Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Daniel T. Hog"'
Autor:
Hilmar Weinmann, Lisa Candish, Daniel T. Hog, Henriette Lämmermann, Lars Wortmann, Karl D. Collins, R. Meier, Alexander Sudau, Daniel Rackl
Publikováno v:
Synlett. 29:2679-2684
The sulfoximine group has been reported as a versatile and beneficial functionality for pharmaceutical or agrochemical entities. Herein, we report the Csp2–H sulfoximidation of electron-rich arenes under the irradiation of blue light using an org
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2920b507571cd37ddaf2f96c70987e82
https://doi.org/10.1055/s-0037-1609656
https://doi.org/10.1055/s-0037-1609656
Autor:
Dirk Trauner, Peter Mayer, Kendall N. Houk, Daniel T. Hog, Gonzalo Jiménez-Osés, Florian M. E. Huber
Publikováno v:
Chemistry - A European Journal. 21:13646-13665
Astellatol and nitidasin belong to a subset of sesterterpenoids that share a sterically encumbered trans-hydrindane motif with an isopropyl substituent. In addition, these natural products feature intriguing polycyclic ring systems, posing significan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8db63da8e7e62b87d36935e1c2d24d21
https://doi.org/10.1002/chem.201501423
https://doi.org/10.1002/chem.201501423
Autor:
Andreas Züttel, Jeffrey C. Gehrig, Elsa Callini, Santhosh Kumar Matam, Andreas Borgschulte, Daniel T. Hog, Cedric L. Hugelshofer
Publikováno v:
The Journal of Physical Chemistry C. 118:15940-15945
An empirical study of the gas–solid reaction of carbon dioxide (CO2) with alanates is presented. This investigation was triggered by reports of hazards related to the reaction of lithium aluminum hydride with carbon dioxide, together with the recen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9fae3434ba4f451b117cef485cce39a
https://doi.org/10.1021/jp505323j
https://doi.org/10.1021/jp505323j
Publikováno v:
Angewandte Chemie. 126:8653-8657
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a567b4b112f0a1bd5262ccc552da78a
https://doi.org/10.1002/ange.201403605
https://doi.org/10.1002/ange.201403605
Autor:
Pavol Jakubec, Peter N. Carlsen, Ian B. Seiple, Filip T. Szczypiński, Peter M. Wright, Kazuo Yabu, William D. Green, Yoshiaki Kitamura, Senkara Rao Allu, Audrey Langlois-Mercier, Andrew G. Myers, Daniel T. Hog, Ziyang Zhang, Xiang Zhou, Takehiro Fukuzaki, Matthew L. Condakes
Publikováno v:
Nature, vol 533, iss 7603
Nature
Nature
The chemical modification of structurally complex fermentation products, a process known as semisynthesis, has been an important tool in the discovery and manufacture of antibiotics for the treatment of various infectious diseases. However, many of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1131e840dbc9c733227cac4f62fc147f
https://escholarship.org/uc/item/4dp8m2jd
https://escholarship.org/uc/item/4dp8m2jd
Autor:
Daniel T. Hog, Feliu Maseras, Antonio M. Echavarren, Elena Herrero-Gómez, Patricia Pérez-Galán, Nolwenn J. A. Martin
Publikováno v:
Chem. Sci.. 2:141-149
The gold(I)-catalyzed intermolecular cyclopropanation of alkenes with 1,6-enynes is an electrophilic process, which is mechanistically related to the well-known Simmons–Smith reaction proceeding through zinc carbenoids. This cyclopropanation is ste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c747893a6ba8025730ab3d63d3124444
https://doi.org/10.1039/c0sc00335b
https://doi.org/10.1039/c0sc00335b
Autor:
Daniel T. Hog, Martin Oestreich
Publikováno v:
European Journal of Organic Chemistry. 2009:5047-5056
We recently employed a silicon-stereogenic silane as astereochemical probe to clarify the mechanism of the B(C6F5)3-catalyzed hydrosilylation of ketones. When using a prochiral ketone, reasonable stereoinduction was seen, originating from the stereog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9449cb82e1c0a493ebc9e184bca3b0d7
https://doi.org/10.1002/ejoc.200900796
https://doi.org/10.1002/ejoc.200900796
Publikováno v:
ChemInform. 46
Nitidasin is a pentacyclic sesterterpenoid with a rare 5-8-6-5 carbon skeleton that was isolated from the Peruvian folk medicine "Hercampuri". It belongs to a small class of sesterterpenoids that feature an isopropyl trans-hydrindane moiety fused to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d5435bda858d2ea4ba5c51807e91a44
https://doi.org/10.1002/chin.201506230
https://doi.org/10.1002/chin.201506230
Publikováno v:
Angewandte Chemie (International ed. in English). 53(32)
Nitidasin is a pentacyclic sesterterpenoid with a rare 5-8-6-5 carbon skeleton that was isolated from the Peruvian folk medicine "Hercampuri". It belongs to a small class of sesterterpenoids that feature an isopropyl trans-hydrindane moiety fused to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e5a21e97c362b93f6b4b010f23f3711
https://pubmed.ncbi.nlm.nih.gov/24962933
https://pubmed.ncbi.nlm.nih.gov/24962933
Publikováno v:
ChemInform. 43
Covering: up to December 2011 Sesterterpenoids account for many bioactive natural products, often with unusual and complex structural features, which makes them attractive targets for synthetic chemists. This review surveys efforts undertaken toward
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba599edb63272be81187389e75982f4a
https://doi.org/10.1002/chin.201236226
https://doi.org/10.1002/chin.201236226