Pure and Applied Chemistry

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• Marek Ilan, Minko Yury, Pasco Morgane, Mejuch Tom, Gilboa Noga, Chechik Helena, Das Jaya P.: All-Carbon Quaternary Stereogenic Centers in Acyclic Systems through the Creation of Several C–C Bonds per Chemical Step. J. Am. Chem. Soc. 2014, 136, 2682. <http://dx.doi.org/10.1021/ja410424g>
• Yang Kai, Liu Li-Juan, Liu Jin-Tao: The Synthesis and Strecker Reaction of 2-Chlorotetrafluoroethanesulfinyl Ketimines. J. Org. Chem. 2014, 79, 3215. <http://dx.doi.org/10.1021/jo500008e>
• de Miranda Amanda S., de Souza Rodrigo O. M. A., Miranda Leandro S. M.: Ammonium formate as a green hydrogen source for clean semi-continuous enzymatic dynamic kinetic resolution of (+/−)-α-methylbenzylamine. RSC Adv. 2014, 4, 13620. <http://dx.doi.org/10.1039/c4ra00462k>
• Lei Qian, Wei Yawen, Talwar Dinesh, Wang Chao, Xue Dong, Xiao Jianliang: Fast Reductive Amination by Transfer Hydrogenation “on Water”. Chem. Eur. J. 2013, 19, 4021. <http://dx.doi.org/10.1002/chem.201204194>
• Sirvent Juan Alberto, Foubelo Francisco, Yus Miguel: Chiral Aminated α-Methylenebenzocycloalkenes from o -Bromoaryl Aldehydes and Ketones. Eur. J. Org. Chem. 2013, 2013, 2461. <http://dx.doi.org/10.1002/ejoc.201201712>
• Yang Yanmei, Huang Yangen, Qing Feng-Ling: Asymmetric synthesis of trifluoromethylated aziridines from CF3-substituted N-tert-butanesulfinyl ketimines. Tetrahedron Letters 2013, 54, 3826. <http://dx.doi.org/10.1016/j.tetlet.2013.05.048>
• Bonazzi Simone, Cheng Bichu, Wzorek Joseph S., Evans David A.: Total Synthesis of (−)-Nakadomarin A. J. Am. Chem. Soc. 2013, 135, 9338. <http://dx.doi.org/10.1021/ja404673s>
• Guijarro David, Pablo Óscar, Yus Miguel: Synthesis of γ-, δ-, and ε-Lactams by Asymmetric Transfer Hydrogenation of N-(tert-Butylsulfinyl)iminoesters. J. Org. Chem. 2013, 78, 3647. <http://dx.doi.org/10.1021/jo400164y>
• Pablo Óscar, Guijarro David, Yus Miguel: Synthesis of Nitrogenated Heterocycles by Asymmetric Transfer Hydrogenation of N-(tert-Butylsulfinyl)haloimines. J. Org. Chem. 2013, 78, 9181. <http://dx.doi.org/10.1021/jo4014386>
• Huang Wei, Ye Jian-Liang, Zheng Wei, Dong Han-Qing, Wei Bang-Guo: Radical Migration–Addition of N-tert-Butanesulfinyl Imines with Organozinc Reagents. J. Org. Chem. 2013, 78, 11229. <http://dx.doi.org/10.1021/jo401640c>
• Pasco Morgane, Gilboa Noga, Mejuch Tom, Marek Ilan: The Renaissance of Zinc Carbenoid in Stereoselective Synthesis in Acyclic Systems. Organometallics 2013, 32, 942. <http://dx.doi.org/10.1021/om301220a>
• de Miranda Amanda S., Miranda Leandro S. M., de Souza Rodrigo O. M. A.: Ethyl acetate as an acyl donor in the continuous flow kinetic resolution of (±)-1-phenylethylamine catalyzed by lipases. Org. Biomol. Chem. 2013, 11, 3332. <http://dx.doi.org/10.1039/c3ob40437d>
