메뉴 건너뛰기




Volumn 14, Issue 6, 2010, Pages 601-613

Polyhydroxylated carbobicyclic sugar mimics. part 2. The Chiron Approach to bicyclic systems

Author keywords

[No Author keywords available]

Indexed keywords

HYDROXYLATION;

EID: 77954931809     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527210790820267     Document Type: Article
Times cited : (6)

References (65)
  • 3
    • 0001946536 scopus 로고    scopus 로고
    • Some progeny of 2,3-unsaturated sugars they little resemble grandfather glucose: Twenty years later
    • and references therein
    • Fraser-Reid, B. Some progeny of 2,3-unsaturated sugars they little resemble grandfather glucose: Twenty years later. Acc. Chem. Res., 1996, 29, 57-66 and references therein.
    • (1996) Acc. Chem. Res , vol.29 , pp. 57-66
    • Fraser-Reid, B.1
  • 4
    • 0032439180 scopus 로고    scopus 로고
    • Indolizidine and quinolizidine alkaloids
    • and references therein
    • Michael, J.P. Indolizidine and quinolizidine alkaloids. Nat. Prod. Rep., 1998, 5, 571-594 and references therein.
    • (1998) Nat. Prod. Rep , vol.5 , pp. 571-594
    • Michael, J.P.1
  • 5
    • 0030592829 scopus 로고    scopus 로고
    • 2-Hydroxycastanospermines (dihydroxy-Lswainsonines) from octonolactones: Inhibition of naringinase (Lrhamnosidase)
    • Bell, A.A.; Pickering, L.; Watson, A.A.; Nash, R.J.; Griffiths, R.C.; Jones, M.G.; Fleet, G.W.J. 2-Hydroxycastanospermines (dihydroxy-Lswainsonines) from octonolactones: Inhibition of naringinase (Lrhamnosidase). Tetrahedron Lett. 1996, 47, 8561-8564.
    • (1996) Tetrahedron Lett , vol.47 , pp. 8561-8564
    • Bell, A.A.1    Pickering, L.2    Watson, A.A.3    Nash, R.J.4    Griffiths, R.C.5    Jones, M.G.6    Fleet, G.W.J.7
  • 6
    • 0002764933 scopus 로고    scopus 로고
    • Stereocontrolled synthesis of a trihydroxylated indolizidine alkaloid, 1-deoxycastanospermine
    • Yoda, H.; Nakajima, T.; Takabe, K. Stereocontrolled synthesis of a trihydroxylated indolizidine alkaloid, 1-deoxycastanospermine. Synlett, 1997, 911-912.
    • (1997) Synlett , pp. 911-912
    • Yoda, H.1    Nakajima, T.2    Takabe, K.3
  • 8
    • 0029784236 scopus 로고    scopus 로고
    • Synthesis of tetrahydroxyquinolizidines: Ringexpanded analogs of the mannosidase inhibitor swainsonine
    • Pearson, W.H.; Hembre, E.J. Synthesis of tetrahydroxyquinolizidines: Ringexpanded analogs of the mannosidase inhibitor swainsonine. J. Org. Chem., 1996, 61, 5537-5545.
    • (1996) J. Org. Chem , vol.61 , pp. 5537-5545
    • Pearson, W.H.1    Hembre, E.J.2
  • 9
    • 0033579586 scopus 로고    scopus 로고
    • Polycyclitols: Stereoselective synthesis of enantiopure polyhydroxylated hydrindanes (annulated carbasugars)
    • Mehta, G.; Ramesh, S.S. Polycyclitols: Stereoselective synthesis of enantiopure polyhydroxylated hydrindanes (annulated carbasugars). Tetrahedron Lett., 1999, 40, 9137-9140.
    • (1999) Tetrahedron Lett , vol.40 , pp. 9137-9140
    • Mehta, G.1    Ramesh, S.S.2
  • 10
    • 0033613795 scopus 로고    scopus 로고
    • Enzymatic resolution of dioxygenated dicyclopentadienes: Enantiopure hydrindanes, hydroisoquinolones, diquinanes and application to a synthesis of (+)-coronofacic acid
    • Mehta, G.; Reddy, D.S. Enzymatic resolution of dioxygenated dicyclopentadienes: Enantiopure hydrindanes, hydroisoquinolones, diquinanes and application to a synthesis of (+)-coronofacic acid. Tetrahedron Lett. 1999, 40, 991-994.
