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Volumn 16, Issue 13, 2012, Pages 1609-1635

Carbon dioxide: Versatile, cheap and safe alternative in the syntheses of organic carbamates+

Author keywords

Amines; Carbamation; Carbon dioxide; Organic carbamates

Indexed keywords

AGRICULTURAL CHEMICALS; BIOCHIPS;

EID: 84862529634     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527212800840982     Document Type: Review
Times cited : (17)

References (232)
  • 1
    • 0009354933 scopus 로고
    • Esters of carbamic acid
    • Adams, P.; Baron, F. A. Esters of carbamic acid. Chem. Rev., 1965, 65, 567-602.
    • (1965) Chem. Rev , vol.65 , pp. 567-602
    • Adams, P.1    Baron, F.A.2
  • 2
    • 0011878207 scopus 로고
    • Acylation by ketenes and isocyanates. A mechanistic comparison
    • Sutchell, D. P. N.; Satchell, R. S. Acylation by ketenes and isocyanates. A mechanistic comparison. Chem. Soc. Rev., 1975, 4, 231-250
    • (1975) Chem. Soc. Rev , vol.4 , pp. 231-250
    • Sutchell, D.P.N.1    Satchell, R.S.2
  • 3
    • 0012397313 scopus 로고
    • Directed ortho metalation: Tertiary amide and O-carbamate di-rectors in synthetic strategies for polysubstituted aromatics
    • Snieckus, V. Directed ortho metalation: Tertiary amide and O-carbamate di-rectors in synthetic strategies for polysubstituted aromatics. Chem. Rev., 1990, 90, 879-933.
    • (1990) Chem. Rev , vol.90 , pp. 879-933
    • Snieckus, V.1
  • 4
    • 0001458108 scopus 로고
    • Homogeneous hydrogenation of carbon dioxide
    • Jessop, P. G.; Ikariya, T.; Noyori, R. Homogeneous hydrogenation of carbon dioxide. Chem. Rev., 1995, 95, 259-272.
    • (1995) Chem. Rev , vol.95 , pp. 259-272
    • Jessop, P.G.1    Ikariya, T.2    Noyori, R.3
  • 5
    • 0001011833 scopus 로고    scopus 로고
    • A review of the selective catalytic reduction of aromatic nitro compounds into aromatic amines, isocyanates, carbamates, and ureas using CO
    • Tafesh, A. M.; Weiguny, J. A review of the selective catalytic reduction of aromatic nitro compounds into aromatic amines, isocyanates, carbamates, and ureas using CO. Chem. Rev., 1996, 96, 2035-2052.
    • (1996) Chem. Rev , vol.96 , pp. 2035-2052
    • Tafesh, A.M.1    Weiguny, J.2
  • 7
    • 0036882403 scopus 로고    scopus 로고
    • Catalytic antibodies as designer proteases and esterases
    • Tanaka, F. Catalytic antibodies as designer proteases and esterases. Chem. Rev., 2002, 102, 4885-4906.
    • (2002) Chem. Rev , vol.102 , pp. 4885-4906
    • Tanaka, F.1
  • 8
    • 0038468227 scopus 로고    scopus 로고
    • 1, 2-Amino alcohols and their heterocyclic derivatives as chiral auxiliaries in asymmetric synthesis
    • Ager, A. J.; Prakash, I.; Schaad, D. R. 1, 2-Amino alcohols and their heterocyclic derivatives as chiral auxiliaries in asymmetric synthesis. Chem. Rev., 1996, 96, 835-876.
    • (1996) Chem. Rev , vol.96 , pp. 835-876
    • Ager, A.J.1    Prakash, I.2    Schaad, D.R.3
  • 9
    • 0034635481 scopus 로고    scopus 로고
    • Advances in asymmetric enolate methodology
    • Arya, P.; Qin, H. Advances in asymmetric enolate methodology. Tetrahedron, 2000, 56, 917-947.
    • (2000) Tetrahedron , vol.56 , pp. 917-947
    • Arya, P.1    Qin, H.2
  • 10
    • 0033936085 scopus 로고    scopus 로고
    • Chiral bis(oxazoline) copper (II) complexes: Versatile catalysts for enantioselective cycloaddition, aldol, michael, and carbonyl ene reactions
    • Johnson, J. S.; Evans, D. A. Chiral bis(oxazoline) copper (II) complexes: Versatile catalysts for enantioselective cycloaddition, aldol, michael, and carbonyl ene reactions. Acc. Chem. Res., 2000, 33, 325-335.
    • (2000) Acc. Chem. Res , vol.33 , pp. 325-335
    • Johnson, J.S.1    Evans, D.A.2
  • 11
    • 0040804064 scopus 로고
    • Reaction of organoaluminum coordination compound with carbon dioxide
    • Inoue, S.; Yokoo, Y. Reaction of organoaluminum coordination compound with carbon dioxide. Bull. Chem. Soc. Jpn., 1972, 45, 3651-3653.
    • (1972) Bull. Chem. Soc. Jpn , vol.45 , pp. 3651-3653
    • Inoue, S.1    Yokoo, Y.2
  • 12
    • 37049074010 scopus 로고
    • Deprotonation of nitroalkanes by bicyclic amidine and guanidine bases: Evidence for molecular recognition within a catalytic cycle for C-C bond formation
    • Boyle, P. H.; Convery, M. A.; Davis, A. P.; Hosken, G. D.; Murray, B. A. Deprotonation of nitroalkanes by bicyclic amidine and guanidine bases: Evidence for molecular recognition within a catalytic cycle for C-C bond formation. J. Chem. Soc. Chem. Comm., 1992, 239-242.
    • (1992) J. Chem. Soc. Chem. Comm , pp. 239-242
    • Boyle, P.H.1    Convery, M.A.2    Davis, A.P.3    Hosken, G.D.4    Murray, B.A.5
  • 16
    • 2642569934 scopus 로고    scopus 로고
    • Application of organic carbamates in drug design. Part 1: Anticancer agents-recent reports
    • Ray, S.; Chaturvedi, D. Application of organic carbamates in drug design. Part 1: anticancer agents-recent reports. Drugs of the Future, 2004, 29, 343-357.
    • (2004) Drugs of the Future , vol.29 , pp. 343-357
    • Ray, S.1    Chaturvedi, D.2
  • 17
    • 20044364380 scopus 로고    scopus 로고
    • Organic carbamates in drug development, Part II: Antimicrobial agents: Recent reports
    • Ray, S.; Pathak, S. R.; Chaturvedi, D. Organic carbamates in drug development, Part II: antimicrobial agents: recent reports. Drugs of the Future, 2005, 30, 161-180.
    • (2005) Drugs of the Future , vol.30 , pp. 161-180
    • Ray, S.1    Pathak, S.R.2    Chaturvedi, D.3
  • 18
    • 42449120174 scopus 로고    scopus 로고
    • The structure-activity relationship of discodermolide analogues
    • Shaw, S. J. The structure-activity relationship of discodermolide analogues. Mini-Rev. Med. Chem., 2008, 8, 276-284.
    • (2008) Mini-Rev. Med. Chem , vol.8 , pp. 276-284
    • Shaw, S.J.1
  • 19
    • 0038811886 scopus 로고    scopus 로고
    • Oxazolidinone antibacterial agents: A critical review
    • Hutchinson, D. K. Oxazolidinone antibacterial agents: A critical review. Curr. Top Med. Chem., 2003, 3, 1021-1042.
    • (2003) Curr. Top Med. Chem , vol.3 , pp. 1021-1042
    • Hutchinson, D.K.1
  • 20
    • 0037797390 scopus 로고    scopus 로고
    • Recent development in macrolide antimicrobial research
    • Asaka, T. Manaka, A.; Sugiyama, H. Recent development in macrolide antimicrobial research. Curr. Top Med. Chem., 2003, 3, 961-989.
    • (2003) Curr. Top Med. Chem , vol.3 , pp. 961-989
    • Asaka, T.1    Manaka, A.2    Sugiyama, H.3
  • 21
    • 85196434859 scopus 로고    scopus 로고
    • 10th ed. Thomlin. C. D. S. ed. Crop. Protection Publication, UK, 1994
    • The Pesticidal Manual, 10th ed. Thomlin. C. D. S. ed. Crop. Protection Publication, UK, 1994.
    • The Pesticidal Manual
  • 22
    • 29244462794 scopus 로고    scopus 로고
    • The high throughput analysis of N-methyl carbamate pesticides in fruits and vegetables by liquid chromatography electrospray ionization tandem mass spectrometry using a short column
    • Goto, T.; Ito, Y.; Yamada, S.; Matsumoto, H.; Oka, H.; Nagase, H. The high throughput analysis of N-methyl carbamate pesticides in fruits and vegetables by liquid chromatography electrospray ionization tandem mass spectrometry using a short column. Anal. Chimica Acta, 2006, 555, 225-232.
    • (2006) Anal. Chimica Acta , vol.555 , pp. 225-232
    • Goto, T.1    Ito, Y.2    Yamada, S.3    Matsumoto, H.4    Oka, H.5    Nagase, H.6
  • 23
    • 33646148695 scopus 로고    scopus 로고
    • Differential responses of eight cyanobacterial and green algal species, to carbamate insecticides
    • Ma, J.; Lu, N.; Qin, W.; Xu, R.; Wang, Y.; Chen, X. Differential responses of eight cyanobacterial and green algal species, to carbamate insecticides. Ecotoxicol. Environmental Safety, 2006, 63, 268-274.
    • (2006) Ecotoxicol. Environmental Safety , vol.63 , pp. 268-274
    • Ma, J.1    Lu, N.2    Qin, W.3    Xu, R.4    Wang, Y.5    Chen, X.6
  • 24
    • 0037144634 scopus 로고    scopus 로고
    • Synthesis of a polymersupported oxazolidine aldehyde for asymmetric chemistry
    • Wills, A. J.; Ghosh, Y. K.; Balasubramanian, S. Synthesis of a polymersupported oxazolidine aldehyde for asymmetric chemistry. J. Org. Chem., 2002, 67, 6646-6652.
    • (2002) J. Org. Chem , vol.67 , pp. 6646-6652
    • Wills, A.J.1    Ghosh, Y.K.2    Balasubramanian, S.3
  • 25
    • 0742321841 scopus 로고    scopus 로고
    • Coppermediated synthesis of N-acyl vinylogous carbamic acids and derivatives: Synthesis of the antibiotic CJ-15,801
    • Han, C.; Shen, R.; Su, S.; Porco, J. A. Coppermediated synthesis of N-acyl vinylogous carbamic acids and derivatives: synthesis of the antibiotic CJ-15,801. Org. Lett., 2004, 6, 27-30.
    • (2004) Org. Lett , vol.6 , pp. 27-30
    • Han, C.1    Shen, R.2    Su, S.3    Porco, J.A.4
  • 27
    • 60849092288 scopus 로고    scopus 로고
    • Total synthesis without protecting groups: Pyrrolidines and cyclic carbamates
    • Dangerfield, E. M.; Timmer, M. S. M.; Stocker, B. L. Total synthesis without protecting groups: Pyrrolidines and cyclic carbamates. Org. Lett., 2009, 11, 535-538.
    • (2009) Org. Lett , vol.11 , pp. 535-538
    • Dangerfield, E.M.1    Timmer, M.S.M.2    Stocker, B.L.3
  • 31
    • 0032473927 scopus 로고    scopus 로고
    • Solid phase synthesis of oxazolidinones via a novel cyclization/cleavage reaction
    • Buchstaller, H. P. Solid phase synthesis of oxazolidinones via a novel cyclization/cleavage reaction. Tetrahedron, 1998, 54, 3465-3470.
