A novel method for protection and deprotection of the carbonyl groups in 1,2-indanedione by conversion to dioxa-dithiapropellanes

Tetrahedron Letters

Volumn 44, Issue 16, 2003, Pages 3285-3288

  Almog, Joseph ^a   Zehavy, Yirmi ^a   Cohen, Shmuel ^a  

^a HEBREW UNIVERSITY OF JERUSALEM   (Israel)

Author keywords

1,2 indanedione; 1,3 oxathiolanes; Deprotection; Dioxa dithiapropellanes; Mercaptoethanol; Protection

Indexed keywords

1,2 BIS(1,3 OXATHIOLANE); ACETONE; CARBONYL DERIVATIVE; CHEMICAL COMPOUND; DIKETONE; DIOXADITHIA[4.4.3]PROPELLANE; DIOXANE DERIVATIVE; INDAN 1,2 DIONE; INDAN DERIVATIVE; THIOL DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL MODIFICATION; CHEMICAL REACTION; INFRARED RADIATION; MASS SPECTROMETRY; PROTON NUCLEAR MAGNETIC RESONANCE; ROOM TEMPERATURE; X RAY CRYSTALLOGRAPHY;

EID: 0037436905     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(03)00622-1     Document Type: Article

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30. 3): δ 7.77 (br.d, J=8.0 Hz, 1H), 7.63 (dt, J=7.6, 1.2 Hz, 1H), 7.44-7.38 (m, 2H), 4.72-4.65 (m, 1H), 4.44-4.37 (m, 1H), 3.62 (d, J=9.6 Hz, 1H), 3.54-3.46 (m, 1H), 3.50 (d, J=9.6 Hz, 1H), 3.36-3.28 (m, 1H).
31. Crystallographic data (excluding structure factors) for the structures in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication numbers CCDC 196209 and 196210. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (Fax: +44(0)-1223-336033 or e-mail: deposit@ccdc.cam.ac.uk).