    • (1999) Tetrahedron Lett , vol.40 , pp. 991-994
    • Mehta, G.1    Reddy, D.S.2
  • 11
    • 0033579640 scopus 로고    scopus 로고
    • Polycyclitols: Stereoselective synthesis of decalin and diquinane based polyols as potential glycomimics
    • Mehta, G.; Reddy, D.S.; Ramesh, S.S.; Tatu, U. Polycyclitols: Stereoselective synthesis of decalin and diquinane based polyols as potential glycomimics. Tetrahedron Lett., 1999, 40, 9141-9144.
    • (1999) Tetrahedron Lett , vol.40 , pp. 9141-9144
    • Mehta, G.1    Reddy, D.S.2    Ramesh, S.S.3    Tatu, U.4
  • 12
    • 0032143883 scopus 로고    scopus 로고
    • Pyrrolizidine alkaloids
    • Liddell, J.R. Pyrrolizidine alkaloids. Nat. Prod. Rep., 1998, 15, 363-370.
    • (1998) Nat. Prod. Rep , vol.15 , pp. 363-370
    • Liddell, J.R.1
  • 13
    • 0001199245 scopus 로고
    • The Chemistry of the nargenicin macrolides
    • Rahman, A.-U., Ed.; Elsevier Science Publisher: Amsterdam
    • Kallmerten, J. The Chemistry of the nargenicin macrolides. In: Studies in natural product chemistry. Rahman, A.-U., Ed.; Elsevier Science Publisher: Amsterdam, 1995, pp. 288-311.
    • (1995) Studies In Natural Product Chemistry , pp. 288-311
    • Kallmerten, J.1
  • 14
    • 0029782961 scopus 로고    scopus 로고
    • Studies On the Synthesis of Nargenicin A1: Highly Stereoselective Synthesis of the Complete Carbon Framework Via The Transannular Dielsalder Reaction of An 18-membered Macrolide
    • The synthesis of nargenicins: Roush, W.R.; Koyama, K.; Curtin, M.L.; Moriarty K.J. Studies on the synthesis of nargenicin A1: Highly stereoselective synthesis of the complete carbon framework via the transannular dielsalder reaction of an 18-membered macrolide. J. Am. Chem. Soc., 1996, 118, 7502-7512.
    • (1996) The Synthesis of Nargenicins, J. Am. Chem. Soc. , vol.118 , pp. 7502-7512
    • Roush, W.R.1    Koyama, K.2    Curtin, M.L.3    Moriarty, K.J.4
  • 15
    • 33845183407 scopus 로고
    • Studies of an intramolecular Diels-Alder approach to the nargenicins: Involvement of boatlike transition states in the cyclizations of substituted 1,7,9-decatrien-3-ones
    • Coe, J.W.; Roush, W.R. Studies of an intramolecular Diels-Alder approach to the nargenicins: involvement of boatlike transition states in the cyclizations of substituted 1,7,9-decatrien-3-ones. J. Org. Chem., 1989, 54, 915-930.
    • (1989) J. Org. Chem , vol.54 , pp. 915-930
    • Coe, J.W.1    Roush, W.R.2
  • 16
    • 0001616071 scopus 로고
    • A rapid esterification by means of mixed anhydride and its application to large-ring lactonization
    • Inanaga, J.; Hirata, K.; Saeki, H.; Katsuki, T.; Yamaguchi, M. A rapid esterification by means of mixed anhydride and its application to large-ring lactonization. Bull. Chem. Soc. Jpn. 1979, 52, 1989-1993.
    • (1979) Bull. Chem. Soc. Jpn. , vol.52 , pp. 1989-1993
    • Inanaga, J.1    Hirata, K.2    Saeki, H.3    Katsuki, T.4    Yamaguchi, M.5
  • 17
    • 24744431637 scopus 로고    scopus 로고
    • Aiming for branimycin: Synthesis of the cis-decalin core
    • Enev, V.S.; Drescher, M.; Kaehling, H.; Mulzer, J. Aiming for branimycin: Synthesis of the cis-decalin core. Synlett, 2005, 14, 2227-2229.
