Jianyou Mao
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Explore the profile of Jianyou Mao including associated specialties, affiliations and a list of published articles.
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45
Citations
176
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Recent Articles
1.
Zhu S H, Wu Y, Mao J, Xu J, Walsh P, Shi H
Chem Soc Rev
. 2025 Feb;
54(5):2520-2542.
PMID: 39911075
Benzylic C-H functionalization is a valuable tool to make complex aromatic molecules from simple, readily available alkylbenzenes. While methods that involve benzylic radicals or cations generated by hydrogen atom transfer...
2.
Jiang M, Wang Y, Gu Y, Ma R, Xiong D, Walsh P, et al.
Org Lett
. 2024 Nov;
26(45):9710-9716.
PMID: 39499791
The one-pot synthesis of diphenylacetylene by the reaction of methyl benzoate with 1-(benzylsulfonyl)-3,5-di(trifluoromethyl)benzene was developed. The combination of LiN(SiMe) and KN(SiMe) is key to promoting the reaction. Simply combining methyl...
3.
Xu L, Zhang F, Wang Y, Bai C, Xiong D, Mao J
Org Lett
. 2024 Oct;
26(43):9288-9293.
PMID: 39431957
A highly regioselective cobalt-catalyzed three-component alkyl arylation of acrylates with alkyl iodides and aryl Grignard reagents has been established. The reaction efficiently provides an alternative strategy for the construction of...
4.
Gao X, Lin T, Wang Y, Xing F, Qiu Y, Xiong D, et al.
Org Lett
. 2024 Oct;
26(41):8792-8797.
PMID: 39377550
An enantioselective 1,2-dicarbofunctionalization of vinyl (hetero)arenes with alkyl bromides and aryl bromides through nickel/photoredox catalysis is described. This three-component enantioselective domino alkyl arylation of vinyl (hetero)arenes could generate a diverse...
5.
Wu Y, Satiro B, Mao J, Walsh P
Angew Chem Int Ed Engl
. 2024 Sep;
64(3):e202415472.
PMID: 39331948
Alkynyl amides play crucial roles in organic synthesis in the production of bioactive compounds and valuable heterocycles. Despite numerous studies on their synthesis, challenges persist due to the necessity of...
6.
Ma R, Gu Y, Wang Y, Fei R, Xiong D, Mao J
Org Lett
. 2024 Jun;
26(24):5082-5086.
PMID: 38848449
Indolin-3-ones are essential heterocycles with wide-ranging biological activities and medicinal values, and therefore, efficient approaches to their synthesis remain in demand. Herein, a novel and operationally simple method to generate...
7.
Shuai S, Mao J, Zhou F, Yan Q, Chen L, Li J, et al.
J Org Chem
. 2024 May;
89(10):6793-6797.
PMID: 38691096
A convenient method for preparing 3-aryl isoquinolines via a base-promoted tandem reaction is presented. Simply combining commercially available 2-methyl-arylaldehydes, benzonitriles, NaN(SiMe), and CsCO enabled the synthesis of a variety of...
8.
Zheng J, Hua R, Wang Y, Lin T, Ou M, Wu Y, et al.
Org Lett
. 2024 Apr;
26(15):2982-2986.
PMID: 38602341
Pd(OAc)/Nixantphos or CoI/Nixantphos catalyzed allylic substitutions with weakly acidic C(sp)-H bonds of azaarylmethylamines are described. This method facilitates access to various kinds of heteroaryl rings containing homoallylamines (39 examples, 30-98%...
9.
Liu Q, Lin T, Wang Y, Liang W, Cao L, Sheng X, et al.
Org Lett
. 2023 Dec;
25(51):9153-9157.
PMID: 38096429
A nickel-catalyzed cross-electrophile coupling of aryl iodides with α-bromo sulfoxide to access a diverse array of aryl benzyl sulfoxides has been discovered. These reactions occurred under mild conditions with excellent...
10.
Xing F, Lin T, Ye Y, Wang Y, Cao X, Gao X, et al.
Chem Commun (Camb)
. 2023 Oct;
59(89):13355-13358.
PMID: 37873615
The first dual nickel/photoredox-catalyzed enantioselective reductive cross-coupling of racemic α-chloro thioesters with aryl iodides has been developed. This strategy avoids the need for organometallic reagents or stoichiometric metal reductants. This...