Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Rebecca J. E. Stetz"'
Autor:
Alison A. Edwards, George E. Tranter, Benjamin Alexander Mayes, George W. J. Fleet, Mark P. Watterson, Christopher W. G. Ansell, Rebecca J. E. Stetz
Circular dichroism studies on a series of linear oligomers derived from a protected 6-amino-6-deoxy-D-galactonate (an ε-amino acid) indicated a predisposition to form a rigid structure in solution, which is comparable to a β-sheet composed of L-ami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0477b7f827f1f443bc43489c885655a8
https://ora.ox.ac.uk/objects/uuid:801e6113-e26a-4fb1-a2dd-c47ab6ff3767
https://ora.ox.ac.uk/objects/uuid:801e6113-e26a-4fb1-a2dd-c47ab6ff3767
Autor:
George W. J. Fleet, Daniel G. Marquess, Janet D. Lloyd, Rebecca J. E. Stetz, Daniel D. Long, Naoki Asano, Ana L. Winters, Robert J. Nash
Publikováno v:
ChemInform. 30
Treatment of D-galactono-1,4-lactone with dimethoxypropane in acetone in the presence of tosic acid forms methyl 2,3:5,6-di-O-isopropylidene-D-galactonate 6 (with only the secondary hydroxy group at C-4 unprotected) and methyl 2,3:4,5-di-O-isopropyli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4955e4d04b37d7abe192aac0150fc2b
https://doi.org/10.1002/chin.199934230
https://doi.org/10.1002/chin.199934230
Publikováno v:
TETRAHEDRON LETTERS. 45(1)
The formation of the 28-membered ring cyclo[(6-amino-6-deoxy-D-galactonic acid)4] by cyclisation of a protected open chain fully hydroxylated nylon 6 linear tetramer in modest yield provides the first example of a new class of carbopeptoid-cyclodextr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3ac1475a9b5ca702d2ec967478b48f5
http://ora.ox.ac.uk/objects/uuid:42b81612-122c-4b9c-b549-daa2676c3361
http://ora.ox.ac.uk/objects/uuid:42b81612-122c-4b9c-b549-daa2676c3361
Autor:
Naoki Asano, Daniel D. Long, Ana L. Winters, Daniel G. Marquess, George W. J. Fleet, Robert J. Nash, Rebecca J. E. Stetz, Janet D. Lloyd
Publikováno v:
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1. (8)
Treatment of D-galactono-1,4-lactone with dimethoxypropane in acetone in the presence of tosic acid forms methyl 2,3:5,6-di-O-isopropylidene-D-galactonate 6 (with only the secondary hydroxy group at C-4 unprotected) and methyl 2,3:4,5-di-O-isopropyli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14072a8148839d655621c30e88452b67
http://ora.ox.ac.uk/objects/uuid:b0e60b4e-4325-4e07-aa00-e13c892ecb2e
http://ora.ox.ac.uk/objects/uuid:b0e60b4e-4325-4e07-aa00-e13c892ecb2e