    • (2005) Synlett , vol.14 , pp. 2227-2229
    • Enev, V.S.1    Drescher, M.2    Kaehling, H.3    Mulzer, J.4
  • 18
    • 33947162951 scopus 로고    scopus 로고
    • Cis-decalins from quinic acid: Toward a synthesis of branimycin
    • Marchart, S.; Mulzer, J.; Enev, V.S. Cis-decalins from quinic acid: toward a synthesis of branimycin. Org. Lett., 2007, 9, 813-816.
    • (2007) Org. Lett. , vol.9 , pp. 813-816
    • Marchart, S.1    Mulzer, J.2    Enev, V.S.3
  • 19
    • 38949125436 scopus 로고    scopus 로고
    • A non-diels-alder approach to the cisdecalin core of branimycin
    • Enev, V.S.; Drescher, M.; Mulzer, J. A non-diels-alder approach to the cisdecalin core of branimycin. Org. Lett., 2008, 10, 413-416.
    • (2008) Org. Lett. , vol.10 , pp. 413-416
    • Enev, V.S.1    Drescher, M.2    Mulzer, J.3
  • 20
    • 67649494474 scopus 로고    scopus 로고
    • A desymmetrization approach toward highly oxygenated cis-decalins
    • Gromov, A.; Valentin Enev, V.S.; Mulzer, J. A desymmetrization approach toward highly oxygenated cis-decalins. Org. Lett., 2009, 11, 2884-2886.
    • (2009) Org. Lett. , vol.11 , pp. 2884-2886
    • Gromov, A.1    Valentin, E.V.S.2    Mulzer, J.3
  • 21
    • 33947162951 scopus 로고    scopus 로고
    • Cis-decalins from quinic acid: Toward a synthesis of branimycin
    • Marchart, S.; Mulzer, J.; Enev, V.S. Cis-decalins from quinic acid: toward a synthesis of branimycin. Org. Lett., 2007, 9, 813-816.
    • (2007) Org. Lett. , vol.9 , pp. 813-816
    • Marchart, S.1    Mulzer, J.2    Enev, V.S.3
  • 22
    • 0041350398 scopus 로고    scopus 로고
    • Stereoselective reactions of a (-)- quinic acid-derived enone: Application to the synthesis of the core of scyphostatin
    • Murray, L.M.; O'Brien, P.; Taylor, R.J.K. Stereoselective reactions of a (-)- quinic acid-derived enone: application to the synthesis of the core of scyphostatin. Org. Lett., 2003, 5, 1943-1946.
    • (2003) Org. Lett. , vol.5 , pp. 1943-1946
    • Murray, L.M.1    O'Brien, P.2    Taylor, R.J.K.3
  • 23
    • 2942589152 scopus 로고    scopus 로고
    • Synthesis of oxygen- and nitrogen-containing heterocycles by ring-closing metathesis
    • Deiters, A.; Martin, S.F. Synthesis of oxygen- and nitrogen-containing heterocycles by ring-closing metathesis. Chem. Rev., 2004, 104, 2199-2238.
    • (2004) Chem. Rev , vol.104 , pp. 2199-2238
    • Deiters, A.1    Martin, S.F.2
  • 24
    • 0142023994 scopus 로고    scopus 로고
    • Molybdenum and tungsten imido alkylidene complexes as efficient olefin-metathesis catalysts
    • Schrock, R.R.; Hoveyda, A.H. Molybdenum and tungsten imido alkylidene complexes as efficient olefin-metathesis catalysts. Angew. Chem., Int. Ed., 2003, 42, 4592-4633.
    • (2003) Angew. Chem., Int. Ed , vol.42 , pp. 4592-4633
    • Schrock, R.R.1    Hoveyda, A.H.2
  • 25
    • 0038215596 scopus 로고    scopus 로고
    • Recent developments in olefin cross-metathesis
    • Connon, S.J.; Blechert, S. Recent developments in olefin cross-metathesis. Angew. Chem. Int. Ed., 2003, 42, 1900-1923.