• Feng Xiangqing, Du Haifeng: Synthesis of Chiral Olefin Ligands and their Application in Asymmetric Catalysis. Asian Journal of Organic Chemistry 2012, 1, 204. <http://dx.doi.org/10.1002/ajoc.201200069>
• Pablo Óscar, Guijarro David, Kovács Gábor, Lledós Agustí, Ujaque Gregori, Yus Miguel: A Versatile Ru Catalyst for the Asymmetric Transfer Hydrogenation of Both Aromatic and Aliphatic Sulfinylimines. Chemistry A European Journal 2012, 18, 1969. <http://dx.doi.org/10.1002/chem.201102426>
• Liu Zhen-Jiang, Zhang Fan, Liu Jin-Tao: Regiospecific and diastereoselective aldol reaction of chiral N-sulfinyl metalloenamines with α,β-unsaturated trifluoromethyl ketones: Asymmetric synthesis of tertiary trifluoromethyl allylic carbinols. J FLUORINE CHEM 2012, 133, 102. <http://dx.doi.org/10.1016/j.jfluchem.2011.09.002>
• Liu Yingle, Huang Yangen, Qing Feng-Ling: Asymmetric synthesis of β-aryl-β-trifluoromethyl-β-aminoarones via Mannich-type reactions of ketone enolates with chiral aryl CF3-substituted N-tert-butanesulfinyl ketimines. Tetrahedron 2012, 68, 4955. <http://dx.doi.org/10.1016/j.tet.2012.04.070>
• Xarnod (Lu-Men Chao) Cholmen, Huang Wei, Ren Rong-Guo, Liu Ru-Cheng, Wei Bang-Guo: A flexible approach to construct three contiguous chiral centers of sphingolipids, and asymmetric synthesis of d-ribo-phytosphingosine and its derivatives. Tetrahedron 2012, 68, 6688. <http://dx.doi.org/10.1016/j.tet.2012.05.120>
• Reddy Leleti Rajender, Gupta Aditya P., Villhauer Eric, Liu Yugang: Rhodium-Catalyzed Asymmetric Arylation of N-(tert-Butanesulfinyl)imines with Sodium Tetraarylborates. J Org Chern 2012, 77, 1095. <http://dx.doi.org/10.1021/jo2024224>
• Collados Juan F., Toledano Estefanía, Guijarro David, Yus Miguel: Microwave-Assisted Solvent-Free Synthesis of Enantiomerically Pure N-(tert-Butylsulfinyl)imines. J. Org. Chem. 2012, 77, 5744. <http://dx.doi.org/10.1021/jo300919x>
• Rajender Reddy Leleti, Prasad Kapa, Prashad Mahavir: A Protocol for an Asymmetric Synthesis of γ-Amino Acids. J. Org. Chem. 2012, 77, 6296. <http://dx.doi.org/10.1021/jo301177f>
• Nie Yanzhao, Yang Jing, Feng Xiangqing, Du Haifeng: Rh(I)-Catalyzed Asymmetric 1,2-Addition to α-Diketones with Chiral Sulfur–Alkene Hybrid Ligands. Org Lett 2012, 14, 624. <http://dx.doi.org/10.1021/ol203238j>
• Yang Cui-Feng, Shen Chen, Wang Jian-Yong, Tian Shi-Kai: A Highly Diastereoselective Decarboxylative Mannich Reaction of β-Keto Acids with Optically Active N-Sulfinyl α-Imino Esters. Org. Lett. 2012, 14, 3092. <http://dx.doi.org/10.1021/ol301180z>
• Izmest’ev E. S., Sudarikov D. V., Rubtsova S. A., Slepukhin P. A., Kuchin A. V.: Asymmetric synthesis of new optically active sulfinamides of menthane series and their derivatives. Rus J Org Chem 2012, 48, 184. <http://dx.doi.org/10.1134/S1070428012020066>
• Firsova Yu. N., Lozinskaya N. A., Sosonyuk S. E., Proskurnina M. V., Zefirov N. S.: Stable synthetic equivalents of N-unsubstituted imines: Part 1. Synthesis. Ref J Chem 2012, 2, 74. <http://dx.doi.org/10.1134/S2079978012010037>
