-
1
-
-
7644242223
-
One-pot stereoselective synthesis of anti 3-alkyl and 3-aryl-N-p-tosyl-aziridine-2-ketones and 3-aryl-N-p-tosyl-aziridine-2- carboxylates
-
Chen D, Timmons C, Guo L, Xu X, Li G. One-pot stereoselective synthesis of anti 3-alkyl and 3-aryl-N-p-tosyl-aziridine-2-ketones and 3-aryl-N-p-tosyl-aziridine-2-carboxylates. Synthesis, 2004, 2479-2484
-
(2004)
Synthesis
, pp. 2479-2484
-
-
Chen, D.1
Timmons, C.2
Guo, L.3
Xu, X.4
Li, G.5
-
2
-
-
15044365017
-
Functionalization of α,β-unsaturated esters and ketones: A facile and highly stereoselective one-pot approach to N-protected α,β-dehydroamino acid derivatives
-
DOI 10.1021/ol050002u
-
D. Chen L. Guo J. Liu S. Kirtane J.F. Cannon G. Li 2005 Functionalization of α,β-unsaturated esters and ketones: a facile and highly stereoselective one-pot approach to N-protected α,β-dehydroamino acid derivatives Org Lett 7 921 924 1:CAS:528:DC%2BD2MXpslSisw%3D%3D 10.1021/ol050002u (Pubitemid 40380259)
-
(2005)
Organic Letters
, vol.7
, Issue.5
, pp. 921-924
-
-
Chen, D.1
Guo, L.2
Liu, J.3
Kirtane, S.4
Cannon, J.F.5
Li, G.6
-
3
-
-
0000567366
-
-
B.M. Trost I. Fleming (eds). Pergamon Press Oxford. 10.1016/B978-0-08- 052349-1.00199-2
-
Kemp JE. In: Trost BM, Fleming I, Eds. Comprehensive Organic Synthesis, Vol. 3. Oxford: Pergamon Press, 1991, 469-513
-
(1991)
Comprehensive Organic Synthesis
, pp. 469-513
-
-
Kemp, J.E.1
-
4
-
-
0034001395
-
A new class of conformationally rigid analogues of 4-amino-5- halopentanoic acids, potent inactivators of γ-aminobutyric acid aminotransferase
-
DOI 10.1021/jm9904755
-
J. Qiu R.B. Silverman 2000 A new class of conformationally rigid analogues of 4-amino-5-halopentanoic acids, potent inactivators of gammaaminobutyric acid aminotransferase J Med Chem 43 706 720 1:CAS:528:DC%2BD3cXotl2htg%3D%3D 10.1021/jm9904755 (Pubitemid 30127165)
-
(2000)
Journal of Medicinal Chemistry
, vol.43
, Issue.4
, pp. 706-720
-
-
Qiu, J.1
Silverman, R.B.2
-
5
-
-
33746588233
-
A general process for the haloamidation of olefins. Scope and mechanism
-
DOI 10.1021/ja063675w
-
Y. Yeung X. Gao E.J. Corey 2006 A general process for the haloamidation of olefins. Scope and mechanism J Am Chem Soc 128 9644 9645 1:CAS:528: DC%2BD28XmvFWitbg%3D 10.1021/ja063675w (Pubitemid 44147944)
-
(2006)
Journal of the American Chemical Society
, vol.128
, Issue.30
, pp. 9644-9645
-
-
Yeung, Y.-Y.1
Gao, X.2
Corey, E.J.3
-
6
-
-
0000288777
-
Total synthesis of allosamidin: An application of the sulfonamidoglycosylation of glycals
-
1:CAS:528:DyaK3MXkslajurc%3D 10.1021/ja00015a051
-
D.A. Griffith S.J. Danishefsky 1991 Total synthesis of allosamidin: An application of the sulfonamidoglycosylation of glycals J Am Chem Soc 113 5863 5864 1:CAS:528:DyaK3MXkslajurc%3D 10.1021/ja00015a051
