Indexed keywords
NUCLEOPHILES;
RING OPENING;
ALCOHOLS;
AMINES;
AMINO ACIDS;
CARBOXYLIC ACIDS;
OLEFINS;
SODIUM COMPOUNDS;
STEREOCHEMISTRY;
2 (BENZYLAMINO) 3 (DIBENZYLAMINO) 4 METHYLHEXYLACETATE;
2 (BENZYLAMINO) 3 (DIBENZYLAMINO) 4 PHENYLBUTYLACETATE;
ALCOHOL;
ALKENE;
AZIRIDINE DERIVATIVE;
CARBOXYLIC ACID DERIVATIVE;
DIAMINE DERIVATIVE;
N1 CYCLOHEXYL N3,N3 DIBENZYL 2 METHOXY 4 PHENYLBUTAN 1,3 DIAMINE;
N1,N1,N2 TRIBENZYL 4 PHENYLBUT 3 EN 1,2 DIAMINE;
N1,N3,N3 TRIBENZYL 2 ISOPROPOXY 4 PHENYLBUTAN 1,3 DIAMINE;
N1,N3,N3 TRIBENZYL 2 ISOPROPOXYBUTAN 1,3 DIAMINE;
N1,N3,N3 TRIBENZYL 2 METHOXY 4 PHENYLBUTAN 1,3 DIAMINE;
N1,N3,N3 TRIBENZYL 2 METHOXY 5 METHYLHEXAN 1,3 DIAMINE;
N3,N1 DIBENZYL N2 CYCLOHEXYL 4 PHENYLBUT 3 EN 1,2 DIAMINE;
PHENYLALANINE;
SODIUM IODIDE;
UNCLASSIFIED DRUG;
ARTICLE;
CHEMICAL REACTION;
CHIRALITY;
REACTION ANALYSIS;
RING OPENING;
STEREOCHEMISTRY;
2
0002054640
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11
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12
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17
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21
0344327894
note
2 is commonly used in Lewis acid-catalyzed ring openings of aziridines. See: (a) Reference 1c.
22
0345190344
note
(b) Reference 2g.
25
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26
0345622528
note
2Ph), respectively.
27
0345622529
note
2 also affords the alcohol 4.
28
0345190343
note
2O afforded 2,3-diaminoalkan-1-ols. See: Reference 5.
29
33748664816
Previously, other N,N-dibenzylated aziridinium salts are proposed as intermediates in reactions of 2,3-epoxyamines: (a) Liu, Q.; Marchington, A. P.; Boden, N.; Rayner, C. M. J. Chem. Soc., Perkin Trans. 1 1997, 511.
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30
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Rayner, C.M.3