K Vosmann
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Explore the profile of K Vosmann including associated specialties, affiliations and a list of published articles.
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13
Citations
32
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Recent Articles
1.
Haase N, Grothe K, Matthaus B, Vosmann K, Lindhauer M
Food Addit Contam Part A Chem Anal Control Expo Risk Assess
. 2012 Jul;
29(8):1230-8.
PMID: 22784192
Heated plant foods may contain compounds with adverse health effects (e.g. acrylamide). On the other hand, health-promoting compounds (e.g. antioxidants) have also been identified in such foods. Therefore, a baking...
2.
Vosmann K, Wiege B, Weitkamp P, Weber N
Appl Microbiol Biotechnol
. 2008 Jun;
80(1):29-36.
PMID: 18542947
Long-chain alkyl benzoates, e.g., lauryl 4-hydroxybenzoate, palmityl 4-hydroxybenzoate, and oleyl 4-hydroxy-3-methoxybenzoate, are formed in high to moderate conversion by lipase-catalyzed transesterification of the corresponding short-chain alkyl benzoates (0.3 to 1...
3.
Fehling E, Klein E, Vosmann K, Bergander K, Weber N
Biotechnol Bioeng
. 2007 Oct;
99(5):1074-84.
PMID: 17969136
Linear copolymeric polyesters (polyoxoesters) containing thioether functions [poly(3,3'-thiodipropionic acid-co-alpha,omega-alkanediols)] were formed in good yield by esterification of an equimolar mixture of 3,3'-thiodipropionic acid (4-thiaheptane-1,7-dioic acid) and 1,6-hexanediol (weight average molecular...
4.
Chemo-enzymatic preparation of copolymeric polythioesters containing branched-chain thioether groups
Fehling E, Klein E, Weber N, Demes C, Vosmann K
Appl Microbiol Biotechnol
. 2006 Nov;
74(2):357-65.
PMID: 17103159
Branched-chain copolymeric polythioesters (PTE) were formed in good yield (approximately 87%) by chemoenzymatic reactions including thiyl radical-induced addition of 1,6-hexanedithiol to the >C=C< double bond of dimethyl 1,18-octadec-9-enedioate and transthioesterification...
5.
Weber N, Bergander K, Fehling E, Klein E, Vosmann K, Mukherjee K
Appl Microbiol Biotechnol
. 2005 Jul;
70(3):290-7.
PMID: 16007456
Linear copolymeric polythioesters [PTE; poly(alpha,omega-alkanedioic acid-co-alpha,omega-alkanedithiols)] were formed in good yield (approximately 69%) by thioesterification of 1,12-dodecanedioic acid with 1,6-hexanedithiol and 1,8-octanedithiol, respectively, catalyzed by immobilized lipase from Rhizomucor miehei...
6.
Tsevegsuren N, Aitzetmuller K, Vosmann K
Lipids
. 2004 Nov;
39(6):571-6.
PMID: 15554157
The occurrence of petroselinic acid (18:1delta6cis) in seed oils was believed to be limited to the Umbelliferae or Apiaceae, and a few other members of the Umbelliflorae. A major occurrence...
7.
Weber N, Klein E, Vosmann K, Mukherjee K
Appl Microbiol Biotechnol
. 2004 Mar;
64(6):800-5.
PMID: 15048592
1- S-Mono-palmitoyl-hexanedithiol and 1- S-mono-palmitoyl-octanedithiol were prepared in high yield (80-90%) by solvent-free lipase-catalyzed thioesterification of palmitic acid with the corresponding alpha,omega-alkanedithiols in vacuo. Similarly, 1,6-di- S-palmitoyl-hexanedithiol and 1,8-di- S-palmitoyl-octanedithiol...
8.
Tsevegsuren N, Aitzetmuller K, Vosmann K
Lipids
. 2004 Jan;
38(11):1173-8.
PMID: 14733363
Seeds of Androsace septentrionalis of the genus Androsace (tribus Primuleae) from the plant family Primulaceae were studied for their oil content and FA composition. The seed oil of A. septentrionalis...
9.
Weber N, Klein E, Vosmann K, Mukherjee K
Chem Phys Lipids
. 2000 May;
105(2):215-23.
PMID: 10823469
The lipase-catalyzed preparation of acyl thioesters from unsaturated fatty acids and alkanethiols is accompanied by the formation of geometrical isomers via stereomutation and of thioether derivatives via addition at the...
10.
Tsevegsuren N, Aitzetmuller K, Vosmann K
Lipids
. 1999 Jun;
34(5):525-9.
PMID: 10380126
Seeds of Youngia tenuicaulis and other species from the plant family Compositae (Asteraceae) were studied for their oil content and fatty acid composition. The seed oil of Y. tenuicaulis growing...