메뉴 건너뛰기




Volumn 8, Issue 11, 2013, Pages 2271-2280

Asymmetric synthesis of amines using tert-butanesulfinamide

Author keywords

[No Author keywords available]

Indexed keywords

(1 ISOPROPYL 1 METHYLPROP 2 YNYL) 2 METHYLPROPANESULFINAMIDE; 1 ISOPROPYL 1 METHYLPROP 2 YNYLAMINE; AMINE; DIAGNOSTIC AGENT; N (1 ISOPROPYL 1 METHYL 3 TRIMETHYLSILANYLPROP 2 YNYL) 2 METHYLPROPANESULFINAMIDE; N (1 ISOPROPYL 1 METHYLPROP 2 YNYL) 2 METHYLPROPANESULFINAMIDE; N (3 METHYL 2 BUTYLIDENE) 2 METHYLPROPANESULFINAMIDE; PEPTIDE; PEPTIDE ISOSTERE; PROTEINASE INHIBITOR; SULFINAMIDE; TERT BUTANESULFINAMIDE; TERTIARY CARBINAMINE; UNCLASSIFIED DRUG;

EID: 84887010336     PISSN: 17542189     EISSN: 17502799     Source Type: Journal    
DOI: 10.1038/nprot.2013.134     Document Type: Article
Times cited : (43)

References (49)
  • 2
    • 56549116899 scopus 로고    scopus 로고
    • Chiral HPLC for efficient resolution of enantiomers
    • Okamoto, Y. & Ikai, T. Chiral HPLC for efficient resolution of enantiomers. Chem. Soc. Rev. 37, 2593-2608 (2008).
    • (2008) Chem. Soc. Rev , vol.37 , pp. 2593-2608
    • Okamoto, Y.1    Ikai, T.2
  • 3
    • 0037124885 scopus 로고    scopus 로고
    • Asymmetric catalysis: Science and opportunities (nobel lecture)
    • DOI 10.1002/1521-3773(20020617)41:12<2008::AID-ANIE2008>3.0.CO;2-4
    • Noyori, R. Asymmetric catalysis: science and opportunities (Nobel lecture). Angew. Chem Intl. Edn. 41, 2008-2022 (2002). (Pubitemid 34746902)
    • (2002) Angewandte Chemie - International Edition , vol.41 , Issue.12 , pp. 2008-2022
    • Noyori, R.1
  • 4
    • 77954797329 scopus 로고    scopus 로고
    • Biocatalytic asymmetric synthesis of chiral amines from ketones applied to sitagliptin manufacture
    • Savile, C.K. et al. Biocatalytic asymmetric synthesis of chiral amines from ketones applied to sitagliptin manufacture. Science 329, 305-309 (2010).
    • (2010) Science , vol.329 , pp. 305-309
    • Savile, C.K.1
  • 5
    • 84878074014 scopus 로고    scopus 로고
    • Asymmetric preparation of prim-, sec-, and tert-amines employing selected biocatalysts
    • Kroutil, W. et al. Asymmetric preparation of prim-, sec-, and tert-amines employing selected biocatalysts. Org. Process Res. Dev. 17, 751-759 (2013).
    • (2013) Org. Process Res. Dev , vol.17 , pp. 751-759
    • Kroutil, W.1
  • 6
    • 33846906752 scopus 로고    scopus 로고
    • Recent developments in asymmetric catalytic addition to C{double bond, long}N bonds
    • DOI 10.1016/j.tet.2006.11.076, PII S0040402006018941
    • Friestad, G.K. & Mathies, A.K. Recent developments in asymmetric catalytic addition to C=N bonds. Tetrahedron 63, 2541-2569 (2007). (Pubitemid 46240099)
    • (2007) Tetrahedron , vol.63 , Issue.12 , pp. 2541-2569
    • Friestad, G.K.1    Mathies, A.K.2
  • 7
    • 79954533009 scopus 로고    scopus 로고
    • Catalytic enantioselective formation of C-C bonds by addition to imines and hydrazones: A ten-year update
    • Kobayashi, S., Mori, Y., Fossey, J.S. & Salter, M.M. Catalytic enantioselective formation of C-C bonds by addition to imines and hydrazones: A ten-year update. Chem. Rev. 111, 2626-2704 (2011).
