Asymmetric cyclopropanation of allylic ethers: cleavage and regeneration of the chiral auxiliary
AB Charette, B Cote
Index: Charette, Andre B.; Cote, Bernard Journal of Organic Chemistry, 1993 , vol. 58, # 4 p. 933 - 936
Full Text: HTML
Citation Number: 47
Abstract
The ring contraction reaction of 2-0-[[(trifluoromethyl) sulfonylloxyl-~-~-glucopyranosides and their corresponding a-anomers is reported. The rearrangement was shown to occur under extremely mild basic conditions to allow isolation of acid-sensitive optically active substituted cyclopropylmethanols. The chiral auxiliary can be regenerated by converting the C-glucofuranoside, byproduct of the rearrangement, into tri-0-benzyl-D-glucal (two steps).
Related Articles:
[Weinig, Hans-Georg; Passacantilli, Pietro; Colapietro, Marcello; Piancatelli, Giovanni Tetrahedron Letters, 2002 , vol. 43, # 26 p. 4613 - 4615]
[Madhusudan, Soni Kamlesh; Agnihotri, Geetanjali; Negi, Devendra S.; Misra, Anup Kumar Carbohydrate Research, 2005 , vol. 340, # 7 p. 1373 - 1377]
[Szeja, W.; Fokt, I.; Grynkiewicz, G. Recueil des Travaux Chimiques des Pays-Bas, 1989 , vol. 108, # 6 p. 224 - 226]
[Boutureira, Omar; Rodriguez, Miguel Angel; Matheu, M. Isabel; Diaz, Yolanda; Castillon, Sergio Organic Letters, 2006 , vol. 8, # 4 p. 673 - 675]
[Skrydstrup, Troels; Jarreton, Olivier; Mazeas, Daniel; Urban, Dominique; Beau, Jean-Marie Chemistry - A European Journal, 1998 , vol. 4, # 4 p. 655 - 671]