Results 1 to 10 of about 3,465 (163)

Application of Hosomi-Sakurai allylation reaction in total synthesis of biologically active natural products [PDF]

open access: yesFrontiers in Chemistry
The Hosomi–Sakurai allylation reaction has been widely applied in the total synthesis of biologically active natural products, especially in synthesising complex polycyclic compounds containing multi-stereogenic centres since its discovery in 1976.
Justice Akwensi   +3 more
doaj   +2 more sources

Copper-Catalyzed Enantioselective Allyl–Allyl Cross-Coupling [PDF]

open access: yesJournal of the American Chemical Society, 2013
A Cu(I)-phosphoramidite-based catalytic system that allows asymmetric allyl-allyl cross-coupling with high enantioselectivity is reported. This transformation tolerates a large variety of functionalized substrates. The versatility of this new reaction is illustrated in the catalytic asymmetric synthesis of the Martinelline alkaloids chromene derivative
Hornillos, Valentin   +3 more
  +8 more sources

Transition-metal-free allylation of 2-azaallyls with allyl ethers through polar and radical mechanisms

open access: yesNature Communications, 2021
Allylation of nucleophiles with less reactive electrophiles, such as carbonates, usually requires a transition-metal catalyst. Here, the authors show a transition-metal-free allylation strategy with allyl ether electrophiles to form homoallylic amine ...
Guogang Deng   +8 more
doaj   +1 more source

Synthesis of Novel Crown Ether-Squaramides and Their Application as Phase-Transfer Catalysts

open access: yesMolecules, 2021
This work presents the synthesis of six new phase-transfer organocatalysts in which the squaramide unit is directly linked to the nitrogen atom of an aza-crown ether.
Zsuzsanna Fehér   +9 more
doaj   +1 more source

DABCO-Catalyzed Mono-/Diallylation of N-Unsubstituted Isatin N,N′-Cyclic Azomethine Imine 1,3-Dipoles with Morita-Baylis-Hillman Carbonates

open access: yesMolecules, 2023
Allylation of N-unsubstituted isatin N,N′-cyclic azomethine imines with Morita-Baylis-Hillman carbonates in the presence of 1–10 mol% DABCO in DCM at room temperature, rapidly gave N-allylated and N, β-diallylated isatin N,N′-cyclic azomethine imine 1,3 ...
Qiumi Wang   +10 more
doaj   +1 more source

Pd-Catalyzed Enantioselective Allyl−Allyl Cross-Coupling [PDF]

open access: yesJournal of the American Chemical Society, 2010
The Pd-catalyzed cross-coupling of allylic carbonates and allylB(pin) is described. The regioselectivity of this reaction is sensitive to the bite angle of the ligand, with small-bite-angle ligands favoring the branched substitution product. This mode of regioselection is consistent with a reaction that operates by a 3,3' reductive elimination reaction.
Ping, Zhang   +2 more
openaire   +2 more sources

Intramolecular Barbier reaction in water: cyclopentane and cyclohexane ring closure [PDF]

open access: yesJournal of the Serbian Chemical Society, 2002
Zinc or indium promoted intramolecular Barbier reactions of aldehydes containing a suitably positioned allylic or propargylic halide unit afford unsaturated cyclic alcohols in moderate yields.
RADOMIR N. SAICIC   +2 more
doaj   +3 more sources

Copper(I)-catalyzed asymmetric 1,6-conjugate allylation

open access: yesNature Communications, 2020
Catalytic asymmetric conjugate allylation of unsaturated carbonyl compounds is usually difficult to achieve due to competing 1,2-addition. Here, the authors report a copper(I)-catalyzed asymmetric 1,6-conjugate allylation of 2,2-dimethyl-6-alkenyl-4H-1,3-
Chang-Yun Shi   +3 more
doaj   +1 more source

A Green Approach for Allylations of Aldehydes and Ketones: Combining Allylborate, Mechanochemistry and Lanthanide Catalyst

open access: yesMolecules, 2016
Secondary and tertiary alcohols synthesized via allylation of aldehydes and ketones are important compounds in bioactive natural products and industry, including pharmaceuticals.
Viviane P. de Souza   +6 more
doaj   +1 more source

Generation and Reactions of ε-Carbonyl Cations via Group 13 Catalysis

open access: yesMolecules, 2022
The generation of ε-carbonyl cations and their reactions with nucleophiles is accomplished readily without transition metal cation stabilization, using the ε-bromide dienoate or dienone starting materials and GaCl3 or InCl3 catalysis.
Page M. Penner, James R. Green
doaj   +1 more source

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