-
(1991)
J Am Chem Soc
, vol.113
, pp. 5863-5864
-
-
Griffith, D.A.1
Danishefsky, S.J.2
-
7
-
-
0000870450
-
Addition of N,N-dichlorosulfonamides to unsaturates
-
1:CAS:528:DyaF1MXkslSjug%3D%3D 10.1021/jo01276a006
-
F.A. Daniher P.E. Butler 1968 Addition of N,N-dichlorosulfonamides to unsaturates J Org Chem 33 4336 4340 1:CAS:528:DyaF1MXkslSjug%3D%3D 10.1021/jo01276a006
-
(1968)
J Org Chem
, vol.33
, pp. 4336-4340
-
-
Daniher, F.A.1
Butler, P.E.2
-
8
-
-
0000668913
-
Addition of N,N-dichlorocarbamtes to conjugated dienes
-
1:CAS:528:DyaF1cXksVegurs%3D 10.1021/jo01271a006
-
F.A. Daniher P.E. Butler 1968 Addition of N,N-dichlorocarbamtes to conjugated dienes J Org Chem 33 2637 2642 1:CAS:528:DyaF1cXksVegurs%3D 10.1021/jo01271a006
-
(1968)
J Org Chem
, vol.33
, pp. 2637-2642
-
-
Daniher, F.A.1
Butler, P.E.2
-
9
-
-
33746051891
-
Evidence for nucleophilicity of N,N-dihalosulfonamide oxygen atoms in addition of N,N-dichlorobenzenesulfonamide to cis- and trans-but-2-ene
-
F.A. Daniher M.T. Melchior P.E. Butler 1968 Evidence for nucleophilicity of N,N-dihalosulfonamide oxygen atoms in addition of N,N- dichlorobenzenesulfonamide to cis- and trans-but-2-ene Chem Commun 16 931 932
-
(1968)
Chem Commun
, vol.16
, pp. 931-932
-
-
Daniher, F.A.1
Melchior, M.T.2
Butler, P.E.3
-
10
-
-
0025743055
-
Stereoselective synthesis of protected amines and diamines from alkenes using N,N-dichloro-tert-butylcarbamate
-
1:CAS:528:DyaK3MXmtVOrsrk%3D 10.1016/0040-4039(91)80624-F
-
B.S. Orlek G. Stemp 1991 Stereoselective synthesis of protected amines and diamines from alkenes using N,N-dichloro-tert-butylcarbamate Tetrahedron Lett 32 4045 4048 1:CAS:528:DyaK3MXmtVOrsrk%3D 10.1016/0040-4039(91)80624-F
-
(1991)
Tetrahedron Lett
, vol.32
, pp. 4045-4048
-
-
Orlek, B.S.1
Stemp, G.2
-
11
-
-
9144225503
-
Palladium(II)-catalyzed intramolecular aminobromination and aminochlorination of olefins
-
1:CAS:528:DC%2BD2cXosVShu78%3D 10.1021/om049432z
-
M.R. Manzoni T.P. Zabawa D. Kasi S.R. Chemler 2004 Palladium(II)- catalyzed intramolecular aminobromination and aminochlorination of olefins Organometallics 23 5618 5621 1:CAS:528:DC%2BD2cXosVShu78%3D 10.1021/om049432z
-
(2004)
Organometallics
, vol.23
, pp. 5618-5621
-
-
Manzoni, M.R.1
Zabawa, T.P.2
Kasi, D.3
Chemler, S.R.4
-
13
-
-
0001071513
-
Transition metal-catalyzed regioselective and stereoselective aminochlorination of cinnamic esters
-
1:CAS:528:DyaK1MXjvFGhurc%3D 10.1021/ol990059e
-
G. Li H. Wei S. Kim M. Neighbors 1999 Transition metal-catalyzed regioselective and stereoselective aminochlorination of cinnamic esters Org Lett 1 395 398 1:CAS:528:DyaK1MXjvFGhurc%3D 10.1021/ol990059e