• Yu Xufen, Lu Xiyan: Cationic Palladium Complex-Catalyzed Diastereoselective Tandem Annulation of 2-Iminoarylboronic Acids with Substituted Alkynes: Enantioselective Synthesis of Aminoindene Derivatives by Double Asymmetric Induction. Synth Catal 2011, 353, 2805. <http://dx.doi.org/10.1002/adsc.201100363>
• Chakravarti Rajashree, Mano Ajayan, Iwai Hideo, Aldeyab Salem S., Kumar R. Pradeep, Kantam M. Lakshmi, Vinu Ajayan: Functionalization of Mesoporous Carbon with Superbasic MgO Nanoparticles for the Efficient Synthesis of Sulfinamides. Chem Eur J 2011, 17, 6673. <http://dx.doi.org/10.1002/chem.201002885>
• Dilman Alexander D., Levin Vitalij V.: Nucleophilic Trifluoromethylation of C=N Bonds. Eur J Org Chem 2011, 2011, 831. <http://dx.doi.org/10.1002/ejoc.201001558>
• Fritz Sven P., Mumtaz Amara, Yar Muhammad, McGarrigle Eoghan M., Aggarwal Varinder K.: Sulfinamides as Highly Effective Amine Protecting Groups and Their Use in the Conversion of Amino Alcohols into Morpholines. Eur J Org Chem 2011, 2011, 3156. <http://dx.doi.org/10.1002/ejoc.201100337>
• Han Zhengxu, Busch Robert, Fandrick Keith R., Meyer Angelica, Xu Yibo, Krishnamurthy Dhileep K., Senanayake Chris H.: Asymmetric synthesis of diverse α,α-diarylmethylamines via aryl Grignard additions to chiral N-2,4,6-triisopropylbenzenesulfinylimines. Tetrahed 2011, 67, 7035. <http://dx.doi.org/10.1016/j.tet.2011.07.019>
• Zhu Rui-Heng, Shi Xiao-Xin: Practical and highly stereoselective method for the preparation of several chiral arylsulfinamides and arylsulfinates based on the spontaneous crystallization of diastereomerically pure N-benzyl-N-(1-phenylethyl)-arylsulfinamides. Tet Asymm 2011, 22, 387. <http://dx.doi.org/10.1016/j.tetasy.2011.01.028>
• Guijarro David, Pablo Óscar, Yus Miguel: Achiral β-amino alcohols as efficient ligands for the ruthenium-catalysed asymmetric transfer hydrogenation of sulfinylimines. Tetrahetron Lett 2011, 52, 789. <http://dx.doi.org/10.1016/j.tetlet.2010.12.031>
• Reddy Leleti Rajender, Gupta Aditya P., Liu Yugang: Asymmetric Synthesis of α-Amino Acids by Reduction of N-tert-Butanesulfinyl Ketimine Esters. J Org Chem 2011, 76, 3409. <http://dx.doi.org/10.1021/jo200401a>
• Feng Xiangqing, Wang Yazhou, Wei Beibei, Yang Jing, Du Haifeng: Simple N-Sulfinyl-Based Chiral Sulfur–Olefin Ligands for Rhodium-Catalyzed Asymmetric 1,4-Additions. Org Lett 2011, 13, 3300. <http://dx.doi.org/10.1021/ol2009494>
• Zhang Fan, Liu Zhen-Jiang, Liu Jin-Tao: Asymmetric aza-Henry reaction of chiral fluoroalkyl α,β-unsaturated N-tert-butanesulfinyl ketoimines: an efficient approach to enantiopure fluoroalkylated α,β-diamines and α,β-diamino acids. Org Biomol Chem 2011, 9, 3625. <http://dx.doi.org/10.1039/c1ob05132f>
