Zobrazeno 1 - 10
of 14
pro vyhledávání: '"John A. Eickhoff"'
Autor:
Eryn Lussier, Rachael Boothe, Genevieve Braus, John W. Eickhoff, Theodore Devito, Larry O. Durbin, Kurt A. Schlomberg, Brenna Birt, Eric D. Schmitz, Tom Ryon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bdfaf939cbb12947497e97edeb72a5b4
https://doi.org/10.2172/1814599
https://doi.org/10.2172/1814599
Publikováno v:
Organic Chemistry Frontiers. 3:330-334
The intramolecular aza-(4 + 3) cycloaddition reactions of in situ generated aza-oxyallylic cations and furans have been reported for the construction of medium sized hydroxamate macrocycles. This method provides direct access to 12–18 membered bicy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ead2a4ede232101c983dd3dcbcf2e42e
https://doi.org/10.1039/c5qo00315f
https://doi.org/10.1039/c5qo00315f
Publikováno v:
The Journal of Organic Chemistry. 80:9989-9999
Facile synthesis of a variety of α-heterosubstituted ketones under mild conditions was achieved by copper-mediated cross-coupling of thioesters with functionalized organostannanes. Application of this coupling methodology provided a concise pathway
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65c2e2c23e1a680f7898c7f4232bcdc0
https://doi.org/10.1021/acs.joc.5b01558
https://doi.org/10.1021/acs.joc.5b01558
Publikováno v:
Journal of the American Chemical Society
Michael addition is a premier synthetic method for carbon–carbon and carbon–heteroatom bond formation. Using chiral dilithium amides as traceless auxiliaries, we report the direct enantioselective Michael addition of carboxylic acids. A free carb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e5752579259b8b6fe543ba2e89e2d9a
https://doi.org/10.1021/ja512213c
https://doi.org/10.1021/ja512213c
Publikováno v:
Synthesis. 45:1825-1836
Polyheterocyclic scaffolds were prepared by intramolecular aza-[4+3] cycloaddition reactions of aza-oxyallylic cations with cyclic dienes. The aza-oxyallylic cation was generated in situ by the dehydrohalogenation of α-halohydroxamates. The highly f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::669e25bc12f11f36eac153e004cf1fd6
https://doi.org/10.1055/s-0033-1338883
https://doi.org/10.1055/s-0033-1338883
Publikováno v:
ChemInform. 47
The intramolecular aza-(4 + 3) cycloaddition reactions of in situ generated aza-oxyallylic cations and furans have been reported for the construction of medium sized hydroxamate macrocycles. This method provides direct access to 12–18 membered bicy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd1532e191218d36edadbcff3ae92bab
https://doi.org/10.1002/chin.201627201
https://doi.org/10.1002/chin.201627201
Autor:
Artur K. Mailyan, John A. Eickhoff, Armen Zakarian, Anastasiia S. Minakova, Ping Lu, Zhenhua Gu
Publikováno v:
ChemInform. 47
The main objective of this review is to provide a comprehensive survey of methods used for stereoselective construction of carbon–nitrogen bonds during the total synthesis of nitrogen-containing natural products that have appeared in the literature
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0307b4f03326afd9397e86c40819eee1
https://doi.org/10.1002/chin.201624258
https://doi.org/10.1002/chin.201624258
Autor:
Zhenhua Gu, Armen Zakarian, Ping Lu, Artur K. Mailyan, John A. Eickhoff, Anastasiia S. Minakova
Publikováno v:
Chemical reviews. 116(7)
The main objective of this review is to provide a comprehensive survey of methods used for stereoselective construction of carbon–nitrogen bonds during the total synthesis of nitrogen-containing natural products that have appeared in the literature
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97d9d84b2565ebd7260b714778739a8c
https://pubmed.ncbi.nlm.nih.gov/27014921
https://pubmed.ncbi.nlm.nih.gov/27014921