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 1900-1923
    • Connon, S.J.1    Blechert, S.2
  • 26
    • 33846427318 scopus 로고    scopus 로고
    • Synthetic Strategies For Converting Carbohydrates Into Carbocycles By the Use of Olefin Metathesis
    • RCM in synthesis of sugar mimetics: Madsen, R. Synthetic strategies for converting carbohydrates into carbocycles by the use of olefin metathesis. Eur. J. Org. Chem., 2007, 399-415.
    • (2007) RCM In Synthesis of Sugar Mimetics, Eur. J. Org. Chem. , pp. 399-415
  • 27
    • 0032838140 scopus 로고    scopus 로고
    • Harvesting diels and alder's garden: Synthetic investigations of. intramolecular [4+2] cycloadditions
    • and references therein
    • Fallis, A.G. Harvesting diels and alder's garden: synthetic investigations of. intramolecular [4+2] cycloadditions. Acc. Chem. Res., 1999, 32, 464-474 and references therein.
    • (1999) Acc. Chem. Res , vol.32 , pp. 464-474
    • Fallis, A.G.1
  • 29
    • 0017857533 scopus 로고
    • Synthesis of anthopleurine, the alarm pheromone from Anthopleura elegantissima
    • Musich, J.A.; Rapoport, H. Synthesis of anthopleurine, the alarm pheromone from Anthopleura elegantissima. J. Am. Chem. Soc., 1978, 100, 4865-4872.
    • (1978) J. Am. Chem. Soc. , vol.100 , pp. 4865-4872
    • Musich, J.A.1    Rapoport, H.2
  • 30
    • 0030824519 scopus 로고    scopus 로고
    • Isopropylidene acetals: Tether control groups for asymmetric intramolecular Diels-Alder reactions
    • Wong, T.; Wilson, P.D.; Woo, S.; Fallis, A.G. Isopropylidene acetals: Tether control groups for asymmetric intramolecular Diels-Alder reactions. Tetrahedron Lett., 1997, 38, 7045-7048.
    • (1997) Tetrahedron Lett , vol.38 , pp. 7045-7048
    • Wong, T.1    Wilson, P.D.2    Woo, S.3    Fallis, A.G.4
  • 31
    • 33749174849 scopus 로고
    • Complete stereoselectivity in the intramolecular Diels-Alder reaction of a triene derivative from DXylose
    • Herczegh, P.; Zsely, M.; Szilagyi, L.; Bognar, R. Complete stereoselectivity in the intramolecular Diels-Alder reaction of a triene derivative from DXylose. Tetrahedron Lett., 1988, 29, 481-484.
    • (1988) Tetrahedron Lett , vol.29 , pp. 481-484
    • Herczegh, P.1    Zsely, M.2    Szilagyi, L.3    Bognar, R.4
  • 32
    • 33746155717 scopus 로고
    • Intramolecular reactions of compounds derived from sugars. Part III. High diastereoselection in the intramolecular Diels-Alder reaction of sugar based 1,7(E,Z),9- decatrienes
    • Herczegh, P.; Zsely, M.; Szilagyi, L.; Dinya, Z.; Bognar, R. Intramolecular reactions of compounds derived from sugars. Part III. High diastereoselection in the intramolecular Diels-Alder reaction of sugar based 1,7(E,Z),9- decatrienes. Tetrahedron, 1989, 45, 5995-6002.
    • (1989) Tetrahedron , vol.45 , pp. 5995-6002
    • Herczegh, P.1    Zsely, M.2    Szilagyi, L.3    Dinya, Z.4    Bognar, R.5
  • 33
    • 23944439719 scopus 로고    scopus 로고
    • Sugar allyltin compounds: Preparation and application in organic synthesis
    • Jarosz, S.; Gaweł, A. Sugar allyltin compounds: preparation and application in organic synthesis. Eur. J. Org. Chem., 2005, 16, 3415-3432.