• Feng Xiangqing, Wei Beibei, Yang Jing, Du Haifeng: Chiral N-tert-butanesulfinyl α,β-unsaturated ketimine: a simple and highly effective olefin/sulfinimide hybrid ligand for asymmetric 1,4-additions. Biomol Chem 2011, 9, 5927. <http://dx.doi.org/10.1039/c1ob05971h>
• Muñoz Lourdes, Rodriguez Anna M., Rosell Gloria, Bosch M. Pilar, Guerrero Angel: Enzymatic enantiomeric resolution of phenylethylamines structurally related to amphetamine. Biomol Chem 2011, 9, 8171. <http://dx.doi.org/10.1039/c1ob06251d>
• Nugent Thomas C., El-Shazly Mohamed: Chiral Amine Synthesis - Recent Developments and Trends for Enamide Reduction, Reductive Amination, and Imine Reduction. Synth Catal 2010, 352, 753. <http://dx.doi.org/10.1002/adsc.200900719>
• Schäfer Sascha, Wirth Thomas: Eine praktische und hochreaktive polyfluorierte hypervalente Iod(III)-Verbindung. angew chemie 2010, 122, 2846. <http://dx.doi.org/10.1002/ange.200907134>
• Schäfer Sascha, Wirth Thomas: A Versatile and Highly Reactive Polyfluorinated Hypervalent Iodine(III) Compound. Angew Chem Int E 2010, 49, 2786. <http://dx.doi.org/10.1002/anie.200907134>
• García Daniel, Foubelo Francisco, Yus Miguel: Reductive Ring-Opening of Phthalan and Isochroman: Application to the Stereoselective Synthesis of Tetrahydroisoquinolines and Tetrahydrobenzazepines. Eur J Org Chem 2010, 2010, 2893. <http://dx.doi.org/10.1002/ejoc.201000111>
• Louvel Julien, Botuha Candice, Chemla Fabrice, Demont Emmanuel, Ferreira Franck, Pérez-Luna Alejandro: Asymmetric Total Synthesis of (+)-6-epi-Castanospermine by the Stereoselective Formation of a syn,anti Acetylenic 2-Amino-1,3-diol Stereotriad. Eur J Org Chem 2010, 2010, 2921. <http://dx.doi.org/10.1002/ejoc.201000202>
• Fousteris Manolis A., Schubert Undine, Roell Daniela, Roediger Julia, Bailis Nikolaos, Nikolaropoulos Sotiris S., Baniahmad Aria, Giannis Athanassios: 20-Aminosteroids as a novel class of selective and complete androgen receptor antagonists and inhibitors of prostate cancer cell growth. Bioorganic & Medicinal Chemistry 2010, 18, 6960. <http://dx.doi.org/10.1016/j.bmc.2010.08.029>
• Almansa Raquel, Collados Juan F., Guijarro David, Yus Miguel: Asymmetric synthesis of α- and β-amino acids by diastereoselective addition of triorganozincates to N-(tert-butanesulfinyl)imines. Tet Asymm 2010, 21, 1421. <http://dx.doi.org/10.1016/j.tetasy.2010.03.046>
• Botuha Candice, Chemla Fabrice, Ferreira Franck, Louvel Julien, Pérez-Luna Alejandro: Allenylzincs and tert-butylsulfinylimines: a fruitful marriage for synthesis. Tet Asymm 2010, 21, 1147. <http://dx.doi.org/10.1016/j.tetasy.2010.04.044>
• Xiao Hengqiao, Huang Yangen, Qing Feng-Ling: Highly diastereoselective synthesis of α-trifluoromethylated α-propargylamines by acetylide addition to chiral CF3-substituted N-tert-butanesulfinyl ketimines. Tetrahedron: Asymmetry 2010, 21, 2949. <http://dx.doi.org/10.1016/j.tetasy.2010.11.028>
