Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Thomas Schwarzlose"'
Publikováno v:
ARKIVOC, Vol 2007, Iss 8, Pp 341-357 (2007)
Externí odkaz:
https://doaj.org/article/bbf9eeab2f024a16ba4c5ba750a6f24e
Autor:
Suresh Moorthy, Hugues Lambert, Neetha Mohan, Thomas Schwarzlose, Werner M. Nau, Elina Kalenius, Tung‐Chun Lee
Publikováno v:
Angewandte Chemie.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fb6586ebc4ab0b5dc9b351d90769c0e
https://doi.org/10.1002/ange.202303491
https://doi.org/10.1002/ange.202303491
Autor:
Fang Huang, Werner M. Nau, Roy N. Dsouza, Thomas Schwarzlose, Elisha Haas, Xiaojuan Wang, Maik H. Jacob
Publikováno v:
The journal of physical chemistry. B. 122(16)
Protein folding can be described as a probabilistic succession of events in which the peptide chain forms loops closed by specific amino acid residue contacts, herein referred to as loop nodes. To measure loop rates, several photophysical methods hav
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af138e95b1b180125bdc327124ae9619
https://pubmed.ncbi.nlm.nih.gov/29617564
https://pubmed.ncbi.nlm.nih.gov/29617564
Publikováno v:
Organic Letters. 10:4089-4092
The derivatization of 3-amino-9-ethylcarbazole with a diamino-alkyl anchor affords a fluorescent dye suitable for indicator displacement from cucurbituril macrocycles. The novel compound 1 shows, due to a complexation-induced pKa shift, a large and p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11a46315dcc0c192c7f5c0044aecef53
https://doi.org/10.1021/ol8016275
https://doi.org/10.1021/ol8016275
Autor:
Werner M. Nau, Roy N. Dsouza, Maik H. Jacob, Thomas Schwarzlose, Indrajit Ghosh, Amir Norouzy
Publikováno v:
The journal of physical chemistry. B. 117(1)
The structural and dynamic properties of a flexible peptidic chain codetermine its biological activity. These properties are imprinted in intrachain site-to-site distances as well as in diffusion coefficients of mutual site-to-site motion. Both dista
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6cf7d3a507acaead2e42ecc49ab6c65
https://pubmed.ncbi.nlm.nih.gov/23215358
https://pubmed.ncbi.nlm.nih.gov/23215358
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 12(18)
The pD dependence of the complexation of p-sulfonatocalix[4]arene (CX4) with the azoalkanes 2,3-diazabicyclo[2.2.1]hept-2-ene (1), 2,3-diazabicyclo[2.2.2]oct-2-ene (2), 2,3-diazabicyclo[2.2.3]non-2-ene (3), and 1-methyl-4-isopropyl-2,3-diazabicyclo-[
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d605e0f4a8e61b9cc4d64df4ad545a91
https://pubmed.ncbi.nlm.nih.gov/16673426
https://pubmed.ncbi.nlm.nih.gov/16673426
Publikováno v:
Organic Letters; Aug2008, Vol. 10 Issue 18, p4089-4092, 4p
Publikováno v:
ResearcherID
ARKIVOC, Vol 2007, Iss 8, Pp 341-357 (2007)
ARKIVOC, Vol 2007, Iss 8, Pp 341-357 (2007)
Two novel derivatives of 2,3-diazabicyclo(2.2.2)oct-2-ene were synthesized, carrying a carboxyl (4) and a methylcarboxyl (5) substituent at the bridgehead position. The photodecomposition quantum yields (51% for 4 and 2.9% for 5) and fluorescence lif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9d5c7a63c410a9b09ac971008c18ef4
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000249060000026&KeyUID=WOS:000249060000026
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000249060000026&KeyUID=WOS:000249060000026
