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Recent advances in multi-component reactions and their mechanistic insights: a triennium review
SE John, S Gulati, N Shankaraiah - Organic Chemistry Frontiers, 2021 - pubs.rsc.org
Multi-component reactions (MCRs) are considered to be an important methodological
arsenal in synthetic and medicinal chemistry. These reactions have been strategically …
arsenal in synthetic and medicinal chemistry. These reactions have been strategically …
Recent approaches in the organocatalytic synthesis of pyrroles
Organocatalysis has emerged as one of the most important tools for the synthesis of diverse
structural scaffolds, and has become one of the most important hot topics of current …
structural scaffolds, and has become one of the most important hot topics of current …
Iodine (V)-Based Oxidants in Oxidation Reactions
The chemistry of hypervalent iodine reagents has now become quite valuable due to the
reactivity of these compounds under mild reaction conditions and their resemblance in …
reactivity of these compounds under mild reaction conditions and their resemblance in …
Iodoxybenzoic acid (IBX) in organic synthesis: a septennial review
This study reviews the oxidative applications of 2-iodoxybenzoic acid (IBX) in organic
synthesis, focusing on CH functionalization, hetero-hetero bond formations, ring cleavage …
synthesis, focusing on CH functionalization, hetero-hetero bond formations, ring cleavage …
NiFe 2 O 4@ SiO 2–Cu as a novel and efficient magnetically recoverable nanocatalyst for regioselective synthesis of β-thiol-1, 2, 3-triazoles under benign conditions
R Eisavi, S Ghadernejad - RSC advances, 2023 - pubs.rsc.org
A green, mild and eco-friendly approach for the three component one-pot regioselective
synthesis of 1, 2, 3-triazoles from thiiranes has been introduced in the presence of …
synthesis of 1, 2, 3-triazoles from thiiranes has been introduced in the presence of …
An Efficient Sequential One‐Pot Approach for the Synthesis of C3‐Functionalized Imidazo[1,2‐a]pyridines under Transition‐Metal Free Conditions
RJ Reddy, A Shankar, AH Kumari - Asian Journal of Organic …, 2019 - Wiley Online Library
A metal‐free sequential one‐pot three‐component protocol is described for the synthesis of
C3‐functionalized imidazo [1, 2‐a] pyridines. A successive construction of imidazo [1, 2‐a] …
C3‐functionalized imidazo [1, 2‐a] pyridines. A successive construction of imidazo [1, 2‐a] …
Direct catalytic synthesis of β-(C3)-substituted pyrroles: a complementary addition to the Paal–Knorr reaction
The synthesis of β-(C3)-functionalized pyrroles is a challenging task and requires a
multistep protocol. An operationally simple direct catalytic synthesis of β-substituted pyrroles …
multistep protocol. An operationally simple direct catalytic synthesis of β-substituted pyrroles …
A simple route to tetracyclic oxazepine-fused pyrroles via metal-free [3+ 2] annulation between dibenzo [b, f][1, 4] oxazepines and aqueous succinaldehyde
S Choudhary, A Singh, J Yadav, NA Mir… - New Journal of …, 2019 - pubs.rsc.org
A direct method for the synthesis of new tetracyclic oxazepine-fused pyrroles has been
developed through [3+ 2] annulation between aqueous succinaldehyde and dibenzo [b, f][1 …
developed through [3+ 2] annulation between aqueous succinaldehyde and dibenzo [b, f][1 …
Sequential multicomponent site-selective synthesis of 4-iodo and 5-iodopyrrole-3-carboxaldehydes from a common set of starting materials by tuning the conditions
S Choudhary, J Yadav, AP Pawar… - Organic & …, 2020 - pubs.rsc.org
A simple and straightforward method for the synthesis of 4-iodo and 5-iodopyrrole-3-
carboxaldehydes is developed from a common set of starting materials by tuning the …
carboxaldehydes is developed from a common set of starting materials by tuning the …
Catalyst-free direct regiospecific multicomponent synthesis of C3-functionalized pyrroles
An operationally simple catalyst-free protocol for the direct regiospecific synthesis of β-(C3)-
substituted pyrroles has been developed. The enamine intermediate, in situ generated from …
substituted pyrroles has been developed. The enamine intermediate, in situ generated from …