-
1
-
-
0032560075
-
Solid phase aldol and conjugate addition reactions using Evans' oxazolidinone chiral auxiliary
-
DOI 10.1016/S0040-4039(98)00230-5, PII S0040403998002305
-
Phoon, C. W.; Abell, C. Solid-phase aldol and conjugate addition reactions using Evans' oxazolidinone chiral auxiliary. Tetrahedron Lett. 1998, 39, 2655-2658. (Pubitemid 28183943)
-
(1998)
Tetrahedron Letters
, vol.39
, Issue.17
, pp. 2655-2658
-
-
Phoon, C.W.1
Abell, C.2
-
2
-
-
0033435122
-
Enantioselective synthesis of (2S,20R)-erythro-methylphenidate
-
Prashad, M.; Liu, Y. G.; Kim, H. Y.; Repic, O.; Blacklock, T. J. Enantioselective synthesis of (2S,20R)-erythro-methylphenidate. Tetrahedron: Asymmetry 1999, 10, 3479-3482.
-
(1999)
Tetrahedron: Asymmetry
, vol.10
, pp. 3479-3482
-
-
Prashad, M.1
Liu, Y.G.2
Kim, H.Y.3
Repic, O.4
Blacklock, T.J.5
-
3
-
-
0037070078
-
Lithiated camphor-derived oxazolidinone S,N-acetals as chiral formyl anion synthons in additions to aldehydes. Asymmetric synthesis of α-hydroxy aldehydes and α-hydroxy acids
-
DOI 10.1016/S0957-4166(02)00043-5, PII S0957416602000435
-
Gawley, R. E.; Campagna, S. A.; Santiago, M.; Ren, T. Lithiated camphor-derived oxazolidinone S,N-acetals as chiral formyl anion synthons in additions to aldehydes: Asymmetric synthesis of a-hydroxy aldehydes and a-hydroxy acids. Tetraherdon: Asymmetry 2002, 13, 29-36. (Pubitemid 34219290)
-
(2002)
Tetrahedron Asymmetry
, vol.13
, Issue.1
, pp. 29-36
-
-
Gawley, R.E.1
Campagna, S.A.2
Santiago, M.3
Ren, T.4
-
4
-
-
0037147984
-
An enantioselective synthesis of sulphonamide hydroxamic acids as matrix metalloproteinase inhibitors
-
DOI 10.1016/S0040-4039(01)02151-7, PII S0040403901021517
-
Watson, R. J.; Batty, D.; Baxter, A. D.; Hannah, D. R.; Owen, D. A.; Montana, J. G. An enantioselective synthesis of sulphonamide hydroxamic acids as matrix metalloproteinase inhibitors. Tetrahedron Lett. 2002, 43, 683-685. (Pubitemid 34085042)
-
(2002)
Tetrahedron Letters
, vol.43
, Issue.4
, pp. 683-685
-
-
Watson, R.J.1
Batty, D.2
Baxter, A.D.3
Hannah, D.R.4
Owen, D.A.5
Montana, J.G.6
-
5
-
-
11144336770
-
Synthetic preparation of N-methyl-aamino acids
-
Aurelio, L.; Brownlee, R. T. C.; Hughus, A. B. Synthetic preparation of N-methyl-aamino acids. Chem. Rev. 2004, 104, 5823-5846.
-
(2004)
Chem. Rev.
, vol.104
, pp. 5823-5846
-
-
Aurelio, L.1
Brownlee, R.T.C.2
Hughus, A.B.3
-
6
-
-
7644221986
-
Synthesis of the first a-fluoro-phosphotyrosyl mimetic
-
Shi, Z. D.; Liu, H. P.; Zhang, M. C.; Yang, D. J.; Burke, Jr., T. R. Synthesis of the first a-fluoro-phosphotyrosyl mimetic. Synth. Commun. 2004, 34, 3883-3889.
-
(2004)
Synth. Commun.