    • (1998) Tetrahedron , vol.54 , pp. 3465-3470
    • Buchstaller, H.P.1
  • 32
    • 27744466783 scopus 로고    scopus 로고
    • Mechanism of carbamate inactivation of FAAH: Implications for the design of covalent inhibitors and in vivo functional probes for enzymes
    • Alaxander, J. P.; Cravatt, B. F. Mechanism of carbamate inactivation of FAAH: Implications for the design of covalent inhibitors and in vivo functional probes for enzymes. Chem. Biol., 2005, 12, 1179-1187.
    • (2005) Chem. Biol , vol.12 , pp. 1179-1187
    • Alaxander, J.P.1    Cravatt, B.F.2
  • 33
    • 28844448724 scopus 로고    scopus 로고
    • Effect of carbamate esters on neurite outgrowth in differentiating human SK-N-SH neuroblastoma cells
    • Chang, P. A.; Wu, Y. J.; Li, W.; Leng, X. F. Effect of carbamate esters on neurite outgrowth in differentiating human SK-N-SH neuroblastoma cells. Chem.-Biol. Interactions, 2006, 159, 65-72.
    • (2006) Chem.-Biol. Interactions , vol.159 , pp. 65-72
    • Chang, P.A.1    Wu, Y.J.2    Li, W.3    Leng, X.F.4
  • 35
    • 34250866214 scopus 로고    scopus 로고
    • Stereo-and regiochemical divergence in the substitution of a lithiated alk-1-en-3-yn-2-yl carbamate: Synthesis of highly enantioenriched vinylallenes or alk-3-en-5-yn-1-ols
    • Chedid, R. B.; Brummer, M.; Wibbeling, B.; Fohlich, R.; Hoppe, D. Stereo-and regiochemical divergence in the substitution of a lithiated alk-1-en-3-yn-2-yl carbamate: Synthesis of highly enantioenriched vinylallenes or alk-3-en-5-yn-1-ols. Angew. Chem. Int. Ed., 2007, 46, 3131-3134.
    • (2007) Angew. Chem. Int , vol.46 , pp. 3131-3134
    • Chedid, R.B.1    Brummer, M.2    Wibbeling, B.3    Fohlich, R.4    Hoppe, D.5
  • 36
    • 34248226223 scopus 로고    scopus 로고
    • Estimation of the kinetic acidity from substrate conformation -stereochemical course of the deprotonation of cyclohexenyl carbamates
    • Becker, J.; Grimme, S.; Frohlich, R.; Hoppe, D. Estimation of the kinetic acidity from substrate conformation -stereochemical course of the deprotonation of cyclohexenyl carbamates. Angew. Chem. Int. Ed., 2007, 46, 1645-1649.
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 1645-1649
    • Becker, J.1    Grimme, S.2    Frohlich, R.3    Hoppe, D.4
  • 37
    • 33846451020 scopus 로고    scopus 로고
    • Bismuth-catalyzed direct substitution of the hydroxy group in alcohols with sulfonamides, carbamates, and carboxamides
    • Qin, H.; Yamagiva, N.; Matsunaga, S.; Shibasaki, M. Bismuth-catalyzed direct substitution of the hydroxy group in alcohols with sulfonamides, carbamates, and carboxamides. Angew. Chem. Int. Ed., 2007, 46, 409-413.
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 409-413
    • Qin, H.1    Yamagiva, N.2    Matsunaga, S.3    Shibasaki, M.4
  • 38
    • 33746094780 scopus 로고    scopus 로고
    • Gold catalyzed intramolecular hydroamination of alkenyl carbamates
    • Han, X.; Widenhoefer, R. A. Gold catalyzed intramolecular hydroamination of alkenyl carbamates. Angew. Chem. Int. Ed., 2006, 45, 1747-1748.
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 1747-1748
    • Han, X.1    Widenhoefer, R.A.2
  • 39
    • 25144513578 scopus 로고    scopus 로고
    • Synthesis of imides, N-acyl vinylogous carbamates and ureas, and nitriles by oxidation of amides and amines with Dess-Martin periodinane
    • Nicolaou, K. C.; Mathison, J. N. Synthesis of imides, N-acyl vinylogous carbamates and ureas, and nitriles by oxidation of amides and amines with Dess-Martin periodinane. Angew. Chem. Int. Ed., 2005, 44, 5992-5996.
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 5992-5996
    • Nicolaou, K.C.1    Mathison, J.N.2
  • 40
    • 2642569934 scopus 로고    scopus 로고
    • Application of organic carbamates in drug design. Part 1: Anticancer agents-recent reports
    • Ray, S.; Chaturvedi, D. Application of organic carbamates in drug design. Part 1: anticancer agents-recent reports. Drugs of the Future, 2004, 29, 343-357.
    • (2004) Drugs of the Future , vol.29 , pp. 343-357
    • Ray, S.1    Chaturvedi, D.2
  • 42
    • 46049096634 scopus 로고    scopus 로고
    • Various approaches for the synthesis of organic carbamates
    • Chaturvedi, D. Ph. D. Thesis, Agra University, India, 2003, Chapter 2: Synthesis of organic carbamates through various approaches
    • Chaturvedi, D. Ph. D. Thesis, Agra University, India, 2003, Chapter 2: Synthesis of organic carbamates through various approaches, Chaturvedi, D.; Mishra, N.; Mishra, V. Various approaches for the synthesis of organic carbamates. Curr. Org. Synth., 2007, 3, 308-320.
    • (2007) Curr. Org. Synth. , vol.3 , pp. 308-320
    • Chaturvedi, D.1    Mishra, N.2    Mishra, V.3
  • 43
    • 2942601813 scopus 로고    scopus 로고
    • Synthesis of carbamate type caged derivatives of a novel glutamate transporter blocker
    • Takaoka, K.; Tatsu, Y.; Yumoto, N.; Nakajima, T.; Shimamoto, K. Synthesis of carbamate type caged derivatives of a novel glutamate transporter blocker. Bioorg. Med. Chem., 2004, 12, 3687-3694.
    • (2004) Bioorg. Med. Chem , vol.12 , pp. 3687-3694
    • Takaoka, K.1    Tatsu, Y.2    Yumoto, N.3    Nakajima, T.4    Shimamoto, K.5
  • 44
    • 18144364379 scopus 로고    scopus 로고
    • New antitubulin derivatives in the combretastanin A4 series: Synthesis and biological evaluation
    • Borrel, C. Thoret, S.; Cachet, X.; Guenard, D.; Tillequin, F.; Koch, M.; Michel, S. New antitubulin derivatives in the combretastanin A4 series: Synthesis and biological evaluation. Bioorg. Med. Chem., 2005, 13, 3853-3864.
    • (2005) Bioorg. Med. Chem , vol.13 , pp. 3853-3864
    • Borrel, C.1    Thoret, S.2    Cachet, X.3    Guenard, D.4    Tillequin, F.5    Koch, M.6    Michel, S.7
  • 46
    • 0021235883 scopus 로고
    • Synthesis, receptor binding, and target-tissue uptake of carbon-11 labeled carbamate derivatives of estradiol and hexestrol
    • Ouellet, R.; Rousseau, J.; Brasseur, N.; Lier, J. E.; Doksic, M.; Westera, G. Synthesis, receptor binding, and target-tissue uptake of carbon-11 labeled carbamate derivatives of estradiol and hexestrol. J. Med. Chem., 1984, 27, 509-513.
    • (1984) J. Med. Chem , vol.27 , pp. 509-513
    • Ouellet, R.1    Rousseau, J.2    Brasseur, N.3    Lier, J.E.4    Doksic, M.5    Westera, G.6
  • 47
    • 33745737662 scopus 로고    scopus 로고
    • Review camptothecin: Current perspectives
    • Li, Q. Y.; Zu, Y. G.; Shi, R. Z.; Yao, L. P. Review camptothecin: Current perspectives Curr. Med. Chem., 2006, 13, 2021-2039.
    • (2006) Curr. Med. Chem , vol.13 , pp. 2021-2039
    • Li, Q.Y.1    Zu, Y.G.2    Shi, R.Z.3    Yao, L.P.4
  • 48
    • 1542351340 scopus 로고    scopus 로고
    • Tumor specific novel taxoid-monoclonal antibody conjugates
    • Wu, X.; Ojima, J. Tumor specific novel taxoid-monoclonal antibody conjugates Curr. Med. Chem., 2004, 11, 429-438.
    • (2004) Curr. Med. Chem , vol.11 , pp. 429-438
    • Wu, X.1    Ojima, J.2
  • 49
    • 0035173131 scopus 로고    scopus 로고
    • Recent developments on ketolides and macrolides
    • Wu, Y. J.; Su, W. G. Recent developments on ketolides and macrolides. Curr. Med. Chem., 2001, 8, 1727-1758.
    • (2001) Curr. Med. Chem , vol.8 , pp. 1727-1758
    • Wu, Y.J.1    Su, W.G.2
  • 50
    • 33750594978 scopus 로고    scopus 로고
    • PPAR-γ activity in the vessel wall: Anti-atherogenic properties
    • Reiss, A. B.; Vagell, M. E. PPAR-γ activity in the vessel wall: Anti-atherogenic properties. Curr. Med. Chem., 2006, 13, 3227-3238.
    • (2006) Curr. Med. Chem , vol.13 , pp. 3227-3238
    • Reiss, A.B.1    Vagell, M.E.2
  • 51
    • 34247574158 scopus 로고    scopus 로고
    • Enhancement of chemotherapeutic efficacy by small molecule inhibition of NF-κB and checkpoint kinases
    • Sharma, V.; Hupp, C. D.; Tepe, J. J. Enhancement of chemotherapeutic efficacy by small molecule inhibition of NF-κB and checkpoint kinases. Curr. Med. Chem., 2007, 14, 1061-1074.
    • (2007) Curr. Med. Chem , vol.14 , pp. 1061-1074
    • Sharma, V.1    Hupp, C.D.2    Tepe, J.J.3
  • 52
    • 0034121289 scopus 로고    scopus 로고
    • Central selective acetylcholinesterase inhibitor with neurotrophic activity: Structure-activity relationships of TAK-147 and related compounds
    • Ishihara, Y.; Goto, G.; Miyamoto, M. Central selective acetylcholinesterase inhibitor with neurotrophic activity: Structure-activity relationships of TAK-147 and related compounds. Curr. Med. Chem., 2000, 7, 341-354.
    • (2000) Curr. Med. Chem , vol.7 , pp. 341-354
    • Ishihara, Y.1    Goto, G.2    Miyamoto, M.3
  • 53
    • 3042663164 scopus 로고    scopus 로고
    • Asymmetric synthesis of β-lactams through the staudinger reaction and their use as building blocks of natural and nonnatural products
    • Palomo, C.; Aizpurua, J. M.; Ganboa, I.; Oiarbiode, M. Asymmetric synthesis of β-lactams through the staudinger reaction and their use as building blocks of natural and nonnatural products. Curr. Med. Chem., 2004, 11, 1837-1872.
    • (2004) Curr. Med. Chem , vol.11 , pp. 1837-1872
    • Palomo, C.1    Aizpurua, J.M.2    Ganboa, I.3    Oiarbiode, M.4
  • 54
    • 14744297865 scopus 로고    scopus 로고
    • Azapeptides as pharmacological agents
    • Zega, A. Azapeptides as pharmacological agents. Curr. Med. Chem., 2005, 12, 589-597.
    • (2005) Curr. Med. Chem , vol.12 , pp. 589-597
    • Zega, A.1
  • 57
    • 33750083620 scopus 로고    scopus 로고
    • Synthesis and antitumor activity of CBI-bearing ester and carbamate prodrugs of CC-1065 analogue
    • Wang, Y.; Li, L.; Tian, Z.; Jiang, W.; Larrick, J. W. Synthesis and antitumor activity of CBI-bearing ester and carbamate prodrugs of CC-1065 analogue. Bioorg. Med. Chem. 2006, 14, 7854-7861.
