Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Petri, M. A."'
Autor:
Sakari Tuokko, Petri M. Pihko
Publikováno v:
Organic Process Research & Development. 18:1740-1751
Stoichiometric quantities of triethylsilane in the presence of activated Pd/C as the catalyst can be used to effect chemo-, regio-, and stereoselective hydrosilylation and transfer hydrogenation reactions. α,β-Unsaturated aldehydes and ketones are
Autor:
Petri M. Pihko, Sakari Tuokko
Publikováno v:
ChemInform. 47
Aldehyde α-hydroperoxides can be accessed from α-substituted acroleins with triethylsilane and water under Pd/C catalysis and aerobic conditions. The reaction is composed of a Pd/C-catalyzed conjugate reduction step and a hydroperoxidation step. Th
Autor:
Sarngadharan Sarath Chand, Kokkuvayil Vasu Radhakrishnan, E. Jijy, Petri M. Pihko, Praveen Prakash, Preethalayam Preethanuj
Publikováno v:
Chemistry - A European Journal. 19:10473-10477
The first utilization of acyclic cyclopropane bearing spirocyclic olefines for the generation of stereospecific complex fused ring systems with an achiral catalyst is reported.
Publikováno v:
Angewandte Chemie International Edition. 52:4818-4822
Autor:
Kokkuvayil Vasu Radhakrishnan, Rani Rajan, Nayana Joseph, N. V. Devika, Jubi John, Shyam Chand, Petri M. Pihko, Eringathodi Suresh
Publikováno v:
RSC Advances. 3(21):7751-7757
A simple and efficient method for the stereoselective ring opening of bicyclic hydrazines with various aryl halides under palladium catalysis has been elaborated. The reactions afforded trans-3,4-disubstituted cyclopentenes or alkylidene cyclopentene
Publikováno v:
Chemistry : A European Journal. 18(4):1259-12594
The Bronsted aids: The first dehydrogenative arylation of β-keto esters with arenes under ambient aerobic conditions is described. Under a Pd(II)/Bronsted acid co-catalytic system, regioselective arylations with alkoxylated arenes and phenols were a
Publikováno v:
Chemistry - A European Journal. 17:8404-8413
A highly versatile and efficient hydrosilylation method by palladium nanoparticle catalysis allows the direct and chemoselective synthesis of 1) enolsilanes of high isomeric purity, 2) saturated aldehydes or ketones, or 3) the corresponding saturated
Akademický článek
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Autor:
Kokkuvayil Vasu Radhakrishnan, E. Jijy, Petri M. Pihko, Praveen Prakash, Preethalayam Preethanuj, Sarngadharan Sarath Chand
Publikováno v:
ChemInform. 44
The first utilization of acyclic cyclopropane bearing spirocyclic olefines for the generation of stereospecific complex fused ring systems with an achiral catalyst is reported.
Publikováno v:
ChemInform. 44
The process tolerates a broad spectrum of substrates and the highly functionalized indole scaffolds are formed under mild conditions with excellent regioselectivity.