, vol.34
, pp. 3883-3889
-
-
Shi, Z.D.1
Liu, H.P.2
Zhang, M.C.3
Yang, D.J.4
Burke Jr., T.R.5
-
7
-
-
14844365696
-
Streptogramins, oxazolidinones, and other inhibitors of bacterial protein synthesis
-
DOI 10.1021/cr030110z
-
Makhtar, T. M.; Wright, G. D. Streptogramins, oxazolidinones, and other inhibitors of bacterial protein synthesis. Chem. Rev. 2005, 105, 529-542. (Pubitemid 40351632)
-
(2005)
Chemical Reviews
, vol.105
, Issue.2
, pp. 529-542
-
-
Mukhtar, T.A.1
Wright, G.D.2
-
8
-
-
25444476745
-
Synthesis of (-)-amphidinolide K fragment C9-C22
-
DOI 10.1021/ol051200o
-
Andreou, T.; Costa, A. M.; Esteban, L.; Gonzalez, L.; Mas, G.; Vilarrasa, J. Synthesis of (-)-amphidinolide k fragment C9-C22. Org. Lett. 2005, 7, 4083-4086. (Pubitemid 41361534)
-
(2005)
Organic Letters
, vol.7
, Issue.19
, pp. 4083-4086
-
-
Andreou, T.1
Costa, A.M.2
Esteban, L.3
Gonzalez, L.4
Mas, G.5
Vilarrasa, J.6
-
9
-
-
0038587681
-
Oxazolidinone structure-activity relationships leading to linezolid
-
DOI 10.1002/anie.200200528
-
Barbachyn, M. R.; Ford, C. W. Oxazolidinone structure-activity relationships leading to linezolid. Angew. Chem. Int. Ed. 2003, 42, 2010-2023. (Pubitemid 36604340)
-
(2003)
Angewandte Chemie - International Edition
, vol.42
, Issue.18
, pp. 2010-2023
-
-
Barbachyn, M.R.1
Ford, C.W.2
-
10
-
-
0037821645
-
Cross-linking in the living cell locates the site of action of oxazolidinone antibiotics
-
DOI 10.1074/jbc.M302109200
-
Colca, J. R.; McDonald, W. G.; Waldon, D. J.; Thomasco, L. M.; Gadwood, R. C.; Lund, E. T.; Cavey, G. S.; Mathews, W. R.; Adams, L. D.; Cecil, E. T.; Pearson, J. D.; Bock, J. H.; Mott, J. E.; Shinabarger, D. L.; Xiong, L.; Mankin, A. S. Cross-linking in the living cell locates the site of action of oxazolidinone antibiotics. J. Biol. Chem. 2003, 278, 21972-21979. (Pubitemid 36792605)
-
(2003)
Journal of Biological Chemistry
, vol.278
, Issue.24
, pp. 21972-21979
-
-
Colca, J.R.1
McDonald, W.G.2
Waldon, D.J.3
Thomasco, L.M.4
Gadwood, R.C.5
Lund, E.T.6
Cavey, G.S.7
Mathews, W.R.8
Adams, L.D.9
Cecil, E.T.10
Pearson, J.D.11
Bock, J.H.12
Mott, J.E.13
Shinabarger, D.L.14
Xiong, L.15
Mankin, A.S.16
-
11
-
-
0037417021
-
Antipneumococcal and antistaphylococcal activities of ranbezolid (RBX 7644), a new oxazolidinone, compared to those of other agents
-
DOI 10.1128/AAC.47.3.1148-1150.2003
-
Hoellman, D. B.; Lin, G.; Ednie, L. M.; Rattan, A.; Jacobs, M. R.; Appelbaum, P. C. Antipneumococcal and antistaphylococcal activities of ranbezolid (RBX 7644), a new oxazolidinone, compared to those of other agents. Antimicrob. Agents Chemother. 2003, 47, 1148-1150. (Pubitemid 36254252)
-
(2003)
Antimicrobial Agents and Chemotherapy
, vol.47
, Issue.3
, pp. 1148-1150
-
-
Hoellman, D.B.1
Lin, G.2
Ednie, L.M.3
Rattan, A.4
Jacobs, M.R.5
Appelbaum, P.C.6
-
12
-
-
0038441366
-