    • (2011) Chem. Rev , vol.111 , pp. 2626-2704
    • Kobayashi, S.1    Mori, Y.2    Fossey, J.S.3    Salter, M.M.4
  • 8
    • 0030924784 scopus 로고    scopus 로고
    • Asymmetric synthesis of amines by nucleophilic 1,2-addition of organometallic reagents to the CN-double bond
    • DOI 10.1016/S0957-4166(97)00208-5, PII S0957416697002085
    • Enders, D. & Reinhold, U. Asymmetric synthesis of amines by nucleophilic 1,2-addition of organometallic reagents to the CN-double bond. Tetrahedron Asymmetry 8, 1895-1946 (1997). (Pubitemid 27277912)
    • (1997) Tetrahedron Asymmetry , vol.8 , Issue.12 , pp. 1895-1946
    • Enders, D.1    Reinhold, U.2
  • 9
    • 77953299014 scopus 로고    scopus 로고
    • Synthesis and applications of tert-butanesulfinamide
    • Robak, M.T., Herbage, M.A. & Ellman, J.A. Synthesis and applications of tert-butanesulfinamide. Chem. Rev. 110, 3600-3740 (2010).
    • (2010) Chem. Rev , vol.110 , pp. 3600-3740
    • Robak, M.T.1    Herbage, M.A.2    Ellman, J.A.3
  • 10
    • 63049135096 scopus 로고    scopus 로고
    • Tert-Butanesulfinimines: Structure, synthesis and synthetic applications
    • Ferreira, F., Botuha, C., Chemla, F. & Perez-Luna, A. tert-Butanesulfinimines: structure, synthesis and synthetic applications. Chem. Soc. Rev. 38, 1162-1186 (2009).
    • (2009) Chem. Soc. Rev , vol.38 , pp. 1162-1186
    • Ferreira, F.1    Botuha, C.2    Chemla, F.3    Perez-Luna, A.4
  • 11
    • 49149123060 scopus 로고    scopus 로고
    • An advance on exploring N-tert-butanesulfinyl imines in asymmetric synthesis of chiral amines
    • Lin, G.-Q., Xu, M.-H., Zhong, Y.-W. & Sun, X.-W. An advance on exploring N-tert-butanesulfinyl imines in asymmetric synthesis of chiral amines. Acc. Chem. Res. 41, 831-840 (2008).
    • (2008) Acc. Chem. Res , vol.41 , pp. 831-840
    • Lin, G.-Q.1    Xu, M.-H.2    Zhong, Y.-W.3    Sun, X.-W.4
  • 12
    • 33747113614 scopus 로고    scopus 로고
    • Chiral non-racemic sulfinimines: Versatile reagents for asymmetric synthesis
    • DOI 10.1016/j.tet.2006.06.107, PII S0040402006010647
    • Morton, D. & Stockman, R.A. Chiral non-racemic sulfinimines: versatile reagents for asymmetric synthesis. Tetrahedron 62, 8869-8905 (2006). (Pubitemid 44218983)
    • (2006) Tetrahedron , vol.62 , Issue.38 , pp. 8869-8905
    • Morton, D.1    Stockman, R.A.2
  • 14
    • 28044452665 scopus 로고    scopus 로고
    • Enantiopure sulfoxides and sulfinamides: Recent developments in their stereoselective synthesis and application to asymmetric synthesis
    • Senanayake, C.H., Krishnamurthy, D., Lu, Z.-H., Han, Z. & Gallon, E. Enantiopure sulfoxides and sulfinamides: recent developments in their stereoselective synthesis and application to asymmetric synthesis. Aldrichim. Acta 38, 93-103 (2005).