• Benamer Mounira, Turcaud Serge, Royer Jacques: Diastereoselective alkynylation of chiral phosphinoylimines: preparation of optically active propargylamines. Tetrahetron Lett 2010, 51, 645. <http://dx.doi.org/10.1016/j.tetlet.2009.11.091>
• Ji Du-Ming, Xu Ming-Hua: Highly diastereoselective Friedel–Crafts reaction of indoles with an N-tert-butanesulfinylimino ester: an efficient and practical approach to enantiomerically enriched α-(3-indolyl)glycines. Chem Commun 2010, 46, 1550. <http://dx.doi.org/10.1039/b914687c>
• Reddy Leleti Rajender, Prashad Mahavir: Asymmetric synthesis of 2-substituted pyrrolidines by addition of Grignard reagents to γ-chlorinated N-tert-butanesulfinyl imine. Chem Commun 2010, 46, 222. <http://dx.doi.org/10.1039/b917435d>
• Leemans Erika, Mangelinckx Sven, De Kimpe Norbert: Asymmetric synthesis of 2-arylpyrrolidines starting from γ-chloro N-(tert-butanesulfinyl)ketimines. Chem Commun 2010, 46, 3122. <http://dx.doi.org/10.1039/b925209f>
• Colpaert Filip, Mangelinckx Sven, Leemans Erika, Denolf Bram, De Kimpe Norbert: Asymmetric synthesis of new chiral N-sulfinyl 2,2-disubstituted aziridines by Grignard additions across α-chloro N-sulfinyl ketimines. Org Biomol Chem 2010, 8, 3251. <http://dx.doi.org/10.1039/c001471k>
• Yus Miguel, Foubelo Francisco, K. Dema Haythem: Enantioselective Synthesis of α-Methylene-γ-butyrolactams Using N-tert-Butanesulfinamides. HETEROCYCLES 2010, 82, 1411. <http://dx.doi.org/10.3987/COM-10-S(E)94>
• Yin Chao, Hui Xin-Ping, Xu Peng-Fei, Niu Liang-Feng, Chen Yong-Fei, Wang Binghe: Development and Application of a New General Method for the Asymmetric Synthesis of (E)-(2-En-3-ynyl)-amines. Adv. Synth. Catal. 2009, 351, 357. <http://dx.doi.org/10.1002/adsc.200800642>
• Höhne Matthias, Bornscheuer Uwe T.: Biocatalytic Routes to Optically Active Amines. ChemCatChem 2009, 1, 42. <http://dx.doi.org/10.1002/cctc.200900110>
• Liu Min, Sun Xing-Wen, Xu Ming-Hua, Lin Guo-Qiang: Highly Efficient Asymmetric Synthesis of Vinylic Amino Alcohols by Zn-Promoted Benzoyloxyallylation of Chiral N-tert-Butanesulfinyl Imines: Facile and Rapid Access to (−)-Cytoxazone. Chem Eur J 2009, 15, 10217. <http://dx.doi.org/10.1002/chem.200900801>
• Almansa Raquel, Guijarro David, Yus Miguel: An improved procedure for the diastereoselective addition of triorganozincates to N-(tert-butanesulfinyl)imines: use of catalytic dialkylzinc. Tetrahetron Lett 2009, 50, 3198. <http://dx.doi.org/10.1016/j.tetlet.2009.01.136>
• Aggarwal Varinder K., Barbero Nekane, McGarrigle Eoghan M., Mickle Greg, Navas Raquel, Suárez José Ramón, Unthank Matthew G., Yar Muhammad: The fate of the tert-butylsulfinyl auxiliary after acid-promoted cleavage—a method for recycling t-BuSONH2. Tetrahetron Lett 2009, 50, 3482. <http://dx.doi.org/10.1016/j.tetlet.2009.03.020>