-
(1999)
Org Lett
, vol.1
, pp. 395-398
-
-
Li, G.1
Wei, H.2
Kim, S.3
Neighbors, M.4
-
14
-
-
12344320218
-
Ionic liquid media resulted in the first asymmetric aminohalogenation reaction of alkenes
-
DOI 10.1021/ol048045i
-
X. Xu S.R.S.S. Kotti J. Liu J.F. Cannon A.D. Headley G. Li 2004 Ionic liquid media resulted in the first asymmetric aminohalogenation reaction of alkenes Org Lett 6 4881 4884 1:CAS:528:DC%2BD2cXhtVGhtr3I 10.1021/ol048045i (Pubitemid 40125833)
-
(2004)
Organic Letters
, vol.6
, Issue.26
, pp. 4881-4884
-
-
Xu, X.1
Kotti, S.R.S.S.2
Liu, J.3
Cannon, J.F.4
Headley, A.D.5
Li, G.6
-
15
-
-
4444347294
-
Regio- and stereoselective copper-catalyzed synthesis of vicinal haloamino ketones from α,β-unsaturated ketones
-
Chen D, Timmons C, Chao S, Li G. Regio- and stereoselective copper-catalyzed synthesis of vicinal haloamino ketones from α,β-unsaturated ketones. Eur J Org Chem, 2004, 3097-3101
-
(2004)
Eur J Org Chem
, pp. 3097-3101
-
-
Chen, D.1
Timmons, C.2
Chao, S.3
Li, G.4
-
16
-
-
33644775515
-
3-catalyzed aminohalogenation of arylmethylenecyclopropanes and arylvinylidenecyclopropanes and corresponding mechanistic studies
-
DOI 10.1021/ol052806f
-
3-catalyzed aminohalogenation of arylmethylenecyclopropanes and arylvinylidenecyclopropanes and corresponding mechanistic studies Org lett 8 625 628 1:CAS:528: DC%2BD28XoslKqtg%3D%3D 10.1021/ol052806f (Pubitemid 43341975)
-
(2006)
Organic Letters
, vol.8
, Issue.4
, pp. 625-628
-
-
Li, Q.1
Shi, M.2
Timmons, C.3
Li, G.4
-
17
-
-
34250618403
-
CuCl-catalyzed regio- and stereoselective aminohalogenation of α,β-unsaturated nitriles
-
Han J, Zhi S, Wang L, Pan Y, Li G. CuCl-catalyzed regio- and stereoselective aminohalogenation of α,β-unsaturated nitriles. Eur J Org Chem, 2007, 1332-1337
-
(2007)
Eur J Org Chem
, pp. 1332-1337
-
-
Han, J.1
Zhi, S.2
Wang, L.3
Pan, Y.4
Li, G.5
-
18
-
-
44949231178
-
Catalytic aminohalogenation reaction of β-nitrostyrenes with N,N-dichloro-4-toluenesulfonamide resulting in dichlorinated halo amides with opposite regiochemistry to previous systems
-
Zhi S, Han J, Lin C, An G, Pan Y, Li G. Catalytic aminohalogenation reaction of β-nitrostyrenes with N,N-dichloro-4-toluenesulfonamide resulting in dichlorinated halo amides with opposite regiochemistry to previous systems. Synthesis, 2008, 1570-1574
-
(2008)
Synthesis
, pp. 1570-1574
-
-
Zhi, S.1
Han, J.2
Lin, C.3
An, G.4
Pan, Y.5
Li, G.6
-
19
-
-
76449098661
-
Regioselective aminohalogenation of β-nitrostyrenes using NCS and NBS as nitrogen/halogen sources
-
1:CAS:528:DC%2BC3cXjslars7w%3D 10.1007/s11426-010-0028-9
-
