메뉴 건너뛰기




Volumn 40, Issue 11, 2010, Pages 1650-1657

Novel stereocontrolled preparation of amino polyols from 2,3-aziridine alcohols

Author keywords

2,3 aziridino alcohols; Amino polyols; Stereocontrolled synthesis

Indexed keywords

2,3 AZIRIDINE ALCOHOL DERIVATIVE; ALCOHOL DERIVATIVE; POLYOL; UNCLASSIFIED DRUG;

EID: 77952053649     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910903161645     Document Type: Article
Times cited : (4)

References (18)
  • 1
    • 34547527847 scopus 로고    scopus 로고
    • Synthesis and anti-influenza activities of carboxyl alkoxyalkyl esters of 4-guanidino-Neu5Ac2en (zanatni-vir)
    • (a)Liu, Z.; Wang, B.; Zhao, L.; Li, Y.; Shao, H.; Yi, H.; You, X.; Li, Z. Synthesis and anti-influenza activities of carboxyl alkoxyalkyl esters of 4-guanidino-Neu5Ac2en (zanatni-vir). Bioorg. Med. Chem. Lett. 2007, 17, 4851-4854;
    • (2007) Bioorg. Med. Chem. Lett. , vol.17 , pp. 4851-4854
    • Liu, Z.1    Wang, B.2    Zhao, L.3    Li, Y.4    Shao, H.5    Yi, H.6    You, X.7    Li, Z.8
  • 2
    • 30344463318 scopus 로고    scopus 로고
    • Improving the membrane permeability of sialic acid derivatives
    • (b)Altamore, T. M.; Duggan, P. J.; Krippner, G. Y. Improving the membrane permeability of sialic acid derivatives. Bioorg. Med. Chem. 2006, 14, 1126-1133;
    • (2006) Bioorg. Med. Chem. , vol.14 , pp. 1126-1133
    • Altamore, T.M.1    Duggan, P.J.2    Krippner, G.Y.3
  • 4
    • 0037288241 scopus 로고    scopus 로고
    • Synthesis of enantiopure amino polyols and pyrrolidine derivatives from 5-bromo-1,2-oxazin-4-ones
    • (a)Pulz, R.; Schade, W.; Reissing, H.-U. Synthesis of enantiopure amino polyols and pyrrolidine derivatives from 5-bromo-1,2-oxazin-4-ones. Synlett 2003, 14, 405-407;
    • (2003) Synlett , vol.14 , pp. 405-407
    • Pulz, R.1    Schade, W.2    Reissing, H.-U.3
  • 5
    • 0034697199 scopus 로고    scopus 로고
    • The synthesis of vicinal amino alcohols
    • (b)Bergmeier, S. C. The synthesis of vicinal amino alcohols. Tetrahedron 2000, 56, 2561-2576;
    • (2000) Tetrahedron , vol.56 , pp. 2561-2576
    • Bergmeier, S.C.1
  • 6
    • 0033588135 scopus 로고    scopus 로고
    • Glycosidase inihibitors: Synthesis of enantiomeri-cally pure aza-sugar from Shiff base amino esters tandem reduction-alkenylation and osmilation
    • (c)Polt, R.; Sames, D.; Chruma, J. Glycosidase inihibitors: Synthesis of enantiomeri-cally pure aza-sugar from Shiff base amino esters tandem reduction-alkenylation and osmilation. J. Org. Chem. 1999, 64, 6147-6158;
    • (1999) J. Org. Chem. , vol.64 , pp. 6147-6158
    • Polt, R.1    Sames, D.2    Chruma, J.3
  • 7
    • 0031796184 scopus 로고    scopus 로고
    • Linear aminopolyhydroxylated structures through rapid domino assembly of a highly functionalized heterotricyclic system and its selective cleavage
    • (d)Righi, P.; Marotta, E.; Rosini, G. Linear aminopolyhydroxylated structures through rapid domino assembly of a highly functionalized heterotricyclic system and its selective cleavage. Chem. Eur. J. 1998, 4, 2501-2508;
    • (1998) Chem. Eur. J. , vol.4 , pp. 2501-2508
    • Righi, P.1    Marotta, E.2    Rosini, G.3
  • 8
    • 77952079147 scopus 로고
    • Stereo-selective synthesis of masked aminopolyols via osmylation of 4,5-dihydro-5-vinylisoxa-zoles
    • (e)Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L.; Restelli, A. Stereo-selective synthesis of masked aminopolyols via osmylation of 4,5-dihydro-5-vinylisoxa-zoles. Helv. Chim. Acta 1985, 68, 1217-1225.
    • (1985) Helv. Chim. Acta , vol.68 , pp. 1217-1225
    • Annunziata, R.1    Cinquini, M.2    Cozzi, F.3    Raimondi, L.4    Restelli, A.5
  • 9
    • 0002426991 scopus 로고    scopus 로고
    • Functionalised epoxides and aziridines: Reactivity with metal halides and synthetic applications
    • Attanasi, O. A.; Spinelli, D. (Eds.); Italian Society of Chemistry: Rome
