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1
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0002831079
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(a) Seebach, D.; Colvin, E. W.; Lehr, F.; Weller, T. Chimia 1979, 33, 1.
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(1979)
Chimia
, vol.33
, pp. 1
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-
Seebach, D.1
Colvin, E.W.2
Lehr, F.3
Weller, T.4
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4
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0031889987
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Dilman, A. D.; Tishkov, A. A.; Lyapkalo, I. M.; Ioffe, S. L.; Strelenko, Yu. A.; Tartakovsky, V. A. Synthesis 1998, 181.
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(1998)
Synthesis
, pp. 181
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Dilman, A.D.1
Tishkov, A.A.2
Lyapkalo, I.M.3
Ioffe, S.L.4
Strelenko, Yu.A.5
Tartakovsky, V.A.6
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5
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0013601215
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Dilman, A. D.; Lyapkalo, I. M.; Strelenko, Yu. A.; Ioffe, S. L.; Tartakovsky, V. A. Mend. Commun. 1997, 133.
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(1997)
Mend. Commun.
, pp. 133
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-
Dilman, A.D.1
Lyapkalo, I.M.2
Strelenko, Yu.A.3
Ioffe, S.L.4
Tartakovsky, V.A.5
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7
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0000654908
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Paquette, L., Ed.; Wiley: New York
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(b) Beck, A. K.; Seebach, D. In Encyclopedia of Reagents for Organic Synthesis, Paquette, L., Ed.; Wiley: New York, 1995; Vol. 7, p 5270.
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(1995)
Encyclopedia of Reagents for Organic Synthesis
, vol.7
, pp. 5270
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Beck, A.K.1
Seebach, D.2
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8
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0344429836
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note
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3N to a mixture of 3 + 4 initiates the C,C-cross-coupling reaction.
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-
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11
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0000346432
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DBU quantitatively deprotonates 1; see : Aizpurua, J. M.; Oiarbide, M.; Palomo, C. Tetrahedron Lett. 1987, 28, 5361.
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(1987)
Tetrahedron Lett.
, vol.28
, pp. 5361
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Aizpurua, J.M.1
Oiarbide, M.2
Palomo, C.3
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12
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0009282226
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Feuer, H., Ed.; Interscience: New York
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Nielsen, A. T. In The Chemistry of the Nitro and Nitroso Groups, Feuer, H., Ed.; Interscience: New York, 1970; Vol. I, pp 417-430.
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(1970)
The Chemistry of the Nitro and Nitroso Groups
, vol.1
, pp. 417-430
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Nielsen, A.T.1
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13
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0030505628
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(a) Aryl or tertiary alkyl nitroso compounds react with salts of aliphatic nitro compounds to give corresponding nitrones, see: Lyapkalo, I. M.; Ioffe, S. L.; Strelenko, Yu. A.; Tartakovsky, V. A. Russ. Chem. Bull. 1996, 45, 856.
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(1996)
Russ. Chem. Bull.
, vol.45
, pp. 856
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Lyapkalo, I.M.1
Ioffe, S.L.2
Strelenko, Yu.A.3
Tartakovsky, V.A.4
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14
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0030866345
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(b) Nitroso alkenes bearing electron withdrawing group at the β-carbon atom (i.e. ON-CH=CH-EWG) react with silyl nitronates as N-electrophiles, see: Ioffe, S. L.; Lyapkalo, I. M.; Tishkov, A. A.; Strelenko, Yu. A.; Tartakovsky, V. A. Tetrahedron 1997, 55, 13085.
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(1997)
Tetrahedron
, vol.55
, pp. 13085
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Ioffe, S.L.1
Lyapkalo, I.M.2
Tishkov, A.A.3
Strelenko, Yu.A.4
Tartakovsky, V.A.5
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15
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0344861576
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note
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3N is basic enough to deprotonate methyl nitroacetate 1e quantitatively.
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-
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16
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0345724511
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note
-
There is no evidence for the assumption that yields of oximes 5 diminish owing to competitive O-alkylation (Scheme 3, path b).
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-
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17
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0345292898
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note
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-, silylnitronate 3 is more reactive than BSENA 4.
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-
-
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18
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0345292897
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note
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2O cannot be used in combination with TBAF at -78°C owing to insolubility of tetrabutylammonium derivatives in this solvent.
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-
-
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20
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21844488339
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Lyapkalo, I. M.; Ioffe, S. L.; Strelenko, Yu. A.; Tartakovsky, V. A. Russ. Chem. Bull. 1995, 44, 1142.
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(1995)
Russ. Chem. Bull.
, vol.44
, pp. 1142
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Lyapkalo, I.M.1
Ioffe, S.L.2
Strelenko, Yu.A.3
Tartakovsky, V.A.4
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21
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0345292896
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US Patent 2 390 918 (Resinous Products & Chemical Co.), 1945
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Brason, H. A. US Patent 2 390 918 (Resinous Products & Chemical Co.), 1945; Chem. Abstr. 1946, 40, 2456.
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Brason, H.A.1
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22
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0000374316
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Brason, H. A. US Patent 2 390 918 (Resinous Products & Chemical Co.), 1945; Chem. Abstr. 1946, 40, 2456.
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(1946)
Chem. Abstr.
, vol.40
, pp. 2456
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24
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84918053039
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Belikov, V. M. Bull. Acad. Sci. USSR. Div. Chem. Sci. 1956, 855; Chem. Abstr. 1957 51, 1837.
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(1957)
Chem. Abstr.
, vol.51
, pp. 1837
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