S. Zhi H. Sun C. Lin G. Zhang G. Li Y. Pan 2010 Regioselective aminohalogenation of β-nitrostyrenes using NCS and NBS as nitrogen/halogen sources Sci China Chem 53 140 146 1:CAS:528:DC%2BC3cXjslars7w%3D 10.1007/s11426-010-0028-9
-
(2010)
Sci China Chem
, vol.53
, pp. 140-146
-
-
Zhi, S.1
Sun, H.2
Lin, C.3
Zhang, G.4
Li, G.5
Pan, Y.6
-
21
-
-
0000360619
-
Sulfonamidoglycosylation of glycals. A route to oligosaccharides with 2-aminohexose subunits
-
1:CAS:528:DyaK3cXltlalsLg%3D 10.1021/ja00171a021
-
D.A. Griffith S.J. Danishefsky 1990 Sulfonamidoglycosylation of glycals. A route to oligosaccharides with 2-aminohexose subunits J Am Chem Soc 112 5811 5819 1:CAS:528:DyaK3cXltlalsLg%3D 10.1021/ja00171a021
-
(1990)
J Am Chem Soc
, vol.112
, pp. 5811-5819
-
-
Griffith, D.A.1
Danishefsky, S.J.2
-
22
-
-
0029956353
-
The total synthesis of allosamidin. Expansions of the methodology of azaglycosylation pursuant to the total synthesis of allosamidin. A surprising enantiotopic sense for a lipase-induced deacetylation
-
DOI 10.1021/ja960526c
-
D.A. Griffith S.J. Danishefsky 1996 The total synthesis of Allosamidin. Expansions of the methodology of aza-glycosidation pursuant to the total synthesis of allosamidin. A surprising enantiotopic sense for a lipase-induced deacetylation J Am Chem Soc 118 9526 9538 1:CAS:528:DyaK28XmtF2isbk%3D 10.1021/ja960526c (Pubitemid 26358309)
-
(1996)
Journal of the American Chemical Society
, vol.118
, Issue.40
, pp. 9526-9538
-
-
Griffith, D.A.1
Danishefsky, S.J.2
-
23
-
-
22144497445
-
Synthesis of novel piperazine based building blocks: 3,7,9- triazabicyclo[3. 3.1]nonane, 3,6,8-triazabicyclo[3.2.2]nonane, 3-oxa-7,9-diazabicyclo[3.3.1] nonane and 3-oxa-6,8-diazabicyclo[3.2.2]nonane
-
DOI 10.1016/j.tetlet.2005.06.020, PII S0040403905012530
-
L. Revesz E. Blum R. Wicki 2005 Synthesis of novel piperazine based building blocks: 3,7,9-triazabicyclo[3.3.1]nonane, 3,6,8-triazabicyclo[3.2.2] nonane, 3-oxa-7,9-diazabicyclo[3.3.1]nonane and 3-oxa-6,8-diazabicyclo[3.2.2] nonane Tetrahedron Lett 46 5577 5580 1:CAS:528:DC%2BD2MXmtFCksrs%3D 10.1016/j.tetlet.2005.06.020 (Pubitemid 40981014)
-
(2005)
Tetrahedron Letters
, vol.46
, Issue.33
, pp. 5577-5580
-
-
Revesz, L.1
Blum, E.2
Wicki, R.3
-
24
-
-
33845555454
-
Palladium-catalyzed cyclization of ω-olefinic tosamides. Synthesis of nonaromatic nitrogen heterocycles
-
1:CAS:528:DyaL38XhvVWju78%3D 10.1021/ja00373a019
-
L.S. Hegedus J.M. McKearin 1982 Palladium-catalyzed cyclization of ω-olefinic tosamides. Synthesis of nonaromatic nitrogen heterocycles J Am Chem Soc 104 2444 2451 1:CAS:528:DyaL38XhvVWju78%3D 10.1021/ja00373a019
-
(1982)
J Am Chem Soc
, vol.104
, pp. 2444-2451