    • (2005) Aldrichim. Acta , vol.38 , pp. 93-103
    • Senanayake, C.H.1    Krishnamurthy, D.2    Lu, Z.-H.3    Han, Z.4    Gallon, E.5
  • 15
    • 0033582571 scopus 로고    scopus 로고
    • Synthesis of enantiomerically pure N-tert-butanesulfinyl imines (tert- butanesulfinimines) by the direct condensation of tert-butanesulfinamide with aldehydes and ketones
    • DOI 10.1021/jo982059i
    • Liu, G., Cogan, D.A., Owens, T.D., Tang, T.P. & Ellman, J.A. Synthesis of enantiomerically pure N-tert-butanesulfinyl imines (tert-butanesulfinimines) by the direct condensation of tert-butanesulfinamide with aldehydes and ketones. J. Org. Chem. 64, 1278-1284 (1999). (Pubitemid 29098570)
    • (1999) Journal of Organic Chemistry , vol.64 , Issue.4 , pp. 1278-1284
    • Liu, G.1    Cogan, D.A.2    Owens, T.D.3    Tang, T.P.4    Ellman, J.A.5
  • 16
    • 77956498791 scopus 로고    scopus 로고
    • Racemization free protocol for the synthesis of N-tert-butanesulfinyl ketimines
    • Datta, G.K. & Ellman, J.A. Racemization free protocol for the synthesis of N-tert-butanesulfinyl ketimines. J. Org. Chem. 75, 6283-6285 (2010).
    • (2010) J. Org. Chem , vol.75 , pp. 6283-6285
    • Datta, G.K.1    Ellman, J.A.2
  • 17
    • 1442311146 scopus 로고    scopus 로고
    • 3 as an Activating and Dehydrating Reagent
    • Higashibayashi, S., Tohmiya, H., Mori, T., Hashimoto, K. & Nakata, M. Synthesis of sulfinimines by direct condensation of sulfinamides with aldehydes using Cs2CO3 as an activating and dehydrating reagent. Synlett 2004, 457-460 (2004). (Pubitemid 38293653)
    • (2004) Synlett , Issue.3 , pp. 457-460
    • Higashibayashi, S.1    Tohmiya, H.2    Mori, T.3    Hashimoto, K.4    Nakata, M.5
  • 18
    • 19944411142 scopus 로고    scopus 로고
    • 4-mediated condensation reactions of tert- butanesulfinamide with aldehydes. Preparation of tert-butanesulfinyl aldimines
    • DOI 10.1055/s-2005-865234, U06005ST
    • Huang, Z., Zhang, M., Wang, Y. & Qin, Y. KHSO4-mediated condensation reactions of tert-butanesulfinamide with aldehydes. Preparation of tert-butanesulfinyl aldimines. Synlett 2005, 1334-1336 (2005). (Pubitemid 40755321)
    • (2005) Synlett , Issue.8 , pp. 1334-1336
    • Huang, Z.1    Zhang, M.2    Wang, Y.3    Qin, Y.4
  • 19
    • 84863609085 scopus 로고    scopus 로고
    • Microwave-assisted solvent-free synthesis of enantiomerically pure N-(tert-butylsulfinyl)imines
    • Collados, J.F., Toledano, E., Guijarro, D. & Yus, M. Microwave-assisted solvent-free synthesis of enantiomerically pure N-(tert-butylsulfinyl)imines. J. Org. Chem. 77, 5744-5750 (2012).
    • (2012) J. Org. Chem , vol.77 , pp. 5744-5750
    • Collados, J.F.1    Toledano, E.2    Guijarro, D.3    Yus, M.4
  • 20
    • 68049084689 scopus 로고    scopus 로고
    • Ruthenium-catalysed asymmetric transfer hydrogenation of N-(tert-butanesulfinyl)imines
    • Guijarro, D., Pablo, Ó. & Yus, M. Ruthenium-catalysed asymmetric transfer hydrogenation of N-(tert-butanesulfinyl)imines. Tetrahedron Lett. 50, 5386-5388 (2009).