    • (a)Righi, G.; Bonini, C. Functionalised epoxides and aziridines: Reactivity with metal halides and synthetic applications. In: Target Heterocyclic Systems, Attanasi, O. A.; Spinelli, D. (Eds.); Italian Society of Chemistry: Rome, 2000, vol.4, pp. 139-165;
    • (2000) Target Heterocyclic Systems , vol.4 , pp. 139-165
    • Righi, G.1    Bonini, C.2
  • 10
    • 1242341160 scopus 로고    scopus 로고
    • Stereocontrolled addition of boron enolates to trans-a,b-aziridine aldehydes: A new route to anti-1,2-amino alcohols
    • (b)Righi, G.; Ciambrone, S. Stereocontrolled addition of boron enolates to trans-a,b-aziridine aldehydes: A new route to anti-1,2-amino alcohols. Tetrahedron Lett. 2004, 45, 2103-2106;
    • (2004) Tetrahedron Lett. , vol.45 , pp. 2103-2106
    • Righi, G.1    Ciambrone, S.2
  • 11
    • 33645324053 scopus 로고    scopus 로고
    • Stereocontrolled transformations of trans-a,b-aziri-dine aldehydes toward different amino hydroxylated structures
    • (c)Righi, G.; Ciambrone, S.; Bonini, C. Stereocontrolled transformations of trans-a,b-aziri-dine aldehydes toward different amino hydroxylated structures. Synth. Commun. 2006, 36, 1157-1165.
    • (2006) Synth. Commun. , vol.36 , pp. 1157-1165
    • Righi, G.1    Ciambrone, S.2    Bonini, C.3
  • 12
    • 84891040700 scopus 로고    scopus 로고
    • Vinyl aziridines in organic synthesis
    • Y. K. Andrei (Ed.); Wiley-VCH: Weinheim, Germany
    • (a)Hiroaki, O. Vinyl aziridines in organic synthesis. In Aziridines and Epoxides in Organic Synthesis; Y. K. Andrei (Ed.); Wiley-VCH: Weinheim, Germany, 2006; pp. 47-54;
    • (2006) Aziridines and Epoxides in Organic Synthesis , pp. 47-54
    • Hiroaki, O.1
  • 13
    • 15244353940 scopus 로고    scopus 로고
    • Selectivity aspects of the ring opening reaction of 2-alkenyl aziridines by carbon nucleophiles
    • (b)Cunha, R. L. O. R.; Diego, D. G.; Simonelli, F.; Comasseto, J. V. Selectivity aspects of the ring opening reaction of 2-alkenyl aziridines by carbon nucleophiles. Tetrahedron Lett. 2005, 46, 2539-2542.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 2539-2542
    • Cunha, R.L.O.R.1    Diego, D.G.2    Simonelli, F.3    Comasseto, J.V.4
  • 14
    • 0028236402 scopus 로고
    • A new procedure for Horner-Wadsworth-Emmons olefination of carbonyl compounds
    • Bonadies, F.; Cardilli, A.; Lattanzi, A.; Orelli, L. R.; Scettri, A. A new procedure for Horner-Wadsworth-Emmons olefination of carbonyl compounds. Tetrahedron Lett. 1994, 35, 3383-3386.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 3383-3386
    • Bonadies, F.1    Cardilli, A.2    Lattanzi, A.3    Orelli, L.R.4    Scettri, A.5
  • 15
    • 0026752267 scopus 로고
    • (2S3S)-2,3-Epoxy-3-trimethylsilylpropanal as a new conjunctive reagent
    • Urabe, H.; Mazzuka, T.; Essato, F. (2S,3S)-2,3-Epoxy-3- trimethylsilylpropanal as a new conjunctive reagent. Tetrahedron Lett. 1992, 34, 4179-4182.
    • (1992) Tetrahedron Lett. , vol.34 , pp. 4179-4182
    • Urabe, H.1    Mazzuka, T.2    Essato, F.3
  • 16
    • 0037068153 scopus 로고    scopus 로고
    • Stereo and regioselective ring opening of alkenyl aziridines with metal halides
    • Righi, G.; Bovicelli, P.; Potini, C. Stereo-and regioselective ring opening of alkenyl aziridines with metal halides. Tetrahedron Lett. 2002, 43, 5867-5869.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 5867-5869
    • Righi, G.1    Bovicelli, P.2    Potini, C.3
  • 17
    • 33748632563 scopus 로고
    • On stereochemistry of osmium tetraoxide oxidation of allylic alcohol systems: Empirical rule
    • Cha, J. K.; Christ, W. J.; Kishi, Y. On stereochemistry of osmium tetraoxide oxidation of allylic alcohol systems: Empirical rule. Tetrahedron 1984, 40, 2247-2255.
    • (1984) Tetrahedron , vol.40 , pp. 2247-2255
    • Cha, J.K.1    Christ, W.J.2    Kishi, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.