Regiochemical control of the ring opening of aziridines by means of chelating processes. 2. Synthesis and ring-opening reactions of aziridines derived from 5,6-dihydro-2H-pyran and of the diastereoisomeric cis- and trans-aziridines derived from 3-(benzyloxy)cyclohexene, 2-(benzyloxy)-3,6-dihydro-, and 2-(benzyloxy)-6-methyl-3,6-dihydro-2H-pyran

Tetrahedron

Volumn 53, Issue 4, 1997, Pages 1417-1438

  Crotti, Paolo ^a   Di Bussolo, Valeria ^a   Favero, Lucilla ^a   Pineschi, Mauro ^a  

^a UNIVERSITY OF PISA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; AZIRIDINE DERIVATIVE; TETRAHYDROPYRAN DERIVATIVE;

ARTICLE; CATALYSIS; DRUG SYNTHESIS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0031036354     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(96)01054-X     Document Type: Article

References (23)

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17. 4 in MeCN.
18. The C-1 and C-2 products nomenclature refers to the attacking site of the nucleophile, i.e. at the C-(1) or C-(2) aziridine carbon of aziridines 5-12, 15-18, and 21-23, in accordance with the arbitrary numbering given in Schemes 3-7.
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