-
-
Hegedus, L.S.1
McKearin, J.M.2
-
25
-
-
34248598925
-
2 in the presence of base: A facile highly stereoselective synthesis of (1E,2E)-3-bromo-4-oxo- N′- tosyl-2-alkenoxylimidic acid ethyl esters
-
DOI 10.1021/jo070239z
-
2 in the presence of base: A facile highly stereoselective synthesis of (1E,2E)-3-bromo-4-oxo-N'-tosyl-2-alkenoxylimidic acid ethyl esters J Org Chem 72 3961 3964 1:CAS:528:DC%2BD2sXktVygsb0%3D 10.1021/jo070239z (Pubitemid 46762496)
-
(2007)
Journal of Organic Chemistry
, vol.72
, Issue.10
, pp. 3961-3964
-
-
Shen, R.1
Huang, X.2
-
26
-
-
33644943196
-
2-promoted aminochlorination of olefins with Chloramine-T
-
DOI 10.1021/ol0600178
-
2-promoted aminochlorination of olefins with chloramines-T Org Lett 8 967 969 1:CAS:528:DC%2BD28Xht1eqsb4%3D 10.1021/ol0600178 (Pubitemid 43412009)
-
(2006)
Organic Letters
, vol.8
, Issue.5
, pp. 967-969
-
-
Minakata, S.1
Yoneda, Y.2
Oderaotoshi, Y.3
Komatsu, M.4
-
27
-
-
34548421434
-
Mechanochemical aminochlorination of electrondeficient olefins with chloramine-T promoted by (diacetoxyiodo) benzene
-
1:CAS:528:DC%2BD2sXhtVels7nI 10.1002/adsc.200700020
-
G. Wang X. Wu 2007 Mechanochemical aminochlorination of electrondeficient olefins with chloramine-T promoted by (diacetoxyiodo) benzene Adv Synth Catal 349 1977 1982 1:CAS:528:DC%2BD2sXhtVels7nI 10.1002/adsc.200700020
-
(2007)
Adv Synth Catal
, vol.349
, pp. 1977-1982
-
-
Wang, G.1
Wu, X.2
-
28
-
-
0034720957
-
2/2-NsNHNa combination as the nitrogen and halogen sources for the synthesis of anti-alkyl 3-chloro-2-(o-nitrobenzenesulfonamido)-3-arylpropionates
-
1:CAS:528:DC%2BD3cXkt1Gqsrg%3D 10.1021/ol000120b
-
2/2-NsNHNa combination as the nitrogen and halogen sources for the synthesis of anti-alkyl 3-chloro-2-(o-nitrobenzenesulfonamido)-3- arylpropionates Org Lett 2 2249 2252 1:CAS:528:DC%2BD3cXkt1Gqsrg%3D 10.1021/ol000120b
-
(2000)
Org Lett
, vol.2
, pp. 2249-2252
-
-
Li, G.1
Wei, H.2
Kim, S.3
-
29
-
-
0034987043
-
Bromosulfonamidation of alkenes using S,S-dimethyl-N-p-toluenesulfonyl- sulfilimine
-
Raghavan S, Reddy SR, Tony KA, Kumar CN, Nanda S. Bromosulfonamidation of alkenes using S,S-dimethyl-N-p-toluenesulfonyl-sulfilimine. Synlett, 2001, 851-853
-
(2001)
Synlett
, pp. 851-853
-
-
Raghavan, S.1
Reddy, S.R.2
Tony, K.A.3
Kumar, C.N.4
Nanda, S.5
-
30
-
-
0036794016
-
The "nonoxidative" chloro-pummerer reaction: Novel stereospecific entry to vicinal chloroamines and aziridines
-
Volonterio A, Bravo P, Panzeri W, Pesenti C, Zanda M. The "nonoxidative" chloro-pummerer reaction: novel stereospecific entry to vicinal chloroamines and aziridines. Eur J Org Chem, 2002, 3336-3340
-
(2002)
Eur J Org Chem
, pp. 3336-3340
-
-