    • (2005) Eur. J. Org. Chem. , vol.16 , pp. 3415-3432
    • Jarosz, S.1    Gaweł, A.2
  • 34
    • 0035626725 scopus 로고    scopus 로고
    • Synthesis of higher carbon sugars via coupling of simple monosaccharides - Wittig, Horner-Emmons and related methods
    • Jarosz, S. Synthesis of higher carbon sugars via coupling of simple monosaccharides - Wittig, Horner-Emmons and related methods. J. Carbohydr. Chem., 2001, 20, 93-107.
    • (2001) J. Carbohydr. Chem , vol.20 , pp. 93-107
    • Jarosz, S.1
  • 35
    • 33748731816 scopus 로고
    • Synthesis of The Trans and Cis Higher Sugar Allylic Alcohols-direct Precursors of Dodecoses
    • Acetylene methodology: Jarosz, S. Synthesis of the trans and cis higher sugar allylic alcohols-direct precursors of dodecoses. J. Carbohydr. Chem., 1993, 12, 1149-1160.
    • (1993) Acetylene methodology: J. Carbohydr. Chem. , vol.12 , pp. 1149-1160
    • Jarosz, S.1
  • 36
    • 0002205209 scopus 로고
    • Approaches to Higher-carbon Sugars, Based On the Use of Sugar-derived, Stabilized Wittig Reagent
    • Phosphorane methodology: Jarosz, S. Mootoo, D.R.; Fraser-Reid, B. Approaches to higher-carbon sugars, based on the use of sugar-derived, stabilized Wittig reagent. Carbohydr. Res., 1986, 147, 59-68.
    • (1986) Phosphorane Methodology: Carbohydr. Res. , vol.147 , pp. 59-68
  • 37
    • 0001706244 scopus 로고
    • Stereoselective reduction of higher sugar enones with zinc borohydride
    • Jarosz, S. Stereoselective reduction of higher sugar enones with zinc borohydride. Carbohydr. Res., 1988, 183, 201-207.
    • (1988) Carbohydr. Res , vol.183 , pp. 201-207
    • Jarosz, S.1
  • 38
    • 33748718389 scopus 로고    scopus 로고
    • Phosphonate versus phosphorane method in the synthesis of higher carbon sugars. Preparation of Derythro-L-manno-D-glucododecitol
    • Phosphonate methodology: Jarosz, S.; Mach, M. Phosphonate versus phosphorane method in the synthesis of higher carbon sugars. Preparation of Derythro-L-manno-D-glucododecitol. J. Chem. Soc., Perkin Trans. I, 1998, 3943-3948.
    • (1998) Phosphonate Methodology: J. Chem. Soc., Perkin Trans. , pp. 3943-3948
    • Jarosz, S.1    Mach, M.2
  • 39
    • 0032510334 scopus 로고    scopus 로고
    • Application of stabilized sugar-derived phosphoranes in the synthesis of higher carbon monosaccharides. First synthesis of a C21-dialdose
    • Jarosz, S.; Sałański, P.; Mach M. Application of stabilized sugar-derived phosphoranes in the synthesis of higher carbon monosaccharides. First synthesis of a C21-dialdose. Tetrahedron, 1998, 54, 2583-2594.
    • (1998) Tetrahedron , vol.54 , pp. 2583-2594
    • Jarosz, S.1    Sałański, P.2    Mach, M.3
  • 40
    • 4243893500 scopus 로고
    • Selective reactions using allylic metals
    • and references therein
    • Yamamoto, Y.; Asao, N. Selective reactions using allylic metals. Chem. Rev., 1993, 93, 2207-2293 and references therein.
    • (1993) Chem. Rev , vol.93 , pp. 2207-2293
    • Yamamoto, Y.1    Asao, N.2
  • 41
    • 0000543015 scopus 로고
    • An observation of diastereoface selectivity in thermal reactions between δ-alkoxyallylstannanes and aldehydes
    • Mortlock, S.V.; Thomas, E.J. An observation of diastereoface selectivity in thermal reactions between δ-alkoxyallylstannanes and aldehydes. Tetrahedron Lett., 1988, 29, 2479-2482.
