메뉴 건너뛰기




Volumn 14, Issue 3, 2010, Pages 479-491

One-pot multicomponent synthesis of two novel thiolactone scaffolds

Author keywords

Isocyanide; Multicomponent reaction (MCR); Thiolactone; Virtual library

Indexed keywords

1 OXO OCTAHYDRO PYRIDO[2,1 C][1,4]THIAZINE 4 CARBOXYLIC ACID (2,4,6 TRIMETHYL PHENYL)AMIDE; 1 OXO OCTAHYDRO PYRIDO[2,1 C][1,4]THIAZINE 4 CARBOXYLIC ACID TERT BUTYLAMIDE; 1(2 OXO TETRAHYDRO THIOPHEN 3 YLAMINO)CYCLOHEXANECARBOXYLIC ACID(2,4,6 TRIMETHYL PHENYL)AMIDE; 2 METHYL 2 (2 OXO TETRAHYDRO THIOPHEN 3 YLAMINO)N(2,4,6 TRIMETHYL PHENYL)PROPIONAMIDE; 3 METHYL 2 (2 OXO TETRAHYDRO THIOPHEN 3 YLAMINO)N(2,4,6 TRIMETHYL PHENYL)BUTYRAMIDE; 4,8 DIMETHYL 2 (2 OXO TETRAHYDRO THIOPHEN 3 YLAMINO)NON 7 ENOIC ACID BENZHYDRYL AMIDE; 5 (2 METHYLSULFANYL ETHYL) 6 OXO THIOMORPHOLINE 3 CARBOXYLIC ACID(1 PROPYL BUTYL)AMIDE; 5 BENZYL 6 OXO THIOMORPHOLINE 3 CARBOXYLIC ACID BENZYLAMIDE; 5 BENZYL 6 OXO THIOMORPHOLINE 3 CARBOXYLIC ACID[(METHYL PHENETHYL CARBAMOYL)METHYL]AMIDE; 5 C(1 HYDROXY ETHYL) 6 OXO THIOMORPHOLINE 3 CARBOXYLIC ACID(2 FLUORO PHENYL) AMIDE; 5 ISOPROPYL 6 OXO THIOMORPHOLINE 3 CARBOXYLIC ACID [2 OXO 2 (4 PHENYL PIPERAZIN 1 YL)ETHYL]AMIDE; 5 METHYL 6 OXO THIOMORPHOLINE 3 CARBOXYLIC ACID(2,4,6 TRIMETHYL PHENYL)AMIDE; 5 SEC BUTYL 6 OXO THIOMORPHOLINE 3 CARBOXYLIC ACID TERT BUTYLAMIDE; [(1 OXO HEXAHYDRO PYRROLO[2,1 C][1,4]THIAZINE 4 CARBONYL)AMINO]ACETIC ACID METHYL ESTER; ERDOSTEINE; MOLECULAR SCAFFOLD; N BENZHYDRYL 2 (2 OXO TETRAHYDRO THIOPHEN 3 YLAMINO) 3 PHENYL PROPIONAMIDE; N BENZYL 2 (2 OXO TETRAHYDRO THIOPHEN 3 YLAMINO) 4 PHENYL BUTYRAMIDE; N BENZYL 2 CYCLOPROPYL 2 (2 OXO TETRAHYDRO THIOPHEN 3 YLAMINO)ACETAMIDE; N TERT BUTYL 2 NAPHTHALEN 2 YL 2 (2 OXO TETRAHYDRO THIOPHEN 3 YLAMINO)ACETAMIDE; N TERT BUTYL 3 (5 METHYL 2,4 DIOXO 3,4 DIHYDRO 2H PYRIMIDIN 1 YL) 2 (2 OXO TETRAHYDRO THIOPHEN 3 YLAMINO)PROPIONAMIDE; N TERT BUTYL 3 METHYL 2 (2 OXOTETRAHYDRO THIOPHEN 3 YLAMINO)BUTYRAMIDE; PRASUGREL; THIOLACTOMYCIN; THIOLACTONE; UNCLASSIFIED DRUG;

EID: 78650176366     PISSN: 13811991     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11030-010-9249-2     Document Type: Article
Times cited : (12)

References (51)
  • 1
    • 0019979856 scopus 로고
    • Thiolactomycin, a new antibiotic. II. Structure elucidation
    • H Sasaki H Oishi T Hayashi I Matsuura K Ando M Sawada 1982 Thiolactomycin, a new antibiotic. II. Structure elucidation J Antibiot (Tokyo) 35 396 400 1:CAS:528:DyaL38Xkt1ems74%3D (Pubitemid 12046393)
    • (1982) Journal of Antibiotics , vol.35 , Issue.4 , pp. 396-400
    • Sasaki, H.1    Oishi, H.2    Hayashi, T.3
  • 2
    • 40049108020 scopus 로고    scopus 로고
    • Changes in blood ROS, e-NO, and some pro-inflammatory mediators in bronchial secretions following erdosteine or placebo: A controlled study in current smokers with mild COPD
    • DOI 10.1016/j.pupt.2007.07.004, PII S1094553907000697
