrieved 14 March 2025.

harvard.edu

ui.adsabs.harvard.edu

Evans, D. A.; Nelson J. V.; Vogel E.; Taber T. R. (1981). "Stereoselective aldol condensations via boron enolates". Journal of the American Chemical Society. 103 (11): 3099–3111. Bibcode:1981JAChS.103.3099E. doi:10.1021/ja00401a031.
Brown, H. C.; Dhar, R. K.; Bakshi, R. K.; Pandiarajan, P. K.; Singaram, B. (1989). "Major effect of the leaving group in dialkylboron chlorides and triflates in controlling the stereospecific conversion of ketones into either E- or Z-enol borinates". Journal of the American Chemical Society. 111 (9): 3441–3442. Bibcode:1989JAChS.111.3441B. doi:10.1021/ja00191a058.
Zimmerman, H. E.; Traxler, M. D. (1957). "The Stereochemistry of the Ivanov and Reformatsky Reactions. I". Journal of the American Chemical Society. 79 (8): 1920–1923. Bibcode:1957JAChS..79.1920Z. doi:10.1021/ja01565a041.
Evans, D. A.; Rieger D. L.; Bilodeau M. T.; Urpi F. (1991). "Stereoselective aldol reactions of chlorotitanium enolates. An efficient method for the assemblage of polypropionate-related synthons". Journal of the American Chemical Society. 113 (3): 1047–1049. Bibcode:1991JAChS.113.1047E. doi:10.1021/ja00003a051.
Masamune S.; Ellingboe J. W.; Choy W. (1982). "Aldol strategy: coordination of the lithium cation with an alkoxy substituent". Journal of the American Chemical Society. 104 (20): 1047–1049. Bibcode:1982JAChS.104.5526M. doi:10.1021/ja00384a062.
Evans, D. A.; Dart M. J.; Duffy J. L.; Rieger D. L. (1995). "Double Stereodifferentiating Aldol Reactions. The Documentation of "Partially Matched" Aldol Bond Constructions in the Assemblage of Polypropionate Systems". Journal of the American Chemical Society. 117 (35): 9073–9074. Bibcode:1995JAChS.117.9073E. doi:10.1021/ja00140a027.
Evans, D. A.; Bartroli J.; Shih T. L. (1981). "Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates". Journal of the American Chemical Society. 103 (8): 2127–2129. Bibcode:1981JAChS.103.2127E. doi:10.1021/ja00398a058.
Evans, D. A.; Bender S. L.; Morris J. (1988). "The total synthesis of the polyether antibiotic X-206". Journal of the American Chemical Society. 110 (8): 2506–2526. Bibcode:1988JAChS.110.2506E. doi:10.1021/ja00216a026.
Crimmins M. T.; King B. W.; Tabet A. E. (1997). "Asymmetric Aldol Additions with Titanium Enolates of Acyloxazolidinethiones: Dependence of Selectivity on Amine Base and Lewis Acid Stoichiometry". Journal of the American Chemical Society. 119 (33): 7883–7884. Bibcode:1997JAChS.119.7883C. doi:10.1021/ja9716721.
Northrup, Alan B.; MacMillan David W. C. (2002). "The First Direct and Enantioselective Cross-Aldol Reaction of Aldehydes" (PDF). Journal of the American Chemical Society. 124 (24): 6798–6799. Bibcode:2002JAChS.124.6798N. doi:10.1021/ja0262378. PMID 12059180.
Evans, D. A.; Tedrow, J. S.; Shaw, J. T.; Downey, C. W. (2002). "Diastereoselective Magnesium Halide-Catalyzed anti-Aldol Reactions of Chiral N-Acyloxazolidinones". Journal of the American Chemical Society. 124 (3): 392–393. Bibcode:2002JAChS.124..392E. doi:10.1021/ja0119548. PMID 11792206.

hathitrust.org

babel.hathitrust.org

Wurtz, C. A. (1872). "Sur un aldéhyde-alcool" [On an aldehyde alcohol]. Bulletin de la Société Chimique de Paris. 2nd series (in French). 17: 436–442.
Wurtz, C. A. (1872). "Ueber einen Aldehyd-Alkohol" [About an aldehyde alcohol]. Journal für Praktische Chemie (in German). 5 (1): 457–464. doi:10.1002/prac.18720050148.
Borodin, A. (1873) "Ueber einen neuen Abkömmling des Valerals" (On a new derivative of valerian aldehyde), Berichte der deutschen chemischen Gesellschaft (in German), 6 : 982–985.