• Almansa Raquel, Guijarro David, Yus Miguel: Application of the addition of triorganozincates to N-(tert-butanesulfinyl)imines to the enantioselective synthesis of α-amino acids. Tetrahetron Lett 2009, 50, 4188. <http://dx.doi.org/10.1016/j.tetlet.2009.05.008>
• García Daniel, Moreno Benjamín, Soler Tatiana, Foubelo Francisco, Yus Miguel: Stereoselective synthesis of 3-substituted tetrahydroisoquinolines from phthalan and chiral N-sulfinylimines. Tetrahetron Lett 2009, 50, 4710. <http://dx.doi.org/10.1016/j.tetlet.2009.06.010>
• Guijarro David, Pablo Óscar, Yus Miguel: Ruthenium-catalysed asymmetric transfer hydrogenation of N-(tert-butanesulfinyl)imines. Tetrahetron Lett 2009, 50, 5386. <http://dx.doi.org/10.1016/j.tetlet.2009.07.044>
• Ferreira Franck, Botuha Candice, Chemla Fabrice, Pérez-Luna Alejandro: tert-Butanesulfinimines: structure, synthesis and synthetic applications. Chem Soc Rev 2009, 38, 1162. <http://dx.doi.org/10.1039/b809772k>
• Reddy A. Veera, Bhaskara Rao S. Udaya, Narasimha G. Lakshmi, Dubey P. K.: Improved Process for the Preparation of Tamsulosin Hydrochloride. Synth Comm 2009, 39, 1451. <http://dx.doi.org/10.1080/00397910802519216>
• Liu Jun, Hu Jinbo: Synthesis of fluorinated chiral amines using N-tert-butylsulfinyl imines. Future Medicinal Chemistry 2009, 1, 875. <http://dx.doi.org/10.4155/fmc.09.62>
• Pei Dong, Zhang Yu, Wei Siyu, Wang Meng, Sun Jian: Rationally-Designed S-Chiral Bissulfinamides as Highly Enantioselective Organocatalysts for Reduction of Ketimines. Adv Synth Catal 2008, 350, 619. <http://dx.doi.org/10.1002/adsc.200700504>
• Marek Ilan: A Shift in Retrosynthetic Paradigm. Chem Eur J 2008, 14, 7460. <http://dx.doi.org/10.1002/chem.200800580>
• Guerrini Andrea, Varchi Greta, Samorì Cristian, Battaglia Arturo: Synthesis of α^2,2,β³-Diamino Acids by Double Stereodifferentiation Aldol Addition of Oxazolidinone Enolates to N-(tert-Butylsulfinyl) Imines. Eur J Org Chem 2008, 2008, 3834. <http://dx.doi.org/10.1002/ejoc.200800356>
• Zani Lorenzo, Eriksson Lars, Adolfsson Hans: Synthesis of Novel Amino-Acid-Derived Sulfinamides and Their Evaluation as Ligands for the Enantioselective Transfer Hydrogenation of Ketones. Eur J Org Chem 2008, 2008, 4655. <http://dx.doi.org/10.1002/ejoc.200800576>
• Almansa Raquel, Guijarro David, Yus Miguel: Triorganozincates as efficient nucleophiles for the diastereoselective addition to N-(tert-butanesulfinyl)imines. Tet Asymm 2008, 19, 603. <http://dx.doi.org/10.1016/j.tetasy.2008.01.038>
• Almansa Raquel, Guijarro David, Yus Miguel: Synthesis of highly enantiomerically enriched amines by the diastereoselective addition of triorganozincates to N-(tert-butanesulfinyl)imines. Tet Asymm 2008, 19, 2484. <http://dx.doi.org/10.1016/j.tetasy.2008.10.012>
• Liu Ru-Cheng, Wei Jin-Hu, Wei Bang-Guo, Lin Guo-Qiang: Concise asymmetric synthesis of (−)-deoxoprosophylline. Tet Asymm 2008, 19, 2731. <http://dx.doi.org/10.1016/j.tetasy.2008.12.014>