    • Dal Negro RW, Visconti M, Micheletto C, Tognella S (2008) Changes in blood ROS, e-NO, and some pro-inflammatory mediators in bronchial secretions following erdosteine or placebo: a controlled study in current smokers with mild COPD. Pulm Pharmacol Ther 21:304-308. doi: S1094-5539(07)00069-7. [pii] doi: 10.1016/j.pupt.2007.07.004 (Pubitemid 351320569)
    • (2008) Pulmonary Pharmacology and Therapeutics , vol.21 , Issue.2 , pp. 304-308
    • Dal Negro, R.W.1    Visconti, M.2    Micheletto, C.3    Tognella, S.4
  • 6
    • 36549013144 scopus 로고    scopus 로고
    • Mercaptopropionaldehyde from homocysteine: Implications for Alzheimer's disease
    • 1:CAS:528:DC%2BD2sXhtlClsb7J 18057557
    • JI Toohey 2007 Mercaptopropionaldehyde from homocysteine: implications for Alzheimer's disease J Alzheimers Dis 12 241 243 1:CAS:528:DC%2BD2sXhtlClsb7J 18057557
    • (2007) J Alzheimers Dis , vol.12 , pp. 241-243
    • Toohey, J.I.1
  • 8
    • 57349166038 scopus 로고    scopus 로고
    • Application of an enantiomerically pure bicyclic thiolactone in the synthesis of a farnesyl transferase inhibitor
    • 10.1021/op700218j 1:CAS:528:DC%2BD1cXitFeht7Y%3D 10.1021/op700218j
    • S Abbas L Ferris AK Norton L Powell GE Robinson P Siedlecki RJ Southworth A Stark EG Williams 2008 Application of an enantiomerically pure bicyclic thiolactone in the synthesis of a farnesyl transferase inhibitor Org Process Res Dev 12 202 212 10.1021/op700218j 1:CAS:528:DC%2BD1cXitFeht7Y%3D 10.1021/op700218j
    • (2008) Org Process Res Dev , vol.12 , pp. 202-212
    • Abbas, S.1    Ferris, L.2    Norton, A.K.3    Powell, L.4    Robinson, G.E.5    Siedlecki, P.6    Southworth, R.J.7    Stark, A.8    Williams, E.G.9
  • 10
    • 0004155427 scopus 로고
    • W.H. Freeman and Company New York
    • Stryer L (1988) Biochemistry. W.H. Freeman and Company, New York
    • (1988) Biochemistry
    • Stryer, L.1
  • 12
    • 34250201064 scopus 로고    scopus 로고
    • Synthesis and cleavage of lactones and thiolactones applications in organic synthesis
    • 1:CAS:528:DC%2BD2sXlsVajt7s%3D 10.1080/00304940709356015
    • Z Paryzek I Skiera 2007 Synthesis and cleavage of lactones and thiolactones applications in organic synthesis Org Prep Proced Int 39 203 296 1:CAS:528:DC%2BD2sXlsVajt7s%3D 10.1080/00304940709356015
    • (2007) Org Prep Proced Int , vol.39 , pp. 203-296
    • Paryzek, Z.1    Skiera, I.2
  • 13
    • 0037413582 scopus 로고    scopus 로고
    • Synthetic analogues of the bacterial signal (quorum sensing) molecule N-(3-oxododecanoyl)-L-homoserine lactone as immune modulators
    • DOI 10.1021/jm020909n
    • SR Chhabra C Harty DS Hooi M Daykin P Williams G Telford DI Pritchard BW Bycroft 2003 Synthetic analogues of the bacterial signal (quorum sensing) molecule N-(3-oxododecanoyl)-L-homoserine lactone as immune modulators J Med Chem 46 97 104 10.1021/jm020909n 1:CAS:528:DC%2BD38XptVagsbY%3D 10.1021/jm020909n 12502363 (Pubitemid 36043789)
    • (2003) Journal of Medicinal Chemistry , vol.46 , Issue.1 , pp. 97-104
    • Chhabra, S.R.1    Harty, C.2    Hooi, D.S.W.3    Daykin, M.4    Williams, P.5    Telford, G.6    Pritchard, D.I.7    Bycroft, B.W.8