nih.gov

pubmed.ncbi.nlm.nih.gov

Crimmins M. T.; Chaudhary K. (2000). "Titanium enolates of thiazolidinethione chiral auxiliaries: Versatile tools for asymmetric aldol additions". Organic Letters. 2 (6): 775–777. doi:10.1021/ol9913901. PMID 10754681.
Crimmins, Michael T.; Shamszad, Mariam (2007). "Highly Selective Acetate Aldol Additions Using Mesityl-Substituted Chiral Auxiliaries". Org. Lett. 9 (1): 149–152. doi:10.1021/ol062688b. PMID 17192107.
S. B. Jennifer Kan; Kenneth K.-H. Ng; Ian Paterson (2013). "The Impact of the Mukaiyama Aldol Reaction in Total Synthesis". Angewandte Chemie International Edition. 52 (35): 9097–9108. doi:10.1002/anie.201303914. PMID 23893491.
Northrup, Alan B.; MacMillan David W. C. (2002). "The First Direct and Enantioselective Cross-Aldol Reaction of Aldehydes" (PDF). Journal of the American Chemical Society. 124 (24): 6798–6799. Bibcode:2002JAChS.124.6798N. doi:10.1021/ja0262378. PMID 12059180.
Evans, D. A.; Tedrow, J. S.; Shaw, J. T.; Downey, C. W. (2002). "Diastereoselective Magnesium Halide-Catalyzed anti-Aldol Reactions of Chiral N-Acyloxazolidinones". Journal of the American Chemical Society. 124 (3): 392–393. Bibcode:2002JAChS.124..392E. doi:10.1021/ja0119548. PMID 11792206.
Evans, David A.; Downey, C. Wade; Shaw, Jared T.; Tedrow, Jason S. (2002). "Magnesium Halide-Catalyzed Anti-Aldol Reactions of Chiral N-Acylthiazolidinethiones". Organic Letters. 4 (7): 1127–1130. doi:10.1021/ol025553o. PMID 11922799.
Northrup A. B.; Mangion I. K.; Hettche F.; MacMillan D. W. C. (2004). "Enantioselective Organocatalytic Direct Aldol Reactions of -Oxyaldehydes: Step One in a Two-Step Synthesis of Carbohydrates". Angewandte Chemie International Edition in English. 43 (16): 2152–2154. doi:10.1002/anie.200453716. PMID 15083470.

orgsyn.org

Bal, B.; Buse, C. T.; Smith, K.; Heathcock, C. H., (2SR,3RS)-2,4-Dimethyl-3-Hydroxypentanoic Acid Archived 2011-06-06 at the Wayback Machine, Org. Synth., Coll. Vol. 7, p.185 (1990); Vol. 63, p.89 (1985).
Gage J. R.; Evans D. A., Diastereoselective Aldol Condensation Using A Chiral Oxazolidinone Auxiliary: (2S*,3S*)-3-Hydroxy-3-Phenyl-2-Methylpropanoic Acid Archived 2012-09-29 at the Wayback Machine, Organic Syntheses, Coll. Vol. 8, p.339 (1993); Vol. 68, p.83 (1990).

orgsynth.org

3-Hydroxy-3-Methyl-1-Phenyl-1-Butanone by Crossed Aldol Reaction Teruaki Mukaiyama and Koichi Narasaka Organic Syntheses, Coll. Vol. 8, p.323 (1993); Vol. 65, p.6 (1987)

sigmaaldrich.com

Evans, D. A. (1982). "Studies in Asymmetric Synthesis: The Development of Practical Chiral Enolate Synthons" (PDF). Aldrichimica Acta. 15: 23.

thieme-connect.de

Molander, G. A., ed. (2011). "Enzymatic Direct Aldol Additions". Stereoselective Synthesis 2: Stereoselective Reactions of Carbonyl and Imino Groups (1 ed.). Stuttgart: Georg Thieme Verlag. doi:10.1055/sos-sd-202-00331. ISBN 978-3-13-154121-5.
Molander, ed. (2011). Stereoselective Synthesis 2: Stereoselective Reactions of Carbonyl and Imino Groups (1 ed.). Stuttgart: Georg Thieme Verlag. doi:10.1055/sos-sd-202-00331. ISBN 978-3-13-154121-5.

web.archive.org

Bal, B.; Buse, C. T.; Smith, K.; Heathcock, C. H., (2SR,3RS)-2,4-Dimethyl-3-Hydroxypentanoic Acid Archived 2011-06-06 at the Wayback Machine, Org. Synth., Coll. Vol. 7, p.185 (1990); Vol. 63, p.89 (1985).
Gage J. R.; Evans D. A., Diastereoselective Aldol Condensation Using A Chiral Oxazolidinone Auxiliary: (2S*,3S*)-3-Hydroxy-3-Phenyl-2-Methylpropanoic Acid Archived 2012-09-29 at the Wayback Machine, Organic Syntheses, Coll. Vol. 8, p.339 (1993); Vol. 68, p.83 (1990).

wiley.com

onlinelibrary.wiley.com

Kane, Robert (1838). "Ueber den Essiggeist und einige davon abgeleitete Verbindungen". Journal für Praktische Chemie. 15: 129–155. doi:10.1002/prac.18380150112. Retrieved 14 March 2025.
Kane, Robert (1838). "Ueber den Essiggeist und einige davon abgeleitete Verbindungen". Journal für Praktische Chemie. 15: 129–155. doi:10.1002/prac.18380150112. Retrieved 14 March 2025.

worldcat.org

search.worldcat.org

Klein, David R. (December 22, 2020). Organic chemistry (4th ed.). Hoboken, NJ: Wiley. p. 1014. ISBN 978-1-119-65959-4. OCLC 1201694230.