Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Koenraad, Vanhessche"'
Autor:
Sandra Moser, Gernot A. Strohmeier, Erich Leitner, Thomas J. Plocek, Koenraad Vanhessche, Harald Pichler
Publikováno v:
Metabolic Engineering Communications, Vol 7, Iss , Pp - (2018)
The triterpenoid (+)-ambrein is a natural precursor for (-)-ambrox, which constitutes one of the most sought-after fragrances and fixatives for the perfume industry. (+)-Ambrein is a major component of ambergris, an intestinal excretion of sperm whal
Externí odkaz:
https://doaj.org/article/4210246e77904ce9973edcf1976b5bb1
Publikováno v:
Yeast. 37:163-172
The triterpenoid (+)-ambrein is the major component of ambergris, a coprolite of the sperm whale that can only be rarely found on shores. Upon oxidative degradation of (+)-ambrein, several fragrance molecules are formed, amongst them (-)-ambrox, one
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d787470ffbef992edfa59485892742e
https://doi.org/10.1002/yea.3444
https://doi.org/10.1002/yea.3444
Autor:
Wolfgang Kroutil, Michael Fuchs, Koenraad Vanhessche, Georg Steinkellner, Karl Gruber, Christoph K. Winkler, Jeyson Cerne, Michael Friess, Lucas Hammerer, Thomas J Plocek
Publikováno v:
ChemCatChem. 11:5642-5649
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f6d0d1cf3c9f7139aa62fd23e836423
https://doi.org/10.1002/cctc.201901679
https://doi.org/10.1002/cctc.201901679
Autor:
Koenraad Vanhessche, Thomas J Plocek, Erich Leitner, Gernot Strohmeier, Sandra Moser, Harald Pichler
Publikováno v:
Metabolic Engineering Communications, Vol 7, Iss, Pp-(2018)
The triterpenoid (+)-ambrein is a natural precursor for (-)-ambrox, which constitutes one of the most sought-after fragrances and fixatives for the perfume industry. (+)-Ambrein is a major component of ambergris, an intestinal excretion of sperm whal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::219a27eed421b0b3c192c52d86404c92
https://doi.org/10.1016/j.mec.2018.e00077
https://doi.org/10.1016/j.mec.2018.e00077
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33801550a49d8367d84e4fb93dbcc0a5
https://doi.org/10.1002/chin.199525286
https://doi.org/10.1002/chin.199525286
Publikováno v:
Synlett. 1991:921-922
(-)-Neplanocin A (9) has been synthesized from L-ribulose (1) in 14 steps and in 15 % overall yield. The key step involves an intramolecular nitrone [2 + 3] cycloaddition reaction.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11bf52255faa1fb4c4ba0eb34362df1f
https://doi.org/10.1055/s-1991-20924
https://doi.org/10.1055/s-1991-20924