-
1
-
-
24344501374
-
The conjugate addition of nantiomerically pure lithium amidesas homochiral ammonia equivalents: Scope, limitations and synthetic applications
-
1:CAS:528:DC%2BD2MXpvVSqs78%3D 10.1016/j.tetasy.2005.08.006
-
S.G. Davies A.D. Smith P.D. Price 2005 The conjugate addition of nantiomerically pure lithium amidesas homochiral ammonia equivalents: Scope, limitations and synthetic applications Tetrahedron: Asymmetry 16 2833 2891 1:CAS:528:DC%2BD2MXpvVSqs78%3D 10.1016/j.tetasy.2005.08.006
-
(2005)
Tetrahedron: Asymmetry
, vol.16
, pp. 2833-2891
-
-
Davies, S.G.1
Smith, A.D.2
Price, P.D.3
-
2
-
-
0037201534
-
Recent advances in the stereoselective synthesis of β-amino acids
-
10.1016/S0040-4020(02)00991-2
-
M. Lui P. Sibi 2002 Recent advances in the stereoselective synthesis of β-amino acids Tetrahedron 58 7991 8035 10.1016/S0040-4020(02)00991-2
-
(2002)
Tetrahedron
, vol.58
, pp. 7991-8035
-
-
Lui, M.1
Sibi, P.2
-
4
-
-
0029016398
-
A convenient preparative method for β-lactams from β-amino acids using sulfenamide/triphenylphosphine
-
1:CAS:528:DyaK2MXmtFCjurc%3D 10.1016/0040-4039(95)00658-Y
-
T. Murayama T. Kobayashi T. Miura 1995 A convenient preparative method for β-lactams from β-amino acids using sulfenamide/triphenylphosphine Tetrahedron Lett 36 3703 3706 1:CAS:528:DyaK2MXmtFCjurc%3D 10.1016/0040-4039(95) 00658-Y
-
(1995)
Tetrahedron Lett
, vol.36
, pp. 3703-3706
-
-
Murayama, T.1
Kobayashi, T.2
Miura, T.3
-
5
-
-
0035799155
-
Synthesis of β-lactams and cyclo-β-dipeptides from β-amino acids: Experimental observations and theoretical analysis
-
1:CAS:528:DC%2BD3MXhsFGhtrs%3D 10.1016/S0040-4020(00)01169-8
-
J. Escalante M.A. González-Tototzin J. Aviña O. Muñoz-Muñiz E. Juaristi 2001 Synthesis of β-lactams and cyclo-β-dipeptides from β-amino acids: Experimental observations and theoretical analysis Tetrahedron 57 1883 1890 1:CAS:528:DC%2BD3MXhsFGhtrs%3D 10.1016/S0040-4020(00)01169-8
-
(2001)
Tetrahedron
, vol.57
, pp. 1883-1890
-
-
Escalante, J.1
González-Tototzin, M.A.2
Aviña, J.3
Muñoz-Muñiz, O.4
Juaristi, E.5
-
6
-
-
0037198777
-
Liquid-phase combinatorial synthesis of alicyclic β-lactams via Ugi four-component reaction
-
1:CAS:528:DC%2BD38XjsVSiu7k%3D 10.1021/ol025986r
-
S. Gedey J. Van der Eycken F. Fülöp 2002 Liquid-phase combinatorial synthesis of alicyclic β-lactams via Ugi four-component reaction Org Lett. 4 1967 1969 1:CAS:528:DC%2BD38XjsVSiu7k%3D 10.1021/ol025986r
-
(2002)
Org Lett.