  • 14
    • 33748685012 scopus 로고    scopus 로고
    • X{double bond, long}Y-ZH compounds as potential 1,3-dipoles. Part 63: Silver catalysed azomethine ylide cycloaddition-the synthesis of spiro homoserine lactone analogues
    • DOI 10.1016/j.tet.2006.08.077, PII S0040402006013792
    • R Grigg MAB Sarker 2006 UK XY-ZH compounds as potential 1,3-dipoles. Part 63: Silver catalysed azomethine ylide cycloaddition-the synthesis of spiro homoserine lactone analogues Tetrahedron 62 10332 10343 10.1016/j.tet.2006.08. 077 1:CAS:528:DC%2BD28XhtVSisrvP 10.1016/j.tet.2006.08.077 (Pubitemid 44397125)
    • (2006) Tetrahedron , vol.62 , Issue.44 , pp. 10332-10343
    • Grigg, R.1    Sarker, M.A.B.2
  • 15
    • 0035855835 scopus 로고    scopus 로고
    • 2′ pockets
    • DOI 10.1021/jm010097f
    • S Hanessian N Moitessier C Gauchet M Viau 2001 N-Aryl sulfonyl homocysteine hydroxamate inhibitors of matrix metalloproteinases: further probing of the S(1), S(1)′, and S(2)′ pockets J Med Chem 44 3066 3073 10.1021/jm010097f 1:CAS:528:DC%2BD3MXls1OktL4%3D 10.1021/jm010097f 11543675 (Pubitemid 32862337)
    • (2001) Journal of Medicinal Chemistry , vol.44 , Issue.19 , pp. 3066-3073
    • Hanessian, S.1    Moitessier, N.2    Gauchet, C.3    Viau, M.4
  • 16
    • 0036179979 scopus 로고    scopus 로고
    • A novel synthesis of a key intermediate for (+)-biotin from l-aspartic acid
    • 10.1055/s-2002-20035 10.1055/s-2002-20035
    • M Seki T Shimizu K Inubushi 2002 A novel synthesis of a key intermediate for (+)-biotin from l-aspartic acid Synthesis 2002 361 364 10.1055/s-2002-20035 10.1055/s-2002-20035
    • (2002) Synthesis , vol.2002 , pp. 361-364
    • Seki, M.1    Shimizu, T.2    Inubushi, K.3
  • 17
    • 0026495944 scopus 로고
    • X=Y-ZH systems as potential 13-dipoles. Part 39 Metallo-azomethine ylides from aliphatic aldimines Facile regio- and stereo-specific cycloaddition reactions
    • 10.1016/S0040-4020(01)88346-0 1:CAS:528:DyaK3sXhs1yqs7k%3D 10.1016/S0040-4020(01)88346-0
    • R Grigg J Montgomery A Somasunderam 1992 X=Y-ZH systems as potential 13-dipoles. Part 39 Metallo-azomethine ylides from aliphatic aldimines Facile regio- and stereo-specific cycloaddition reactions Tetrahedron 48 10431 10442 10.1016/S0040-4020(01)88346-0 1:CAS:528:DyaK3sXhs1yqs7k%3D 10.1016/S0040- 4020(01)88346-0
    • (1992) Tetrahedron , vol.48 , pp. 10431-10442
    • Grigg, R.1    Montgomery, J.2    Somasunderam, A.3
  • 18
    • 0035969010 scopus 로고    scopus 로고
    • Thiophenes act as dienophiles in novel cycloadditions with masked o-benzoquinones
    • DOI 10.1016/S0040-4039(01)01648-3, PII S0040403901016483
    • C-H Lai S Ko P Dharma Rao C-C Liao 2001 Thiophenes act as dienophiles in novel cycloadditions with masked o-benzoquinones Tetrahedron Lett 42 7851 7854 10.1016/S0040-4039(01)01648-3 1:CAS:528:DC%2BD3MXnsV2rsL0%3D 10.1016/S0040-4039(01)01648-3 (Pubitemid 32971801)
    • (2001) Tetrahedron Letters , vol.42 , Issue.44 , pp. 7851-7854