    • (1988) Tetrahedron Lett , vol.29 , pp. 2479-2482
    • Mortlock, S.V.1    Thomas, E.J.2
  • 42
    • 0001411625 scopus 로고
    • Synthesis of higher sugars via allyltin derivatives of simple monosaccharides
    • Jarosz, S.; Fraser-Reid, B. Synthesis of higher sugars via allyltin derivatives of simple monosaccharides. J. Org. Chem., 1989, 54, 4011-4013.
    • (1989) J. Org. Chem , vol.54 , pp. 4011-4013
    • Jarosz, S.1    Fraser-Reid, B.2
  • 43
    • 0343957013 scopus 로고
    • From sugar allyltin derivatives to chiral dienoaldehydes and trienoates
    • Kozłowska, E.; Jarosz, S. From sugar allyltin derivatives to chiral dienoaldehydes and trienoates. J. Carbohydr. Chem., 1994, 13, 889-898.
    • (1994) J. Carbohydr. Chem. , vol.13 , pp. 889-898
    • Kozłowska, E.1    Jarosz, S.2
  • 44
    • 2942536403 scopus 로고    scopus 로고
    • Reaction of sugar allyltins with aldehydes under high pressure
    • Jarosz, S.; Szewczyk, K.; Gaweł, A.; Luboradzki, R. Reaction of sugar allyltins with aldehydes under high pressure. Tetrahedron Asymmetry, 2004, 15, 1719-1727.
    • (2004) Tetrahedron Asymmetry , vol.15 , pp. 1719-1727
    • Jarosz, S.1    Szewczyk, K.2    Gaweł, A.3    Luboradzki, R.4
  • 45
    • 0342314537 scopus 로고    scopus 로고
    • A convenient route to enantiomerically pure, conjugated dienes from sugar allyltin derivatives
    • Jarosz, S.; Skóra, S.; Szewczyk, K. A convenient route to enantiomerically pure, conjugated dienes from sugar allyltin derivatives. Tetrahedron Asymmetry, 2000, 11, 1997-2006.
    • (2000) Tetrahedron Asymmetry , vol.11 , pp. 1997-2006
    • Jarosz, S.1    Skóra, S.2    Szewczyk, K.3
  • 46
    • 0009533111 scopus 로고
    • Deoxygenation of allylic alcohols to terminal olefins via stannylation/destannylation
    • Ueno, Y.; Sano, H.; Okawara, M. Deoxygenation of allylic alcohols to terminal olefins via stannylation/destannylation. Tetrahedron Lett., 1980, 21, 1767-1770.
    • (1980) Tetrahedron Lett , vol.21 , pp. 1767-1770
    • Ueno, Y.1    Sano, H.2    Okawara, M.3
  • 47
    • 85022591503 scopus 로고
    • A new method for the 1,3-hydroxytransposition in allylic alcohols via allylic stannanes
    • Ueno, Y.; Sano, H.; Okawara, M. A new method for the 1,3-hydroxytransposition in allylic alcohols via allylic stannanes. Synthesis, 1980, 1011-1013.
    • (1980) Synthesis , pp. 1011-1013
    • Ueno, Y.1    Sano, H.2    Okawara, M.3
  • 48
    • 0030807653 scopus 로고    scopus 로고
    • Tri-n-butyltin cuprate as a tool for the preparation of stannyl derivatives of carbohydrates
    • Jarosz, S. Tri-n-butyltin cuprate as a tool for the preparation of stannyl derivatives of carbohydrates. Tetrahedron, 1997, 53, 10765-10774.
    • (1997) Tetrahedron , vol.53 , pp. 10765-10774
    • Jarosz, S.1
  • 49
    • 0347389221 scopus 로고    scopus 로고
    • Intramolecular Diels-Alder reaction of chiral, highly oxygenated trienoates derived from sugar allyltins
    • Jarosz, S.; Kozłowska, E.; Jeżewski, A. Intramolecular Diels-Alder reaction of chiral, highly oxygenated trienoates derived from sugar allyltins. Tetrahedron, 1997, 53, 10775-10782.