, vol.4
, pp. 1967-1969
-
-
Gedey, S.1
Van Der Eycken, J.2
Fülöp, F.3
-
7
-
-
0141869057
-
Recent developments in the catalytic asymmetric synthesis of α- And β-amino acids
-
1:CAS:528:DC%2BD3sXotVWqu70%3D 10.1002/anie.200301600
-
J.A. Ma 2003 Recent developments in the catalytic asymmetric synthesis of α- and β-amino acids Angew Chem Int Ed 42 4290 4299 1:CAS:528:DC%2BD3sXotVWqu70%3D 10.1002/anie.200301600
-
(2003)
Angew Chem Int Ed
, vol.42
, pp. 4290-4299
-
-
Ma, J.A.1
-
8
-
-
63849265966
-
Scalable synthesis of β-amino esters via Reformatsky reaction with N-tert-butanesulfinyl imines
-
10.1055/s-0028-1087964
-
K. Brinner B. Doughan D.J. Poon 2009 Scalable synthesis of β-amino esters via Reformatsky reaction with N-tert-butanesulfinyl imines Synlett 6 991 993 10.1055/s-0028-1087964
-
(2009)
Synlett
, vol.6
, pp. 991-993
-
-
Brinner, K.1
Doughan, B.2
Poon, D.J.3
-
9
-
-
67549143961
-
The use of samarium enolates, a novel alternative in the addition reactions to imines. Synthesis of 3-amino esters, amides and enantiopure 3,4-diamino esters
-
1:CAS:528:DC%2BD1MXos1arur0%3D 10.1002/adsc.200900189
-
J.M. Concellon H. Rodriguez-Solla C. Simal 2009 The use of samarium enolates, a novel alternative in the addition reactions to imines. Synthesis of 3-amino esters, amides and enantiopure 3,4-diamino esters Adv Synth Catal 351 1238 1242 1:CAS:528:DC%2BD1MXos1arur0%3D 10.1002/adsc.200900189
-
(2009)
Adv Synth Catal
, vol.351
, pp. 1238-1242
-
-
Concellon, J.M.1
Rodriguez-Solla, H.2
Simal, C.3
-
10
-
-
0035532121
-
Asymmtric addition of Reformatsky-type reagent to imines utilizing diisopropyl tartrate as a chirlauxiliary
-
Ukaji Y, Takenaka S, Horita Y, Inomata K. Asymmtric addition of Reformatsky-type reagent to imines utilizing diisopropyl tartrate as a chirlauxiliary. Chem Lett, 2001, 254-255
-
(2001)
Chem Lett
, pp. 254-255
-
-
Ukaji, Y.1
Takenaka, S.2
Horita, Y.3
Inomata, K.4
-
11
-
-
0033550271
-
Enantioselective synthesis of α,α-difluoro-β-amino acid and 3,3-difluoroazetidin-2-one via the Reformatsky-type reaction of ethyl bromodifluoroacetate with chiral 1,3-oxazolidines
-
1:CAS:528:DyaK1MXnt1Sht7Y%3D 10.1021/jo990868b
-
S. Marcotte X. Pannecoucke C. Feasson J.C. Quirion 1999 Enantioselective synthesis of α,α-difluoro-β-amino acid and 3,3- difluoroazetidin-2-one via the Reformatsky-type reaction of ethyl bromodifluoroacetate with chiral 1,3-oxazolidines J Org Chem 64 8461 8464 1:CAS:528:DyaK1MXnt1Sht7Y%3D 10.1021/jo990868b
-
(1999)
J Org Chem
, vol.64
, pp. 8461-8464
-
-
Marcotte, S.1
Pannecoucke, X.2
Feasson, C.3
Quirion, J.C.4
-
12
-
-
0029972809
-
6arene) chromium (0) complexes as chiral auxiliaries: Asymmetric synthesis of β-aminoesters and β-lactams by Reformatsky condensation
-
1:CAS:528:DyaK28XhvFOmt7w%3D 10.1016/0040-4020(96)00156-1
-
6arene) chromium (0) complexes as chiral auxiliaries: Asymmetric synthesis of β-aminoesters and β-lactams by Reformatsky condensation Tetrahedron 52 4849 4856 1:CAS:528:DyaK28XhvFOmt7w%3D 10.1016/0040-4020(96)00156-1
-
(1996)
Tetrahedron
, vol.52