    • Lai, C.-H.1    Ko, S.2    Dharma Rao, P.3    Liao, C.-C.4
  • 19
    • 78650178156 scopus 로고
    • Über die Synthese der optisch aktiven Diastereomeren Cystathionin und Allocystathionin und über Methoden zu deren Trennung
    • 1:CAS:528:DyaG2sXktlWgtg%3D%3D 10.1002/jlac.19565990104
    • A Schoberl G Tauber 1956 Über die Synthese der optisch aktiven Diastereomeren Cystathionin und Allocystathionin und über Methoden zu deren Trennung Justus Liebigs Ann Chem 599 23 37 1:CAS:528:DyaG2sXktlWgtg%3D%3D 10.1002/jlac.19565990104
    • (1956) Justus Liebigs Ann Chem , vol.599 , pp. 23-37
    • Schoberl, A.1    Tauber, G.2
  • 20
    • 37349030716 scopus 로고    scopus 로고
    • Thiocarbonyl induced heterocumulenic Pauson-Khand type reaction: Expedient synthetic method for thieno[2,3-b]indol-2-ones
    • DOI 10.1039/b712739a
    • Saito T, Nihei H, Otani T, Suyama T, Furukawa N, Saito M (2008) Thiocarbonyl induced heterocumulenic Pauson-Khand type reaction: expedient synthetic method for thieno[2,3-b]indol-2-ones. Chem Commun (Camb):172-174. doi: 10.1039/b712739a (Pubitemid 350294095)
    • (2008) Chemical Communications , Issue.2 , pp. 172-174
    • Saito, T.1    Nihei, H.2    Otani, T.3    Suyama, T.4    Furukawa, N.5    Saito, M.6
  • 22
    • 31544434530 scopus 로고    scopus 로고
    • Recent developments in isocyanide based multicomponent reactions in applied chemistry
    • DOI 10.1021/cr0505728
    • A Domling 2006 Recent developments in isocyanide based multicomponent reactions in applied chemistry Chem Rev 106 17 89 10.1021/cr0505728 10.1021/cr0505728 16402771 (Pubitemid 43159621)
    • (2006) Chemical Reviews , vol.106 , Issue.1 , pp. 17-89
    • Domling, A.1
  • 23
    • 45149100138 scopus 로고    scopus 로고
    • New end-on thiolactone scaffold by an isocyanide-based multicomponent reaction
    • 10.3987/COM-07-S(U)17 1:CAS:528:DC%2BD1cXhs1Sisg%3D%3D 10.3987/COM-07-S(U)17
    • B Beck S Srivastava A Domling 2007 New end-on thiolactone scaffold by an isocyanide-based multicomponent reaction Heterocycles 73 177 182 10.3987/COM-07-S(U)17 1:CAS:528:DC%2BD1cXhs1Sisg%3D%3D 10.3987/COM-07-S(U)17
    • (2007) Heterocycles , vol.73 , pp. 177-182
    • Beck, B.1    Srivastava, S.2    Domling, A.3
  • 24
    • 0031000559 scopus 로고    scopus 로고
    • A simple procedure for the solid phase synthesis of diketopiperazine and diketomorpholine derivatives
    • DOI 10.1016/S0040-4020(97)00218-4, PII S0040402097002184
    • AK Szardenings TS Burkoth HH Lu DW Tien DA Campbell 1997 A simple procedure for the solid phase synthesis of diketopiperazine and diketomorpholine derivatives Tetrahedron 53 6573 6593 10.1016/S0040-4020(97)00218-4 1:CAS:528:DyaK2sXjtlKhsLc%3D 10.1016/S0040-4020(97)00218-4 (Pubitemid 27193297)
    • (1997) Tetrahedron , vol.53 , Issue.19 , pp. 6573-6593
    • Szardenings, A.K.1    Burkoth, T.S.2    Lu, H.H.3    Tien, D.W.4    Campbell, D.A.5
  • 25
    • 0033575465 scopus 로고    scopus 로고
    • Novel applications of ethyl glyoxalate with the Ugi MCR
