不斉補助剤 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "不斉補助剤" in Japanese language version.

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27doi.org

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acs.org

pubs.acs.org

Brunel, Jean Michel. “BINOL: A Versatile Chiral Reagent”. Chemical Reviews 105 (3): 857–898. 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 105 (19): 6154–6155. doi:10.1021/ja00357a033.
Buchi, George; Vogel, Dennis E.. “A new method for the preparation of .gamma.,.delta.-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.; Trauner, Dirk. “Total Synthesis of (−)-Heptemerone B and (−)-Guanacastepene E”. Journal of the American Chemical Society 128 (51): 17057–17062. 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 16 (19): 5104–5107. doi:10.1021/ol502454r.

doi.org

Glorius, F.; Gnas, Y. (2006). “Chiral Auxiliaries — Principles and Recent Applications”. Synthesis 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. doi:10.1021/ja00856a074.
Miller, J. P. (2013). “ChemInform Abstract: Recent Advances in Asymmetric Diels-Alder Reactions”. ChemInform 44 (48). 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. “BINOL: A Versatile Chiral Reagent”. Chemical Reviews 105 (3): 857–898. 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 105 (19): 6154–6155. 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.
Buchi, George; Vogel, Dennis E.. “A new method for the preparation of .gamma.,.delta.-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.; Trauner, Dirk. “Total Synthesis of (−)-Heptemerone B and (−)-Guanacastepene E”. Journal of the American Chemical Society 128 (51): 17057–17062. 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 16 (19): 5104–5107. doi:10.1021/ol502454r.
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. 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. 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” (英語). Molecules 17 (11): 13330–13344. doi:10.3390/molecules171113330.
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. (2012). “Pseudoephenamine: A Practical Chiral Auxiliary for Asymmetric Synthesis”. Angew. Chem. 124: 4646–4649. doi:10.1002/ange.201200370.
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: 13231–13233. doi:10.1021/ja806021y.
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: 984–995. doi:10.1021/ar020066u.
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. (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: 3467–3476. doi:10.1021/jm9802158.
Roth, B. D. ' (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: 357–366. doi:10.1021/jm00105a056.

mdpi.com

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” (英語). Molecules 17 (11): 13330–13344. doi:10.3390/molecules171113330.

sciencedirect.com

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.
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.