Volonterio, A.1
Bravo, P.2
Panzeri, W.3
Pesenti, C.4
Zanda, M.5
-
31
-
-
0141739359
-
2 and NBS as nitrogen and bromine sources
-
DOI 10.1021/ol027530f
-
2 and NBS as nitrogen and bromine sources Org Lett 5 861 864 1:CAS:528: DC%2BD3sXhtlSrurY%3D 10.1021/ol027530f (Pubitemid 37130636)
-
(2003)
Organic Letters
, vol.5
, Issue.6
, pp. 861-864
-
-
Thakur, V.V.1
Talluri, S.K.2
Sudalai, A.3
-
32
-
-
38549115115
-
2 and NBS as the nitrogen and bromine sources mediated by hypervalent iodine in a ball mill
-
DOI 10.1039/b717333d
-
2 and NBS as the nitrogen and bromine sources mediated by hypervalent iodine in a ball mill Org Biomol Chem 6 548 553 1:CAS:528: DC%2BD1cXhtVWht7c%3D 10.1039/b717333d (Pubitemid 351161745)
-
(2008)
Organic and Biomolecular Chemistry
, vol.6
, Issue.3
, pp. 548-553
-
-
Wu, X.-L.1
Xia, J.-J.2
Wang, G.-W.3
-
34
-
-
55449127973
-
2-catalyzed aminobromination of alkenes using amides or sulfonamides and NBS as the nitrogen and bromine sources
-
2-catalyzed aminobromination of alkenes using amides or sulfonamides and NBS as the nitrogen and bromine sources. Synlett, 2008, 2667-2670
-
(2008)
Synlett
, pp. 2667-2670
-
-
Wang, Z.1
Zhang, Y.M.2
Fu, H.3
Jiang, Y.Y.4
Zhao, Y.F.5
-
35
-
-
70349100400
-
Hypervalent iodine-mediated aminobromination of olefins in water
-
1:CAS:528:DC%2BD1MXhtFGgu7nP 10.1016/j.tet.2009.08.069
-
X.L. Wu G.W. Wang 2009 Hypervalent iodine-mediated aminobromination of olefins in water Tetrahedron 65 8802 8807 1:CAS:528:DC%2BD1MXhtFGgu7nP 10.1016/j.tet.2009.08.069
-
(2009)
Tetrahedron
, vol.65
, pp. 8802-8807
-
-
Wu, X.L.1
Wang, G.W.2
-
37
-
-
64549155327
-
2 and NBS as nitrogen and halogen sources
-
1:CAS:528:DC%2BD1cXhsFChsb%2FM 10.1021/jo8023768
-
2 and NBS as nitrogen and halogen sources J Org Chem 74 1371 1373 1:CAS:528:DC%2BD1cXhsFChsb%2FM 10.1021/jo8023768
-
(2009)
J Org Chem
, vol.74
, pp. 1371-1373
-
-
Chen, Z.G.1
Wei, J.F.2
Li, R.T.3
Shi, X.Y.4
Zhao, P.F.5
-
39
-
-
64549112553
-
Titanium superoxide: A heterogeneous catalyst for anti-Markovnikov aminobromination of olefins
-
1:CAS:528:DC%2BD1MXkslyjsro%3D 10.1016/j.tetlet.2009.03.169
-
T.M. Shaikh P.U. Karabal G. Suryavanshi A. Sudalai 2009 Titanium superoxide: a heterogeneous catalyst for anti-Markovnikov aminobromination of olefins Tetrahedron Lett 50 2815 2817 1:CAS:528:DC%2BD1MXkslyjsro%3D 10.1016/j.tetlet.2009.03.169
-
(2009)
Tetrahedron Lett
, vol.50
, pp. 2815-2817
-
-
Shaikh, T.M.1
Karabal, P.U.2
Suryavanshi, G.3
Sudalai, A.4
-
40
-
-
0034605847
-
α,β-Differentiated tandem diamination of cinnamic esters using N,N-dichloro-2-nitrobenzenesulfonamide and acetonitrile as the nitrogen sources
-
1:CAS:528:DC%2BD3cXovVWksLg%3D 10.1016/S0040-4039(00)01579-3