    • (1997) Tetrahedron , vol.53 , pp. 10775-10782
    • Jarosz, S.1    Kozłowska, E.2    Jezewski, A.3
  • 50
    • 0035973780 scopus 로고    scopus 로고
    • Reaction of sugar allyltins with aldehydes. A remarkable difference in reactivity between furanose and pyranose organometallic derivatives
    • Jarosz, S.; Skóra, S.; Szewczyk, K.; Ciunik, Z. Reaction of sugar allyltins with aldehydes. A remarkable difference in reactivity between furanose and pyranose organometallic derivatives. Tetrahedron Asymmetry, 2001, 12, 1895-1905.
    • (2001) Tetrahedron Asymmetry , vol.12 , pp. 1895-1905
    • Jarosz, S.1    Skóra, S.2    Szewczyk, K.3    Ciunik, Z.4
  • 51
    • 0000212392 scopus 로고
    • Transmetalation reactions of higher order cyanocuprates: Direct formation of trialkyltin cuprates from tin hydrides which bypasses organolithium intermediates
    • Lipshutz, B.H.; Ellsworth, E.L.; Dimock, S.H.; Reuter, D.C. Transmetalation reactions of higher order cyanocuprates: Direct formation of trialkyltin cuprates from tin hydrides which bypasses organolithium intermediates. Tetrahedron Lett., 1989, 30, 2065-2068.
    • (1989) Tetrahedron Lett , vol.30 , pp. 2065-2068
    • Lipshutz, B.H.1    Ellsworth, E.L.2    Dimock, S.H.3    Reuter, D.C.4
  • 52
    • 0037867624 scopus 로고    scopus 로고
    • Synthesis and thermal stability of secondary sugar allyltin derivatives
    • Jarosz, S.; Szewczyk, K.; Zawisza, A. Synthesis and thermal stability of secondary sugar allyltin derivatives Tetrahedron Asymmetry, 2003, 14, 1715-1723.
    • (2003) Tetrahedron Asymmetry , vol.14 , pp. 1715-1723
    • Jarosz, S.1    Szewczyk, K.2    Zawisza, A.3
  • 53
    • 4444345959 scopus 로고    scopus 로고
    • Mechanism of the fragmentation of secondary sugar allyltin derivatives
    • Jarosz, S.; Szewczyk, K.; Sitkowski, J.; Gaweł, A. Mechanism of the fragmentation of secondary sugar allyltin derivatives. Tetrahedron Asymmetry, 2004, 15, 2653-2656.
    • (2004) Tetrahedron Asymmetry , vol.15 , pp. 2653-2656
    • Jarosz, S.1    Szewczyk, K.2    Sitkowski, J.3    Gaweł, A.4
  • 54
    • 0343134568 scopus 로고    scopus 로고
    • A convenient route to enantiomerically pure bicyclo[ 4.3.0]nonanes from sugar allyltin derivatives
    • Jarosz, S.; Skóra, S. A convenient route to enantiomerically pure bicyclo[ 4.3.0]nonanes from sugar allyltin derivatives. Tetrahedron Asymmetry, 2000, 11, 1425-1432.
    • (2000) Tetrahedron Asymmetry , vol.11 , pp. 1425-1432
    • Jarosz, S.1    Skóra, S.2
  • 55
    • 0037529981 scopus 로고    scopus 로고
    • Synthesis of highly oxygenated enantiomerically pure cis-bicyclo[4.3.0]nonanes from secondary sugar allyltin derivatives
    • Jarosz, S.; Szewczyk, K.; Zawisza, A. Synthesis of highly oxygenated enantiomerically pure cis-bicyclo[4.3.0]nonanes from secondary sugar allyltin derivatives. Tetrahedron Asymmetry, 2003, 14, 1709-1713.
    • (2003) Tetrahedron Asymmetry , vol.14 , pp. 1709-1713
    • Jarosz, S.1    Szewczyk, K.2    Zawisza, A.3
  • 56
    • 0343505805 scopus 로고    scopus 로고
    • A convenient route to enantiomerically pure highly oxygenated decalins from sugar allyltin derivatives
    • Jarosz, S.; Skóra, S. A convenient route to enantiomerically pure highly oxygenated decalins from sugar allyltin derivatives. Tetrahedron Asymmetry, 2000, 11, 1433-1448.
