Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Anna L. Win"'
Autor:
Mattie S. M. Timmer, Emma M. Dangerfield, Stephen G. Withers, Seino A. K. Jongkees, Bridget L. Stocker, Anna L. Win-Mason
Publikováno v:
Carbohydrate Research. 367:29-32
The ability of a series of pyrrolidines to inhibit several glycosidases was investigated. Using Fleet’s ‘mirror-image postulate’, it was proposed that enantiomeric derivatives of 1,4-dideoxy-1,4-imino- d -lyxitol (a known α- d -galactosidase i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61cc48be6d2b2cacdbdf84b44b9824f8
https://doi.org/10.1016/j.carres.2012.11.011
https://doi.org/10.1016/j.carres.2012.11.011
Autor:
Peter C. Tyler, Emma M. Dangerfield, Mattie S. M. Timmer, Bridget L. Stocker, Anna L. Win-Mason
Publikováno v:
European Journal of Organic Chemistry. 2011:4008-4014
An efficient and highly stereoselective synthesis of L-ido-aminoiminosugar 3 has been described. Key in the synthesis is the application of a diastereoselective Strecker reaction and the extension of our carbamate annulation methodology to protected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae9f1fee97302aeb34375a767c02d22b
https://doi.org/10.1002/ejoc.201100523
https://doi.org/10.1002/ejoc.201100523
Autor:
Catherine H. Plunkett, Emma M. Dangerfield, Bridget L. Stocker, Anna L. Win-Mason, Mattie S. M. Timmer
Publikováno v:
The Journal of Organic Chemistry. 75:5470-5477
New methodology for the protecting-group-free synthesis of primary amines is presented. By optimizing the metal hydride/ammonia mediated reductive amination of aldehydes and hemiacetals, primary amines were selectively prepared with no or minimal for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::040d8ff95846c0c76253911704cc3a19
https://doi.org/10.1021/jo100004c
https://doi.org/10.1021/jo100004c
Autor:
Emma M. Dangerfield, Mattie S. M. Timmer, Gregory W. Haslett, Anna L. Win-Mason, Bridget L. Stocker
Publikováno v:
European Journal of Organic Chemistry. 2010:1615-1637
As noted inhibitors of glycosidases, iminosugars have enormous therapeutic potential in the treatment of a number of diseases such as cancer, diabetes, and lysosomal storage disorders. Accordingly, much effort has been expended over the past decades
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9abda3f303e03c6d65fa5a3b86117525
https://doi.org/10.1002/ejoc.200901320
https://doi.org/10.1002/ejoc.200901320
Publikováno v:
ChemInform. 43
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e1965d0aa87ffface9b2439b686efb7
https://doi.org/10.1002/chin.201237227
https://doi.org/10.1002/chin.201237227
Publikováno v:
Carbohydrate research. 356
The I 2 -mediated carbamate annulation provides an efficient and highly stereoselective route for the synthesis of a variety of pyrrolidines and piperidines, both in the presence and absence of protecting groups. Evidence for the formation of an iodo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebb704fcf53e49cc16e0f0562e40e499
https://pubmed.ncbi.nlm.nih.gov/22513135
https://pubmed.ncbi.nlm.nih.gov/22513135
Autor:
Mattie S. M. Timmer, Anna L. Win-Mason, Stephen G. Withers, Seino A. K. Jongkees, Bridget L. Stocker, Peter C. Tyler
Publikováno v:
The Journal of organic chemistry. 76(23)
New methodology for the preparation of a variety of aminoiminohextitols is described. Key in the synthesis is the application of a diastereoselective Strecker reaction and the extension of our carbamate annulation methodology to protected and functio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c700c11ad578488a794a1f890ead82a4
https://pubmed.ncbi.nlm.nih.gov/22022891
https://pubmed.ncbi.nlm.nih.gov/22022891
Autor:
Catherine H. Plunkett, Anna L. Win-Mason, Bridget L. Stocker, Mattie S. M. Timmer, Emma M. Dangerfield
Publikováno v:
ChemInform. 41
New methodology for the protecting-group-free synthesis of primary amines is presented. By optimizing the metal hydride/ammonia mediated reductive amination of aldehydes and hemiacetals, primary amines were selectively prepared with no or minimal for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::117491676b6e44a83f367cf4d9b6df0d
https://doi.org/10.1002/chin.201050060
https://doi.org/10.1002/chin.201050060
Autor:
Emma M. Dangerfield, Gregory W. Haslett, Anna L. Win-Mason, Mattie S. M. Timmer, Bridget L. Stocker
Publikováno v:
ChemInform. 41
As noted inhibitors of glycosidases, iminosugars have enormous therapeutic potential in the treatment of a number of diseases such as cancer, diabetes, and lysosomal storage disorders. Accordingly, much effort has been expended over the past decades
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fed4b3da21a1d417d3868e668f532619
https://doi.org/10.1002/chin.201025204
https://doi.org/10.1002/chin.201025204
Autor:
Anna L. Win, Lars Kröger, Ruth Falshaw, Joachim Thiem, Erzsébet Farkas, Andrew Falshaw, Joanne B. Hart
Publikováno v:
Carbohydrate research. 339(11)
The products from the enzymatic β- d -galactopyranosylation of 1 d - chiro -inositol, 1 d -pinitol, 1 d -3- O -allyl-4- O -methyl- chiro -inositol, 1 d -3,4-di- O -methyl- chiro -inositol, 1 l - chiro -inositol and myo -inositol in combined yields r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48bc921972ea8b88c68a80362464e21b
https://pubmed.ncbi.nlm.nih.gov/15261579
https://pubmed.ncbi.nlm.nih.gov/15261579