Results 1 to 10 of about 10,321 (224)

Total Syntheses of Sappanin-Based Natural Products Enabled by Pattern Recognition Analysis and Brominative Aromatization. [PDF]

Chem Asian J
Zhao WT, Liang JY, Wu YK.
europepmc   +1 more source

DDQ-catalyzed oxidative α-allylation of isochromans under aerobic conditions. [PDF]

RSC Adv
Lee S, Jung S, Hyeon S, Kim K, Min SJ.
europepmc   +1 more source

Scalable Total Synthesis of Bastimolide A Enabled by Asymmetric Allylborations Catalyzed by Chiral Brønsted Acids. [PDF]

JACS Au
Umemiya S, Shinagawa N, Fujimoto A, Terada M.   +3 more
europepmc   +1 more source

Facile, general allylation of unactivated alkyl halides <i>via</i> electrochemically enabled radical-polar crossover. [PDF]

Chem Sci
Chen H, Rueping M.
europepmc   +1 more source

DFT Calculation-Assisted Virtual Screening to Refine Chiral Phosphoric Acid-Catalyzed Allylboration Enabling Organocatalytic Synthesis of Tetrafibricin C21-C40 Fragment. [PDF]

JACS Au
Umemiya S, Hirata T, Terada M.
europepmc   +1 more source

Kinetics and Mechanisms of the Allyl + Allyl and Allyl + Propargyl Recombination Reactions

The Journal of Physical Chemistry A, 2011
The kinetics and mechanisms of the self-reaction of allyl radicals and the cross-reaction between allyl and propargyl radicals were studied both experimentally and theoretically. The experiments were carried out over the temperature range 295-800 K and the pressure range 20-200 Torr (maintained by He or N(2)).
Akira, Matsugi, Kohsuke, Suma, Akira, Miyoshi   +2 more
openaire   +2 more sources

Allylation of Epoxides with Allylic Indium Reagents.

ChemInform, 2004
Allylindium sesquihalide reacts with epoxide to give homoallyl alcohol via a 1,2-shift reaction. In contrast, allylindate gives the ring-opening product without rearrangement.
Tsunehisa Hirashita, Kazuma Mitsui, Yousuke Hayashi, Shuki Araki   +3 more
openaire   +1 more source

Triflimide-catalyzed allyl–allyl cross-coupling: a metal-free allylic alkylation

Chemical Communications, 2012
A highly efficient metal-free intermolecular C(sp3)-C(sp3) allyl-allyl cross-coupling protocol between allyl acetates and allyltrimethylsilanes, which proceeded smoothly in the presence of catalytic triflimide to form 1,5-dienes with good to excellent regioselectivity, has been developed.
Ding, Feiqing, William, Ronny, Wang, Fei, Liu, Xue-Wei   +3 more
openaire   +3 more sources

Telomerization Studies with Allyl Ethene Sulfonate and Allyl Allyl Sulfonate

Journal of Macromolecular Science: Part A - Chemistry, 1971
Abstract Telomerization of allyl ethene sulfonate (AES) in the presence of butyl mercaptan yielded a mixture of two products: the first was a five-membered ring sultone containing a sulfide group and the second a five-membered ring sulfonium salt formed by reaction of the sultone of the Just product with its own sulfide function.
E. De Witte, E. J. Goethals
openaire   +1 more source