    • (2009) Tetrahedron Lett , vol.50 , pp. 5386-5388
    • Guijarro, D.1    Pablo, Ó.2    Yus, M.3
  • 21
    • 13644262210 scopus 로고    scopus 로고
    • Diastereoselective and enantioselective Rh(I)-catalyzed additions of arylboronic acids to N-tert-butanesulfinyl and N-diphenylphosphinoyl aldimines
    • DOI 10.1021/ja044003d
    • Weix, D.J., Shi, Y. & Ellman, J.A. Diastereoselective and enantioselective Rh(I)-catalyzed additions of arylboronic acids to N-tert-butanesulfinyl and N-diphenylphosphinoyl aldimines. J. Am. Chem. Soc. 127, 1092-1093 (2005). (Pubitemid 40228670)
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.4 , pp. 1092-1093
    • Weix, D.J.1    Shi, Y.2    Ellman, J.A.3
  • 22
    • 33646590315 scopus 로고    scopus 로고
    • Asymmetric synthesis of protected arylglycines by rhodium-catalyzed addition of arylboronic acids to N-tert-butanesulfinyl imino esters
    • DOI 10.1021/ja060529h
    • Beenen, M.A., Weix, D.J. & Ellman, J.A. Asymmetric synthesis of protected arylglycines by rhodium-catalyzed addition of arylboronic acids to N-tert-butanesulfinyl imino esters. J. Am. Chem. Soc. 128, 6304-6305 (2006). (Pubitemid 43727253)
    • (2006) Journal of the American Chemical Society , vol.128 , Issue.19 , pp. 6304-6305
    • Beenen, M.A.1    Weix, D.J.2    Ellman, J.A.3
  • 23
    • 34547946031 scopus 로고    scopus 로고
    • Diastereoselective synthesis of arylglycine derivatives by cationic palladium(II)-catalyzed addition of arylboronic acids to N-tert-butanesulfinyl imino esters
    • Dai, H. & Lu, X. Diastereoselective synthesis of arylglycine derivatives by cationic palladium(II)-catalyzed addition of arylboronic acids to N-tert-butanesulfinyl imino esters. Org. Lett. 9, 3077-3080 (2007).
    • (2007) Org. Lett , vol.9 , pp. 3077-3080
    • Dai, H.1    Lu, X.2
  • 25
    • 17844392594 scopus 로고    scopus 로고
    • A room-temperature protocol for the rhodium(I)-catalyzed addition of arylboron compounds to sulfinimines
    • DOI 10.1021/ol050014f
    • Bolshan, Y. & Batey, R.A. A room-temperature protocol for the Rhodium(I)-catalyzed addition of arylboron compounds to sulfinimines. Org. Lett. 7, 1481-1484 (2005). (Pubitemid 40585911)
    • (2005) Organic Letters , vol.7 , Issue.8 , pp. 1481-1484
    • Bolshan, Y.1    Batey, R.A.2
  • 26
    • 44949200996 scopus 로고    scopus 로고
    • Conversion of 1,3-disubstituted arenes to chiral ?,?-diaryl methylammonium chlorides using arene borylation
    • Boebel, T.A. & Hartwig, J.F. Conversion of 1,3-disubstituted arenes to chiral ?,?-diaryl methylammonium chlorides using arene borylation. Tetrahedron 64, 6824-6830 (2008).