    • DOI 10.1016/S0040-4039(99)00960-0, PII S0040403999009600
    • C Hulme M-P Cherrier 1999 Novel applications of ethyl glyoxalate with the Ugi MCR Tetrahedron Lett 40 5295 5299 10.1016/S0040-4039(99)00960-0 1:CAS:528:DyaK1MXksVyntr0%3D 10.1016/S0040-4039(99)00960-0 (Pubitemid 29317671)
    • (1999) Tetrahedron Letters , vol.40 , Issue.29 , pp. 5295-5299
    • Hulme, C.1    Cherrier, M.-P.2
  • 26
    • 0035148292 scopus 로고    scopus 로고
    • Studies on isocyanides and related compounds; A facile synthesis of 4-phenyl-1-(2h)phthalazinone-2-alkanoic acid amides
    • 10.1055/s-2001-9745 10.1055/s-2001-9745
    • S Marcaccini R Pepino C Polo MC Pozo 2001 Studies on isocyanides and related compounds; a facile synthesis of 4-phenyl-1-(2h)phthalazinone-2-alkanoic acid amides Synthesis 2001 85 89 10.1055/s-2001-9745 10.1055/s-2001-9745
    • (2001) Synthesis , vol.2001 , pp. 85-89
    • Marcaccini, S.1    Pepino, R.2    Polo, C.3    Pozo, M.C.4
  • 27
    • 0037932800 scopus 로고    scopus 로고
    • Short and diverse route toward complex natural product-like macrocycles
    • DOI 10.1021/ol034077e
    • B Beck G Larbig B Mejat M Magnin-Lachaux A Picard E Herdtweck A Domling 2003 Short and diverse route toward complex natural product-like macrocycles Org Lett 5 1047 1050 10.1021/ol034077e 1:CAS:528:DC%2BD3sXhvFeku7c%3D 10.1021/ol034077e 12659570 (Pubitemid 37141032)
    • (2003) Organic Letters , vol.5 , Issue.7 , pp. 1047-1050
    • Beck, B.1    Larbig, G.2    Mejat, B.3    Magnin-Lachaux, M.4    Picard, A.5    Herdtweck, E.6    Domling, A.7
  • 28
    • 0037139571 scopus 로고    scopus 로고
    • Ammonium chloride-promoted four-component synthesis of pyrrolo[3,4-b] pyridin-5-one
    • DOI 10.1021/ja017563a
    • P Janvier X Sun H Bienayme J Zhu 2002 Ammonium chloride-promoted four-component synthesis of pyrrolo[3,4-b]pyridin-5-one J Am Chem Soc 124 2560 2567 10.1021/ja017563a 1:CAS:528:DC%2BD38Xht1ers7s%3D 10.1021/ja017563a 11890807 (Pubitemid 34251770)
    • (2002) Journal of the American Chemical Society , vol.124 , Issue.11 , pp. 2560-2567
    • Janvier, P.1    Sun, X.2    Bienayme, H.3    Zhu, J.4
  • 29
    • 33744941075 scopus 로고    scopus 로고
    • Supramolecular compounds from multiple ugi multicomponent macrocyclizations: Peptoid-based cryptands, cages, and cryptophanes
    • DOI 10.1021/ja060720r
    • DG Rivera LA Wessjohann 2006 Supramolecular compounds from multiple Ugi multicomponent macrocyclizations: peptoid-based cryptands, cages, and cryptophanes J Am Chem Soc 128 7122 7123 10.1021/ja060720r 1:CAS:528: DC%2BD28XksFGgsL4%3D 10.1021/ja060720r 16734440 (Pubitemid 43849089)
    • (2006) Journal of the American Chemical Society , vol.128 , Issue.22 , pp. 7122-7123
    • Rivera, D.G.1    Wessjohann, L.A.2
  • 30
    • 33847396935 scopus 로고    scopus 로고
    • New Ugi/Pictet-Spengler multicomponent formation of polycyclic diketopiperazines from isocyanides and α-keto acids
    • DOI 10.1055/s-2007-968026
