References analysis of the Wikipedia article "Chiral auxiliary" in the English version

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Jamali, Fakhreddin (1993). "Chapter 14: Stereochemically Pure Drugs: An Overview". In Wainer, Irving W. (ed.). Drug Stereochemistry: Analytical Methods and Pharmacology. Marcel Dekker, Inc. pp. 375–382. ISBN 978-0-8247-8819-3.

Caron, Stéphane (2011). "Chapter 15: Synthetic Route Development of Selected Contemporary Pharmaceutical Drugs". In Caron, Stéphane (ed.). Practical Synthetic Organic Chemistry. John Wiley & Sons, Inc. pp. 666–670. ISBN 978-0-470-03733-1.

doi.org

Glorius, F.; Gnas, Y. (2006). "Chiral Auxiliaries — Principles and Recent Applications". Synthesis. 2006 (12): 1899–1930. doi:10.1055/s-2006-942399.

Corey, E. J.; Ensley, H. E. (1975). "Preparation of an Optically Active Prostaglandin Intermediate via Asymmetric Induction". J. Am. Chem. Soc. 97 (23): 6908–6909. Bibcode:1975JAChS..97.6908C. doi:10.1021/ja00856a074. PMID 1184891.

Miller, J. P. (2013). "ChemInform Abstract: Recent Advances in Asymmetric Diels-Alder Reactions". ChemInform. 44 (48): no. doi:10.1002/chin.201348243.

Corey, E. J.; Ensley, H. E.; Parnell, C. A. (1978). "Convenient Synthesis of a Highly Efficient and Recyclable Chiral Director for Asymmetric Induction". J. Org. Chem. 43 (8): 1610–1611. doi:10.1021/jo00402a037.

Whitesell, J. K.; Chen, H. H.; Lawrence, R. M. (1985). "trans-2-Phenylcyclohexanol. A powerful and readily available chiral auxiliary". J. Org. Chem. 50 (23): 4663–4664. doi:10.1021/jo00223a055.

Comins, D. L.; Salvador, J. D. (1993). "Efficient Synthesis and Resolution of trans-2-(1-Aryl-1-methylethyl)cyclohexanols: Practical Alternatives to 8-P henylmenthol". J. Org. Chem. 58 (17): 4656–4661. doi:10.1021/jo00069a031.

Brunel, Jean Michel (2005). "BINOL: A Versatile Chiral Reagent". Chemical Reviews. 105 (3): 857–898. doi:10.1021/cr040079g. PMID 15755079.

Sakane, Soichi; Fujiwara, Junya; Maruoka, Keiji; Yamamoto, Hisashi (1983). "Chiral leaving group. Biogenetic-type asymmetric synthesis of limonene and bisabolenes". Journal of the American Chemical Society. 105 (19): 6154–6155. Bibcode:1983JAChS.105.6154S. doi:10.1021/ja00357a033.

Tanaka, Kiyoshi; Ahn, Mija; Watanabe, Yukari; Fuji, Kaoru (1996-06-01). "Asymmetric synthesis of uncommon α-amino acids by diastereoselective alkylations of a chiral glycine equivalent". Tetrahedron: Asymmetry. 7 (6): 1771–1782. doi:10.1016/0957-4166(96)00212-1.

Maglioli, Paola; De Lucchi, Ottorino; Delogu, Giovanna; Valle, Giovanni (1992-01-01). "Highly diastereoselective reduction and addition of nucleophiles to binaphthol-protected arylglyoxals". Tetrahedron: Asymmetry. 3 (3): 365–366. doi:10.1016/S0957-4166(00)80276-1.

Mondal, Anirban; Thiel, Niklas O.; Dorel, Ruth; Feringa, Ben L. (January 2022). "P-chirogenic phosphorus compounds by stereoselective Pd-catalysed arylation of phosphoramidites". Nature Catalysis. 5 (1): 10–19. doi:10.1038/s41929-021-00697-9. S2CID 245426891.