    • (2008) Tetrahedron , vol.64 , pp. 6824-6830
    • Boebel, T.A.1    Hartwig, J.F.2
  • 27
    • 44449138158 scopus 로고    scopus 로고
    • Asymmetric copper-catalyzed synthesis of α-amino boronate esters from N-tert-butanesulfinyl aldimines
    • DOI 10.1021/ja800829y
    • Beenen, M.A., An, C. & Ellman, J.A. Asymmetric copper-catalyzed synthesis of ?-amino boronate esters from N-tert-butanesulfinyl aldimines. J. Am. Chem. Soc. 130, 6910-6911 (2008). (Pubitemid 351770116)
    • (2008) Journal of the American Chemical Society , vol.130 , Issue.22 , pp. 6910-6911
    • Beenen, M.A.1    An, C.2    Ellman, J.A.3
  • 28
    • 0030694323 scopus 로고    scopus 로고
    • Catalytic asymmetric synthesis of tert-butanesulfinamide. Application to the asymmetric synthesis of amines
    • DOI 10.1021/ja972012z
    • Liu, G.C., Cogan, D.A. & Ellman, J.A. Catalytic asymmetric synthesis of tert-butanesulfinamide. Application to the asymmetric synthesis of amines. J. Am. Chem. Soc. 119, 9913-9914 (1997). (Pubitemid 27466867)
    • (1997) Journal of the American Chemical Society , vol.119 , Issue.41 , pp. 9913-9914
    • Liu, G.1    Cogan, D.A.2    Ellman, J.A.3
  • 29
    • 33750128847 scopus 로고    scopus 로고
    • Asymmetric synthesis of α,α-dibranched propargylamines by acetylide additions to N-tert-butanesulfinyl ketimines
    • DOI 10.1021/jo061160h
    • Patterson, A.W. & Ellman, J.A. Asymmetric synthesis of ?,?-dibranched propargylamines by acetylide additions to N-tert-butanesulfinyl ketimines. J. Org. Chem. 71, 7110-7112 (2006). (Pubitemid 44645702)
    • (2006) Journal of Organic Chemistry , vol.71 , Issue.18 , pp. 7110-7112
    • Patterson, A.W.1    Ellman, J.A.2
  • 30
    • 75649145831 scopus 로고    scopus 로고
    • Silver(i)-mediated highly enantioselective synthesis of axially chiral allenes under thermal and microwave-assisted conditions
    • Lo, V.K.-Y., Zhou, C.-Y., Wong, M.-K. & Che, C.-M. Silver(i)-mediated highly enantioselective synthesis of axially chiral allenes under thermal and microwave-assisted conditions. Chem. Commun. 46, 213-215 (2010).
    • (2010) Chem. Commun , vol.46 , pp. 213-215
    • Lo, V.K.-Y.1    Zhou, C.-Y.2    Wong, M.-K.3    Che, C.-M.4
  • 32
    • 4544326574 scopus 로고    scopus 로고
    • Stereocontrolled total synthesis of (+)-streptazolin by a palladium-catalyzed reductive diyne cyclization
    • DOI 10.1002/anie.200460058
    • Trost, B.M., Chung, C.K. & Pinkerton, A.B. Stereocontrolled total synthesis of (+)-streptazolin by a palladium-catalyzed reductive diyne cyclization. Angew. Chem. Intl. Edn. 43, 4327-4329 (2004). (Pubitemid 39257411)
    • (2004) Angewandte Chemie - International Edition , vol.43 , Issue.33 , pp. 4327-4329
    • Trost, B.M.1    Chung, C.K.2    Pinkerton, A.B.3
  • 33
    • 2542566677 scopus 로고    scopus 로고
    • Stereoselective synthesis of D-desosamine and related glycals via tungsten-catalyzed alkynol cycloisomerization
    • DOI 10.1021/ol049630m
    • Davidson, M.H. & McDonald, F.E. Stereoselective synthesis of d-desosamine and related glycals via tungsten-catalyzed alkynol cycloisomerization. Org. Lett. 6, 1601-1603 (2004). (Pubitemid 38698461)
    • (2004) Organic Letters , vol.6 , Issue.10 , pp. 1601-1603
    • Davidson, M.H.1    McDonald, F.E.2
  • 34
    • 0242298263 scopus 로고    scopus 로고
    • Formal synthesis of (+)-lactacystin based on a novel radical cyclisation of an α-ethynyl substituted serine
    • DOI 10.1016/j.tetlet.2003.10.022
    • Brennan, C.J., Pattenden, G. & Rescourio, G. Formal synthesis of (+)-lactacystin based on a novel radical cyclisation of an ?-ethynyl substituted serine. Tetrahedron Lett. 44, 8757-8760 (2003). (Pubitemid 37363305)
    • (2003) Tetrahedron Letters , vol.44 , Issue.49 , pp. 8757-8760
    • Brennan, C.J.1    Pattenden, G.2    Rescourio, G.3
  • 35
    • 48249146974 scopus 로고    scopus 로고
    • Synthesis and conformational analysis of a cyclic peptide obtained via i to i+4 intramolecular side-chain to side-chain azide-alkyne 1,3-dipolar cycloaddition
    • Cantel, S. et al. Synthesis and conformational analysis of a cyclic peptide obtained via i to i+4 intramolecular side-chain to side-chain azide-alkyne 1,3-dipolar cycloaddition. J. Org. Chem. 73, 5663-5674 (2008).