Worldwide assessment of linezolid's clinical safety and tolerability: Comparator-controlled phase III studies
-
DOI 10.1128/AAC.47.6.1824-1831.2003
-
Rubinstein, E.; Isturiz, R.; Standiford, H. C.; Smith, L. G.; Oliphant, T. H.; Cammarata, S.; Hafkin, B.; Le, V.; Remington, J. Worldwide assessment of linezolid's clinical safety and tolerability: Comparator-controlled phase III studies. Antimicrob. Agents Chemother. 2003, 47, 1824-1831. (Pubitemid 36637801)
-
(2003)
Antimicrobial Agents and Chemotherapy
, vol.47
, Issue.6
, pp. 1824-1831
-
-
Rubinstein, E.1
Isturiz, R.2
Standiford, H.C.3
Smith, L.G.4
Oliphant, T.H.5
Cammarata, S.6
Hafkin, B.7
Le, V.8
Remington, J.9
-
13
-
-
0035027126
-
Oxazolidinones: New players in the battle against multi-resistant Gram-positive bacteria
-
Kaatz, G. W.; Rybak, M. J. Oxazolidinones: New players in the battle against multi-resistant Gram-positive bacteria. Emerging Drugs 2001, 6, 43-55. (Pubitemid 32381376)
-
(2001)
Emerging Drugs
, vol.6
, Issue.1
, pp. 43-55
-
-
Kaatz, G.W.1
Rybak, M.J.2
-
14
-
-
0036668114
-
In vitro activity of AZD2563, a novel oxazolidinone, against European Gram-positive cocci
-
Fluit, A. C.; Schmitz, F. J.; Verhoef, J.; Milatovic, D. In vitro activity of AZD2563, a novel oxazolidinone, against European Gram-positive cocci. J. Antimicrob. Chemother. 2002, 50, 271-276. (Pubitemid 34918860)
-
(2002)
Journal of Antimicrobial Chemotherapy
, vol.50
, Issue.2
, pp. 271-276
-
-
Fluit, A.C.1
Schmitz, F.-J.2
Verhoef, J.3
Milatovic, D.4
-
15
-
-
0343083490
-
The reactions of b-hydroxyethylamides and b-hydroxyethylcarbamates with phosgene
-
Ben-Ishai, D. The reactions of b-hydroxyethylamides and b-hydroxyethylcarbamates with phosgene. J. Am. Chem. Soc. 1956, 78, 4962-4965.
-
(1956)
J. Am. Chem. Soc.
, vol.78
, pp. 4962-4965
-
-
Ben-Ishai, D.1
-
16
-
-
0010188497
-
Formation of tetrahydro-oxazoles from a-hydroxy-banilino-a,b- diphenylethane and its homologs
-
Crowther, H. L.; McCombie, H. Formation of tetrahydro-oxazoles from a-hydroxy-banilino-a,b-diphenylethane and its homologs. J. Chem. Soc. 1913, 103, 27-31.
-
(1913)
J. Chem. Soc.
, vol.103
, pp. 27-31
-
-
Crowther, H.L.1
McCombie, H.2
-
17
-
-
0042745641
-
Chemical development on the chiral auxiliary (S)-4-(phenylmethyl)-2- oxazolidinone utilizing automated synthesis and DoE
-
DOI 10.1021/op034033l
-
Vo, L.; Ciula, J.; Gooding, O. W. Chemical development on the chiral auxiliary (S)-4-(phenylmethyl)-2-oxazolidinone utilizing automated synthesis and doe. Org. Process Res. Dev. 2003, 7, 514-520. (Pubitemid 36928387)
-
(2003)
Organic Process Research and Development
, vol.7
, Issue.4
, pp. 514-520
-
-
Vo, L.1
Ciula, J.2
Gooding, O.W.3
-
18
-
-
0002302741
-
Anticonvulsant drugs . IV: Some 2-oxazolidones
-
Close, W. J. Anticonvulsant drugs, IV: Some 2-oxazolidones. J. Am. Chem. Soc. 1951, 73, 95-98.
