Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Vaidotas Navickas"'
Autor:
Bian Wu, Rohana Abu, Cyntia M. Palacio, Sebastian Bartsch, Ciprian G. Crismaru, Vaidotas Navickas, Kai Baldenius, Dick B. Janssen, John M. Woodley, Klaus Ditrich, Michael Breuer
Publikováno v:
Biotechnology and Bioengineering. 113:1853-1861
We constructed an enzymatic network composed of three different enzymes for the synthesis of valuable ether amines. The enzymatic reactions are interconnected to catalyze the oxidation and subsequent transamination of the substrate and to provide cof
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c55ab5ff6eea887dbb012a09bafbea2e
https://doi.org/10.1002/bit.25954
https://doi.org/10.1002/bit.25954
Autor:
Vaidotas Navickas, Martin E. Maier
Publikováno v:
Asymmetric Synthesis II: More Methods and Applications
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1f341806a7a669a29dcd7311ed74ced
https://doi.org/10.1002/9783527652235.ch18
https://doi.org/10.1002/9783527652235.ch18
Publikováno v:
Organic Letters. 13:2334-2337
The synthesis of the 16-membered core structure of leiodermatolide 40 has been achieved in 26 linear steps starting from (R)-Roche ester. The key steps in the synthesis of 40 are a Stille cross-coupling between two main fragments 11 and 33 having rou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9559158eb9b9e908fd7f2468abeefdd4
https://doi.org/10.1021/ol200584a
https://doi.org/10.1021/ol200584a
Publikováno v:
Synlett. 2011:191-194
The synthesis of three key fragments of the novel 16-membered macrolide leiodermatolide is described. The stereotetrad-containing building block was prepared via a Marshall-Tamaru reaction on an aldehyde obtained by organocatalysis. For a second buil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87fc6d32381c70d08c0c9efabab6e7b6
https://doi.org/10.1055/s-0030-1259286
https://doi.org/10.1055/s-0030-1259286
Publikováno v:
Organic Letters. 12:3418-3421
A cyclic carbonyl ylide with a trans-annulated cyclopentane ring was generated by a Rh(2)(OAc)(4)-catalyzed reaction from a diazoketone precursor and trapped with allyl propiolate. The 1,3-dipolar cycloaddition led to the stereoselective formation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::104a625b24ee86f7374498c2d2724822
https://doi.org/10.1021/ol1012185
https://doi.org/10.1021/ol1012185
Autor:
Martin E. Maier, Vaidotas Navickas
Publikováno v:
Tetrahedron. 66:94-101
The proposed structure of the benzolactone queenslandon ( 6 ) was synthesized utilizing a triol containing building block prepared from d -ribose. While a ring-closing metathesis approach did not lead to the macrocycle, alkylation of a benzyl(phenyl)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7d9b1dc60cac93ef9ffc0ef5f2c359cc
https://doi.org/10.1016/j.tet.2009.11.024
https://doi.org/10.1016/j.tet.2009.11.024
Autor:
Cyntia M, Palacio, Ciprian G, Crismaru, Sebastian, Bartsch, Vaidotas, Navickas, Klaus, Ditrich, Michael, Breuer, Rohana, Abu, John M, Woodley, Kai, Baldenius, Bian, Wu, Dick B, Janssen
Publikováno v:
Biotechnology and bioengineering. 113(9)
We constructed an enzymatic network composed of three different enzymes for the synthesis of valuable ether amines. The enzymatic reactions are interconnected to catalyze the oxidation and subsequent transamination of the substrate and to provide cof
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::03e845c226fc8ddd3077a2c45196fcba
https://pubmed.ncbi.nlm.nih.gov/26915048
https://pubmed.ncbi.nlm.nih.gov/26915048
Autor:
Markus Ströbele, Vaidotas Navickas, Florenz Sasse, Martin E. Maier, Dmitry B. Ushakov, Cäcilia Maichle-Mössmer
Publikováno v:
Organic letters. 13(8)
An effective total synthesis of (-)-9-deoxy-englerin (4), an analogue of the natural guaiane sesquiterpene englerin A (1), has been achieved. The synthesis features a transannular epoxide opening to construct the 5,7-fused ring system followed by tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c17149de33ee3c8edcbdbf52afaba27
https://pubmed.ncbi.nlm.nih.gov/21413694
https://pubmed.ncbi.nlm.nih.gov/21413694
Publikováno v:
ChemInform. 41
The ester (I), readily available in 5 steps from (-)-carvone, is used as starting material in the sequence.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a54a718cf9a570b1fa00fe6dd36db79
https://doi.org/10.1002/chin.201048187
https://doi.org/10.1002/chin.201048187
Publikováno v:
Organic Letters; May2011, Vol. 13 Issue 9, p2334-2337, 4p