    • L El Kaim M Gageat L Gaultier L Grimaud 2007 New Ugi/Pictet-Spengler multicomponent formation of polycyclic diketopiperazines from isocyanides and α-keto acids Synlett 2007 500 502 10.1055/s-2007-968026 10.1055/s-2007-968026 (Pubitemid 46340234)
    • (2007) Synlett , Issue.3 , pp. 500-502
    • El Kaim, L.1    Gageat, M.2    Gaultier, L.3    Grimaud, L.4
  • 31
    • 4243141892 scopus 로고    scopus 로고
    • Synthesis of tetrazolopiperazine building blocks by a novel multi-component reaction
    • DOI 10.1016/j.tetlet.2004.06.133, PII S004040390401456X
    • M Umkehrer J Kolb C Burdack G Ross W Hiller 2004 Synthesis of tetrazolopiperazine building blocks by a novel multi-component reaction Tetrahedron Lett 45 6421 6424 10.1016/j.tetlet.2004.06.133 1:CAS:528: DC%2BD2cXmt1Kjtrc%3D 10.1016/j.tetlet.2004.06.133 (Pubitemid 39106815)
    • (2004) Tetrahedron Letters , vol.45 , Issue.34 , pp. 6421-6424
    • Umkehrer, M.1    Kolb, J.2    Burdack, C.3    Ross, G.4    Hiller, W.5
  • 32
    • 0001419996 scopus 로고    scopus 로고
    • A novel multicomponent synthesis of polysubstituted 5-aminooxazole and its new scaffold-generating reaction to pyrrolo[3,4-b]pyridine
    • DOI 10.1021/ol007055q
    • X Sun P Janvier G Zhao H Bienayme J Zhu 2001 A novel multicomponent synthesis of polysubstituted 5-aminooxazole and its new scaffold-generating reaction to pyrrolo[3,4-b]pyridine Org Lett 3 877 880 10.1021/ol007055q 1:CAS:528:DC%2BD3MXhsVakt7o%3D 10.1021/ol007055q 11263905 (Pubitemid 33629416)
    • (2001) Organic Letters , vol.3 , Issue.6 , pp. 877-880
    • Sun, X.1    Janvier, P.2    Zhao, G.3    Bienayme, H.4    Zhu, J.5
  • 33
    • 0037145162 scopus 로고    scopus 로고
    • An efficient synthesis of α-amino-δ-valerolactones by the Ugi five-center three-component reaction
    • 1:CAS:528:DC%2BD38XotVGqsrk%3D 10.5012/bkcs.2002.23.9.1277
    • YB Kim SJ Park G Keum MS Jang SB Kang DH Lee Y Kim 2002 An efficient synthesis of α-amino-δ-valerolactones by the Ugi five-center three-component reaction Korean Chem Soc 23 1277 1284 1:CAS:528: DC%2BD38XotVGqsrk%3D 10.5012/bkcs.2002.23.9.1277
    • (2002) Korean Chem Soc , vol.23 , pp. 1277-1284
    • Kim, Y.B.1    Park, S.J.2    Keum, G.3    Jang, M.S.4    Kang, S.B.5    Lee, D.H.6    Kim, Y.7
  • 34
    • 0020211577 scopus 로고
    • From isocyanides via four-component condensations to antibiotic syntheses
    • DOI 10.1002/anie.198208101
    • I Ugi 1982 From isocyanides via four-component condensations to antibiotic syntheses Angew Chem Int Ed Engl 21 810 819 10.1002/anie.198208101 10.1002/anie.198208101 (Pubitemid 13212197)
    • (1982) Angewandte Chemie - International Edition in English , vol.21 , Issue.11 , pp. 810-819
    • Ugi, I.1
  • 35
    • 0347132249 scopus 로고    scopus 로고
    • Ugi reaction in aqueous solutions: A simple protocol for libraries production
    • DOI 10.1023/B:MODI.0000006758.61294.57