-
(1951)
J. Am. Chem. Soc.
, vol.73
, pp. 95-98
-
-
Close, W.J.1
-
21
-
-
67649346460
-
A new synthesis of heterocycles via carbonylation of amines with carbon monoxide in the presence of selenium
-
Yoshida, T.; Kambe, N.; Ogawa, A.; Sonoda, N. A new synthesis of heterocycles via carbonylation of amines with carbon monoxide in the presence of selenium. Phosphorus, Sulfur Silicon Relat. Elem. 1988, 38, 137-148.
-
(1988)
Phosphorus, Sulfur Silicon Relat. Elem.
, vol.38
, pp. 137-148
-
-
Yoshida, T.1
Kambe, N.2
Ogawa, A.3
Sonoda, N.4
-
22
-
-
0005515593
-
Base-catalysed direct introduction of carbon dioxide into acetylenic amines
-
Costa, M.; Chiusoli, G. P.; Rizzardi, M. Base-catalysed direct introduction of carbon dioxide into acetylenic amines. Chem. Commun. 1996, 14, 1699-1701.
-
(1996)
Chem. Commun.
, vol.14
, pp. 1699-1701
-
-
Costa, M.1
Chiusoli, G.P.2
Rizzardi, M.3
-
23
-
-
0037059469
-
Transition-metal-catalyzed reactions of propargylamine with carbon dioxide and carbon disulfide
-
DOI 10.1021/jo0014966
-
Shi, M.; Shen, Y. M. Transition-metal-catalyzed reactions of propargylamine with carbon dioxide and carbon disulfide. J. Org. Chem. 2002, 67, 16-21. (Pubitemid 34052414)
-
(2002)
Journal of Organic Chemistry
, vol.67
, Issue.1
, pp. 16-21
-
-
Shi, M.1
Shen, Y.-M.2
-
24
-
-
24944587192
-
2. Synthesis of 5-methylene-1,3-oxazolidin-2-ones
-
DOI 10.1021/jo0511804
-
Feroci, M.; Orsini, M.; Sotgiu, G.; Rossi, L.; Inesi, A. Electrochemically promoted C-N bond formation from acetylenic amines and CO2: Synthesis of 5-methylene-1,3-oxazolidin-2-ones. J. Org. Chem. 2005, 70, 7795-7798. (Pubitemid 41318549)
-
(2005)
Journal of Organic Chemistry
, vol.70
, Issue.19
, pp. 7795-7798
-
-
Feroci, M.1
Orsini, M.2
Sotgiu, G.3
Rossi, L.4
Inesi, A.5
-
25
-
-
24144465852
-
Ionic liquid as an efficient promoting medium for fixation of carbon dioxide: A clean method for the synthesis of 5-methylene-1,3-oxazolidin-2-ones from propargylic alcohols, amines, and carbon dioxide catalyzed by Cu(I) under mild conditions
-
DOI 10.1021/jo050802i
-
Gu, Y. L.; Zhang, Q. H.; Duan, Z. Y.; Zhang, J.; Zhang, S. G.; Deng, Y. Q. Ionic liquid as an efficient promoting medium for fixation of carbon dioxide: A clean method for the synthesis of 5-methylene-1,3-oxazolidin-2-ones from propargylic alcohols, amines, and carbon dioxide catalyzed by Cu(I) under mild conditions. J. Org. Chem. 2005, 70, 7376-7380. (Pubitemid 41233279)
-
(2005)
Journal of Organic Chemistry
, vol.70
, Issue.18
, pp. 7376-7380
-
-
Gu, Y.1
Zhang, Q.2
Duan, Z.3
Zhang, J.4
Zhang, S.5
Deng, Y.6
-
26
-
-
56949102894
-
Silver-catalyzed activation of internal propargylic alcohols in supercritical carbon dioxide: Efficient and eco-friendly synthesis of 4-alkylidene-1,3-oxazolidin-2-ones
-
Jiang, H. F.; Zhao, J. W. Silver-catalyzed activation of internal propargylic alcohols in supercritical carbon dioxide: Efficient and eco-friendly synthesis of 4-alkylidene-1,3-oxazolidin-2-ones. Tetrahedron Lett. 2009, 50, 60-62.
