Zobrazeno 1 - 8
of 8
pro vyhledávání: '"George Douglas Ii Hiler"'
Autor:
Guochuan Yin, David Johnathan Kitko, Daryle H. Busch, George Douglas Ii Hiler, William Michael Scheper, Henry T. He, John David Carter, Victor W. Day
Publikováno v:
Journal of Coordination Chemistry. 61:45-59
Two ultra rigid, o-xylylene cross-bridged macrobicyclic ligands, 1,10,13,19-tetraazatricyclo[8.6.6.03,8]docosa-3,5,7-triene (H2XBC), and 13,19-dimethyl-1,10,13,19-tetraazatricyclo[8.6.6.03,8]docosa-3,5,7-triene (Me2XBC), have been synthesized and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13479fd26e32bd227a8f4afe95e89080
https://doi.org/10.1080/00958970701730331
https://doi.org/10.1080/00958970701730331
Autor:
George Douglas Ii Hiler, M. Joseph. Mohlenkamp, Tracy D. Wilkins, Adam W. Mazur, Roger L. Van Tassell
Publikováno v:
Journal of Agricultural and Food Chemistry. 41:1925-1930
This paper describes the rationale by which nonnutritive food products may be developed and examines an in vitro fermentation model in which large numbers of compounds may be easily screened, early in their development, for their potential to be ferm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb26a961dae6b4a8805b8cfc152ac170
https://doi.org/10.1021/jf00035a022
https://doi.org/10.1021/jf00035a022
Publikováno v:
The Journal of Physical Chemistry. 97:11344-11349
Freeze-fracture transmission electron microscopy (FF/TEM) is employed in this work to image association structures formed spontaneously from amphiphilic reaction products during the heterogeneous hydrolysis of trioctanoate with 1,3-specific lipase. D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b1f85a5fd57f4582389a9cfbd921d54
https://doi.org/10.1021/j100145a037
https://doi.org/10.1021/j100145a037
Publikováno v:
Polymer. 33:5343-5345
2 H n.m.r. spectroscopy is employed to characterize the mesomorphic behaviour of hydroxypropyl cellulose (HPC) in D 2 O. This analysis is further extended to ternary solutions containing HPC and xanthan gum (XG). A compositional range over which addi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::589afb7597ad275c2aaa8627e1b1b5f6
https://doi.org/10.1016/0032-3861(92)90825-h
https://doi.org/10.1016/0032-3861(92)90825-h
Autor:
George Douglas Ii Hiler, Adam W. Mazur
Publikováno v:
The Journal of organic chemistry. 62(13)
Synthesis of 5-C-(hydroxymethyl)hexoses, carbohydrates resistant to metabolism, is described. These compounds are obtained in the reaction of hexose 6-aldehydes with formaldehyde. 5-C-(Hydroxymethyl)-l-arabino-hexopyranoses can be efficiently obtaine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fd870c531f5a6316d09e1c4ab336bb3
https://pubmed.ncbi.nlm.nih.gov/11671776
https://pubmed.ncbi.nlm.nih.gov/11671776
Publikováno v:
ACS Symposium Series ISBN: 9780841218963
Microemulsions and Emulsions in Foods
Microemulsions and Emulsions in Foods
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c1db9ddd20ee0a069420865fb729ef4
https://doi.org/10.1021/bk-1991-0448.ch003
https://doi.org/10.1021/bk-1991-0448.ch003
Autor:
George Douglas Ii Hiler, Molly P. Armstrong, Susannie S.C. Lee, Jack D. Wendel, Adam W. Mazur
Publikováno v:
Chemistry and physics of lipids. 60(2)
A methodology for regio- and stereoselective preparation of acyl glycerol derivatives is presented. It offers easy access to specific 1,2-, 1,3-diglycerides and triglycerides as well as alkyl glycerol esters, phospholipids and glycolipids. These comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::573aace762324905c1bc9c7007c0a73c
https://pubmed.ncbi.nlm.nih.gov/1814641
https://pubmed.ncbi.nlm.nih.gov/1814641
Autor:
Adam W. Mazur, George Douglas Ii Hiler
Publikováno v:
Carbohydrate Research. 168:146-150
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da73e89307b95c992940a161d660d9a9
https://doi.org/10.1016/0008-6215(87)80018-6
https://doi.org/10.1016/0008-6215(87)80018-6