    • MA Mironov MN Ivantsova VS Mokrushin 2003 Ugi reaction in aqueous solutions: a simple protocol for libraries production Mol Divers 6 193 197 10.1023/B:MODI.0000006758.61294.57 1:CAS:528:DC%2BD3sXpsFOgt7w%3D 10.1023/B:MODI.0000006758.61294.57 15068081 (Pubitemid 38089855)
    • (2003) Molecular Diversity , vol.6 , Issue.3-4 , pp. 193-197
    • Mironov, M.A.1    Ivantsova, M.N.2    Mokrushin, V.S.3
  • 36
    • 0030603133 scopus 로고    scopus 로고
    • Ugi reactions with trifunctional α-amino acids, aldehydes, isocyanides and alcohols
    • DOI 10.1016/0040-4020(96)00647-3
    • I Ugi A Demharter W Horl T Schmid 1996 Ugi reactions with trifunctional α-amino acids, aldehydes, isocyanides and alcohols Tetrahedron 52 11657 11664 10.1016/0040-4020(96)00647-3 1:CAS:528:DyaK28XltlGrurY%3D 10.1016/0040-4020(96)00647-3 (Pubitemid 26267634)
    • (1996) Tetrahedron , vol.52 , Issue.35 , pp. 11657-11664
    • Ugi, I.1    Demharter, A.2    Horl, W.3    Schmid, T.4
  • 37
    • 0347915136 scopus 로고    scopus 로고
    • Synthesis of chiral 1,1prime-iminodicarboxylic acid derivatives from alpha-amino acids, aldehydes, isocyanides, and alcohols by the diastereoselective five-center-four-component reaction
    • doi: 10.1002/anie.199601731
    • Demharter A, Hörl W, Herdtweck E, Ugi I (1996) Synthesis of chiral 1,1prime-iminodicarboxylic acid derivatives from alpha-amino acids, aldehydes, isocyanides, and alcohols by the diastereoselective five-center-four-component reaction. Angew Chem Int Ed Engl 35. doi: 10.1002/anie.199601731
    • (1996) Angew Chem Int Ed Engl , vol.35
    • Demharter A, H.1
  • 38
    • 0346501858 scopus 로고    scopus 로고
    • Application of MCR: Facile one-pot diastereoselective syntheses of novel chiral α,α′-iminodiacetic acid analogues
    • DOI 10.1023/B:MODI.0000006783.21086.0d
    • K Sung FL Chen MJ Chung 2003 Application of MCR: facile one-pot diastereoselective syntheses of novel chiral alpha,alpha'-iminodiacetic acid analogues Mol Divers 6 213 221 10.1023/B:MODI.0000006783.21086.0d 1:CAS:528:DC%2BD3sXpsFOgtL4%3D 10.1023/B:MODI.0000006783.21086.0d 15068084 (Pubitemid 38089858)
    • (2003) Molecular Diversity , vol.6 , Issue.3-4 , pp. 213-221
    • Sung, K.1    Chen, F.-L.2    Chung, M.-J.3
  • 39
    • 0032563923 scopus 로고    scopus 로고
    • A facile synthesis of N-carbamoylmethyl-α-aminobutyrolactones by the Ugi multicomponent condensation reaction
    • DOI 10.1016/S0040-4039(98)01509-3, PII S0040403998015093
    • SJ Park G Keum SB Kang HY Koh Y Kim DH Lee 1998 A facile synthesis of N-carbamoylmethyl-α-aminobutyrolactones by the Ugi multicomponent condensation reaction Tetrahedron Lett 39 7109 7112 10.1016/S0040-4039(98)01509- 3 1:CAS:528:DyaK1cXmtVemtLw%3D 10.1016/S0040-4039(98)01509-3 (Pubitemid 28414795)
    • (1998) Tetrahedron Letters , vol.39 , Issue.39 , pp. 7109-7112
    • Park, S.J.1    Keum, G.2    Kang, S.B.3    Koh, H.Y.4    Kim, Y.5    Duck Hyung, L.6
  • 40
    • 33646024927 scopus 로고    scopus 로고
    • Isoindoles and dihydroisoquinolines by gold-catalyzed intramolecular hydroamination of alkynes
    • doi: 10.1039/b516017k