Buchi, George; Vogel, Dennis E. (1985). "A new method for the preparation of γ,δ-unsaturated ketones via Claisen rearrangement". The Journal of Organic Chemistry. 50 (23): 4664–4665. doi:10.1021/jo00223a056.

Miller, Aubry K.; Hughes, Chambers C.; Kennedy-Smith, Joshua J.; Gradl, Stefan N.; Dirk Trauner (2006). "Total Synthesis of (−)-Heptemerone B and (−)-Guanacastepene E". Journal of the American Chemical Society. 128 (51): 17057–17062. Bibcode:2006JAChS.12817057M. doi:10.1021/ja0660507. PMID 17177458.

Al Hazmi, Ali M.; Sheikh, Nadeem S.; Bataille, Carole J. R.; Al-Hadedi, Azzam A. M.; Watkin, Sam V.; Luker, Tim J.; Camp, Nicholas P.; Brown, Richard C. D. (2014). "trans-2-Tritylcyclohexanol as a Chiral Auxiliary in Permanganate-Mediated Oxidative Cyclization of 2-Methylenehept-5-enoates: Application to the Synthesis of trans-(+)-Linalool Oxide". Organic Letters. 16 (19): 5104–5107. doi:10.1021/ol502454r. PMID 25225741.

Evans, D. A.; Bartroli, J.; Shih, T. L. (1981). "Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates". J. Am. Chem. Soc. 103 (8): 2127–2129. Bibcode:1981JAChS.103.2127E. doi:10.1021/ja00398a058.

Evans, D. A.; Ennis, M. D.; Mathre, D. J. (1982). "Asymmetric Alkylation Reactions of Chiral Imide Enolates. A Practical Approach to the Enantioselective Synthesis of a-Substituted Carboxylic Acid Derivatives". J. Am. Chem. Soc. 104 (6): 1737–1739. doi:10.1021/ja00370a050.

Evans, D. A.; Chapman, K. T.; Bisaha, J. (1984). "New Asymmetric Diels-Alder Cycloaddition Reactions. Chiral α,β-Unsaturated Carboximides as Practical Chiral Acrylate and Crotonate Dienophile Synthons". J. Am. Chem. Soc. 106 (15): 4261–4263. Bibcode:1984JAChS.106.4261E. doi:10.1021/ja00327a031.

Evans, D. A.; Chapman, K. T.; Hung, D. T.; Kawaguchi, A. T. (1987). "Transition State π-Solvation by Aromatic Rings: An Electronic Contribution to Diels-Alder Reaction Diastereoselectivity". Angew. Chem. Int. Ed. 26 (11): 1184–1186. doi:10.1002/anie.198711841.

Shinada, Tetsuro; Oe, Kentaro; Ohfune, Yasufumi (2012-06-27). "Efficient total synthesis of manzacidin B". Tetrahedron Letters. 53 (26): 3250–3253. doi:10.1016/j.tetlet.2012.04.042.

Tsai, Wen-Jiuan; Lin, Yi-Tsong; Uang, Biing-Jiun (1994-07-01). "Asymmetric Michael addition of thiols to (1R,2R,4R)-(−)-2,10-N-enoylcamphorsultam". Tetrahedron: Asymmetry. 5 (7): 1195–1198. doi:10.1016/0957-4166(94)80155-X.

Takao, Ken-ichi; Sakamoto, Shu; Touati, Marianne Ayaka; Kusakawa, Yusuke; Tadano, Kin-ichi (2012-11-08). "Asymmetric Construction of All-Carbon Quaternary Stereocenters by Chiral-Auxiliary-Mediated Claisen Rearrangement and Total Synthesis of (+)-Bakuchiol". Molecules. 17 (11): 13330–13344. doi:10.3390/molecules171113330. PMC 6268616. PMID 23138536.