    • (2000) Tetrahedron Asymmetry , vol.11 , pp. 1433-1448
    • Jarosz, S.1    Skóra, S.2
  • 57
    • 12944325309 scopus 로고    scopus 로고
    • Synthesis of complex carbobicyclic compounds from sugar allyltins: Functionalization of the allylic position in bicyclo[4.3.0]nonene derivatives
    • Jarosz, S.; Boryczko, B.; Cmoch, P.; Gomez, A.M.; Lopez, C. Synthesis of complex carbobicyclic compounds from sugar allyltins: functionalization of the allylic position in bicyclo[4.3.0]nonene derivatives. Tetrahedron Asymmetry, 2005, 16, 513-518.
    • (2005) Tetrahedron Asymmetry , vol.16 , pp. 513-518
    • Jarosz, S.1    Boryczko, B.2    Cmoch, P.3    Gomez, A.M.4    Lopez, C.5
  • 58
    • 0035806470 scopus 로고    scopus 로고
    • Sugar allyltins in the synthesis of carbobicycles. Preparation of highly oxygenated enantiomerically pure decalins. Tetrahedron
    • Jarosz, S.; Skóra, S. Sugar allyltins in the synthesis of carbobicycles. Preparation of highly oxygenated enantiomerically pure decalins. Tetrahedron Asymmetry, 2001, 12, 1651-1656.
    • (2001) Asymmetry , vol.12 , pp. 1651-1656
    • Jarosz, S.1    Skóra, S.2
  • 59
    • 0000269981 scopus 로고
    • Über steroide und sexualhormone. 160. Mitteilung. 2α, 3α- und 2β, 3β-Oxido-chlolestane; Konfiguration der 2-Oxy-cholestane
    • Fürst, A.; Plattner, P.A. Über steroide und sexualhormone. 160. Mitteilung. 2α, 3α- und 2β, 3β-Oxido-chlolestane; Konfiguration der 2-Oxy-cholestane. Helv. Chim. Acta, 1949, 32, 275-283.
    • (1949) Helv. Chim. Acta , vol.32 , pp. 275-283
    • Fürst, A.1    Plattner, P.A.2
  • 62
    • 0007590568 scopus 로고
    • Mild procedure for the conversion of epoxides to allylic alcohols. First organoselenium reagent
    • Sharpless, K.B.; Lauer, R.F. Mild procedure for the conversion of epoxides to allylic alcohols. First organoselenium reagent. J. Am. Chem. Soc., 1973, 95, 2697-2699.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 2697-2699
    • Sharpless, K.B.1    Lauer, R.F.2
  • 63
    • 33745131803 scopus 로고    scopus 로고
    • Approach towards highly oxygenated cisdecalins from sugar allyltins
    • Jarosz, S.; Nowogródzki, M. Approach towards highly oxygenated cisdecalins from sugar allyltins. J. Carbohydr. Chem., 2006, 25, 139-149.
    • (2006) J. Carbohydr. Chem. , vol.25 , pp. 139-149
    • Jarosz, S.1    Nowogródzki, M.2
  • 64
    • 43649096286 scopus 로고    scopus 로고
    • Synthesis of highly oxygenated bicyclo[ 4.3.0]nonanes from sugar allyltins: Model transformations of the adduct derived from the D-mannose
    • Jarosz, S.; Błońska, A.; Cmoch, P. Synthesis of highly oxygenated bicyclo[ 4.3.0]nonanes from sugar allyltins: model transformations of the adduct derived from the D-mannose. Tetrahedron Asymmetry, 2008, 19, 1127-1133.
    • (2008) Tetrahedron Asymmetry , vol.19 , pp. 1127-1133
    • Jarosz, S.1    Błońska, A.2    Cmoch, P.3
  • 65
    • 52949095415 scopus 로고    scopus 로고
    • From higher carbon sugars to carbocyclic sugar mimics
    • Jarosz, S. From higher carbon sugars to carbocyclic sugar mimics. Curr. Org. Chem., 2008, 12, 985-994.
    • (2008) Curr. Org. Chem , vol.12 , pp. 985-994
    • Jarosz, S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.