    • (2006) Bioorg. Med. Chem , vol.14 , pp. 7854-7861
    • Wang, Y.1    Li, L.2    Tian, Z.3    Jiang, W.4    Larrick, J.W.5
  • 59
    • 75949122408 scopus 로고    scopus 로고
    • Mitomycins syntheses: A recent update
    • avaliable online. (mdoi:10.3762/bjoc.5.33)
    • Andez, J. C. Mitomycins syntheses: a recent update. Beilstein J. Org. Chem., 2009, 5. avaliable online. (mdoi:10.3762/bjoc.5.33)
    • (2009) Beilstein J. Org. Chem , pp. 5
    • Andez, J.C.1
  • 63
    • 68649104244 scopus 로고    scopus 로고
    • Novel semisynthetic derivatives of betulin and betulinic acid with cytotoxic activity
    • Santos, R. C.; Salvador, J. A. R.; Marin, S.; Cascante, M. Novel semisynthetic derivatives of betulin and betulinic acid with cytotoxic activity. Bioorg. Med. Chem. 2009, 17, 6241-6250.
    • (2009) Bioorg. Med. Chem , vol.17 , pp. 6241-6250
    • Santos, R.C.1    Salvador, J.A.R.2    Marin, S.3    Cascante, M.4
  • 64
    • 43049140828 scopus 로고    scopus 로고
    • New targeting system for antimycotic drugs: β-Glucosidase sensitive Amphotericin B-star poly(ethylene glycol) conjugate
    • Sedlak, M.; Dravina, P.; Bilkova, E.; Simunek, P.; Buchta, V. New targeting system for antimycotic drugs: β-Glucosidase sensitive Amphotericin B-star poly(ethylene glycol) conjugate. Bioorg. Med. Chem. Lett. 2008, 18, 2952-2956.
    • (2008) Bioorg. Med. Chem. Lett , vol.18 , pp. 2952-2956
    • Sedlak, M.1    Dravina, P.2    Bilkova, E.3    Simunek, P.4    Buchta, V.5
  • 65
    • 3142592640 scopus 로고    scopus 로고
    • New broad-spectrum parenteral cephalosporins exhibiting potent activity against both methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa. Part 3:7β-[2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-ethoxyiminoacetamido]-cephalosporins bearing 4-[3-(aminoalkyl)-ureido]-1-pyridinium at C-3'
    • Yoshizawa, H.; Kubota, T.; Itani, H.; Minami, K.; Miwa, H.; Nishitani, H. New broad-spectrum parenteral cephalosporins exhibiting potent activity against both methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa. Part 3:7β-[2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-ethoxyiminoacetamido]-cephalosporins bearing 4-[3-(aminoalkyl)-ureido]-1-pyridinium at C-3'. Bioorg. Med. Chem. 2004, 12, 4221-4231.
    • (2004) Bioorg. Med. Chem , vol.12 , pp. 4221-4231
    • Yoshizawa, H.1    Kubota, T.2    Itani, H.3    Minami, K.4    Miwa, H.5    Nishitani, H.6
  • 70
    • 0030758320 scopus 로고    scopus 로고
    • Total Syntheses and Anticholinesterase Activities of (3aS)-N(8)-Norphysostigmine, (3aS)-N(8)-Norphenserine, Their Antipodal Isomers, and Other N(8)-Substituted Analogues
    • Yu, Q. S.; Pei, X. F.; Holloway, H. W.; Greig, N. H. Total Syntheses and Anticholinesterase Activities of (3aS)-N(8)-Norphysostigmine, (3aS)-N(8)-Norphenserine, Their Antipodal Isomers, and Other N(8)-Substituted Analogues. J. Med. Chem. 1997, 40, 2895-2901.
    • (1997) J. Med. Chem , vol.40 , pp. 2895-2901
    • Yu, Q.S.1    Pei, X.F.2    Holloway, H.W.3    Greig, N.H.4
  • 71
    • 7044269372 scopus 로고    scopus 로고
    • Syntheses of photolabile novobiocin analogues
    • Shen, G.; Yu, X. M.; Blagg, B. S. J. Syntheses of photolabile novobiocin analogues. Bioorg. Med. Chem. Lett. 2004, 14, 5903-5906.
    • (2004) Bioorg. Med. Chem. Lett , vol.14 , pp. 5903-5906
    • Shen, G.1    Yu, X.M.2    Blagg, B.S.J.3
  • 73
    • 1942534224 scopus 로고    scopus 로고
    • New cationic lipids for gene transfer with high efficiency and low toxicity: T-shape cholesterol ester derivatives
    • Lee, Y.; Koo, H.; Lim, Y. B.; Lee, Y.; Moa, H.; Park, H. J. New cationic lipids for gene transfer with high efficiency and low toxicity: T-shape cholesterol ester derivatives. Bioorg. Med. Chem. Lett. 2004, 14, 2637-2641.
    • (2004) Bioorg. Med. Chem. Lett , vol.14 , pp. 2637-2641
    • Lee, Y.1    Koo, H.2    Lim, Y.B.3    Lee, Y.4    Moa, H.5    Park, H.J.6
  • 75
    • 0242662279 scopus 로고    scopus 로고
    • Synthesis and evaluation of methyl ether derivatives of the vancomycin, teicoplanin, and ristocetin aglycon methyl esters
    • McComas, C.; Crowley, B. M.; Hwang, I.; Boger, D. L. Synthesis and evaluation of methyl ether derivatives of the vancomycin, teicoplanin, and ristocetin aglycon methyl esters. Bioorg. Med. Chem. Lett. 2003, 13, 2933-2936.
    • (2003) Bioorg. Med. Chem. Lett , vol.13 , pp. 2933-2936
    • McComas, C.1    Crowley, B.M.2    Hwang, I.3    Boger, D.L.4
  • 76
    • 33847011665 scopus 로고    scopus 로고
    • High-affinity carbamate analogues of morphinan at opioid receptors
    • Peng, X.; Knapp, B. I.; Bidlack, J. M.; Neumeyer, J. N. High-affinity carbamate analogues of morphinan at opioid receptors. Bioorg. Med. Chem. Lett. 2007, 17, 1508-1511.
    • (2007) Bioorg. Med. Chem. Lett , vol.17 , pp. 1508-1511
    • Peng, X.1    Knapp, B.I.2    Bidlack, J.M.3    Neumeyer, J.N.4
  • 81
    • 33947588806 scopus 로고    scopus 로고
    • Synthesis of carbamate derivatives of iejimalides. Retention of normal antiproliferative activity and localization of binding in cancer cells
    • Schweitzer, D.; Zhu, J.; Jarori, G.; Tanaka, J.; Higa, T.; Davissona, V. J.; Helquist, P. Synthesis of carbamate derivatives of iejimalides. Retention of normal antiproliferative activity and localization of binding in cancer cells. Biorg. Med. Chem. 2007, 15, 3208-3216.
    • (2007) Biorg. Med. Chem , vol.15 , pp. 3208-3216
    • Schweitzer, D.1    Zhu, J.2    Jarori, G.3    Tanaka, J.4    Higa, T.5    Davissona, V.J.6    Helquist, P.7
  • 83
    • 22844436226 scopus 로고    scopus 로고
    • Recent advances in tumortargeting anticancer drug conjugates
    • Jaracz, S.; Chen, J.; Kuznetsova, L. V.; Ojima, I. Recent advances in tumortargeting anticancer drug conjugates. Bioorg. Med. Chem. 2005, 13, 5043-5054.
    • (2005) Bioorg. Med. Chem , vol.13 , pp. 5043-5054
    • Jaracz, S.1    Chen, J.2    Kuznetsova, L.V.3    Ojima, I.4
  • 84
    • 18144364379 scopus 로고    scopus 로고
    • New antitubulin derivatives in the combretastatin A4 series: Synthesis and biological evaluation
    • Borrel, C.; Thoret, S.; Cachet, X.; Guénard, D.; Tillequin, F.; Kocha, M.; Michel, S. New antitubulin derivatives in the combretastatin A4 series: synthesis and biological evaluation. Bioorg. Med. Chem. 2005, 13, 3853-3864.
    • (2005) Bioorg. Med. Chem , vol.13 , pp. 3853-3864
    • Borrel, C.1    Thoret, S.2    Cachet, X.3    Guénard, D.4    Tillequin, F.5    Kocha, M.6    Michel, S.7
  • 85
    • 16244388265 scopus 로고    scopus 로고
    • Novel cyclosporin derivatives featuring enhanced skin penetration despite increased molecular weight
    • Billich, A.; Vyplel, H.; Grassberger, M.; Schmook, F. P.; Steck, A. Stuetz, A. Novel cyclosporin derivatives featuring enhanced skin penetration despite increased molecular weight. Bioorg. Med. Chem. 2005, 13, 3157-3167.
    • (2005) Bioorg. Med. Chem , vol.13 , pp. 3157-3167
    • Billich, A.1    Vyplel, H.2    Grassberger, M.3    Schmook, F.P.4    Steck, A.5    Stuetz, A.6
  • 87
    • 33845362839 scopus 로고    scopus 로고
    • Design, synthesis, and preliminary evaluation of doxazolidine carbamates as prodrugs activated by carboxylesterases
    • Burkhart, D. J.; Barthel, B. L.; Post, G. C.; Kalet, B. T.; Nafie, J. W.; Shoemaker, R. K.; Koch, T. H. Design, synthesis, and preliminary evaluation of doxazolidine carbamates as prodrugs activated by carboxylesterases. J. Med. Chem. 2006, 49, 7002-7012.
    • (2006) J. Med. Chem , vol.49 , pp. 7002-7012
    • Burkhart, D.J.1    Barthel, B.L.2    Post, G.C.3    Kalet, B.T.4    Nafie, J.W.5    Shoemaker, R.K.6    Koch, T.H.7
  • 88
    • 73249148673 scopus 로고    scopus 로고
    • Carbamate Analogues of Fumagillin as Potent, Targeted Inhibitors of Methionine Aminopeptidase-2
    • C. C.; Benjamin, D. R.; Caiazzo, T. M.; Centrella, P. A.; Contonio, B. D.; Cook, C. M.; Doyle, E. G.; Hannig, G.; Labenski, M. T.; Searle, L. L.; Lind, K.; Morgan, B. A.; Olson, G.; Paradise, C. L.; Self, C.; Skinner, S. R.; Sluboski, B.; Svendsen, J. L.; Thompson, C. D.; Westlin, W.; White, K. F. Carbamate Analogues of Fumagillin as Potent, Targeted Inhibitors of Methionine Aminopeptidase-2. J. Med. Chem. 2009, 52, 8047-8056.
    • (2009) J. Med. Chem , vol.52 , pp. 8047-8056
  • 89
    • 44849120199 scopus 로고    scopus 로고
    • TrkA kinase inhibitors from a library of modified and isosteric Staurosporine aglycone
    • Tripathi, R.; Angeles, T. S.; Yang, S. X.; Mallamo, J. P. TrkA kinase inhibitors from a library of modified and isosteric Staurosporine aglycone. Bioorg. Med. Chem. Lett. 2008, 18, 3551-3555.
    • (2008) Bioorg. Med. Chem. Lett , vol.18 , pp. 3551-3555
    • Tripathi, R.1    Angeles, T.S.2    Yang, S.X.3    Mallamo, J.P.4
  • 90
    • 0037797390 scopus 로고    scopus 로고
    • Recent developments in macrolide antimicrobial research
    • Asaka, T.; Manaka, A.; Sugiyama, H. Recent developments in macrolide antimicrobial research. Curr. Top. Med. Chem. 2003, 3, 961-989.
    • (2003) Curr. Top. Med. Chem , vol.3 , pp. 961-989
    • Asaka, T.1    Manaka, A.2    Sugiyama, H.3
  • 91
    • 0038474136 scopus 로고    scopus 로고
    • Structural consideration of macrolide antibiotics in relation to the ribosomal interaction and drug design
    • Takashima, H. Structural consideration of macrolide antibiotics in relation to the ribosomal interaction and drug design. Curr. Top. Med. Chem., 2003, 3, 991-999.
