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pro vyhledávání: '"Oliver T. Holton"'
Autor:
Joseph W. Stevenson, Oliver T. Holton
Publikováno v:
Platinum Metals Review. 57:259-271
Johnson Matthey, Orchard Road, Royston, Hertfordshire SG8 5HE, UK Email: *oliver.holton@matthey.com; **joe.stevenson@matthey.com Proton exchange membrane fuel cells (PEMFCs) dominate the transportation fuel cell market and platinum (Pt) is the cataly
Autor:
Amber L. Thomson, C. Adam Russell, Craig D. Campbell, P. Ross Walker, Helen A. Chapman, Rebecca L. Greenaway, Greg Carr, Oliver T. Holton, Edward A. Anderson
Publikováno v:
ChemInform. 47
A plenty of azacycles is obtained by a cascade sequence of carbopalladation followed by cross-coupling/electrocyclization, or reduction processes.
Autor:
Craig D. Campbell, Helen A. Chapman, Oliver T. Holton, Rebecca L. Greenaway, Edward A. Anderson
Publikováno v:
ChemInform. 45
Cascade reaction of bromoenynamides such as (I) and (V) equipped with an additional alkyne or ynamide substituent affords azatricyclic products (II) and (VI), respectively.
Autor:
Edward A. Anderson, Oliver T. Holton, Craig D. Campbell, Rebecca L. Greenaway, Helen A. Chapman
Publikováno v:
Chemical communications (Cambridge, England). 50(40)
Palladium-catalyzed cascade cyclization of bromoenynamides equipped with an additional alkyne or ynamide substituent affords azatricyclic products. Using 5- to 7-membered ring tethers, this chemistry offers a regiospecific route to highly-functionali
Autor:
Edward A. Anderson, Oliver T. Holton, Rebecca L. Greenaway, Craig D. Campbell, C. Adam Russell
Publikováno v:
ChemInform. 43
Bromoenynamides can serve as substrates for the synthesis of a diverse range of bicyclic aminodienes using a palladium cascade cyclization.
Autor:
Edward A. Anderson, Oliver T. Holton, C. Adam Russell, Craig D. Campbell, Rebecca L. Greenaway
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 17(51)
Cascade reactions: A modular assembly of azabicycles by using a cascade cyclization/Suzuki coupling/6π-electrocyclization of bromoenynamides is reported. The reaction offers a wide substituent scope on the bicyclic aminodiene products, which can be