-
G. Li S. Kim H. Wei 2000 α,β-Differentiated tandem diamination of cinnamic esters using N,N-dichloro-2-nitrobenzenesulfonamide and acetonitrile as the nitrogen sources Tetrahedron Lett 41 8699 8703 1:CAS:528:DC%2BD3cXovVWksLg%3D 10.1016/S0040-4039(00)01579-3
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 8699-8703
-
-
Li, G.1
Kim, S.2
Wei, H.3
-
41
-
-
33746099286
-
Recent development of regio- and stereoselective aminohalogenation reaction of alkenes
-
Liu J, Wang Y, Li G. Recent development of regio- and stereoselective aminohalogenation reaction of alkenes. Eur J Org Chem, 2006, 3112-3115
-
(2006)
Eur J Org Chem
, pp. 3112-3115
-
-
Liu, J.1
Wang, Y.2
Li, G.3
-
42
-
-
73449130535
-
Catalyst-free aminobromination of alkenes with N-methyl-p- toluenesulfonamide as nitrogen resource
-
1:CAS:528:DC%2BC3cXjtVGksw%3D%3D 10.1016/j.tetlet.2009.12.059
-
G.Q. Zhang G.H. An J. Zheng Y. Pan G. Li 2010 Catalyst-free aminobromination of alkenes with N-methyl-p-toluenesulfonamide as nitrogen resource Tetrahedron Lett 51 987 989 1:CAS:528:DC%2BC3cXjtVGksw%3D%3D 10.1016/j.tetlet.2009.12.059
-
(2010)
Tetrahedron Lett
, vol.51
, pp. 987-989
-
-
Zhang, G.Q.1
An, G.H.2
Zheng, J.3
Pan, Y.4
Li, G.5
-
43
-
-
0002457459
-
The synthesis of p-substituted D,L-phenylglycines by the amidoalkylation of benzylchloride and N-benzylbenzamide
-
1:CAS:528:DyaE1cXhslSntrY%3D 10.1016/0040-4020(77)80295-0
-
D. Ben-Ishai J. Altman N. Peled 1977 The synthesis of p-substituted D,L-phenylglycines by the amidoalkylation of benzylchloride and N-benzylbenzamide Tetrahedron 33 2715 2717 1:CAS:528:DyaE1cXhslSntrY%3D 10.1016/0040-4020(77)80295-0
-
(1977)
Tetrahedron
, vol.33
, pp. 2715-2717
-
-
Ben-Ishai, D.1
Altman, J.2
Peled, N.3
-
44
-
-
0000486777
-
Total synthesis of cyclobutane amino acids from atelia Herbert smithii
-
1:CAS:528:DyaL1cXlsFSjs7s%3D 10.1021/jo00255a024
-
P. Hughes J. Clardy 1988 Total synthesis of cyclobutane amino acids from atelia Herbert smithii J Org Chem 53 4793 4796 1:CAS:528:DyaL1cXlsFSjs7s%3D 10.1021/jo00255a024
-
(1988)
J Org Chem
, vol.53
, pp. 4793-4796
-
-
Hughes, P.1
Clardy, J.2
-
45
-
-
0031055494
-
Total synthesis of (+)-duocarmycin A, epi-(+)-duocarmycin A and their unnatural enantiomers: Assessment of chemical and biological properties
-
DOI 10.1021/ja962431g, PII S0002786396024316
-
D.L. Boger J.A. Mckie T. Nishi T. Ogiku 1997 Total synthesis of (+)-duocarmycin A, epi-(+)-duocarmycin A and their unnatural enantiomers: Assessment of chemical and biological properties J Am Chem Soc 119 311 325 1:CAS:528:DyaK2sXhtFyrtbk%3D 10.1021/ja962431g (Pubitemid 27079482)
-
(1997)
Journal of the American Chemical Society