    • (2003) Curr. Top. Med. Chem , vol.3 , pp. 991-999
    • Takashima, H.1
  • 94
    • 72049120150 scopus 로고    scopus 로고
    • Antioxidant activity of benzoxazolinonic and benzothiazolinonic derivatives in the LDL oxidation model
    • Yekini, I.; Hammoudi, F.; Martin-Nizard, F.; Yous, S.; Lebegue, N.; Berthelot, P.; Carato, P. Antioxidant activity of benzoxazolinonic and benzothiazolinonic derivatives in the LDL oxidation model. Bioorg. Med. Chem. 2009, 17, 7823-7830.
    • (2009) Bioorg. Med. Chem , vol.17 , pp. 7823-7830
    • Yekini, I.1    Hammoudi, F.2    Martin-Nizard, F.3    Yous, S.4    Lebegue, N.5    Berthelot, P.6    Carato, P.7
  • 96
    • 33847681052 scopus 로고    scopus 로고
    • Antituberculosis drugs: Ten years of research
    • Janin, Y. L. Antituberculosis drugs: Ten years of research. Bioorg. Med. Chem. 2007, 15, 2479-2513.
    • (2007) Bioorg. Med. Chem , vol.15 , pp. 2479-2513
    • Janin, Y.L.1
  • 100
    • 71849107576 scopus 로고    scopus 로고
    • Novel estrogen receptor (ER) modulators: Carbamate and thiocarbamate derivatives with mcarborane bisphenol structure
    • Ohta, K.; Ogawa, T.; Suzuki, T.; Ohta, S.; Endo, Y. Novel estrogen receptor (ER) modulators: Carbamate and thiocarbamate derivatives with mcarborane bisphenol structure. Bioorg. Med. Chem. 2009, 17, 7958-7963.
    • (2009) Bioorg. Med. Chem , vol.17 , pp. 7958-7963
    • Ohta, K.1    Ogawa, T.2    Suzuki, T.3    Ohta, S.4    Endo, Y.5
  • 103
    • 35348839769 scopus 로고    scopus 로고
    • Versatile use of carbon dioxide in the synthesis of organic carbamates
    • Chaturvedi, D.; Ray, S. Versatile use of carbon dioxide in the synthesis of organic carbamates. Curr. Org. Chem., 2007, 11, 987-998.
    • (2007) Curr. Org. Chem , vol.11 , pp. 987-998
    • Chaturvedi, D.1    Ray, S.2
  • 105
    • 2342477255 scopus 로고    scopus 로고
    • Organic carbonates
    • Shaikh, A. G.; Sivaram, S. Organic carbonates. Chem. Rev., 1996, 96, 951-976.
    • (1996) Chem. Rev , vol.96 , pp. 951-976
    • Shaikh, A.G.1    Sivaram, S.2
  • 106
    • 0034644564 scopus 로고    scopus 로고
    • Perspectives on alkyl carbonates in organic synthesis
    • Parrish, J. P.; Salvatore, R. N.; Jung, K. W. Perspectives on alkyl carbonates in organic synthesis. Tetrahedron, 2000, 56, 8207-8237.
    • (2000) Tetrahedron , vol.56 , pp. 8207-8237
    • Parrish, J.P.1    Salvatore, R.N.2    Jung, K.W.3
  • 107
    • 34447102805 scopus 로고    scopus 로고
    • Transformation of carbon dioxide
    • Sakakura, T.; Choi, J. C.; Yashuda, H. Transformation of carbon dioxide. Chem. Rev., 2007, 107, 2365-2387.
    • (2007) Chem. Rev , vol.107 , pp. 2365-2387
    • Sakakura, T.1    Choi, J.C.2    Yashuda, H.3
  • 108
    • 34250371029 scopus 로고    scopus 로고
    • A high yielding one-pot synthesis of dialkyl carbonates from alcohols using Mitsunobu's reagent
    • Chaturvedi, D.; Mishra, N.; Mishra, V. A high yielding one-pot synthesis of dialkyl carbonates from alcohols using Mitsunobu's reagent. Tetrahedron Lett., 2007, 48, 5043-5045.
    • (2007) Tetrahedron Lett , vol.48 , pp. 5043-5045
    • Chaturvedi, D.1    Mishra, N.2    Mishra, V.3
  • 110
    • 61849159942 scopus 로고    scopus 로고
    • The syn thesis of organic carbonates from carbon dioxide
    • Sakakura, T.; Kohno, K. The syn thesis of organic carbonates from carbon dioxide. Chem. Commun., 2009, 1312-1330.
    • (2009) Chem. Commun , pp. 1312-1330
    • Sakakura, T.1    Kohno, K.2
  • 111
    • 8344224465 scopus 로고    scopus 로고
    • 2 in supramolecular chemistry: Preparation of switchable supramolecular polymers
    • 2 in supramolecular chemistry: Preparation of switchable supramolecular polymers. Chem. Eur. J., 2004, 10, 5432-5442.
    • (2004) Chem. Eur. J , vol.10 , pp. 5432-5442
    • Xu, H.1    Rudkevich, D.M.2
  • 112
    • 34447135655 scopus 로고    scopus 로고
    • Biocatalysis in supercritical fluids, in fluorous solvents, and under solvent free conditions
    • Hobbs, H. R.; Thomas, N. R. Biocatalysis in supercritical fluids, in fluorous solvents, and under solvent free conditions. Chem. Rev., 2007, 107, 2786-2820.
    • (2007) Chem. Rev , vol.107 , pp. 2786-2820
    • Hobbs, H.R.1    Thomas, N.R.2
  • 113
    • 39349087755 scopus 로고    scopus 로고
    • An efficient, one-pot synthesis of S-alkyl thiocarbamates from the corresponding thiols using the Mitsunobu reagent
    • Chaturvedi, D.; Mishra, N.; Mishra, V. An efficient, one-pot synthesis of S-alkyl thiocarbamates from the corresponding thiols using the Mitsunobu reagent. Synthesis, 2008, 355-357.
    • (2008) Synthesis , pp. 355-357
    • Chaturvedi, D.1    Mishra, N.2    Mishra, V.3
  • 114
    • 39749092344 scopus 로고    scopus 로고
    • A high yielding, one-pot, synthesis of substituted ureas from the corresponding amines using Mitsunobu's reagent
    • Chaturvedi, D.; Mishra, N.; Mishra, V. A high yielding, one-pot, synthesis of substituted ureas from the corresponding amines using Mitsunobu's reagent. Monatsh. Chem., 2008, 139, 267-270.
    • (2008) Monatsh. Chem , vol.139 , pp. 267-270
    • Chaturvedi, D.1    Mishra, N.2    Mishra, V.3
  • 115
    • 54349121353 scopus 로고    scopus 로고
    • Triton-B catalyzed, one-pot synthesis of carbazates through alcoholic tosylates
    • Chaturvedi, D.; Chaturvedi, A. K.; Mishra, N.; Mishra, V. Triton-B catalyzed, one-pot synthesis of carbazates through alcoholic tosylates. Synth. Commun., 2008, 38, 4013-4022.
    • (2008) Synth. Commun , vol.38 , pp. 4013-4022
    • Chaturvedi, D.1    Chaturvedi, A.K.2    Mishra, N.3    Mishra, V.4
  • 116
    • 70349266468 scopus 로고    scopus 로고
    • Basic resin mediated, efficient, one-pot, synthesis of carbazates from the corresponding alkyl halides
    • Chaturvedi, D.; Chaturvedi, A. K.; Mishra, N.; Mishra, V. Basic resin mediated, efficient, one-pot, synthesis of carbazates from the corresponding alkyl halides. J. Iran. Chem. Soc., 2009, 6, 510-513.
    • (2009) J. Iran. Chem. Soc , vol.6 , pp. 510-513
    • Chaturvedi, D.1    Chaturvedi, A.K.2    Mishra, N.3    Mishra, V.4
  • 117
    • 77955967758 scopus 로고    scopus 로고
    • A high yielding one-pot synthesis of S,S-dialkyldithiocarbonates through the corresponding thiols using Mitsunobu's reagent
    • Chaturvedi, A. K.; Chaturvedi, D.; Mishra, N.; Mishra, V. A high yielding one-pot synthesis of S,S-dialkyldithiocarbonates through the corresponding thiols using Mitsunobu's reagent. J. Iran. Chem. Soc., 2010, 7, 702-706.
    • (2010) J. Iran. Chem. Soc , vol.7 , pp. 702-706
    • Chaturvedi, A.K.1    Chaturvedi, D.2    Mishra, N.3    Mishra, V.4
  • 118
    • 0001656606 scopus 로고
    • Reactions of alkyl amines with carbon dioxide
    • Wright, H. B.; Moore, M. B. Reactions of alkyl amines with carbon dioxide. J. Am. Chem. Soc., 1948, 70, 3865-3866.
    • (1948) J. Am. Chem. Soc , vol.70 , pp. 3865-3866
    • Wright, H.B.1    Moore, M.B.2
  • 119
    • 0242389015 scopus 로고
    • A direct synthesis of carbamic ester from carbon dioxide, vinyl ether and amine
    • Yoshida, Y.; Inoue, S. A direct synthesis of carbamic ester from carbon dioxide, vinyl ether and amine. Chem. Lett., 1977, 6, 1375-1376.
    • (1977) Chem. Lett , vol.6 , pp. 1375-1376
    • Yoshida, Y.1    Inoue, S.2
  • 120
    • 0006580439 scopus 로고
    • A direct synthesis of carbamate ester from carbon dioxide, amine and alkyl halide
    • Yoshida, Y.; Ishii, S.; Yamashita, T. A direct synthesis of carbamate ester from carbon dioxide, amine and alkyl halide. Chem. Lett., 1984, 13, 1571-1572.
    • (1984) Chem. Lett , vol.13 , pp. 1571-1572
    • Yoshida, Y.1    Ishii, S.2    Yamashita, T.3
  • 121
    • 0000776151 scopus 로고
    • Novel synthesis of carbamate ester from carbon dioxide, amines, and alkyl halides
    • Yoshida, Y.; Ishii, S.; Watanabe, M.; Yamashita, T. Novel synthesis of carbamate ester from carbon dioxide, amines, and alkyl halides. Bull. Chem. Soc. Jpn., 1989, 62, 1534-1538.
    • (1989) Bull. Chem. Soc. Jpn , vol.62 , pp. 1534-1538
    • Yoshida, Y.1    Ishii, S.2    Watanabe, M.3    Yamashita, T.4
  • 122
    • 84886331052 scopus 로고
    • Novel synthesis of carbamic ester from carbon dioxide, amine, and ortho ester
    • Ishii, S.; Nakayama, H.; Yoshida, Y.; Yamashita, T. Novel synthesis of carbamic ester from carbon dioxide, amine, and ortho ester. Bull. Chem. Soc. Jpn., 1989, 62, 455-458.
    • (1989) Bull. Chem. Soc. Jpn , vol.62 , pp. 455-458
    • Ishii, S.1    Nakayama, H.2    Yoshida, Y.3    Yamashita, T.4
  • 123
    • 0242294505 scopus 로고
    • A direct synthesis of monocarbamic ester of 1,2-diol from carbon dioxide, epoxide and amine
    • Yoshida, Y.; Inoue, S. A direct synthesis of monocarbamic ester of 1,2-diol from carbon dioxide, epoxide and amine. Chem. Lett., 1978, 7, 139-140.