, pp. 4849-4856
-
-
Baldoli, C.1
Buttero, P.D.2
Licandro, E.3
Papagni, A.4
-
13
-
-
0029882551
-
Synthesis of an optically pure 3-unsubstituted β-lactam using an asymmetric Reformatsky reaction and its conversion to cholesterol absorption inhibitors
-
1:CAS:528:DyaK28XjslKlt7w%3D 10.1016/0040-4039(96)00764-2
-
B.B. Shankar M.P. Kirkup S.W. McCombie J.W. Clader A.K. Ganguly 1996 Synthesis of an optically pure 3-unsubstituted β-lactam using an asymmetric Reformatsky reaction and its conversion to cholesterol absorption inhibitors Tetrahedron Lett 37 4095 4098 1:CAS:528:DyaK28XjslKlt7w%3D 10.1016/0040-4039(96) 00764-2
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 4095-4098
-
-
Shankar, B.B.1
Kirkup, M.P.2
McCombie, S.W.3
Clader, J.W.4
Ganguly, A.K.5
-
14
-
-
20644448209
-
Highly enantioselective one-pot, three-component imino-Reformatsky reaction
-
1:CAS:528:DC%2BD2MXlsVyktL4%3D 10.1002/anie.200462757
-
P.G. Cozzi E. Rivalta 2005 Highly enantioselective one-pot, three-component imino-Reformatsky reaction Angew Chem Int Ed 44 3600 3603 1:CAS:528:DC%2BD2MXlsVyktL4%3D 10.1002/anie.200462757
-
(2005)
Angew Chem Int Ed
, vol.44
, pp. 3600-3603
-
-
Cozzi, P.G.1
Rivalta, E.2
-
15
-
-
77953299014
-
Synthesis and applications of tert-butanesulfinamide
-
1:CAS:528:DC%2BC3cXltFChsbs%3D 10.1021/cr900382t
-
M.T. Robak M.A. Herbage J.A. Ellman 2010 Synthesis and applications of tert-butanesulfinamide Chem Rev 110 3600 3740 1:CAS:528:DC%2BC3cXltFChsbs%3D 10.1021/cr900382t
-
(2010)
Chem Rev
, vol.110
, pp. 3600-3740
-
-
Robak, M.T.1
Herbage, M.A.2
Ellman, J.A.3
-
16
-
-
67649641727
-
Chiral N-phosphonyl imine chemistry: Asymmetric synthesis of α, β-diamino ester by reacting phosphonyl imines with glycine enolates
-
1:CAS:528:DC%2BD1MXosVGnt7c%3D 10.1016/j.bmcl.2009.03.001
-
T. Ai G.G. Li 2009 Chiral N-phosphonyl imine chemistry: Asymmetric synthesis of α, β-diamino ester by reacting phosphonyl imines with glycine enolates Bioorg Med Chem Lett 19 3967 3969 1:CAS:528: DC%2BD1MXosVGnt7c%3D 10.1016/j.bmcl.2009.03.001
-
(2009)
Bioorg Med Chem Lett
, vol.19
, pp. 3967-3969
-
-
Ai, T.1
Li, G.G.2
-
17
-
-
77149145199
-
Chiral N-phosphonyl imine chemistry: An efficient asymmetric synthesis of chiral N-phosphonyl propargylamines
-
1:CAS:528:DC%2BC3cXitFGkt7w%3D 10.1039/b923914f
-
P. Kaur G. Shakya H. Sun Y. Pan G.G. Li 2010 Chiral N-phosphonyl imine chemistry: An efficient asymmetric synthesis of chiral N-phosphonyl propargylamines Org Biomol Chem 8 1091 1096 1:CAS:528:DC%2BC3cXitFGkt7w%3D 10.1039/b923914f
-
(2010)
Org Biomol Chem
, vol.8
, pp. 1091-1096
-
-
Kaur, P.1
Shakya, G.2
Sun, H.3
Pan, Y.4
Li, G.G.5
-
18
-
-
77953313259
-
2AlCN using amino alcohols and BINOLs as catalysts
-
1:CAS:528:DC%2BC3cXntVentrc%3D 10.1039/c0cc00287a
-
2AlCN using amino alcohols and BINOLs as catalysts Chem Commun 46 4330 4332 1:CAS:528: DC%2BC3cXntVentrc%3D 10.1039/c0cc00287a
-
(2010)
Chem Commun
, vol.46
, pp. 4330-4332
-
-
Kaur, P.1
Pindi, S.2
Wever, W.3
Rajale, T.4
Li, G.G.5
-
19
-
-
77955135426
-
