References analysis of the Wikipedia article "手性助剂" in the Chinese version

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

Jamali, Fakhreddin. Chapter 14: Stereochemically Pure Drugs: An Overview. Wainer, Irving W. (编). Drug Stereochemistry: Analytical Methods and Pharmacology. Marcel Dekker, Inc. 1993: 375–382. ISBN 0-8247-8819-2.

Evans, D. A.; Helmchen, G.; Rüping, M. Chiral Auxiliaries in Asymmetric Synthesis. Christmann, M (编). Asymmetric Synthesis — The Essentials. Wiley-VCH Verlag GmbH & Co. 2007: 3–9. ISBN 978-3-527-31399-0.

Caron, Stéphane. Chapter 15: Synthetic Route Development of Selected Contemporary Pharmaceutical Drugs. Caron, Stéphane (编). Practical Synthetic Organic Chemistry

. John Wiley & Sons, Inc. 2011: 666–670. ISBN 978-0-470-03733-1.

Jie Jack Li, Douglas S. Johnson, Drago R. Sliskovic, Bruce D. Roth. Chapter 9. Atorvastatin Calcium (Lipitor). Contemporary Drug Synthesis. John Wiley & Sons, Inc. 2004: 113–125. ISBN 0-471-21480-9.

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

Miller, J. P. ChemInform Abstract: Recent Advances in Asymmetric Diels-Alder Reactions. ChemInform. 2013, 44 (48). doi:10.1002/chin.201348243.

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

Corey, E. J.; Ensley, H. E.; Parnell, C. A. Convenient Synthesis of a Highly Efficient and Recyclable Chiral Director for Asymmetric Induction. J. Org. Chem. 1978, 43 (8): 1610–1611. doi:10.1021/jo00402a037. 引文使用过时参数coauthors (帮助)

Whitesell, J. K.; Chen, H. H.; Lawrence, R. M. trans-2-Phenylcyclohexanol. A powerful and readily available chiral auxiliary. J. Org. Chem. 1985, 50 (23): 4663–4664. doi:10.1021/jo00223a055. 引文使用过时参数coauthors (帮助)

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

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

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

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

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

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

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

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

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. 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. 2014, 16 (19): 5104–5107. PMID 25225741. doi:10.1021/ol502454r.

Evans, D. A.; Bartroli, J.; Shih, T. L. Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates. J. Am. Chem. Soc. 1981, 103 (8): 2127–2129. doi:10.1021/ja00398a058. 引文使用过时参数coauthors (帮助)

Evans, D. A.; Ennis, M D.; Mathre, D. J. Asymmetric Alkylation Reactions of Chiral Imide Enolates. A Practical Approach to the Enantioselective Synthesis of a-Substituted Carboxylic Acid Derivatives. J. Am. Chem. Soc. 1982, 104 (7): 1737–1739. doi:10.1021/ja00370a050. 引文使用过时参数coauthors (帮助)

Evans, D. A.; Chapman, K. T.; Bisaha, J. New Asymmetric Diels-Alder Cycloaddition Reactions. Chiral α,β-Unsaturated Carboximides as Practical Chiral Acrylate and Crotonate Dienophile Synthons. J. Am. Chem. Soc. 1984, 106 (15): 4261–4263. doi:10.1021/ja00327a031. 引文使用过时参数coauthors (帮助)

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

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

Tsai, Wen-Jiuan; Lin, Yi-Tsong; Uang, Biing-Jiun. Asymmetric Michael addition of thiols to (1R,2R,4R)-(−)-2,10-N-enoylcamphorsultam. Tetrahedron: Asymmetry. 1994-07-01, 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. Asymmetric Construction of All-Carbon Quaternary Stereocenters by Chiral-Auxiliary-Mediated Claisen Rearrangement and Total Synthesis of (+)-Bakuchiol. Molecules. 2012-11-08, 17 (11): 13330–13344. PMC 6268616 

. PMID 23138536. doi:10.3390/molecules171113330 

（英语）.

Myers, A. G., et al., Pseudoephedrine as a Practical Chiral Auxiliary for the Synthesis of Highly Enantiomerically Enriched Carboxylic Acids, Alcohols, Aldehydes, and Ketones, J. Am. Chem. Soc., 1997, 119, 6496-6511.doi:10.1021/ja970402f

Myers, A. G.; Morales, M. R.; Mellem, K. T. Pseudoephenamine: A Practical Chiral Auxiliary for Asymmetric Synthesis. Angew. Chem. 2012, 124: 4646–4649. doi:10.1002/ange.201200370. 引文使用过时参数coauthors (帮助)

Myers, A. G.; Yang, B. H.; McKinstry, L.; Kopecky, D. J.; Gleason, J. L. Pseudoephedrine as a Practical Chiral Auxiliary for the Synthesis of Highly Enantiomerically Enriched Carboxylic Acids, Alcohols, Aldehydes, and Ketones. J. Am. Chem. Soc. 1997, 119: 6496–6511. doi:10.1021/ja970402f. 引文使用过时参数coauthors (帮助)

Kummer, D. A.; Chain, W. J.; Morales, M. R.; Quiroga, O.; Myers, A. G. Stereocontrolled Alkylative Construction of Quaternary Carbon Centers. J. Am. Chem. Soc. 2008, 130: 13231–13233. doi:10.1021/ja806021y. 引文使用过时参数coauthors (帮助)

Ellman, J. A.; Owens, T. D.; Tang, T. P. N-tert-Butanesulfinyl Imines: Versatile Intermediates for the Asymmetric Synthesis of Amines. Acc. Chem. Res. 2002, 35: 984–995. doi:10.1021/ar020066u. 引文使用过时参数coauthors (帮助)

Corey, E. J., Enders, D. 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. 1976, 17 (1): 3–6. doi:10.1016/s0040-4039(00)71307-4.

Turner, S. T.; et al. 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. 1998, 41: 3467–3476. doi:10.1021/jm9802158.

Roth, B. D. et al.' '. 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. 1991, 34: 357–366. doi:10.1021/jm00105a056.

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