    • (1978) Chem. Lett , vol.7 , pp. 139-140
    • Yoshida, Y.1    Inoue, S.2
  • 124
    • 0242389014 scopus 로고
    • Synthesis of carbamic ester by a reaction of carbon dioxide, tetrakis(dimethylamido)titanium(IV) and epoxide
    • Yoshida, Y.; Inoue, S. Synthesis of carbamic ester by a reaction of carbon dioxide, tetrakis(dimethylamido)titanium(IV) and epoxide. Bull. Chem. Soc. Jpn., 1978, 51, 559-560.
    • (1978) Bull. Chem. Soc. Jpn , vol.51 , pp. 559-560
    • Yoshida, Y.1    Inoue, S.2
  • 125
    • 0242294506 scopus 로고
    • Formation of carbamate derivatives by reaction of chloromethyloxirane or phenyloxirane with carbon dioxide and aliphatic amines
    • Asano, T.; Saito, N.; Ito, S.; Hatakeda, K.; Toda, T. Formation of carbamate derivatives by reaction of chloromethyloxirane or phenyloxirane with carbon dioxide and aliphatic amines. Chem. Lett., 1978, 7, 311-312.
    • (1978) Chem. Lett , vol.7 , pp. 311-312
    • Asano, T.1    Saito, N.2    Ito, S.3    Hatakeda, K.4    Toda, T.5
  • 126
    • 37049098911 scopus 로고
    • A new synthesis of carbamic esters from carbon dioxide, epoxides, and amines
    • Yoshida, Y.; Inoue, S. J. A new synthesis of carbamic esters from carbon dioxide, epoxides, and amines. Chem. Soc. Perkin Trans. I, 1979, 3146-3150.
    • (1979) Chem. Soc. Perkin Trans. I , pp. 3146-3150
    • Yoshida, Y.1    Inoue, S.J.2
  • 127
    • 33845374417 scopus 로고
    • Fixation and activation of carbon dioxide on aluminum porphyrin: Catalytic formation of a carbamic ester from carbon dioxide, amine, and epoxide
    • Christ, E.; Kojima, F.; Aida, T.; Inoue, S. Fixation and activation of carbon dioxide on aluminum porphyrin: Catalytic formation of a carbamic ester from carbon dioxide, amine, and epoxide. J. Am. Chem. Soc. 1986, 108, 391-395.
    • (1986) J. Am. Chem. Soc , vol.108 , pp. 391-395
    • Christ, E.1    Kojima, F.2    Aida, T.3    Inoue, S.4
  • 128
    • 6144237039 scopus 로고
    • Reaction of carbon dioxide with α-bromoacylophenones: Formation of oxazolidone derivatives
    • Toda, T. Reaction of carbon dioxide with α-bromoacylophenones: Formation of oxazolidone derivatives. Chem. Lett., 1977, 6, 957-958.
    • (1977) Chem. Lett , vol.6 , pp. 957-958
    • Toda, T.1
  • 129
    • 0000715112 scopus 로고
    • Formation of bis(2-oxazolidinone) derivatives by reactions of 2-methoxy-3,3-dimethyl-2-phenyloxirane or α-bromoisobutyrophenone with carbon dioxide and aliphatic α,ω-diamines
    • Saito, N.; Hatakeda, K.; Ito, S.; Asano, T.; Toda, T. Formation of bis(2-oxazolidinone) derivatives by reactions of 2-methoxy-3,3-dimethyl-2-phenyloxirane or α-bromoisobutyrophenone with carbon dioxide and aliphatic α,ω-diamines. Bull. Chem. Soc. Jpn., 1986, 59, 1629-1631.
    • (1986) Bull. Chem. Soc. Jpn , vol.59 , pp. 1629-1631
    • Saito, N.1    Hatakeda, K.2    Ito, S.3    Asano, T.4    Toda, T.5
  • 130
    • 22144440435 scopus 로고
    • Selective synthesis of five-and sixmembered cyclic carbamates by the reaction of 2-(1-haloalkyl)oxiranes with carbon dioxide and aliphatic primary amines
    • Yoshida, M.; Ohshima, M.; Toda, T. Selective synthesis of five-and sixmembered cyclic carbamates by the reaction of 2-(1-haloalkyl)oxiranes with carbon dioxide and aliphatic primary amines. Heterocycles, 1993, 35, 623-626.
    • (1993) Heterocycles , vol.35 , pp. 623-626
    • Yoshida, M.1    Ohshima, M.2    Toda, T.3
  • 131
    • 0022696514 scopus 로고
    • Novel organic synthesis using DBU [1,8-diazabicyclo[5.4.0]undec-7-ene] Facile synthesis of dialkylcarbonates and carbamates using carbon dioxide
    • Hori, Y.; Nagano, Y.; Nakao, J.; Fukuhara, T.; Taniguchi, H. Novel organic synthesis using DBU [1,8-diazabicyclo[5.4.0]undec-7-ene] Facile synthesis of dialkylcarbonates and carbamates using carbon dioxide. Chem. Express., 1986, 224-227.
    • (1986) Chem. Express , pp. 224-227
    • Hori, Y.1    Nagano, Y.2    Nakao, J.3    Fukuhara, T.4    Taniguchi, H.5
  • 132
    • 0026596070 scopus 로고
    • 2 and alkyl halides in the presence of crown-ethers
    • 2 and alkyl halides in the presence of crown-ethers. Tetrahedron, 1992, 48, 1515-1530.
    • (1992) Tetrahedron , vol.48 , pp. 1515-1530
    • Aresta, M.1    Quaranta, E.2
  • 134
    • 0001390549 scopus 로고
    • Palladium-catalyzed generation of O-allylic urethanes and carbonates from amines/alcohols, carbon dioxide, and allylic chlorides
    • McGhee, W. D.; Riley, D. P.; Christ, M. K. M. Palladium-catalyzed generation of O-allylic urethanes and carbonates from amines/alcohols, carbon dioxide, and allylic chlorides. Organometallics, 1993, 12, 1429-1433.
    • (1993) Organometallics , vol.12 , pp. 1429-1433
    • McGhee, W.D.1    Riley, D.P.2    Christ, M.K.M.3
  • 136
    • 0003060192 scopus 로고
    • Formation of cyclic urethanes from amino alcohols and carbon dioxide using phosphorus (III) reagents and halogenoalkanes
    • Kubota, Y.; Kodaka, M.; Tomohiro, T.; Okuno, H. Formation of cyclic urethanes from amino alcohols and carbon dioxide using phosphorus (III) reagents and halogenoalkanes. J. Chem. Soc. Perkin. Trans. I, 1993, 5-6.
    • (1993) J. Chem. Soc. Perkin. Trans. I , pp. 5-6
    • Kubota, Y.1    Kodaka, M.2    Tomohiro, T.3    Okuno, H.4
  • 138
    • 4444239165 scopus 로고    scopus 로고
    • Carboxylation and Mitsunobu's reaction of amines to give carbamates: Retention vs inversion of configuration is substituent dependent
    • Dinsmore, C. J.; Mercer, S. P. Carboxylation and Mitsunobu's reaction of amines to give carbamates: Retention vs inversion of configuration is substituent dependent. Org. Lett., 2004, 6, 2885-2888.
    • (2004) Org. Lett , vol.6 , pp. 2885-2888
    • Dinsmore, C.J.1    Mercer, S.P.2
  • 139
    • 31344438428 scopus 로고    scopus 로고
    • A high yielding, one-pot, Triton-B catalyzed, expeditious synthesis of carbamate esters by four component coupling methodology
    • Chaturvedi, D.; Ray, S. A high yielding, one-pot, Triton-B catalyzed, expeditious synthesis of carbamate esters by four component coupling methodology. Monatsh. Chem., 2006, 137, 201-206.
    • (2006) Monatsh. Chem , vol.137 , pp. 201-206
    • Chaturvedi, D.1    Ray, S.2
  • 140
    • 33645553201 scopus 로고    scopus 로고
    • Triton-B catalyzed, efficient, one-pot, synthesis of carbamate esters from alcoholic tosylates
    • Chaturvedi, D.; Ray, S. Triton-B catalyzed, efficient, one-pot, synthesis of carbamate esters from alcoholic tosylates. Monatsh. Chem., 2006, 137, 459-463.
    • (2006) Monatsh. Chem , vol.137 , pp. 459-463
    • Chaturvedi, D.1    Ray, S.2
  • 141
    • 33751057334 scopus 로고    scopus 로고
    • An efficient, one-pot, basic resin catalyzed, novel synthesis of carbamate esters through alcoholic tosylates
    • Chaturvedi, D.; Ray, S. An efficient, one-pot, basic resin catalyzed, novel synthesis of carbamate esters through alcoholic tosylates. Lett. Org. Chem., 2005, 2, 742-744.
    • (2005) Lett. Org. Chem , vol.2 , pp. 742-744
    • Chaturvedi, D.1    Ray, S.2
  • 142
    • 33751069833 scopus 로고    scopus 로고
    • An efficient and novel synthesis of carbamate esters from the coupling of amines, halides, carbon dioxide in the presence of basic resin
    • Chaturvedi, D.; Mishra, N.; Mishra, V. An efficient and novel synthesis of carbamate esters from the coupling of amines, halides, carbon dioxide in the presence of basic resin. Chin. Chem. Lett., 2006, 17, 1309-1312.
    • (2006) Chin. Chem. Lett , vol.17 , pp. 1309-1312
    • Chaturvedi, D.1    Mishra, N.2    Mishra, V.3
  • 143
    • 0141852869 scopus 로고    scopus 로고
    • A high yielding, one-pot, novel synthesis of carbamate esters from alcohols using Mitsunobu's reagent
    • Chaturvedi, D.; Kumar, A.; Ray, S. A high yielding, one-pot, novel synthesis of carbamate esters from alcohols using Mitsunobu's reagent. Tetrahedron Lett., 2003, 44, 7637-7639.
    • (2003) Tetrahedron Lett , vol.44 , pp. 7637-7639
    • Chaturvedi, D.1    Kumar, A.2    Ray, S.3
  • 144
    • 33845984315 scopus 로고    scopus 로고
    • An efficient, one-pot, synthesis of carbamates from the corresponding alcohols using Mitsunobu's reagent
    • Chaturvedi, D.; Mishra, N.; Mishra, V. An efficient, one-pot, synthesis of carbamates from the corresponding alcohols using Mitsunobu's reagent. Monatsh. Chem., 2007, 138, 57-60.
    • (2007) Monatsh. Chem , vol.138 , pp. 57-60
    • Chaturvedi, D.1    Mishra, N.2    Mishra, V.3
  • 145
    • 3142743924 scopus 로고    scopus 로고
    • Phosgene-free synthesis of carbamates over zeolite-based catalysts
    • Srivastava, R.; Manju, M. D.; Srinivas, D.; Ratnasamy, P. Phosgene-free synthesis of carbamates over zeolite-based catalysts. Catal. Lett., 2004, 97, 41-47.
    • (2004) Catal. Lett , vol.97 , pp. 41-47
    • Srivastava, R.1    Manju, M.D.2    Srinivas, D.3    Ratnasamy, P.4
  • 147
    • 34547931646 scopus 로고    scopus 로고
    • Mild and convenient synthesis of organic carbamates from amines and carbon dioxide using tetraethylammonium superoxide
    • Singh, K. N. Mild and convenient synthesis of organic carbamates from amines and carbon dioxide using tetraethylammonium superoxide. Synth. Commun., 2007, 37, 2651-2654.
    • (2007) Synth. Commun , vol.37 , pp. 2651-2654
    • Singh, K.N.1
  • 148
    • 57749183844 scopus 로고    scopus 로고
    • An efficient use of microwavesuperoxide combination for the synthesis of organic carbamates and dithiocarbamates
    • Singh, S. K.; Verma, M.; Singh, K. N. An efficient use of microwavesuperoxide combination for the synthesis of organic carbamates and dithiocarbamates. Ind. J. Chem., 2008, 47B, 1545-1548.
