Results 111 to 120 of about 8,483 (210)

Auxin activity of 3-hydroxymethyl oxindole and 3-methylene oxindole in oat

open access: yesBiologia Plantarum, 1986
Two photooxidation products of indol-3-ylacetic acid (IAA), 3-hydroxymethyl oxindole (HMO) and 3-methylene oxindole (Meox) were almost as effective as IAA in stimulation of growth of oat (Avena saliva cv. Kent) coleoptile sections. The IAA failed to give stimulation of growth after pretreatment of the coleoptiles with chemicals inhibiting oxidation of ...
R. N. Bhattacharyya   +2 more
openaire   +1 more source

Asymmetric α-amination of 3-substituted oxindoles using chiral bifunctional phosphine catalysts

open access: yesBeilstein Journal of Organic Chemistry, 2016
A highly enantioselective α-amination of 3-substituted oxindoles with azodicarboxylates catalyzed by amino acids-derived chiral phosphine catalysts is reported. The corresponding products containing a tetrasubstituted carbon center attached to a nitrogen
Qiao-Wen Jin   +4 more
doaj   +1 more source

Organocatalytic asymmetric Michael addition of unprotected 3-substituted oxindoles to 1,4-naphthoquinone

open access: yesBeilstein Journal of Organic Chemistry, 2012
We reported the first example of organocatalytic Michael addition of unprotected 3-prochiral oxindoles 1 to 1,4-naphthoquinone. Quinidine derivative (DHQD)2PYR was found to be able to catalyze this reaction in up to 83% ee, with moderate to excellent ...
Jin-Sheng Yu   +3 more
doaj   +1 more source

Domino Reactions Enable Zn-Mediated Direct Synthesis of Spiro-Fused 2-Oxindole-α-Methylene-γ-Butyrolactones/Lactams from Isatin Derivatives and 2-(Bromomethyl)acrylates

open access: yesMolecules
Isatin-derived spirocyclic cores are found in several biologically active molecules. Here, we report nucleophilic domino reactions for the synthesis of α-methylene-γ-butyrolactone/lactam containing spirocyclic oxindoles. The Zn-mediated one-step reaction
Prathap Reddy Mukthapuram   +1 more
doaj   +1 more source

Facile synthesis of functionalized spiro[indoline-3,2'-oxiran]-2-ones by Darzens reaction

open access: yesBeilstein Journal of Organic Chemistry, 2013
A series of functionalized spiro[indoline-3,2'-oxiran]-2-ones was efficiently synthesized by Darzens reaction of phenacyl bromides with isatins both with N-alkyl groups and without N-substituent in the presence of potassium carbonate as a base catalyst ...
Qin Fu, Chao-Guo Yan
doaj   +1 more source

Chemistry [PDF]

open access: yes
Photoactivatable fluorophores are essential tools for studying the dynamic molecular interactions within important biological systems with high spatiotemporal resolution.

core  

Oxindoles. V. Selective Solvolysis Reactions of Oxindole-Spirodimer

open access: yesYAKUGAKU ZASSHI, 1985
YOSHIKAZU KONDO   +2 more
openaire   +2 more sources

Alcaloïdes de l'Uncaria guianensis [PDF]

open access: yes, 1983
Bruneton, J.   +2 more
core   +1 more source

Palladium-Catalyzed Construction of Quaternary Stereocenters by Enantioselective Arylation of γ-Lactams with Aryl Chlorides and Bromides [PDF]

open access: yes, 2019
Herein, we report the first Pd‐catalyzed enantioselective arylation of α‐substituted γ‐lactams. Two sets of conditions were developed for this transformation, allowing for the use of either aryl chlorides or bromides as electrophiles.
Bachman, Shoshana   +7 more
core   +1 more source

Synthese des Oxindols [PDF]

open access: yesBerichte der deutschen chemischen Gesellschaft, 1878
openaire   +1 more source

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