@article {3718,
	title = {Structural studies of organoboron compounds .64. Boron chelate formation with glycolohydroxamic acids, and the crystal and molecular structure of 5-(1-hydroxycyclohexyl)-2,2-diphenyl-1,3-dioxa-4-azonia-2-borata-4-cyclo pentane},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {74},
	number = {3},
	year = {1996},
	note = {ISI Document Delivery No.: UF848Times Cited: 4Cited Reference Count: 26},
	month = {Mar},
	pages = {445-452},
	type = {Article},
	abstract = {{The syntheses of representative diphenyl- and difluoroboron chelates of 2-hydroxycarbohydroxamic acids (glycolohydroxamic acids) are reported. Crystals of 5-(1-hydroxycyclohexyl)-2,2-diphenyl-1,3-dioxa-4-azonia-2-borata-4-cyclo pentene, 2a, are triclinic},
	keywords = {BOND LENGTHS RELATIONS, crystal structure, HETERO-PI-SYSTEMS, hydroxamatoborate, HYDROXAMIC ACIDS, organoboron compound},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1996UF84800018},
	author = {Kliegel, W. and Schumacher, U. and Rettig, S. J. and Trotter, J.}
}
@article {7053,
	title = {STRUCTURAL STUDIES OF ORGANOBORON COMPOUNDS .43. 4-[(1-HYDROXYCYCLOHEXYL)METHYL]-2,2,5-TRIPHENYL-1,3-DIOXA-4-AZONIA-2-BOR ATA-4-CYCLOPENTENE},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {69},
	number = {3},
	year = {1991},
	note = {ISI Document Delivery No.: FE808Times Cited: 7Cited Reference Count: 23},
	month = {Mar},
	pages = {545-549},
	type = {Article},
	abstract = {{The reaction of N{\textquoteright}-hydroxy-N-[1-hydroxycyclohexyl)methyl]benzamide and diphenylborinic anhydride gives 4-[(1-hydroxycyclohexyl)methyl]-2,2,5-triphenyl-1,3-dioxa-4-azonia-2-bor ata-4-cyclopentene in nearly quantitative yield. Crystals of the product are monoclinic},
	keywords = {BOND LENGTHS RELATIONS, BORON COMPOUND, CN-BONDS, CO-BONDS, CRYSTAL, crystal structure, HETERO-PI-SYSTEMS, MOLECULAR-STRUCTURES, organoboron compound},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1991FE80800027},
	author = {Kliegel, W. and Schumacher, U. and Tajerbashi, M. and Rettig, S. J. and Trotter, J.}
}