• Kattuboina Adiseshu, Li Guigen: Chiral N-phosphonyl imine chemistry: new reagents and their applications for asymmetric reactions. Tetrahetron Lett 2008, 49, 1573. <http://dx.doi.org/10.1016/j.tetlet.2008.01.028>
• Kattuboina Adiseshu, Kaur Parminder, Nguyen Thao, Li Guigen: Chiral N-phosphonyl imine chemistry: asymmetric 1,2-additions of allylmagnesium bromides. Tetrahetron Lett 2008, 49, 3722. <http://dx.doi.org/10.1016/j.tetlet.2008.04.038>
• Liu Zhen-Jiang, Liu Jin-Tao: Asymmetric synthesis of either diastereomer of trifluoromethylated allylic amines by the selective reduction of trifluoromethyl α,β-unsaturated N-tert-butanesulfinyl ketoimines. Chem Commun 2008, 5233. <http://dx.doi.org/10.1039/b810459j>
• Solà Jordi, Revés Marc, Riera Antoni, Verdaguer Xavier: N-Phosphino Sulfinamide Ligands: An Efficient Manner To Combine Sulfur Chirality and Phosphorus Coordination Behavior. Angew Chem 2007, 119, 5108. <http://dx.doi.org/10.1002/ange.200701040>
• Kolodney Goren, Sklute Genia, Perrone Sylvie, Knochel Paul, Marek Ilan: Diastereodivergent Synthesis of Enantiomerically Pure Homoallylic Amine Derivatives Containing Quaternary Carbon Stereocenters. Angew Chem 2007, 119, 9451. <http://dx.doi.org/10.1002/ange.200702981>
• Solà Jordi, Revés Marc, Riera Antoni, Verdaguer Xavier: N-Phosphino Sulfinamide Ligands: An Efficient Manner To Combine Sulfur Chirality and Phosphorus Coordination Behavior. Angew Chem Int Ed 2007, 46, 5020. <http://dx.doi.org/10.1002/anie.200701040>
• Kolodney Goren, Sklute Genia, Perrone Sylvie, Knochel Paul, Marek Ilan: Diastereodivergent Synthesis of Enantiomerically Pure Homoallylic Amine Derivatives Containing Quaternary Carbon Stereocenters. Angew Chem Int Ed 2007, 46, 9291. <http://dx.doi.org/10.1002/anie.200702981>
• Wakchaure Vijay N., Mohanty Rashmi R., Shaikh Ahson J., Nugent Thomas C.: A One-Pot Asymmetric Sequential Amination-Alkylation of Aldehydes: Expedient Synthesis of Aliphatic Chiral Amines. Eur J Org Chem 2007, 2007, 959. <http://dx.doi.org/10.1002/ejoc.200600781>
• Kuduk Scott D., DiPardo Robert M., Chang Ronald K., Di Marco Christina N., Murphy Kathy L., Ransom Richard W., Reiss Duane R., Tang Cuyue, Prueksaritanont Thomayant, Pettibone Douglas J.: Bradykinin B1 antagonists: Biphenyl SAR studies in the cyclopropanecarboxamide series. Biorg Med Chem Lett 2007, 17, 3608. <http://dx.doi.org/10.1016/j.bmcl.2007.04.040>
• Guerrini Andrea, Varchi Greta, Daniele Rizzo, Samorì Cristian, Battaglia Arturo: Synthesis of chiral β2,2,3-3-amino-2-hydroxyalkanoates and 3-alkyl-3-hydroxy-β-lactams by double asymmetric induction. Tetrahedron 2007, 63, 7949. <http://dx.doi.org/10.1016/j.tet.2007.05.069>
• Grajewska Agnieszka, Rozwadowska Maria D.: Total synthesis of (R)-(+)-salsolidine by hydride addition to (R)-N-tert-butanesulfinyl ketimine. Tet Asymm 2007, 18, 557. <http://dx.doi.org/10.1016/j.tetasy.2007.01.033>