    • (2008) J. Org. Chem , vol.73 , pp. 5663-5674
    • Cantel, S.1
  • 37
    • 77649200180 scopus 로고    scopus 로고
    • Nonpeptidic tetrafluorophenoxymethyl ketone cruzain inhibitors as promising new leads for Chagas disease chemotherapy
    • Brak, K. et al. Nonpeptidic tetrafluorophenoxymethyl ketone cruzain inhibitors as promising new leads for Chagas disease chemotherapy. J. Med. Chem. 53, 1763-1773 (2010).
    • (2010) J. Med. Chem , vol.53 , pp. 1763-1773
    • Brak, K.1
  • 38
    • 84861610305 scopus 로고    scopus 로고
    • A nonpeptidic cathepsin S activity-based probe for noninvasive optical imaging of tumor-associated macrophages
    • Verdoes, M. et al. A nonpeptidic cathepsin S activity-based probe for noninvasive optical imaging of tumor-associated macrophages. Chem. Biol. 19, 619-628 (2012).
    • (2012) Chem. Biol , vol.19 , pp. 619-628
    • Verdoes, M.1
  • 39
    • 78649341457 scopus 로고    scopus 로고
    • Identification and evaluation of small molecule pan-caspase inhibitors in Huntington's disease models
    • Leyva, M.J. et al. Identification and evaluation of small molecule pan-caspase inhibitors in Huntington?s disease models. Chem. Biol. 17, 1189-1200 (2010).
    • (2010) Chem. Biol , vol.17 , pp. 1189-1200
    • Leyva, M.J.1
  • 40
    • 77956051319 scopus 로고    scopus 로고
    • Functional studies of Plasmodium falciparum dipeptidyl aminopeptidase i using small molecule inhibitors and active site probes
    • Deu, E. et al. Functional studies of Plasmodium falciparum dipeptidyl aminopeptidase I using small molecule inhibitors and active site probes. Chem. Biol. 17, 808-819 (2010).
    • (2010) Chem. Biol , vol.17 , pp. 808-819
    • Deu, E.1
  • 41
    • 27644555726 scopus 로고    scopus 로고
    • Substrate activity screening: A fragment-based method for the rapid identification of nonpeptidic protease inhibitors
    • DOI 10.1021/ja0547230
    • Wood, W.J., Patterson, A.W., Tsuruoka, H., Jain, R.K. & Ellman, J.A. Substrate activity screening: A fragment-based method for the rapid identification of nonpeptidic protease inhibitors. J. Am. Chem. Soc. 127, 15521-15527 (2005). (Pubitemid 41572526)
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.44 , pp. 15521-15527
    • Wood, W.J.L.1    Patterson, A.W.2    Tsuruoka, H.3    Jain, R.K.4    Ellman, J.A.5
  • 42
  • 43
    • 34250219213 scopus 로고    scopus 로고
    • Characterization and optimization of selective, nonpeptidic inhibitors of cathepsin S with an unprecedented binding mode
    • DOI 10.1021/jm070111+
    • Inagaki, H. et al. Characterization and optimization of selective, nonpeptidic inhibitors of cathepsin S with an unprecedented binding mode. J. Med. Chem. 50, 2693-2699 (2007). (Pubitemid 46896077)
    • (2007) Journal of Medicinal Chemistry , vol.50 , Issue.11 , pp. 2693-2699
    • Inagaki, H.1    Tsuruoka, H.2    Hornsby, M.3    Lesley, S.A.4    Spraggon, G.5    Ellman, J.A.6
  • 44
    • 84869092523 scopus 로고    scopus 로고
    • Exploration of cathepsin S inhibitors characterized by a triazole P1-P2 amide replacement
    • Moss, N. et al. Exploration of cathepsin S inhibitors characterized by a triazole P1-P2 amide replacement. Bioorg. Med. Chem. Lett. 22, 7189-7193 (2012).
