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Title: Chelation-assisted regioselective C-O bond clevage reactions

Conference ·
OSTI ID:250136
; ;  [1]
  1. National Taiwan Univ., Taipei (China); and others

Chelation demonstrates a unique role to direct the chemo- and regioselectivity on a variety of fascinating transformations. The strategy has been extensively employed in the regioselective intramolecular addition of an organometallic species to a coordinated double bond and in the activation of a neighboring C-H bond. In this paper, the authors present the recent progress on applications of the chelation-assisted C-O bond cleavage reactions in acetals. Thus, treatments of various acetonides of monosaccharide and inositol derivatives with the Grignard reagent afford regioselectively the corresponding products having only one free hydroxy group.

OSTI ID:
250136
Report Number(s):
CONF-9508100-; TRN: 96:002623-0074
Resource Relation:
Conference: 8. IUPAC symposium on organometallic chemistry directed towards organic synthesis, Santa Barbara, CA (United States), 6-10 Aug 1995; Other Information: PBD: 1995; Related Information: Is Part Of Eight IUPAC symposium on organometallic chemistry directed towards organic synthesis (OMCOS 8); PB: 375 p.
Country of Publication:
United States
Language:
English