Zobrazeno 1 - 10
of 111
pro vyhledávání: '"Peter Spiteller"'
Autor:
Hedda Schrey, Tarek Scheele, Conrad Ulonska, Dana Leoni Nedder, Tim Neudecker, Peter Spiteller, Marc Stadler
Publikováno v:
Journal of Natural Products. 85:2363-2371
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::729c6ab7d47f2aa77d8deed0456a44ef
https://doi.org/10.1021/acs.jnatprod.2c00554
https://doi.org/10.1021/acs.jnatprod.2c00554
Autor:
Fidele Ntie-Kang, Ikhlas A. Khan, Omonike O. Ogbole, Pascal Wafo, Peter Spiteller, F. Uzor Philip, Zulfiqar Ali, Ramsay Soup Teoua Kamdem
Publikováno v:
Physical Sciences Reviews. 6:9-26
Bacteria and fungi have a high potential to produce compounds that display large structural change and diversity, thus displaying an extensive range of biological activities. Secondary metabolism or specialized metabolism is a term for pathways and s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08aba0b6454bab58c01527ea9c76a123
https://doi.org/10.1515/psr-2018-0170
https://doi.org/10.1515/psr-2018-0170
Publikováno v:
Fitoterapia. 167:105478
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fba899fcbcacd767965d3d4af856b5d7
https://doi.org/10.1016/j.fitote.2023.105478
https://doi.org/10.1016/j.fitote.2023.105478
Autor:
Patrick Swieca, Peter Spiteller
Publikováno v:
European Journal of Organic Chemistry. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d68819c73413bf2e15f5ef755915ae22
https://doi.org/10.1002/ejoc.202101576
https://doi.org/10.1002/ejoc.202101576
Autor:
Peter Spiteller, Robert J. R. Jaeger, Zeljka Rupcic, Jana Backenköhler, Silke Wagner, Marc Stadler, Michèle-Laure Lieunang Watat, Rieke Himstedt
Publikováno v:
ChemBioChem
Chembiochem
Chembiochem
Mycenarubin C, a previously unknown red pyrroloquinoline alkaloid, was isolated from fruiting bodies of the mushroom Mycena rosea and its structure was elucidated mainly by NMR spectroscopy and mass spectrometry. Unlike mycenarubin A, the major pyrro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdf573fea52413a1833b58839e5e377f
https://doi.org/10.1002/cbic.201900733
https://doi.org/10.1002/cbic.201900733
Autor:
Ramsay Soup Teoua Kamdem, Omonike Ogbole, Pascal Wafo, Philip F. Uzor, Zulfiqar Ali, Fidele Ntie-Kang, Ikhlas A. Khan, Peter Spiteller
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8b11641e702f96f8b07eb1d54d7873a
https://doi.org/10.1515/9783110668896-009
https://doi.org/10.1515/9783110668896-009
Publikováno v:
Journal of the Serbian Chemical Society, Vol 70, Iss 10, Pp 1133-1136 (2005)
The aldol condensation product of 1H-indan-1-one, (2E)-2-(2,3-dihydro-1H-inden-1-ylidene)-2,3-dihydro-1H-inden-1-one, subjected to Huang–Minlon reduction conditions was shown, via 1D and 2DNMRanalysis, to be amixture of (1S,1aR,6aR)-2’,3’,6,6a-
Externí odkaz:
https://doaj.org/article/88793c536e9e499e85e2c7e64db1afe5
Publikováno v:
Chemistry – A European Journal. 25:10333-10341
(5S,6S)-Aminotenuazonic acid, a new 3-acyltetramic acid, related to the well-known mycotoxin tenuazonic acid has been isolated from fruiting bodies of Laccaria bicolor. Its structure was mostly established by analysis of its 2D NMR and HR-(+)-ESI-MS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77731034021d79fe0b9c99a753436c57
https://doi.org/10.1002/chem.201901405
https://doi.org/10.1002/chem.201901405
Publikováno v:
Journal of the Serbian Chemical Society, Vol 66, Iss 11-12, Pp 753-763 (2001)
1H, 13C and two dimensional NMR analyses were applied to determine the NMR parameters of 2-(2,3-dihydro-1H-inden-1-yl)-1H-indene. The chemical shifts of all the H- and C-atoms, as well as the appropriate coupling constants were determined and the com
Externí odkaz:
https://doaj.org/article/fb90a096cd644039882e58b5f14a26eb
Autor:
Wolfgang Steglich, Peter Spiteller, Julia S. Lohmann, Monika von Nussbaum, Wolfgang Brandt, Julia Mülbradt
Publikováno v:
Tetrahedron. 74:5113-5118
Rosellin A and B, two red diketopiperazine alkaloids with unprecedented structures, have been isolated from the fruiting bodies of the mushroom Mycena rosella. The structures of the rosellins were mainly deduced from their 2D NMR and HRMS (ESI) spect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac585a8049f116bd7a4feb836845ccef
https://doi.org/10.1016/j.tet.2018.06.049
https://doi.org/10.1016/j.tet.2018.06.049