, vol.119
, Issue.2
, pp. 311-325
-
-
Boger, D.L.1
McKie, J.A.2
Nishi, T.3
Ogiku, T.4
-
46
-
-
33745110538
-
Vicinal diamino functionalities as privileged structural elements in biologically active compounds and exploitation of their synthetic chemistry
-
DOI 10.1111/j.1747-0285.2006.00347.x
-
S.R.S.S. Kotti C. Timmons G. Li 2006 Vicinal diamino functionalities as privileged structural elements in biologically active compounds and exploitation of their synthetic chemistry Chem Biol Drug Design 67 101 114 1:CAS:528:DC%2BD28XktFSjsr4%3D 10.1111/j.1747-0285.2006.00347.x (Pubitemid 43881372)
-
(2006)
Chemical Biology and Drug Design
, vol.67
, Issue.2
, pp. 101-114
-
-
Saibabu Kotti, S.R.S.1
Timmons, C.2
Li, G.3
-
47
-
-
0001067327
-
Synthesis of arylnitronorbornenes by Diels-Alder cyclization of arylnitroethylenes and cyclopentadiene. Support of the stereochemistry and relative reactivity by the CNDO/II method. Preparation of aminoarylnorbornenes
-
1:CAS:528:DyaL28XhtVylu7c%3D 10.1139/v85-390
-
J. Bourguignon G. Le Nard G. Queguiner 1985 Synthesis of arylnitronorbornenes by Diels-Alder cyclization of arylnitroethylenes and cyclopentadiene. Support of the stereochemistry and relative reactivity by the CNDO/II method. Preparation of aminoarylnorbornenes Can J Chem 63 2354 2361 1:CAS:528:DyaL28XhtVylu7c%3D 10.1139/v85-390
-
(1985)
Can J Chem
, vol.63
, pp. 2354-2361
-
-
Bourguignon, J.1
Le Nard, G.2
Queguiner, G.3
-
48
-
-
33748654251
-
Mechanism of the yeast mediated reduction of nitrostyrenes in light petroleum
-
McAnda AF, Roberts KD, Smallridge AJ, Ten A, Trewhella M A. Mechanism of the yeast mediated reduction of nitrostyrenes in light petroleum. J Chem Soc Perkin Trans 1, 1998, 501-504
-
(1998)
J Chem Soc Perkin Trans
, vol.1
, pp. 501-504
-
-
McAnda, A.F.1
Roberts, K.D.2
Smallridge, A.J.3
Ten, A.4
Trewhella, M.A.5
-
49
-
-
0035959474
-
One-pot synthesis of trans-β-alkylstyrenes
-
DOI 10.1016/S0040-4039(01)01185-6, PII S0040403901011856
-
J.T. Liu C.F. Yao 2001 One-pot synthesis of trans-β-alkylstyrenes Tetrahedron Lett 42 6147 6150 1:CAS:528:DC%2BD3MXlvFaqs7c%3D 10.1016/S0040-4039(01)01185-6 (Pubitemid 32735525)
-
(2001)
Tetrahedron Letters
, vol.42
, Issue.35
, pp. 6147-6150
-
-
Liu, J.-T.1
Yao, C.-F.2
-
50
-
-
9344265208
-
Lewis acid catalyzed dipolar cycloadditions of an activated imidate
-
DOI 10.1021/jo0485536
-
R.K. Bowman J.S. Johnson 2004 Lewis acid-catalyzed dipolar cycloadditions of an activated imidate J Org Chem 69 8537 8540 1:CAS:528:DC%2BD2cXpt1Sktbg%3D 10.1021/jo0485536 (Pubitemid 39557231)
-
(2004)
Journal of Organic Chemistry
, vol.69
, Issue.24
, pp. 8537-8540
-
-
Bowman, R.K.1
Johnson, J.S.2
|