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th ed., Wiley-Interscience, New York, 1992, pp. 533-34, 812-16 and references cited therein. Merkushev, E. B. Synthesis 1988, 923. Christie, S. D. R. J. Chem. Soc., Perkin Trans, 1 1999, 737. Gyulnazarian, A. Kh.; Sahakyan, T,. A. Khim. Zh. Arm. 1999, 52, 49; Chem. Abstr. 1999, 131, 285976. Kryska, A.; Skulski, L. J. Chem. Res., Synop. 1999, 590; (M) 2501. Barluenga, J. Pure Appl. Chem. 1999, 71, 431.
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th ed., Wiley-Interscience, New York, 1992, pp. 533-34, 812-16 and references cited therein. Merkushev, E. B. Synthesis 1988, 923. Christie, S. D. R. J. Chem. Soc., Perkin Trans, 1 1999, 737. Gyulnazarian, A. Kh.; Sahakyan, T,. A. Khim. Zh. Arm. 1999, 52, 49; Chem. Abstr. 1999, 131, 285976. Kryska, A.; Skulski, L. J. Chem. Res., Synop. 1999, 590; (M) 2501. Barluenga, J. Pure Appl. Chem. 1999, 71, 431.
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Anandasundaresan, P.1
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Nagarajan, K.3
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Venkatasubramanian, N.5
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13
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0033583110
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See e. g. Zajc, B. J. Org. Chem. 1999, 64, 1902. Dolenc, D.; Sket, B. Synlett 1995, 327.
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Zajc, B.1
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14
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33750198614
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See e. g. Zajc, B. J. Org. Chem. 1999, 64, 1902. Dolenc, D.; Sket, B. Synlett 1995, 327.
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Synlett
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Dolenc, D.1
Sket, B.2
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18
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0343230877
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note
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3S: C 25.70, H 1.85, N 4.28, found C 25.67, H 1.61, N 4.19.
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19
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0342361352
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note
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6INO: C 30.10, H 2.02, N 3.51, found: C 30.38, H 1.78, N 3.47.
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20
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0342361353
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note
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11 The 5% excess of NISac was usually used, except for reactions with volatile alkenes, where alkenes were in 5-10% excess.
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