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 60-62
-
-
Jiang, H.F.1
Zhao, J.W.2
-
27
-
-
3242723482
-
(Salen)chromium(III)/DMAP: An efficient catalyst system for the selective synthesis of 5-substituted oxazolidinones from carbon dioxide and aziridines
-
DOI 10.1021/ol049689t
-
Miller, A. W.; Nguyen, S. T. (Salen)chromium(III)=DMAP: An efficient catalyst system for the selective synthesis of 5-substituted oxazolidinones from carbon dioxide and aziridines. Org. Lett. 2004, 6, 2301-2304. (Pubitemid 38952525)
-
(2004)
Organic Letters
, vol.6
, Issue.14
, pp. 2301-2304
-
-
Miller, A.W.1
Nguyen, S.T.2
-
28
-
-
67649378629
-
Zirconyl chloride: An efficient recyclable catalyst for synthesis of 5-aryl-2-oxazolidines from aziridines and CO2 under solvent-free conditions
-
Wu, Y.; He, L. N.; Du, Y.; Wang, J. Q.; Miao, C. X.; Li, W. Zirconyl chloride: An efficient recyclable catalyst for synthesis of 5-aryl-2- oxazolidines from aziridines and CO2 under solvent-free conditions. Tetrahedron 2009, 65, 6204-6210.
-
(2009)
Tetrahedron
, vol.65
, pp. 6204-6210
-
-
Wu, Y.1
He, L.N.2
Du, Y.3
Wang, J.Q.4
Miao, C.X.5
Li, W.6
-
29
-
-
73449108431
-
Naturally occuring a-amino acid: A simple and inexpensive catalyst for the selective synthesis of 5-aryl-2-oxazolidinones from CO2 and aziridines under solvent-free conditions
-
Jiang, H. F.; Ye, J. W.; Qi, C. R.; Huang, L. B. Naturally occuring a-amino acid: A simple and inexpensive catalyst for the selective synthesis of 5-aryl-2-oxazolidinones from CO2 and aziridines under solvent-free conditions. Tetrahedron Lett. 2010, 51, 928-932.
-
(2010)
Tetrahedron Lett.
, vol.51
, pp. 928-932
-
-
Jiang, H.F.1
Ye, J.W.2
Qi, C.R.3
Huang, L.B.4
-
30
-
-
4544249177
-
Chemical fixation of carbon dioxide co-catalyzed by a combination of Schiff bases or phenols and organic bases
-
Shen, Y. M.; Duan, W. L.; Shi, M. Chemical fixation of carbon dioxide co-catalyzed by a combination of Schiff bases or phenols and organic bases. Eur. J. Org. Chem. 2004, 3080-3089.
-
(2004)
Eur. J. Org. Chem.
, pp. 3080-3089
-
-
Shen, Y.M.1
Duan, W.L.2
Shi, M.3
-
31
-
-
0037863152
-
A convenient and inexpensive conversion of an aziridine to an oxazolidinone
-
DOI 10.1016/S0040-4039(03)01325-X
-
Hancock, M. T.; Pinhas, A. R. A convenient and inexpensive conversion of an aziridine to an oxazolidinone. Tetrahedron Lett. 2003, 44, 5457-5460. (Pubitemid 36782223)
-
(2003)
Tetrahedron Letters
, vol.44
, Issue.29
, pp. 5457-5460
-
-
Hancock, M.T.1
Pinhas, A.R.2
-
32
-
-
1642578982
-
N-Tosylaziridine, a new substrate for chemical fixation of carbon dioxide via ring expansion reaction under atmospheric pressure
-
DOI 10.1016/j.tetlet.2003.12.052
-
Sudo, T.; Morioka, Y.; Sanda, F.; Endo, T. N-Tosylaziridine, a new substrate for chemical fixation of carbon dioxide via ring-expansion reaction under atmospheric pressure. Tetrahedron Lett. 2004, 45, 1363-1365. (Pubitemid 38134306)
-
(2004)
Tetrahedron Letters
, vol.45
, Issue.7
, pp. 1363-1365
-
-
Sudo, A.1
Morioka, Y.2
Sanda, F.3
Endo, T.4
-
33
-
-
0141537065
-
Highly efficient chemical fixations of carbon dioxide and carbon disulfide by cycloaddition to aziridine under atmospheric pressure
-
DOI 10.1016/j.tetlet.2003.09.011
-
Sudo, A.; Morioka, Y.; Koizumi, E.; Sanda, F.; Endo, T. Highly efficient chemical fixations of carbon dioxide and carbon disulfide by cycloaddition to aziridine under atmospheric pressure. Tetrahedron Lett. 2003, 44, 7889-7891. (Pubitemid 37186940)