    • (2008) Ind. J. Chem , vol.47 B , pp. 1545-1548
    • Singh, S.K.1    Verma, M.2    Singh, K.N.3
  • 149
    • 0035824061 scopus 로고    scopus 로고
    • Halogen-free process for the conversion of carbon dioxide to urethanes by homogeneous catalysis
    • Alba, M.; Choi, J. C.; Sakakura, T. Halogen-free process for the conversion of carbon dioxide to urethanes by homogeneous catalysis. Chem. Commun., 2001, 2238-2239.
    • (2001) Chem. Commun , pp. 2238-2239
    • Alba, M.1    Choi, J.C.2    Sakakura, T.3
  • 151
    • 0000677554 scopus 로고
    • Ruthenium-catalyzed synthesis of vinyl carbamates from carbon dioxide, acetylene, and secondary amines
    • Sasaki, Y.; Dixneuf, P. H. Ruthenium-catalyzed synthesis of vinyl carbamates from carbon dioxide, acetylene, and secondary amines. J. Org. Chem., 1987, 52, 314-315.
    • (1987) J. Org. Chem , vol.52 , pp. 314-315
    • Sasaki, Y.1    Dixneuf, P.H.2
  • 152
    • 0000525363 scopus 로고
    • Ruthenium catalyzed reaction of carbon dioxide, amine and acetylenic alcohol
    • Sasaki, Y.; Dixneuf, P. H. Ruthenium catalyzed reaction of carbon dioxide, amine and acetylenic alcohol. J. Org. Chem., 1987, 52, 4389-4391.
    • (1987) J. Org. Chem , vol.52 , pp. 4389-4391
    • Sasaki, Y.1    Dixneuf, P.H.2
  • 153
    • 0000839405 scopus 로고
    • Ruthenium catalyzed selective synthesis of enol carbamates by fixation of carbon dioxide
    • Matsudo, T.; Hori, Y.; Yamakawa, Y.; Watanabe, Y. Ruthenium catalyzed selective synthesis of enol carbamates by fixation of carbon dioxide. Tetrahedron Lett., 1987, 28, 4417-4418.
    • (1987) Tetrahedron Lett , vol.28 , pp. 4417-4418
    • Matsudo, T.1    Hori, Y.2    Yamakawa, Y.3    Watanabe, Y.4
  • 154
    • 0001757623 scopus 로고
    • Catalytic synthesis of vinyl carbamates from carbon dioxide and alkynes with ruthenium complexes
    • Mahe, R.; Sasaki, Y.; Bruneau, C.; Dixneuf, P. H. Catalytic synthesis of vinyl carbamates from carbon dioxide and alkynes with ruthenium complexes. J. Org. Chem., 1989, 54, 1518-1523.
    • (1989) J. Org. Chem , vol.54 , pp. 1518-1523
    • Mahe, R.1    Sasaki, Y.2    Bruneau, C.3    Dixneuf, P.H.4
  • 158
    • 77955394676 scopus 로고    scopus 로고
    • Efficient synthesis of α-oxoalkyl carbamates from carbon dioxide, internal propargylic alcohols, and secondary amines catalyzed by silver salts and DBU
    • Qi, C.; Huang, L.; Jiang, H. Efficient synthesis of α-oxoalkyl carbamates from carbon dioxide, internal propargylic alcohols, and secondary amines catalyzed by silver salts and DBU Synthesis, 2010, 1433-1440.
    • (2010) Synthesis , pp. 1433-1440
    • Qi, C.1    Huang, L.2    Jiang, H.3
  • 159
    • 44249097483 scopus 로고    scopus 로고
    • Ruthenium tris(2,2,6,6-tetramethyl-3,5-heptanedionate) catalyzed synthesis of vinyl carbamates using carbon dioxide, amines and alkynes
    • Patil, Y. P.; Tambade, P. J.; Nandurkar, N. S.; Bhanage, B. M. Ruthenium tris(2,2,6,6-tetramethyl-3,5-heptanedionate) catalyzed synthesis of vinyl carbamates using carbon dioxide, amines and alkynes. Catal. Commun., 2008, 9, 2068-2072.
    • (2008) Catal. Commun , vol.9 , pp. 2068-2072
    • Patil, Y.P.1    Tambade, P.J.2    Nandurkar, N.S.3    Bhanage, B.M.4
  • 160
    • 0000774487 scopus 로고
    • Carbamate esters: A simple, mild method of formation
    • Butcher, K. J. Carbamate esters: a simple, mild method of formation. Synlett., 1994, 825-826.
    • (1994) Synlett , pp. 825-826
    • Butcher, K.J.1
  • 161
    • 0034618290 scopus 로고    scopus 로고
    • 3 promoted efficient carbonate and carbamate synthesis on solid phase
    • 3 promoted efficient carbonate and carbamate synthesis on solid phase. Org Lett., 2000, 2, 2797-2800.
    • (2000) Org Lett , vol.2 , pp. 2797-2800
    • Salvatore, R.N.1    Flander, V.L.2    Ha, D.3    Jung, K.W.4
  • 166
    • 0036346669 scopus 로고    scopus 로고
    • An efficient, one-pot synthesis of carbamate esters through alcoholic tosylates
    • Chaturvedi, D.; Kumar, A.; Ray, S. An efficient, one-pot synthesis of carbamate esters through alcoholic tosylates. Synth. Commun., 2002, 32, 2651-2655.
    • (2002) Synth. Commun , vol.32 , pp. 2651-2655
    • Chaturvedi, D.1    Kumar, A.2    Ray, S.3
  • 170
    • 0000778345 scopus 로고    scopus 로고
    • Electrogenerated -superoxide activated carbon dioxide: A new mild and safe approach to carbamates
    • Casadei, M. A.; Moracci, F. M.; Zappia, G.; Inesi, A.; Rossi, L. Electrogenerated -superoxide activated carbon dioxide: A new mild and safe approach to carbamates. J. Org. Chem., 1997, 62, 6754-6759.
    • (1997) J. Org. Chem , vol.62 , pp. 6754-6759
    • Casadei, M.A.1    Moracci, F.M.2    Zappia, G.3    Inesi, A.4    Rossi, L.5
  • 171
    • 0034606884 scopus 로고    scopus 로고
    • The reaction of amines with an electrogenerated base: Improved synthesis of arylcarbamic esters
    • Feroci, M.; Inesi, A.; Rosii, L. The reaction of amines with an electrogenerated base: Improved synthesis of arylcarbamic esters. Tetrahedron Lett., 2000, 41, 963-966.
    • (2000) Tetrahedron Lett , vol.41 , pp. 963-966
    • Feroci, M.1    Inesi, A.2    Rosii, L.3
  • 172
    • 0037068116 scopus 로고    scopus 로고
    • Synthesis of chiral oxazolidin-2-ones by 1,2-amino alcohols, carbon dioxide and electrogenerated acetonitrile anion
    • Feroci, M.; Gennaro, A.; Inesi, A.; Orsini, M.; Palombi, L. Synthesis of chiral oxazolidin-2-ones by 1,2-amino alcohols, carbon dioxide and electrogenerated acetonitrile anion. Tetrahedron Lett., 2002, 43, 5863-5865.
    • (2002) Tetrahedron Lett , vol.43 , pp. 5863-5865
    • Feroci, M.1    Gennaro, A.2    Inesi, A.3    Orsini, M.4    Palombi, L.5
  • 173
    • 0242432418 scopus 로고    scopus 로고
    • Cynomethyl anion/ carbon dioxide system: An electrogenerating carboxylating reagent. Synthesis of carbamates under mild and safe conditions
    • Feroci, M.; Casadei, A. M.; Orsini, M.; Palombi, L.; Inesi, I. Cynomethyl anion/ carbon dioxide system: An electrogenerating carboxylating reagent. Synthesis of carbamates under mild and safe conditions. J. Org. Chem., 2003, 68, 1548-1551.
    • (2003) J. Org. Chem , vol.68 , pp. 1548-1551
    • Feroci, M.1    Casadei, A.M.2    Orsini, M.3    Palombi, L.4    Inesi, I.5
  • 174
    • 33846072582 scopus 로고    scopus 로고
    • Electrochemically promoted C-N bond formation of amines and CO2 in ionic liquid [Bmim] BF4: Synthesis of carbamates
    • Feroci, M.; Orsini, M.; Rossi, L.; Sotqiu, G.; Inesi, A. Electrochemically promoted C-N bond formation of amines and CO2 in ionic liquid [Bmim] BF4: Synthesis of carbamates. J. Org. Chem., 2007, 72, 200-203.
    • (2007) J. Org. Chem , vol.72 , pp. 200-203
    • Feroci, M.1    Orsini, M.2    Rossi, L.3    Sotqiu, G.4    Inesi, A.5
  • 175
    • 0034696597 scopus 로고    scopus 로고
    • Electrosynthesis of cyclic carbamates from aziridines and carbon dioxide
    • Tascedda, P.; Dunach, E. Electrosynthesis of cyclic carbamates from aziridines and carbon dioxide. Chem. Commun., 2000, 449-450.
    • (2000) Chem. Commun , pp. 449-450
    • Tascedda, P.1    Dunach, E.2
  • 177
    • 0034695653 scopus 로고    scopus 로고
    • Catalytic production of urethanes from amines and alkyl halides in supercritical carbon dioxide
    • Yoshida, M.; Hara, N.; Okuyama, S. Catalytic production of urethanes from amines and alkyl halides in supercritical carbon dioxide. Chem. Commun., 2000, 151-151.
    • (2000) Chem. Commun , pp. 151
    • Yoshida, M.1    Hara, N.2    Okuyama, S.3
  • 178
    • 57249111542 scopus 로고    scopus 로고
    • Solvent-free ruthenium-catalyzed vinylcarbamate synthesis from phenylacetylene and diethylamine in 'supercritical' carbon dioxide
    • Rohr, M.; Geyer, C.; Wandeler, R.; Schnieder, M. S.; Murphy, E. F.; Baiker, A. Solvent-free ruthenium-catalyzed vinylcarbamate synthesis from phenylacetylene and diethylamine in 'supercritical' carbon dioxide. Green Chem., 2001, 3, 123-125.
    • (2001) Green Chem , vol.3 , pp. 123-125
    • Rohr, M.1    Geyer, C.2    Wandeler, R.3    Schnieder, M.S.4    Murphy, E.F.5    Baiker, A.6
  • 179
    • 40849085595 scopus 로고    scopus 로고
    • An efficiently and eco-friendly process for the conversion of carbon dioxide into oxazolones and oxazolidinones under supercritical conditions
    • Jiang, H.; Zhao, J.; Wang, A. An efficiently and eco-friendly process for the conversion of carbon dioxide into oxazolones and oxazolidinones under supercritical conditions. Synthesis, 2008, 763-769.
    • (2008) Synthesis , pp. 763-769
    • Jiang, H.1    Zhao, J.2    Wang, A.3
  • 181
    • 77956942530 scopus 로고    scopus 로고
    • Palladium-catalyzed carboxylative cyclization of α-allenyl amines in dense carbon dioxide
    • Kayaki, Y.; Mori, N.; Ikariya, T. Palladium-catalyzed carboxylative cyclization of α-allenyl amines in dense carbon dioxide. Tetrahedron Lett., 2009, 50, 6491-6493.
    • (2009) Tetrahedron Lett , vol.50 , pp. 6491-6493
    • Kayaki, Y.1    Mori, N.2    Ikariya, T.3
  • 182
    • 67651167979 scopus 로고    scopus 로고
    • Synthesis of organic carbamates without using phosgene: Carbonylation of amines with carbonic acid diesters
    • Carafa, M.; Quaranta, E. Synthesis of organic carbamates without using phosgene: carbonylation of amines with carbonic acid diesters. Mini-Rev. Org. Chem., 2009, 6, 168-183.
