Results 111 to 120 of about 108,077 (187)

Cobalt-Catalyzed Cyclohydrocarbonylations: Syntheses of Saturated Heterocycles Promoted by Light. [PDF]

J Am Chem Soc
Rodriguez MR, Jung M, Faculak MS, Handlin AD, Liu S, Alexanian EJ.   +5 more
europepmc   +1 more source

Enantioselective Carbonyl Crotylation of Alcohol Proelectrophiles via Ruthenium-Catalyzed Hydrogen Autotransfer: Innovation Inspired by Polyketide Total Synthesis. [PDF]

ACS Catal
Meares PW, Santana CG, Krische MJ.
europepmc   +1 more source

Mechanistic elucidation of the uncatalyzed allylation of carbonyl compounds: a combined DFT and nudged elastic band study. [PDF]

J Mol Model
Da Silva WDAB, Da Silva JAB, Freitas JCR, Dias RP, Da Silva JCS.   +4 more
europepmc   +1 more source

Alternative pathways for Heck intermediates: palladium-catalyzed oxyarylation of homoallylic alcohols. [PDF]

Angew Chem Int Ed Engl, 2011
Zhu C, Falck JR.
europepmc   +1 more source

Adamantyl-BOX Ligand Enabling Stereoselective Synthesis of Axially Chiral Aldehydes Bearing Vicinal Stereogenic Centers. [PDF]

ACS Cent Sci
Hao EJ, Ding XB, Shan JR, Wu Z, Wang X, Cao R, Jin F, Houk KN, Shi L.   +8 more
europepmc   +1 more source

Catalytic Asymmetric (<i>ene</i>-<i>endo</i>)-Carbonyl-Ene Type Cyclizations. [PDF]

J Am Chem Soc
Shi L, Tsuji N, Zhu C, Leutzsch M, Grimm JAA, List B.   +5 more
europepmc   +1 more source

Dual Co/Photoredox-Catalyzed Regio- and Stereoselective Allyl Homocoupling Providing Functionalized 1,5-Dienes. [PDF]

Org Lett
Gao F, Armellin G, Amos SGE, Kleij AW.
europepmc   +1 more source

Enantioselective Alkyne-Mediated Aldehyde Allylation of Alcohol Proelectrophiles Using RuHCl(CO)(PPh₃)₃ as Precatalyst. [PDF]

Org Lett
Evarts MM, Nguyen TN, Krische MJ.
europepmc   +1 more source

Enantioselective Butadiene-Mediated Aldehyde Crotylation of Alcohol Proelectrophiles: RuHCl(CO)(PPh₃)₃ as a Precatalyst. [PDF]

Org Lett
Santana CG, Pfaffinger DE, Meares PW, Krische MJ.   +3 more
europepmc   +1 more source

Catalyst-controlled Wacker-type oxidation of homoallylic alcohols in the absence of protecting groups. [PDF]

J Org Chem, 2011
McCombs JR, Michel BW, Sigman MS.
europepmc   +1 more source