    • (2012) Bioorg. Med. Chem. Lett , vol.22 , pp. 7189-7193
    • Moss, N.1
  • 45
    • 79955563074 scopus 로고    scopus 로고
    • Solid-phase synthesis and chemical space analysis of a 190-membered alkaloid/terpenoid-like library
    • Moura-Letts, G., Diblasi, C.M., Bauer, R.A. & Tan, D.S. Solid-phase synthesis and chemical space analysis of a 190-membered alkaloid/terpenoid-like library. Proc. Natl. Acad. Sci. USA 108, 6745-6750 (2011).
    • (2011) Proc. Natl. Acad. Sci. USA , vol.108 , pp. 6745-6750
    • Moura-Letts, G.1    Diblasi, C.M.2    Bauer, R.A.3    Tan, D.S.4
  • 46
    • 0033575410 scopus 로고    scopus 로고
    • Asymmetric synthesis of chiral amines by highly diastereoselective 1,2- additions of organometallic reagents to N-tert-butanesulfinyl imines
    • DOI 10.1016/S0040-4020(99)00451-2, PII S0040402099004512
    • Cogan, D.A., Liu, G. & Ellman, J. Asymmetric synthesis of chiral amines by highly diastereoselective 1,2-additions of organometallic reagents to N-tert-butanesulfinyl imines. Tetrahedron 55, 8883-8904 (1999). (Pubitemid 29314612)
    • (1999) Tetrahedron , vol.55 , Issue.29 , pp. 8883-8904
    • Cogan, D.A.1    Liu, G.2    Ellman, J.3
  • 47
    • 0035829093 scopus 로고    scopus 로고
    • Asymmetric synthesis of α,α-diaryl and α-aryl-α- heteroaryl alkylamines by organometallic additions to N-tert-butanesulfinyl ketimines
    • DOI 10.1016/S0040-4039(01)01513-1, PII S0040403901015131
    • Shaw, A.W. & deSolms, S.J. Asymmetric synthesis of ?,?-diaryl and ?-aryl-?-heteroaryl alkylamines by organometallic additions to N-tert-butanesulfinyl ketimines. Tetrahedron Lett. 42, 7173-7176 (2001). (Pubitemid 32913211)
    • (2001) Tetrahedron Letters , vol.42 , Issue.41 , pp. 7173-7176
    • Shaw, A.W.1    DeSolms, S.J.2
  • 48
    • 75749144634 scopus 로고    scopus 로고
    • Highly diastereoselective addition of alkynylmagnesium chlorides to N-tert-butanesulfinyl aldimines: A practical and general access to chiral ?-branched amines
    • Chen, B.-L., Wang, B. & Lin, G.-Q. Highly diastereoselective addition of alkynylmagnesium chlorides to N-tert-butanesulfinyl aldimines: A practical and general access to chiral ?-branched amines. J. Org. Chem. 75, 941-944 (2009).
    • (2009) J. Org. Chem , vol.75 , pp. 941-944
    • Chen, B.-L.1    Wang, B.2    Lin, G.-Q.3
  • 49
    • 33744491803 scopus 로고    scopus 로고
    • Highly diastereoselective synthesis of N-tert- butylsulfinylpropargylamines through direct addition of alkynes to N-tert-butanesulfinimines
    • DOI 10.1055/s-2006-939076
    • Ding, C.-H., Chen, D.-D., Luo, Z.-B., Dai, L.-X. & Hou, X.-L. Highly diastereoselective synthesis of N-tert-butylsulfinylpropargylamines through direct addition of alkynes to N-tert-butanesulfinimines. Synlett 2006, 1272-1274 (2006). (Pubitemid 43797905)
    • (2006) Synlett , Issue.8 , pp. 1272-1274
    • Ding, C.-H.1    Chen, D.-D.2    Luo, Z.-B.3    Dai, L.-X.4    Hou, X.-L.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.