    • (2009) Mini-Rev. Org. Chem , vol.6 , pp. 168-183
    • Carafa, M.1    Quaranta, E.2
  • 183
    • 0036738434 scopus 로고    scopus 로고
    • The chemistry of dimethyl carbonate
    • Tundo, P.; Selva, M. The chemistry of dimethyl carbonate. Acc. Chem. Res., 2002, 35, 706-716.
    • (2002) Acc. Chem. Res , vol.35 , pp. 706-716
    • Tundo, P.1    Selva, M.2
  • 184
    • 0001105291 scopus 로고
    • Reactions of diethyl carbonate with amines catalyzed by metal centers
    • Porta, F.; Cenini, S.; Pizzoti, M.; Crotti, C. Reactions of diethyl carbonate with amines catalyzed by metal centers. Gazz. Chim. Ital., 1985, 115, 275-277.
    • (1985) Gazz. Chim. Ital , vol.115 , pp. 275-277
    • Porta, F.1    Cenini, S.2    Pizzoti, M.3    Crotti, C.4
  • 185
    • 0002761728 scopus 로고
    • Dimethyl carbonate: A new and versatile intermediate product
    • Romano, U.; Rivetti, F. Dimethyl carbonate: a new and versatile intermediate product. Chimica Oggi, 1984, 37-41.
    • (1984) Chimica Oggi , pp. 37-41
    • Romano, U.1    Rivetti, F.2
  • 186
    • 0002751604 scopus 로고
    • Dimethyl carbonate: A new building block for organic chemicals production
    • Mauri, M. M.; Romano, U.; Rivetti, Franco. Dimethyl carbonate: a new building block for organic chemicals production. Quad. Chim. Ital., 1985, 21, 6-12
    • (1985) Quad. Chim. Ital , vol.21 , pp. 6-12
    • Mauri, M.M.1    Romano, U.2    Franco, R.3
  • 187
    • 0000686412 scopus 로고
    • Reactivity of phosphacarbamates: Transfer of the carbamate group promoted by metal assisted electrophilic attack at the carbon dioxide moiety
    • Aresta, M.; Quaranta, E. Reactivity of phosphacarbamates: Transfer of the carbamate group promoted by metal assisted electrophilic attack at the carbon dioxide moiety. J. Org. Chem., 1988, 53, 4153-4154.
    • (1988) J. Org. Chem , vol.53 , pp. 4153-4154
    • Aresta, M.1    Quaranta, E.2
  • 189
    • 37049098823 scopus 로고
    • Preparation of urethanes from carbon dioxide via a coppercarbamato-complex
    • Tsuda, T.; Washita, H.; Watanabe, K.; Miwa, M.; Saegusa, T. Preparation of urethanes from carbon dioxide via a coppercarbamato-complex. Chem. Commun., 1978, 815-816.
    • (1978) Chem. Commun , pp. 815-816
    • Tsuda, T.1    Washita, H.2    Watanabe, K.3    Miwa, M.4    Saegusa, T.5
  • 190
    • 0006580439 scopus 로고
    • A direct synthesis of carbamate ester from amine, carbon dioxide and alkyl halide
    • Yoshida, Y.; Ishi, S.; Yamashita, T. A direct synthesis of carbamate ester from amine, carbon dioxide and alkyl halide. Chem. Lett., 1984, 13, 1571-1572.
    • (1984) Chem. Lett , vol.13 , pp. 1571-1572
    • Yoshida, Y.1    Ishi, S.2    Yamashita, T.3
  • 191
    • 49049127243 scopus 로고
    • Convenient methods for the syntheses of active carbamates, ureas and nitroso-ureas using N,N-disuccinimido carbonate
    • Takeda, K.; Akagi, Y.; Saiki, A.; Tsukahara, T.; Ogura, H. Convenient methods for the syntheses of active carbamates, ureas and nitroso-ureas using N,N-disuccinimido carbonate. Tetrahedron Lett., 1983, 24, 4569-4572.
    • (1983) Tetrahedron Lett , vol.24 , pp. 4569-4572
    • Takeda, K.1    Akagi, Y.2    Saiki, A.3    Tsukahara, T.4    Ogura, H.5
  • 192
    • 0007488939 scopus 로고
    • A synthesis of new type of alkoxy carbonylating reagents from 1,1-bis[6-(trifluoromethyl)benzotriazolyl]carbonate (BTBC) and their reactions
    • Takeda, K.; Tsuboyama, K.; Hoshino, M.; Kishino, M.; Ogura, H. A synthesis of new type of alkoxy carbonylating reagents from 1,1-bis[6-(trifluoromethyl)benzotriazolyl]carbonate (BTBC) and their reactions. Synthesis, 1987, 557-560.
    • (1987) Synthesis , pp. 557-560
    • Takeda, K.1    Tsuboyama, K.2    Hoshino, M.3    Kishino, M.4    Ogura, H.5
  • 193
    • 37049086530 scopus 로고
    • An efficient synthesis of functionalized urethanes from azides
    • Ghosh, A. K.; Mckee, S. P.; Doung, T. T.; Thompson, W. J. An efficient synthesis of functionalized urethanes from azides. Chem. Commun., 1992, 1308-1309.
    • (1992) Chem. Commun , pp. 1308-1309
    • Ghosh, A.K.1    McKee, S.P.2    Doung, T.T.3    Thompson, W.J.4
  • 194
    • 0026681169 scopus 로고
    • N,NDissuccinimidyl carbonate: A useful reagent for alkoxycarbonylation of amines
    • Ghosh, A. K.; Doung, T. T.; McKee, S. P.; Thomson, W. J. N,NDissuccinimidyl carbonate: a useful reagent for alkoxycarbonylation of amines. Tetrahedron Lett., 1992, 33, 2781-2784.
    • (1992) Tetrahedron Lett , vol.33 , pp. 2781-2784
    • Ghosh, A.K.1    Doung, T.T.2    McKee, S.P.3    Thomson, W.J.4
  • 195
    • 0027161772 scopus 로고
    • Chiral carbamates through an enzymatic alkoxycarbonylation reaction
    • Pozo, M.; Gotor, V. Chiral carbamates through an enzymatic alkoxycarbonylation reaction. Tetrahedron, 1993, 49, 4321-4326.
    • (1993) Tetrahedron , vol.49 , pp. 4321-4326
    • Pozo, M.1    Gotor, V.2
  • 196
    • 0027372682 scopus 로고
    • Chemo-enzymatic synthesis of 2′-deoxynucleoside urethanes
    • Garcia-Alles, L. F.; Morris, F.; Gotor, V. Chemo-enzymatic synthesis of 2′-deoxynucleoside urethanes. Tetrahedron Lett., 1993, 34, 6337-6340.
    • (1993) Tetrahedron Lett , vol.34 , pp. 6337-6340
    • Garcia-Alles, L.F.1    Morris, F.2    Gotor, V.3
  • 197
    • 0029053394 scopus 로고
    • Biomimetic building-up of the carbamic moiety: The intermediacy of carboxyphosphate analogues in the synthesis of N-aryl carbamate esters from arylamines and organic carbonates promoted by phosphorus acids
    • Aresta, M.; Berloco, C.; Quaranta, E. Biomimetic building-up of the carbamic moiety: the intermediacy of carboxyphosphate analogues in the synthesis of N-aryl carbamate esters from arylamines and organic carbonates promoted by phosphorus acids. Tetrahedron, 1995, 51, 8073-8088.
    • (1995) Tetrahedron , vol.51 , pp. 8073-8088
    • Aresta, M.1    Berloco, C.2    Quaranta, E.3
  • 198
    • 0032481022 scopus 로고    scopus 로고
    • One-pot conversion of azides to Boc-protected amines with trimethylphosphine and Boc-ON
    • Ariza, X.; Urpi, F.; Viladomat, C.; Vilarrasa, J. One-pot conversion of azides to Boc-protected amines with trimethylphosphine and Boc-ON. Tetrahedron Lett., 1998, 39, 9101-9102.
    • (1998) Tetrahedron Lett , vol.39 , pp. 9101-9102
    • Ariza, X.1    Urpi, F.2    Viladomat, C.3    Vilarrasa, J.4
  • 199
    • 0034339554 scopus 로고    scopus 로고
    • Direct conversion of azides and benzyl carbamates to t-butyl carbamates using polymethylhydrosiloxane and Pd-C
    • Chandrasekher, S.; Chandrauch, L.; Reddy, C. R.; Reddy, M. V. Direct conversion of azides and benzyl carbamates to t-butyl carbamates using polymethylhydrosiloxane and Pd-C. Chem. Lett., 2000, 780-781.
    • (2000) Chem. Lett , pp. 780-781
    • Chandrasekher, S.1    Chandrauch, L.2    Reddy, C.R.3    Reddy, M.V.4
  • 200
    • 0141576954 scopus 로고    scopus 로고
    • Enzymatic amidation and alkoxycarbonylation of amines using native and immobilised lipases with different origins: A comparative study
    • Castro, M. S.; Douningnez, P.; Sinisterra, J. V. Enzymatic amidation and alkoxycarbonylation of amines using native and immobilised lipases with different origins: a comparative study. Tetrahedron, 2000, 56, 1387-1391.
    • (2000) Tetrahedron , vol.56 , pp. 1387-1391
    • Castro, M.S.1    Douningnez, P.2    Sinisterra, J.V.3
  • 201
  • 202
    • 0035930766 scopus 로고    scopus 로고
    • Carbamate synthesis by solid-base catalyzed reaction of disubstituted ureas and carbonates
    • Gupte, S. P.; Shivarkar, A. B.; Chaudhari, R. V. Carbamate synthesis by solid-base catalyzed reaction of disubstituted ureas and carbonates. Chem. Commun., 2001, 2620-2621.
    • (2001) Chem. Commun , pp. 2620-2621
    • Gupte, S.P.1    Shivarkar, A.B.2    Chaudhari, R.V.3
  • 203
    • 57249096935 scopus 로고    scopus 로고
    • Catalytic activity of MCM-41-TBD in the selective preparation of carbamates and unsymmetrical alkyl carbonates from diethyl carbonate
    • Carloni, S.; Vos, D. E. D.; Jacobs, P. A.; Maggi, R.; Sartori, G.; Sartorio, R. Catalytic activity of MCM-41-TBD in the selective preparation of carbamates and unsymmetrical alkyl carbonates from diethyl carbonate. J. Catal., 2002, 205, 199-204.
    • (2002) J. Catal , vol.205 , pp. 199-204
    • Carloni, S.1    Vos, D.E.D.2    Jacobs, P.A.3    Maggi, R.4    Sartori, G.5    Sartorio, R.6
  • 204
    • 0037060049 scopus 로고    scopus 로고
    • The synthesis of alkyl carbamates from primary aliphatic amines and dialkyl carbonates in supercritical carbon dioxide
    • Selva, M.; Tundo, P.; Perosa, A. The synthesis of alkyl carbamates from primary aliphatic amines and dialkyl carbonates in supercritical carbon dioxide. Tetrahedron Lett., 2002, 43, 1217-1219.
    • (2002) Tetrahedron Lett , vol.43 , pp. 1217-1219
    • Selva, M.1    Tundo, P.2    Perosa, A.3
  • 205
    • 0344110744 scopus 로고    scopus 로고
    • Solutionphase parallel synthesis of carbamates using polymer-bound Nhydroxysuccinimide
    • Sumiyoshi, H.; Shimizu, T.; Katoh, M.; Baba, Y.; Sodeoka, M. Solutionphase parallel synthesis of carbamates using polymer-bound Nhydroxysuccinimide. Org. Lett., 2002, 4, 3923-3926.
