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Volumn 10, Issue 12, 2004, Pages 2942-2952

Synthetic and spectroscopic investigation of N-acylated sulfoximines

Author keywords

Acylation; Amides; Hydrolysis; Sulfodiimines; Sulfoximines

Indexed keywords

ACIDITY; CRYSTAL STRUCTURE; HYDROGEN; INFRARED SPECTROSCOPY; ISOMERIZATION; NITROGEN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SULFUR COMPOUNDS; SYNTHESIS (CHEMICAL); X RAY ANALYSIS;

EID: 3042826615     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200306016     Document Type: Article
Times cited : (62)

References (104)
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    • note
    • In this paper we mostly depict the N-S and O-S bonds of sulfoximines as double bonds, even though we are aware that the bonding situation can also be expressed differently. C.B. appreciates a stimulating discussion with Professor Herberich on this topic.
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    • note
    • 10c was first revealed by 2D-COSY NMR spectroscopy, which showed a "W" coupling between the α-hydrogen and norbornene bridgehead hydrogen atoms. An analogous analysis confirmed the assignement of the norbornane derivative 10d.
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    • note
    • CCDC-216313 (endo,exo-11) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html (or from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB21EZ, UK; fax: (+44)1223-336-033; or deposit@ccdc. cam.uk).
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    • The interactions of carbonyl groups with various substituents and especially with the amino group has been the subject of quite a few papers in the past, which have in part been reviewed in K. B. Wiberg, Acc. Chem. Res. 1999, 32, 922.
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    • note
    • tot(B) is the difference between the total energies of the cation and the base including correlation and zero-point energies.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.