• Piggott Andrew M., Karuso Peter: Hydrolysis rates of alkyl and aryl sulfinamides: evidence of general acid catalysis. Tetrahetron Lett 2007, 48, 7452. <http://dx.doi.org/10.1016/j.tetlet.2007.08.081>
• Constable David J. C., Dunn Peter J., Hayler John D., Humphrey Guy R., Leazer, Jr. Johnnie L., Linderman Russell J., Lorenz Kurt, Manley Julie, Pearlman Bruce A., Wells Andrew: Key green chemistry research areas?a perspective from pharmaceutical manufacturers. Green Chem 2007, 9, 411. <http://dx.doi.org/10.1039/b703488c>
• Risseeuw Martijn D. P., Mazurek Jaroslaw, van Langenvelde Arjan, van der Marel Gijsbert A., Overkleeft Herman S., Overhand Mark: Synthesis of alkylated sugar amino acids: conformationally restricted l-Xaa-l-Ser/Thr mimics. Org Biomol Chem 2007, 5, 2311. <http://dx.doi.org/10.1039/b705750d>
• Li Zhenjiang, Ren Xinhua, Shi Yuhu, Ouyang Pingkai: Practical and General Entry to N‐Tosyl Aryl Aldimines Promoted by Sulfamic Acid in Water and Alcohol. Synth Comm 2007, 37, 713. <http://dx.doi.org/10.1080/00397910601131387>
• Morton Daniel, Stockman Robert A.: Chiral non-racemic sulfinimines: versatile reagents for asymmetric synthesis. Tetrahedron 2006, 62, 8869. <http://dx.doi.org/10.1016/j.tet.2006.06.107>
• Grigg Ronald, McCaffrey Shaun, Sridharan Visuvanathar, Fishwick Colin W.G., Kilner Colin, Korn Stewart, Bailey Kevin, Blacker John: Enantioselective synthesis of non-proteinogenic 2-arylallyl-α-amino acids via Pd/In catalytic cascades. Tetrahedron 2006, 62, 12159. <http://dx.doi.org/10.1016/j.tet.2006.09.098>
• Kościołowicz Agnieszka, Rozwadowska Maria D.: Diastereoselective Pomeranz–Fritsch–Bobbitt synthesis of (S)-(−)-salsolidine using (R)-N-tert-butanesulfinylimine as a substrate. Tet Asymm 2006, 17, 1444. <http://dx.doi.org/10.1016/j.tetasy.2006.05.011>
• Xiao Dong, Wang Cheng, Palani Anandan, Reichard Gregory, Aslanian Robert, Shih Neng-Yang, Buevich Alexei: Two complementary, diversity-driven asymmetric syntheses of a 2,2-disubstituted piperidine NK1 antagonist. Tet Asymm 2006, 17, 2596. <http://dx.doi.org/10.1016/j.tetasy.2006.09.022>
• Kuduk Scott D., Marco Christina Ng Di, Pitzenberger Steven M., Tsou Nancy: Asymmetric addition reactions of Grignard reagents to chiral 2-trifluoromethyl tert-butyl (Ellman) sulfinimine–ethanol adducts. Tetrahetron Lett 2006, 47, 2377. <http://dx.doi.org/10.1016/j.tetlet.2006.01.154>
• Denolf Bram, Mangelinckx Sven, Törnroos Karl W., De Kimpe Norbert: Use of α-Chlorinated N-(tert-Butanesulfinyl)imines in the Synthesis of Chiral Aziridines. Org Lett 2006, 8, 3129. <http://dx.doi.org/10.1021/ol0611245>
• Li Zhenjiang, Ren Xinghua, Wei Ping, Wan Honggui, Shi Yuhu, Ouyang Pingkai: A convenient preparation of aliphatic and aromatic N-sulfonylimines mediated by sulfamic acid in aqueous media. Green Chem 2006, 8, 433. <http://dx.doi.org/10.1039/b517864a>
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