2AlCN for asymmetric catalytic Strecker reaction
-
1:CAS:528:DC%2BC3cXotlSnsbY%3D 10.1021/jo100865q
-
2AlCN for asymmetric catalytic Strecker reaction J Org Chem 75 5144 5150 1:CAS:528:DC%2BC3cXotlSnsbY%3D 10.1021/jo100865q
-
(2010)
J Org Chem
, vol.75
, pp. 5144-5150
-
-
Kaur, P.1
Pindi, S.2
Wever, W.3
Rajale, T.4
Li, G.G.5
-
20
-
-
8744311540
-
Samarium diiodide-induced asymmetric synthesis of optically pure unsymmetrical vicinal diamines by reductive cross-coupling of nitrones with N-tert-butanesulfinyl imines
-
1:CAS:528:DC%2BD2cXotVShs7Y%3D 10.1021/ol048444d
-
Y.W. Zhong M.H. Xu G.Q. Lin 2004 Samarium diiodide-induced asymmetric synthesis of optically pure unsymmetrical vicinal diamines by reductive cross-coupling of nitrones with N-tert-butanesulfinyl imines Org Lett 6 3953 3956 1:CAS:528:DC%2BD2cXotVShs7Y%3D 10.1021/ol048444d
-
(2004)
Org Lett
, vol.6
, pp. 3953-3956
-
-
Zhong, Y.W.1
Xu, M.H.2
Lin, G.Q.3
-
21
-
-
11444270931
-
2-symmetrical vicinal diamines by reductive homocoupling of chiral aromatic N-tert-butanesulfinyl imines
-
1:CAS:528:DC%2BD2cXpslegtrY%3D 10.1021/ol0479803
-
2-symmetrical vicinal diamines by reductive homocoupling of chiral aromatic N-tert-butanesulfinyl imines Org Lett 6 4747 4750 1:CAS:528:DC%2BD2cXpslegtrY%3D 10.1021/ol0479803
-
(2004)
Org Lett
, vol.6
, pp. 4747-4750
-
-
Zhong, Y.W.1
Izumi, K.2
Xu, M.H.3
Lin, G.Q.4
-
22
-
-
24144490041
-
A highly efficient and direct approach for synthesis of enantiopure β-amino alcohols by reductive cross-coupling of chiral N-tert- Butanesulfinyl imines with aldehydes
-
1:CAS:528:DC%2BD2MXntVertL4%3D 10.1021/ja054401w
-
Y.W. Zhong Y.Z. Dong K. Fang K. Izumi M.H. Xu G.Q. Lin 2005 A highly efficient and direct approach for synthesis of enantiopure β-amino alcohols by reductive cross-coupling of chiral N-tert-Butanesulfinyl imines with aldehydes J Am Chem Soc 127 11956 11957 1:CAS:528:DC%2BD2MXntVertL4%3D 10.1021/ja054401w
-
(2005)
J Am Chem Soc
, vol.127
, pp. 11956-11957
-
-
Zhong, Y.W.1
Dong, Y.Z.2
Fang, K.3
Izumi, K.4
Xu, M.H.5
Lin, G.Q.6
-
23
-
-
0032547296
-
Catalytic asymmetric oxidation of tert-butyl disulfide. Synthesis of tertbutanesulfinamides, tert-butyl sulfoxides, and tert-butanesulfinimines
-
1:CAS:528:DyaK1cXkvF2gt7c%3D 10.1021/ja9809206
-
D.A. Cogan G.C. Liu K. Kim B.J. Backes J.A. Ellman 1998 Catalytic asymmetric oxidation of tert-butyl disulfide. Synthesis of tertbutanesulfinamides, tert-butyl sulfoxides, and tert-butanesulfinimines J Am Chem Soc 120 8011 8019 1:CAS:528:DyaK1cXkvF2gt7c%3D 10.1021/ja9809206
-
(1998)
J Am Chem Soc
, vol.120
, pp. 8011-8019
-
-
Cogan, D.A.1
Liu, G.C.2
Kim, K.3
Backes, B.J.4
Ellman, J.A.5
-
24
-
-
0033582571
-
Synthesis of enantiomerically pure N-tert-Butanesulfinyl imines (tert-butanesulfinimines) by the direct condensation of tert-butanesulfinamide with aldehydes and ketones
-
1:CAS:528:DyaK1MXns1SisQ%3D%3D 10.1021/jo982059i
-
G.C. Liu D.A. Cogan T.D. Owens T.P. Tang J.A. Ellman 1999 Synthesis of enantiomerically pure N-tert-Butanesulfinyl imines (tert-butanesulfinimines) by the direct condensation of tert-butanesulfinamide with aldehydes and ketones J Org Chem 64 1278 1284 1:CAS:528:DyaK1MXns1SisQ%3D%3D 10.1021/jo982059i