-
(2003)
Tetrahedron Letters
, vol.44
, Issue.43
, pp. 7889-7891
-
-
Sudo, A.1
Morioka, Y.2
Koizumi, E.3
Sanda, F.4
Endo, T.5
-
34
-
-
0037140896
-
Regioselectivity and selective enhancement of carbon dioxide fixation of 2-substituted aziridines to 2-oxazolidinones under supercritical conditions
-
DOI 10.1016/S0040-4039(02)00676-7, PII S0040403902006767
-
Kawanami, H.; Ikushima, Y. Regioselectivity and selective enhancement of carbon dioxide fixation of 2-substituted aziridines to 2-oxazolidinones under supercritical conditions. Tetrahedron Lett. 2002, 43, 3841-3844. (Pubitemid 34463044)
-
(2002)
Tetrahedron Letters
, vol.43
, Issue.21
, pp. 3841-3844
-
-
Kawanami, H.1
Ikushima, Y.2
-
35
-
-
17144423642
-
2 fixation with aziridine to 2-oxazolidinone
-
DOI 10.1246/cl.2005.60
-
Kawanami, H.; Matsumoto, H.; Ikushima, Y. Effective scCO2-ionic liquid reaction system based on symmetric aliphatic ammonium salts for the rapid CO2 fixation with aziridine to 2-oxazolidinone. Chem. Lett. 2005, 34, 60-61. (Pubitemid 40522891)
-
(2005)
Chemistry Letters
, vol.34
, Issue.1
, pp. 60-61
-
-
Kawanami, H.1
Matsumoto, H.2
Ikushima, Y.3
-
36
-
-
0034696597
-
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, 6, 449-450. (Pubitemid 30169617)
-
(2000)
Chemical Communications
, Issue.6
, pp. 449-450
-
-
Tascedda, P.1
Dunach, E.2
-
37
-
-
1042279652
-
Synthesis of Thermoresponsive Polyurethane from 2-Methylaziridine and Supercritical Carbon Dioxide
-
DOI 10.1002/anie.200352215
-
Ihata, O.; Kayaki, Y.; Ikariya, T. Synthesis of thermoresponsive polyurethane from 2-methylaziridine and supercritical carbon dioxide. Angew. Chem. Int. Ed. 2004, 43, 717-719. (Pubitemid 38197051)
-
(2004)
Angewandte Chemie - International Edition
, vol.43
, Issue.6
, pp. 717-719
-
-
Ihata, O.1
Kayaki, Y.2
Ikariya, T.3
-
38
-
-
23744476108
-
Aliphatic poly(urethane-amine)s synthesized by copolymerization of aziridines and supercritical carbon dioxide
-
DOI 10.1021/ma050549o
-
Ihata, O.; Kayaki, Y. Aliphatic poly(urethane-amine)s synthesized by copolymerization of aziridines and supercritical carbon dioxide. Macromolecules 2005, 38, 6429-6434. (Pubitemid 41118703)
-
(2005)
Macromolecules
, vol.38
, Issue.15
, pp. 6429-6434
-
-
Ihata, O.1
Kayaki, Y.2
Ikariya, T.3
-
39
-
-
45249084548
-
Quaternary ammonium bromide functionalized polyethylene glycol: A highly efficient and recyclable catalyst for selective synthesis of 5-aryl-2-oxazolidinones from carbon dioxide and aziridines under solvent-free conditions
-
DOI 10.1021/jo800269v
-
Du, Y.; Wu, Y.; Liu, A. H.; He, L. N. Quaternary ammonium bromide functionalized polyethylene glycol: A highly efficient and recyclable catalyst for selective synthesis of 5-Aryl-2-oxazolidinones from carbon dioxide and aziridines under solvent-free conditions. J. Org. Chem. 2008, 73, 4709-4712. (Pubitemid 351842496)
-
(2008)
Journal of Organic Chemistry
, vol.73
, Issue.12
, pp. 4709-4712
-
-
Du, Y.1
Wu, Y.2
Liu, A.-H.3
He, L.-N.4
-
40
-
-
53849109164
-
Copper-catalyzed four-component coupling between aldehydes, amines, alkynes, and carbon dioxide
-
Yoo, W. J.; Li, C. J. Copper-catalyzed four-component coupling between aldehydes, amines, alkynes, and carbon dioxide. Adv. Synth. Catal. 2008, 350, 1503-1506.
