Ligand-controlled stereodivergent 1, 3-dipolar cycloaddition of azomethine ylides with 3-methyl-4-nitro-5-styrylisoxazoles
K Liu, Y Xiong, ZF Wang, HY Tao… - Chemical …, 2016 - pubs.rsc.org
An unprecedented Ag (I)-catalyzed ligand-controlled stereodivergent 1, 3-dipolar
cycloaddition of azomethine ylides with 3-methyl-4-nitro-5-styrylisoxazoles has been …
cycloaddition of azomethine ylides with 3-methyl-4-nitro-5-styrylisoxazoles has been …
1, 3-Dipolar cycloaddition of N-allyl substituted polycyclic derivatives of isoindole-1, 3-dione with nitrones and nitrile oxides: An experimental and theoretical …
MM Efremova, AP Molchanov, AS Novikov, GL Starova… - Tetrahedron, 2020 - Elsevier
Cycloaddition reactions of N-allyl substituted polycyclic derivatives of isoindole-1, 3-dione
with nitrones proceeds regio-and stereoselectively on the double bond of the N-allyl …
with nitrones proceeds regio-and stereoselectively on the double bond of the N-allyl …
Progress in reductive Heck reaction
X Yang, S Ma, TY Du Yanni - Chinese Journal of Organic Chemistry, 2013 - sioc-journal.cn
Reductive Heck reaction is a coupling reaction which unsaturated halides react with olefinic
compounds at the similar Heck conditions to form the addition products. In this paper, the …
compounds at the similar Heck conditions to form the addition products. In this paper, the …
[PDF][PDF] Reductive Heck Reactions and [3+ 2] Cycloadditions of Unsaturated N, N'-Bistricyclic Imides
The C–C coupling of N, N'-bis (5-norbornene-2, 3-dicarboximide)(3) and N, N'-bis (7-oxa-5-
norbornene-2, 3-dicarboximide)(6) with aryl and heteroaryl iodides gave under reductive …
norbornene-2, 3-dicarboximide)(6) with aryl and heteroaryl iodides gave under reductive …
Synthesis of new aryl (hetaryl)-substituted tandospirone analogues with potential anxiolytic activity via reductive Heck type hydroarylations
Tandospirone (I), developed as an anxiolytic drug, is an aryl-piperazine compound that
binds to both 5-HT1A and dopamine D4 receptors. Palladium-catalysed hydroarylation …
binds to both 5-HT1A and dopamine D4 receptors. Palladium-catalysed hydroarylation …
还原型Heck 反应的研究进展
杨晓梅， 马莎， 杜艳妮， 陶云海 - 有机化学, 2013 - sioc-journal.cn
Untitled Page 1 Page 2 Page 3 有机化学 Chinese Journal of Organic Chemistry REVIEW * E-mail:
cloudsea2000@163.com Received March 31, 2013; revised May 20, 2013; published online …
cloudsea2000@163.com Received March 31, 2013; revised May 20, 2013; published online …
Suzuki-Miyaura cross-coupling of 3, 4-disubstituted 5-bromoisoxazoles: An efficient access to trisubstituted isoxazoles
M Tsuda, T Morita, H Nakamura - Tetrahedron Letters, 2021 - Elsevier
Abstract The Suzuki-Miyaura cross-coupling of 3, 4-disubstituted 5-bromoisoxazoles 1 at the
C5 position has successfully proceeded in the presence of Pd 2 (dba) 3 and P (t-Bu) 3· HBF …
C5 position has successfully proceeded in the presence of Pd 2 (dba) 3 and P (t-Bu) 3· HBF …
Synthesis of new tandospirone analogues carrying 1-(3-(trifluoromethyl) phenyl) piperazine
OT Gunkara, BO Sucu, M Guleli… - Synthetic Communications, 2014 - Taylor & Francis
New tandospirone analogues containing a 1-[3-(trifluoromethyl) phenyl] piperazine (TFMPP)
moiety have been synthesized by hydroarylation reactions with Pd (OAc) 2. The …
moiety have been synthesized by hydroarylation reactions with Pd (OAc) 2. The …
Evaluation of the Antioxidative Properties of N‐Acylamino‐Substituted Tricyclic Imides
New N‐acylamino‐substituted tricyclic imides have been screened for scavenging ability
against the free radical 2, 2‐diphenyl‐1‐picryl‐hydrazyl (DPPH•), chelating activity on …
against the free radical 2, 2‐diphenyl‐1‐picryl‐hydrazyl (DPPH•), chelating activity on …
Hydroarylation reactions of N-acylaminosubstituted tricyclic imides
Hydroarylation reactions of N-acylaminosubstituted tricyclic imides Page 1 JOURNAL OF
CHEMICAL RESEARCH 2013 RESEARCH PAPER 345 JUNE, 345–350 Hydroarylation reactions …
CHEMICAL RESEARCH 2013 RESEARCH PAPER 345 JUNE, 345–350 Hydroarylation reactions …