-
(1999)
J Org Chem
, vol.64
, pp. 1278-1284
-
-
Liu, G.C.1
Cogan, D.A.2
Owens, T.D.3
Tang, T.P.4
Ellman, J.A.5
-
25
-
-
33744786759
-
A new route to enantiopure β-aryl-substituted β-amino acids and 4-aryl-substituted β-lactams through lipase-catalyzed enantioselective ring cleavage of β-lactams
-
10.1002/adsc.200505434
-
E. Forro T. Paal G. Tasnadi F. Fulop 2009 A new route to enantiopure β-aryl-substituted β-amino acids and 4-aryl-substituted β-lactams through lipase-catalyzed enantioselective ring cleavage of β-lactams Adv Synth Catal 348 917 923 10.1002/adsc.200505434
-
(2009)
Adv Synth Catal
, vol.348
, pp. 917-923
-
-
Forro, E.1
Paal, T.2
Tasnadi, G.3
Fulop, F.4
-
26
-
-
50149112406
-
Chlorosulfonyl isocyanate addition to o-dial-kylaminostyrenes: Preparation of 6-(o-dialkylaminophenyl) uracils
-
H. Frank S. Hans H. Roy 1982 Chlorosulfonyl isocyanate addition to o-dial-kylaminostyrenes: Preparation of 6-(o-dialkylaminophenyl) uracils Synthesis 8 662 665
-
(1982)
Synthesis
, vol.8
, pp. 662-665
-
-
Frank, H.1
Hans, S.2
Roy, H.3
-
27
-
-
79251560159
-
A simple synthesis of the first 3-amino-1-indanones
-
A. Sylvain D. Patrick R. Max 1987 A simple synthesis of the first 3-amino-1-indanones Bull Soc Chim de France 6 1079 1083
-
(1987)
Bull Soc Chim de France
, vol.6
, pp. 1079-1083
-
-
Sylvain, A.1
Patrick, D.2
Max, R.3
-
28
-
-
0032099613
-
Evidence for new non-steroidal human aromatase inhibitorsand comparison with equine aromatase inhibition for an understanding of the mammalian active site
-
1:CAS:528:DyaK1cXmsFChtrk%3D 10.1016/S0223-5234(98)80046-9
-
P. Auvray S. Moslemi P. Sourdaine S. Galopin G.E. Seralini C. Enguehard P. Dallemagne R. Bureaub P. Sonnetb S. Rault 1998 Evidence for new non-steroidal human aromatase inhibitorsand comparison with equine aromatase inhibition for an understanding of the mammalian active site Eur J Med Chem 33 451 462 1:CAS:528:DyaK1cXmsFChtrk%3D 10.1016/S0223-5234(98)80046-9
-
(1998)
Eur J Med Chem
, vol.33
, pp. 451-462
-
-
Auvray, P.1
Moslemi, S.2
Sourdaine, P.3
Galopin, S.4
Seralini, G.E.5
Enguehard, C.6
Dallemagne, P.7
Bureaub, R.8
Sonnetb, P.9
Rault, S.10
-
29
-
-
85064697204
-
2-Mediated Reformatsky reaction on aldonolactones
-
2-Mediated Reformatsky reaction on aldonolactones. Synlett, 1994, 865-867
-
(1994)
Synlett
, pp. 865-867
-
-
Hanessian, S.1
Girard, C.2
-
30
-
-
0028929020
-
2: Reformatsky reaction type selfcondensation
-
1:CAS:528:DyaK2MXktl2ru7c%3D 10.1016/0040-4039(95)00127-X
-
2: Reformatsky reaction type selfcondensation Tetrahedron Lett 36 1673 1674 1:CAS:528:DyaK2MXktl2ru7c%3D 10.1016/0040-4039(95) 00127-X
-
(1995)
Tetrahedron Lett
, vol.36
, pp. 1673-1674
-
-
Park, H.S.1
Lee, I.S.2
Kim, Y.H.3
-
31
-
-
0030029670
-
Synthesis of succinic diesters via reductive coupling of α-haloesters using samarium (II) iodide and HMPA
-
1:CAS:528:DyaK28XpslSktg%3D%3D 10.1016/0040-4039(95)02299-6
-