    • Kadzimirsz D, Hildebrandt D, Merz K, Dyker G (2006) Isoindoles and dihydroisoquinolines by gold-catalyzed intramolecular hydroamination of alkynes. Chem Commun (Camb):661-662. doi: 10.1039/b516017k
    • (2006) Chem Commun (Camb) , pp. 661-662
    • Kadzimirsz, D.1    Hildebrandt, D.2    Merz, K.3    Dyker, G.4
  • 41
    • 0001220302 scopus 로고    scopus 로고
    • An efficient synthesis of morpholin-2-one derivatives using glycolaldehyde dimer by the Ugi multicomponent reaction
    • DOI 10.1021/ol016716w
    • YB Kim EH Choi G Keum SB Kang DH Lee HY Koh Y Kim 2001 An efficient synthesis of morpholin-2-one derivatives using glycolaldehyde dimer by the Ugi multicomponent reaction Org Lett 3 4149 4152 10.1021/ol016716w 1:CAS:528:DC%2BD3MXos12isbw%3D 10.1021/ol016716w 11784164 (Pubitemid 33627233)
    • (2001) Organic Letters , vol.3 , Issue.26 , pp. 4149-4152
    • Kim, Y.B.1    Choi, E.H.2    Keum, G.3    Kang, S.B.4    Lee, D.H.5    Koh, H.Y.6    Kim, Y.7
  • 43
    • 78650176404 scopus 로고    scopus 로고
    • Crysalis data collection software and data processing software for Oxford Xcalibur diffractometer. Oxford Diffraction Ltd., Oxfordshire (2005)
    • Crysalis data collection software and data processing software for Oxford Xcalibur diffractometer. Oxford Diffraction Ltd., Oxfordshire (2005)
  • 44
    • 0000604488 scopus 로고
    • SIR92-a program for automatic solution of crystal structures by direct methods
    • doi: 10.1107/S002188989400021X
    • Altomare A, Cascarano G, Giacovazzo C, Guagliardi A, Burla MC, Polidori GMC (1994) SIR92-a program for automatic solution of crystal structures by direct methods. J Appl Cryst 27. doi: 10.1107/S002188989400021X
    • (1994) J Appl Cryst , vol.27
    • Altomare, A.1    Cascarano, G.2    Giacovazzo, C.3    Guagliardi, A.4    Burla, M.C.5    Gmc, P.6
  • 46
    • 70449680564 scopus 로고    scopus 로고
    • University of Göttingen Göttingen
    • Sheldrick G (1998) M. SHELXL-97. University of Göttingen, Göttingen
    • (1998) M. SHELXL-97
    • Sheldrick, G.1
  • 48
    • 0141452964 scopus 로고    scopus 로고
    • WinGX (version 1.70.01 January 2005)
    • 1:CAS:528:DyaK1MXlsVSlurk%3D 10.1107/S0021889899006020
    • LJ Farrugia 1999 WinGX (version 1.70.01 January 2005) J Appl Cryst 32 837 838 1:CAS:528:DyaK1MXlsVSlurk%3D 10.1107/S0021889899006020
    • (1999) J Appl Cryst , vol.32 , pp. 837-838
    • Farrugia, L.J.1
  • 51
    • 0031051939 scopus 로고    scopus 로고
    • Radiation protection by alpha-methyl-homocysteine thiolactone in vitro
    • DOI 10.1016/S0024-3205(96)00515-2, PII S0024320596005152
    • KE Koch JC Roberts G Lubec 1997 Radiation protection by alpha-methyl-homocysteine thiolactone in vitro Life Sci 60 341 350 10.1016/S0024-3205(96)00515-2 1:CAS:528:DyaK2sXnvVGktw%3D%3D 10.1016/S0024-3205(96)00515-2 9031679 (Pubitemid 27090531)
    • (1997) Life Sciences , vol.60 , Issue.6 , pp. 341-350
    • Koch, K.E.1    Roberts, J.C.2    Lubec, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.