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 1503-1506
-
-
Yoo, W.J.1
Li, C.J.2
-
41
-
-
33847042273
-
Naturally occurring a-amino acid-catalyzed coupling of carbon dioxide with epoxides to afford cyclic carbonates
-
Qi, C. R.; Jiang, H. F.; Wang, Z. Y.; Zou, B.; Yang, S. R. Naturally occurring a-amino acid-catalyzed coupling of carbon dioxide with epoxides to afford cyclic carbonates. Synlett 2007, 2, 255-258.
-
(2007)
Synlett
, vol.2
, pp. 255-258
-
-
Qi, C.R.1
Jiang, H.F.2
Wang, Z.Y.3
Zou, B.4
Yang, S.R.5
-
42
-
-
50849134879
-
Coupling of carbon dioxide with epoxides catalyzed by amino acid hydrochloride salts
-
Jiang, H. F.; Qi, C. R.; Yuan, B. Z. Coupling of carbon dioxide with epoxides catalyzed by amino acid hydrochloride salts. Chin. J. Chem. 2008, 26, 1305-1308.
-
(2008)
Chin. J. Chem.
, vol.26
, pp. 1305-1308
-
-
Jiang, H.F.1
Qi, C.R.2
Yuan, B.Z.3
-
43
-
-
0037170944
-
Amino acids and peptides as asymmetric organocatalysts
-
DOI 10.1016/S0040-4020(02)00122-9, PII S0040402002001229
-
Jarvo, E. R.; Miller, S. J. Amino acids and peptides as asymmetric organocatalysts. Tetrahedron 2002, 58, 2481-2495. (Pubitemid 34251135)
-
(2002)
Tetrahedron
, vol.58
, Issue.13
, pp. 2481-2495
-
-
Jarvo, E.R.1
Miller, S.J.2
-
44
-
-
0032546129
-
Development and applications of amino acid-derived chiral acylnitroso hetero Diels-Alder reactions
-
DOI 10.1016/S0040-4020(97)10072-2, PII S0040402097100722
-
Vogt, P. F.; Miller, M. J. Development and applications of amino acid-derived chiral acylnitroso hetero Diels-Alder reactions. Tetrahedron 1998, 54, 1317-1348. (Pubitemid 28052880)
-
(1998)
Tetrahedron
, vol.54
, Issue.8
, pp. 1317-1348
-
-
Vogt, P.F.1
Miller, M.J.2
-
45
-
-
31544472868
-
Amino acid-catalyzed asymmetric carbohydrate formation: Organocatalytic one-step de novo synthesis of keto and amino sugars
-
DOI 10.1002/adsc.200505323
-
Ibrahem, I.; Zou, W. B.; Xu, Y. M.; Cordova, A. Amino acid-catalyzed asymmetric carbohydrate formation: Organocatalytic one-step De Novo synthesis of keto and amino sugars. Adv. Synth. Catal. 2006, 348, 211-222. (Pubitemid 43155993)
-
(2006)
Advanced Synthesis and Catalysis
, vol.348
, Issue.1-2
, pp. 211-222
-
-
Ibrahem, I.1
Zou, W.2
Xu, Y.3
Cordova, A.4
-
46
-
-
0037043180
-
Proline-catalyzed asymmetric reactions
-
DOI 10.1016/S0040-4020(02)00516-1, PII S0040402002005161
-
List, B. Proline-catalyzed asymmetric reactions. Tetrahedron 2002, 58, 5573-5590. (Pubitemid 34722894)
-
(2002)
Tetrahedron
, vol.58
, Issue.28
, pp. 5573-5590
-
-
List, B.1
-
47
-
-
4344693780
-
Direct proline-catalyzed asymmetric α-aminoxylation of aldehydes and ketones