Myers, A. G.; et al. (1997). "Pseudoephedrine as a Practical Chiral Auxiliary for the Synthesis of Highly Enantiomerically Enriched Carboxylic Acids, Alcohols, Aldehydes, and Ketones". J. Am. Chem. Soc. 119 (28): 6496–6511. Bibcode:1997JAChS.119.6496M. doi:10.1021/ja970402f.

Myers, A. G.; Morales, M. R.; Mellem, K. T. (2012). "Pseudoephenamine: A Practical Chiral Auxiliary for Asymmetric Synthesis" (PDF). Angew. Chem. 124 (19): 4646–4649. Bibcode:2012AngCh.124.4646M. doi:10.1002/ange.201200370. PMC 3854953. PMID 22461381.

Mellem, Kevin T.; Myers, Andrew G. (2013). "A Simple, Scalable Synthetic Route to (+)- and (−)-Pseudoephenamine". Organic Letters. 15 (21): 5594–5597. doi:10.1021/ol402815d. ISSN 1523-7060. PMC 3864801. PMID 24138164.

Myers, A. G.; Yang, B. H.; McKinstry, L.; Kopecky, D. J.; Gleason, J. L. (1997). "Pseudoephedrine as a Practical Chiral Auxiliary for the Synthesis of Highly Enantiomerically Enriched Carboxylic Acids, Alcohols, Aldehydes, and Ketones". J. Am. Chem. Soc. 119 (28): 6496–6511. Bibcode:1997JAChS.119.6496M. doi:10.1021/ja970402f.

Kummer, D. A.; Chain, W. J.; Morales, M. R.; Quiroga, O.; Myers, A. G. (2008). "Stereocontrolled Alkylative Construction of Quaternary Carbon Centers". J. Am. Chem. Soc. 130 (40): 13231–13233. Bibcode:2008JAChS.13013231K. doi:10.1021/ja806021y. PMC 2666470. PMID 18788739.

Liu, Guangcheng; Cogan, Derek A.; Ellman, Jonathan A. (October 1997). "Catalytic Asymmetric Synthesis of tert -Butanesulfinamide. Application to the Asymmetric Synthesis of Amines". Journal of the American Chemical Society. 119 (41): 9913–9914. Bibcode:1997JAChS.119.9913L. doi:10.1021/ja972012z. ISSN 0002-7863.

Ellman, J. A.; Owens, T. D.; Tang, T. P. (2002). "N-tert-Butanesulfinyl Imines: Versatile Intermediates for the Asymmetric Synthesis of Amines". Acc. Chem. Res. 35 (11): 984–995. doi:10.1021/ar020066u. PMID 12437323.

Corey, E. J.; Enders, D. (1976). "Applications of N,N-dimethylhydrazones to synthesis. Use in efficient, positionally and stereochemically selective C-C bond formation; oxidative hydrolysis to carbonyl compounds". Tetrahedron Letters. 17 (1): 3–6. doi:10.1016/s0040-4039(00)71307-4.

Turner, S. T.; et al. (1998). "Tipranavir (PNU-140690): A Potent, Orally Bioavailable Nonpeptidic HIV Protease Inhibitor of the 5,6-Dihydro-4-hydroxy-2-pyrone Sulfonamide Class". J. Med. Chem. 41 (18): 3467–3476. doi:10.1021/jm9802158. PMID 9719600.

Roth, B. D.; et al. (1991). "Inhibitors of Cholesterol Biosynthesis. 3. Tetrahydro-4-hydroxy-6-[2-(lH-pyrrol-l-yl)ethyl]-2H-pyran-2-one Inhibitors of HMG-CoA Reductase. 2. Effects of Introducing Substituents at Positions Three and Four of the Pyrrole Nucleus". J. Med. Chem. 34 (1): 357–366. doi:10.1021/jm00105a056. PMID 1992137.

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Brunel, Jean Michel (2005). "BINOL: A Versatile Chiral Reagent". Chemical Reviews. 105 (3): 857–898. doi:10.1021/cr040079g. PMID 15755079.

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Chiral auxiliary (English Wikipedia)