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期刊名:Organic letters

缩写:ORG LETT

ISSN:1523-7060

e-ISSN:1523-7052

IF/分区:5.0/Q1

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共收录本刊相关文章索引32031
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Dan Liu,Juan Hu,Qu Luo et al. Dan Liu et al.
The development of methods to form anilines has been a long-standing interest in the synthesis field driven by the prevalence of these motifs in natural products, pharmaceuticals, and functional organic materials. Here, a successful protoco...
Meiqun Lu,Enqi Xie,Wenjie Song et al. Meiqun Lu et al.
Here introduces a novel method for the electrochemical decarboxylative primary alkylarylation of alkenes using quaternary ammonium salts from fatty acids, eliminating the need for external oxidants or metal catalysts to facilitates the effi...
Ashutosh Nath,Jiaming Zhu,Lydia Seki et al. Ashutosh Nath et al.
A new Friedel-Crafts-type reaction involving the formation and ring expansion of spiro-β-lactam is discovered in the synthesis of imidazopyridine- and indole-fused azepinones. The Groebke-Blackburn-Bienaymé (GBB) reaction adducts undergo ...
Peiyi Jin,Jia Hui Ng,Edward R T Tiekink et al. Peiyi Jin et al.
The isoxazole ring transformation was effectively applied for the synthesis of diverse pyrimidines by using a three-component reaction of 5-aminoisoxazole-4-carbonitrile with primary amines and orthoesters. The one-pot rearrangement of the ...
Yongli Zhang,Hao Guan,Qin Duan et al. Yongli Zhang et al.
Three BODIPY dimers fused with five- and six-membered N-heterocycles were synthesized via an SNAr and C-H activation strategy. N-Heterocycle size enables precise modulation of electronic delocalization and excited-state character. The six-m...
Gui-Hao Zhang,Zhong-Ping Cai,Tian Ye et al. Gui-Hao Zhang et al.
Deconstructive alkylation of unstrained cyclic amines is achieved through a boryl radical-enabled spin-center shift (SCS) strategy. Mechanistic studies, including control experiments and DFT calculations, support a pathway involving boryl r...
Yanxia Huang,Yuanping Li,Na Huang et al. Yanxia Huang et al.
Ferrocene-anthracene-fused ladder-type molecules (2Fc-anti and 2Fc-syn) were achieved via a C-H activation/annulation strategy. This design extends the π-conjugated system through molecular ladderization, effectively elongating the molecul...
Bingyang Han,Zihui Gong,Zhaofeng Wang Bingyang Han
We report herein a Rh-catalyzed tandem reaction between a pivaloyl-substituted sulfoxonium-iodonium ylide and diverse nucleophiles, enabling the efficient synthesis of γ-sulfoxonium carbonyl compounds, which were previously inaccessible. T...
Joakim Bøgelund Jakobsen,Xinkai Wu,Markus Staudt et al. Joakim Bøgelund Jakobsen et al.
Interconversion of functional groups in organic chemistry is a key task. Here we have developed an oxidative transformation of aldehydes to nitriles using lithium bis(trimethylsilyl)amide as a nitrogen source and copper iodide as an inexpen...
Kang Guo,Bin Chen,Yongchao Lu et al. Kang Guo et al.
A [4 + 2] annulation with 1,3-dienes, AgSCF3, and KI has been established, affording a variety of CF3S-substituted 2H-thiopyrans with high chemo- and regioselectivities. The intermediate (CF3S)2C═S is generated in situ via the reaction of ...