-
DOI 10.1021/jo049338s
-
Hayashi, Y.; Yamaguchi, J.; Sumiya, T.; Hibino, K.; Shoji, M. Direct proline-catalyzed asymmetric a-aminoxylation of aldehydes and ketones. J. Org. Chem. 2004, 69, 5966-5973. (Pubitemid 39145672)
-
(2004)
Journal of Organic Chemistry
, vol.69
, Issue.18
, pp. 5966-5973
-
-
Hayashi, Y.1
Yamaguchi, J.2
Sumiya, T.3
Hibino, K.4
Shoji, M.5
-
48
-
-
27844446612
-
Development and applications of amino acid derived organometallics
-
DOI 10.1055/s-2005-918950, A38805ST
-
Rilatt, I.; Caggiano, L.; Jackson, R. F. W. Development and applications of amino acid derived organometallics. Synlett 2005, 18, 2701-2719. (Pubitemid 41654278)
-
(2005)
Synlett
, Issue.18
, pp. 2701-2719
-
-
Rilatt, I.1
Caggiano, L.2
Jackson, R.F.W.3
-
49
-
-
45249123858
-
Organocatalytic asymmetric synthesis using proline and related molecules, part 2
-
Kotsuki, H.; Ikishima, H.; Okuyama, A. Organocatalytic asymmetric synthesis using proline and related molecules, part 2. Heterocycles 2008, 75, 757-797.
-
(2008)
Heterocycles
, vol.75
, pp. 757-797
-
-
Kotsuki, H.1
Ikishima, H.2
Okuyama, A.3
-
50
-
-
43849098896
-
Organocatalytic asymmetric synthesis using proline and related molecules, part 1
-
Kotsuki, H.; Ikishima, H.; Okuyama, A. Organocatalytic asymmetric synthesis using proline and related molecules, part 1. Heterocycles 2008, 75, 493-529.
-
(2008)
Heterocycles
, vol.75
, pp. 493-529
-
-
Kotsuki, H.1
Ikishima, H.2
Okuyama, A.3
-
51
-
-
0015976969
-
Copolymerization of carbon dioxide with propyleneimine
-
Soga, K.; Chiang, W. Y.; Ikeda, S. Copolymerization of carbon dioxide with propyleneimine. J. Polym. Sci. Polym. Chem. Ed. 1974, 12, 121-131.
-
(1974)
J. Polym. Sci. Polym. Chem. Ed.
, vol.12
, pp. 121-131
-
-
Soga, K.1
Chiang, W.Y.2
Ikeda, S.3
-
52
-
-
77954215842
-
Facile synthesis of oxazolidinones catalyzed by n-Bu4NBr3=n-Bu4NBr directly from olefins, chloramine-T, and carbon dioxide
-
Kong, D. L.; He, L. N.; Wang, J. Q. Facile synthesis of oxazolidinones catalyzed by n-Bu4NBr3=n-Bu4NBr directly from olefins, chloramine-T, and carbon dioxide. Catal. Commun. 2010, 11, 992-995.
-
(2010)
Catal. Commun.
, vol.11
, pp. 992-995
-
-
Kong, D.L.1
He, L.N.2
Wang, J.Q.3
-
53
-
-
24044445511
-
Directed ortho lithiation of N-alkylphenylaziridines
-
DOI 10.1021/ol051412l
-
Capriati, V.; Florio, S.; Luisi, R.; Musio, B. Directed ortho lithiation of N-alkylphenylaziridines. Org. Lett. 2005, 7, 3749-3752. (Pubitemid 41224566)
-
(2005)
Organic Letters
, vol.7
, Issue.17
, pp. 3749-3752
-
-
Capriati, V.1
Florio, S.2
Luisi, R.3
Musio, B.4
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