A novel method for protection and deprotection of the carbonyl groups in 1, 2-indanedione by conversion to dioxa-dithiapropellanes
J Almog, Y Zehavy, S Cohen
Index: Almog, Joseph; Zehavy, Yirmi; Cohen, Shmuel Tetrahedron Letters, 2003 , vol. 44, # 16 p. 3285 - 3288
Full Text: HTML
Citation Number: 8
Abstract
1, 2-Indanedione reacts with two equivalents of 2-mercaptoethanol to produce, instead of the expected 1, 2-bis (1, 3-oxathiolane), a dioxa-dithia [4.4. 3] propellane. Other 1, 2- indanediones produce analogous compounds. The protecting groups are removed at room temperature with NBS in aqueous acetone, to produce the original diketone.
Related Articles:
[Petrovskaia; Taylor; Hauze; Carroll; Joullie Journal of Organic Chemistry, 2001 , vol. 66, # 23 p. 7666 - 7675]
[De Vos, Dirk E.; De Wildeman, Stefaan; Sels, Bert F.; Grobet, Piet J.; Jacobs, Pierre A. Angewandte Chemie - International Edition, 1999 , vol. 38, # 7 p. 980 - 983]
[Dayan, Sharon; Almog, Joseph; Khodzhaev, Oleg; Rozen, Shlomo Journal of Organic Chemistry, 1998 , vol. 63, # 8 p. 2752 - 2754]
[Gruber, Christian C.; Nestl, Bettina M.; Gross, Johannes; Hildebrandt, Petra; Bornscheuer, Uwe T.; Faber, Kurt; Kroutil, Wolfgang Chemistry - A European Journal, 2007 , vol. 13, # 29 p. 8271 - 8276]
[Journal of Organic Chemistry, , vol. 60, p. 5686 - 5689]