    • (2002) Org. Lett , vol.4 , pp. 3923-3926
    • Sumiyoshi, H.1    Shimizu, T.2    Katoh, M.3    Baba, Y.4    Sodeoka, M.5
  • 206
    • 0036411008 scopus 로고    scopus 로고
    • Selective synthesis of carbamate protected polyamines using alkyl phenyl carbonates
    • Pittelkow, M.; Lewinsky, R.; Christensen, J. B. Selective synthesis of carbamate protected polyamines using alkyl phenyl carbonates. Synthesis, 2002, 2195-2202.
    • (2002) Synthesis , pp. 2195-2202
    • Pittelkow, M.1    Lewinsky, R.2    Christensen, J.B.3
  • 207
    • 0037043070 scopus 로고    scopus 로고
    • Carbamate synthesis from amines and dimethyl carbonate under ytterbium triflate catalysis
    • Curini, M.; Epifano, F.; Malterse, F.; Rosate, O. Carbamate synthesis from amines and dimethyl carbonate under ytterbium triflate catalysis. Tetrahedron Lett., 2002, 43, 4895-4897.
    • (2002) Tetrahedron Lett , vol.43 , pp. 4895-4897
    • Curini, M.1    Epifano, F.2    Malterse, F.3    Rosate, O.4
  • 208
    • 0037020638 scopus 로고    scopus 로고
    • The syntheses of carbamates from reactions of primary and secondary aliphatic amines with dimethyl carbonate in ionic liquids
    • Sima, T.; Guo, S.; Shi, F.; Deng, Y. The syntheses of carbamates from reactions of primary and secondary aliphatic amines with dimethyl carbonate in ionic liquids. Tetrahedron Lett., 2002, 43, 8145-8147.
    • (2002) Tetrahedron Lett , vol.43 , pp. 8145-8147
    • Sima, T.1    Guo, S.2    Shi, F.3    Deng, Y.4
  • 209
    • 0037175470 scopus 로고    scopus 로고
    • Chemoselective conversion of azides to t-butyl carbamates and amines
    • Jung, Y. J.; Chang, Y. M.; Lee, J. H.; Yoon, C. M. Chemoselective conversion of azides to t-butyl carbamates and amines. Tetrahedron Lett., 2002, 43, 8735-8739.
    • (2002) Tetrahedron Lett , vol.43 , pp. 8735-8739
    • Jung, Y.J.1    Chang, Y.M.2    Lee, J.H.3    Yoon, C.M.4
  • 210
    • 0037416885 scopus 로고    scopus 로고
    • Single-step conversion of Nbenzyl, N-trityl and N-diphenylmethyl amines to t-butyl carbamates using polymethylhydrosiloxane
    • Chadrasekhar, S.; Babu, B. N.; Reddy, C. R. Single-step conversion of Nbenzyl, N-trityl and N-diphenylmethyl amines to t-butyl carbamates using polymethylhydrosiloxane. Tetrahedron Lett., 2003, 44, 2057-2059.
    • (2003) Tetrahedron Lett , vol.44 , pp. 2057-2059
    • Chadrasekhar, S.1    Babu, B.N.2    Reddy, C.R.3
  • 211
    • 7444251569 scopus 로고    scopus 로고
    • Carbamate synthesis via transfunctionalization of substituted ureas and carbonates
    • Shivarkar, A. B.; Gupte, S. P.; Chaudhari, R. V. Carbamate synthesis via transfunctionalization of substituted ureas and carbonates. J. Mol. Catal. A: Chem., 2004, 223, 85-92.
    • (2004) J. Mol. Catal. A: Chem , vol.223 , pp. 85-92
    • Shivarkar, A.B.1    Gupte, S.P.2    Chaudhari, R.V.3
  • 213
    • 0742320252 scopus 로고    scopus 로고
    • Group 3 metal (Sc, La) triflates as catalysts for the carbomethoxylation of aliphatic amines with dimethylcarbonate under mild conditions
    • Distaso, M.; Quaranta, E. Group 3 metal (Sc, La) triflates as catalysts for the carbomethoxylation of aliphatic amines with dimethylcarbonate under mild conditions. Tetrahedron, 2004, 60, 1531-1539.
    • (2004) Tetrahedron , vol.60 , pp. 1531-1539
    • Distaso, M.1    Quaranta, E.2
  • 214
    • 6344278275 scopus 로고    scopus 로고
    • Carbomethoxylating reactivity of methyl phenyl carbonate toward aromatic amines in the presence of group 3 metal (Sc, La) triflate catalysts
    • Distaso, M.; Quaranta, E. Carbomethoxylating reactivity of methyl phenyl carbonate toward aromatic amines in the presence of group 3 metal (Sc, La) triflate catalysts. J. Catal., 2004, 228, 36-42.
    • (2004) J. Catal , vol.228 , pp. 36-42
    • Distaso, M.1    Quaranta, E.2
  • 217
    • 34248231984 scopus 로고    scopus 로고
    • Synthesis of carbamates from aliphatic amines and dimethyl carbonate catalyzed by acid functional ionic liquids
    • Zhou, H.; Shi, F.; Tian, X.; Zhang, Q.; Deng, Y. Synthesis of carbamates from aliphatic amines and dimethyl carbonate catalyzed by acid functional ionic liquids. J. Mol. Catal. A: Chem., 2007, 271, 89-92.
    • (2007) J. Mol. Catal. A: Chem , vol.271 , pp. 89-92
    • Zhou, H.1    Shi, F.2    Tian, X.3    Zhang, Q.4    Deng, Y.5
  • 218
    • 33847099508 scopus 로고    scopus 로고
    • Synthesis of methyl N-phenyl carbamate from dimethyl carbonate and 1,3-diphenyl urea under mild conditions
    • Gao, J. J.; Li, H. Q.; Zhang, Y. Synthesis of methyl N-phenyl carbamate from dimethyl carbonate and 1,3-diphenyl urea under mild conditions. Chin. Chem. Lett., 2007, 18, 149-151.
    • (2007) Chin. Chem. Lett , vol.18 , pp. 149-151
    • Gao, J.J.1    Li, H.Q.2    Zhang, Y.3
  • 220
    • 34247506339 scopus 로고    scopus 로고
    • Synthesis of carbamates and ureas using Zr(IV)-catalyzed exchange processes
    • Han, C.; Porco, J. A. Synthesis of carbamates and ureas using Zr(IV)-catalyzed exchange processes. Org. Lett., 2007, 9, 1517-1520.
    • (2007) Org. Lett , vol.9 , pp. 1517-1520
    • Han, C.1    Porco, J.A.2
  • 221
    • 54049097048 scopus 로고    scopus 로고
    • Non-phosgene route for the synthesis of methyl phenyl carbamate using ordered AlSBA-15 catalyst
    • Lucas, N.; Amrute, A. P.; Palraj, K.; Shanvag, G. V.; Vinu, A.; Halligudi, S. B. Non-phosgene route for the synthesis of methyl phenyl carbamate using ordered AlSBA-15 catalyst. J. Mol. Catal A: Chem., 2008, 295, 29-33.
    • (2008) J. Mol. Catal A: Chem , vol.295 , pp. 29-33
    • Lucas, N.1    Amrute, A.P.2    Palraj, K.3    Shanvag, G.V.4    Vinu, A.5    Halligudi, S.B.6
  • 222
    • 47049131787 scopus 로고    scopus 로고
    • 2-fixation reaction of 4-(benzylamino)-2-butynyl carbonates and benzoates
    • 2-fixation reaction of 4-(benzylamino)-2-butynyl carbonates and benzoates. Org. Lett., 2008, 10, 2083-2086.
    • (2008) Org. Lett , vol.10 , pp. 2083-2086
    • Yoshida, M.1    Komatsuzaki, Y.2    Ihara, M.3
  • 224
    • 58149336789 scopus 로고    scopus 로고
    • Nheterocyclic carbomethoxylation catalyzed by ionic liquids in the presence of dimethyl carbonate
    • Fu, X.; Zhang, Z.; Li, C.; Wang, L.; Ji, H.; Yang, Y.; Zhou, T.; Gao, G. Nheterocyclic carbomethoxylation catalyzed by ionic liquids in the presence of dimethyl carbonate. Cat. Commun., 2009, 10, 665-668.
    • (2009) Cat. Commun , vol.10 , pp. 665-668
    • Fu, X.1    Zhang, Z.2    Li, C.3    Wang, L.4    Ji, H.5    Yang, Y.6    Zhou, T.7    Gao, G.8
  • 225
    • 70349227448 scopus 로고    scopus 로고
    • Efficient synthesis of N-Fmocaminoalkoxy pentafluorophenyl carbonates: Application for the synthesis of oligopeptidyl carbamates
    • Sureshbabu, V. V.; Hemantha, H. P. Efficient synthesis of N-Fmocaminoalkoxy pentafluorophenyl carbonates: Application for the synthesis of oligopeptidyl carbamates. Synth. Commun., 2009, 39, 3555-3566.
    • (2009) Synth. Commun , vol.39 , pp. 3555-3566
    • Sureshbabu, V.V.1    Hemantha, H.P.2
  • 226
    • 70349611519 scopus 로고    scopus 로고
    • Amberlyst-15: A mild, efficient and reusable heterogeneous catalyst for N-tert-butoxycarbonylation of amines
    • Kumar, K. S.; Iqbal, J.; Pal, M. Amberlyst-15: A mild, efficient and reusable heterogeneous catalyst for N-tert-butoxycarbonylation of amines. Tetrahedron Lett., 2009, 50, 6244-6346.
    • (2009) Tetrahedron Lett , vol.50 , pp. 6244-6346
    • Kumar, K.S.1    Iqbal, J.2    Pal, M.3
  • 227
    • 77954311340 scopus 로고    scopus 로고
    • An expeditious, efficient green methodology for the Boc protection of amines and silyl protection of alcohols over tungstophosphoric acid-doped mesoporous silica. Tetrahedron Lett., 2010, phosphoric acid-doped mesoporous silica
    • Karmakar, B.; Banerji, J. An expeditious, efficient green methodology for the Boc protection of amines and silyl protection of alcohols over tungstophosphoric acid-doped mesoporous silica. Tetrahedron Lett., 2010, phosphoric acid-doped mesoporous silica. Tetrahedron Lett., 2010, 51, 3855-3858.
    • (2010) Tetrahedron Lett , vol.51 , pp. 3855-3858
    • Karmakar, B.1    Banerji, J.2
  • 229
    • 79151484737 scopus 로고    scopus 로고
    • Carbamate synthesis from amines and dialkyl carbonate over inexpensive and clean acidic catalyst-sulfamic acid
    • Wang, B.; He, J.; Sun, R. C. Carbamate synthesis from amines and dialkyl carbonate over inexpensive and clean acidic catalyst-sulfamic acid. Chin. Chem. Lett., 2010, 21, 794-797.
    • (2010) Chin. Chem. Lett , vol.21 , pp. 794-797
    • Wang, B.1    He, J.2    Sun, R.C.3
  • 230
    • 77953274673 scopus 로고    scopus 로고
    • Synthesis of carbamates from amines and dialkyl carbonates: Influence of leaving and entering groups
    • Tundo, P.; McElroy, C. R.; Arico, F. Synthesis of carbamates from amines and dialkyl carbonates: influence of leaving and entering groups. Synlett., 2010, 1567-1571.
    • (2010) Synlett , pp. 1567-1571
    • Tundo, P.1    McElroy, C.R.2    Arico, F.3
  • 232
    • 0034065213 scopus 로고    scopus 로고
    • Reaction of various oxiranes and carbon dioxide. synthesis and aminolysis of five-membered cyclic carbonates
    • Iwasaki, T.; Kihara, N.; Eudo, T. Reaction of various oxiranes and carbon dioxide. synthesis and aminolysis of five-membered cyclic carbonates. Bull. Chem. Soc. Jpn., 2000, 73, 713-719.
    • (2000) Bull. Chem. Soc. Jpn , vol.73 , pp. 713-719
    • Iwasaki, T.1    Kihara, N.2    Eudo, T.3


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