E. Balaux R. Ruel 1996 Synthesis of succinic diesters via reductive coupling of α-haloesters using samarium (II) iodide and HMPA Tetrahedron Lett 37 801 804 1:CAS:528:DyaK28XpslSktg%3D%3D 10.1016/0040-4039(95)02299-6
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 801-804
-
-
Balaux, E.1
Ruel, R.2
-
32
-
-
0025906166
-
An efficient β-amino acid cyclodehydation using methanesulfonyl chloride to thienamycin intermediate 3-[1-hydroxyethyl]-4- [methoxycarbonylmethyl]-azetidin-2-one
-
1:CAS:528:DyaK3MXkslWhsrw%3D 10.1016/S0040-4039(00)79908-4
-
M.F. Loewe R.J. Cvetovich G.G. Hazen 1991 An efficient β-amino acid cyclodehydation using methanesulfonyl chloride to thienamycin intermediate 3-[1-hydroxyethyl]-4-[methoxycarbonylmethyl]-azetidin-2-one Tetrahedron Lett 32 2299 2302 1:CAS:528:DyaK3MXkslWhsrw%3D 10.1016/S0040-4039(00)79908-4
-
(1991)
Tetrahedron Lett
, vol.32
, pp. 2299-2302
-
-
Loewe, M.F.1
Cvetovich, R.J.2
Hazen, G.G.3
-
33
-
-
0033534429
-
The tert-butanesulfinyl group: An ideal chiral directing group and boc-surrogate for the asymmetric aynthesis and application of β-amino acids
-
1:CAS:528:DyaK1cXotVCrsrk%3D 10.1021/jo9820824
-
T.P. Tang J.A. Ellman 1999 The tert-butanesulfinyl group: An ideal chiral directing group and boc-surrogate for the asymmetric aynthesis and application of β-amino acids J Org Chem 64 12 13 1:CAS:528:DyaK1cXotVCrsrk%3D 10.1021/jo9820824
-
(1999)
J Org Chem
, vol.64
, pp. 12-13
-
-
Tang, T.P.1
Ellman, J.A.2
-
34
-
-
0037178982
-
β-Lactams as building blocks in the synthesis of macrocyclic spermine and spermidine alkaloids
-
1:CAS:528:DC%2BD38XmsFWns74%3D 10.1016/S0040-4020(02)00731-7
-
H.H. Wasserman H. Matsuyama R.P. Robinson 2002 β-Lactams as building blocks in the synthesis of macrocyclic spermine and spermidine alkaloids Tetrahedron 58 7177 7190 1:CAS:528:DC%2BD38XmsFWns74%3D 10.1016/S0040-4020(02) 00731-7
-
(2002)
Tetrahedron
, vol.58
, pp. 7177-7190
-
-
Wasserman, H.H.1
Matsuyama, H.2
Robinson, R.P.3
-
35
-
-
32144454169
-
Stereoselective synthesis of 3-aminoindan-1-ones and subsequent incorporation into HIV-1 protease inhibitors
-
1:CAS:528:DC%2BD2MXhtlGjsL7L 10.1021/jo0521504
-
A. Arefalk J. Wannberg M. Larhed A. Hallberg 2006 Stereoselective synthesis of 3-aminoindan-1-ones and subsequent incorporation into HIV-1 protease inhibitors J Org Chem 71 1265 1268 1:CAS:528:DC%2BD2MXhtlGjsL7L 10.1021/jo0521504
-
(2006)
J Org Chem
, vol.71
, pp. 1265-1268
-
-
Arefalk, A.1
Wannberg, J.2
Larhed, M.3
Hallberg, A.4
-
36
-
-
0026015149
-
One-pot scyclization of alkoxy-3-aminoindan-1-ones
-
1:CAS:528:DyaK38XlvV2juw%3D%3D 10.1016/0040-4039(91)80160-8
-
P. Dallemagne S. Rault J.C. Pilo M.P. Foloppe M. Robba 1991 One-pot scyclization of alkoxy-3-aminoindan-1-ones Tetrahedron Lett 32 6327 6328 1:CAS:528:DyaK38XlvV2juw%3D%3D 10.1016/0040-4039(91)80160-8
-
(1991)
Tetrahedron Lett
, vol.32
, pp. 6327-6328
-
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Dallemagne, P.1
Rault, S.2
Pilo, J.C.3
Foloppe, M.P.4
Robba, M.5
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