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For: Deng Y, Chu W, Shang Y, Yu K, Jia Z, Fan C. P(NMe 2 ) 3 -Mediated Umpolung Spirocyclopropanation Reaction of p -Quinone Methides: Diastereoselective Synthesis of Spirocyclopropane-Cyclohexadienones. Org Lett 2020;22:8376-81. [DOI: 10.1021/acs.orglett.0c02998] [Cited by in Crossref: 11] [Cited by in F6Publishing: 6] [Article Influence: 5.5] [Reference Citation Analysis]
Number Citing Articles
1 Li J, Wang K, Wu J, Zhang H, Chen Y, Liu Q, Xu J, Yi W. Elemental Sulfur‐Promoted Synthesis of 4‐Hydroxybenzophenones from p ‐Quinone Methides under Metal‐Free Condition. European J Organic Chem 2022;2022. [DOI: 10.1002/ejoc.202200158] [Reference Citation Analysis]
2 Qiu ZW, Xu XT, Pan HP, Jia ZS, Ma AJ, Peng JB, Du JY, Feng N, Li BQ, Zhang XZ. Brønsted Acid-Catalyzed Formal (3+3)-Annulation of Propargylic (Aza)-para-Quinone Methides with 4-Hydroxycoumarins and 1,3-Dicarbonyl Compounds. J Org Chem 2021;86:6075-89. [PMID: 33820419 DOI: 10.1021/acs.joc.0c02844] [Reference Citation Analysis]
3 Ali A, Jajoria R, Harit HK, Singh RP. Diastereoselective 1,6-Addition of α-Phosphonyloxy Enolates to para-Quinone Methides. J Org Chem 2022. [PMID: 35378040 DOI: 10.1021/acs.joc.2c00030] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Zuo H, Ji X, Guo C, Tu S, Hao W, Jiang B. Cu-Catalyzed radical-triggered spirotricyclization of enediynes and enyne-nitriles for the synthesis of pentacyclic spiroindenes. Org Chem Front 2021;8:1496-502. [DOI: 10.1039/d0qo01640c] [Cited by in Crossref: 4] [Article Influence: 4.0] [Reference Citation Analysis]
5 Son Y, Hwang S, Bak S, Kim HE, Choi JH, Chung WJ. α-Fluoroamine synthesis via P(III)-mediated deoxygenative geminal fluorosulfonimidation of 1,2-diketones. Org Biomol Chem 2022;20:3263-7. [PMID: 35354199 DOI: 10.1039/d2ob00498d] [Reference Citation Analysis]
6 Gulotty EM, Rodriguez KX, Parker EE, Ashfeld BL. Oxyphosphonium Enolate Equilibria in a (4+1)-Cycloaddition Approach toward Quaternary C3-Spirooxindole Assembly. Chemistry 2021;27:10349-55. [PMID: 33861491 DOI: 10.1002/chem.202100355] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Tan P, Wang H, Wang SR. Nucleophilic Migratory Cyclopropenation of Activated Alkynes: A Nonmetal Approach to Unbiased Cyclopropenes. Org Lett 2021;23:2590-4. [PMID: 33754741 DOI: 10.1021/acs.orglett.1c00498] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
8 Qiu ZW, Li BQ, Liu HF, Zhu ZQ, Pan HP, Feng N, Ma AJ, Peng JB, Zhang XZ. Formal (3 + 4)-Annulation of Propargylic p-Quinone Methides with 2-Indolylmethanols: Synthesis of Polysubstituted Indole-Fused Oxepines. J Org Chem 2021;86:7490-9. [PMID: 34004118 DOI: 10.1021/acs.joc.1c00484] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Yu KY, Ge XM, Fan YJ, Liu XT, Yang X, Yang YH, Zhao XH, An XT, Fan CA. Iron(III)-catalyzed tandem annulation of indolyl-substituted p-quinone methides with ynamides for the synthesis of cyclopenta[b]indoles. Chem Commun (Camb) 2022. [PMID: 35833607 DOI: 10.1039/d2cc03252j] [Reference Citation Analysis]
10 Qu CH, Gao LX, Tang Y, Liu Y, Luo XQ, Song GT. Metal-Free Reductive Coupling of para-Quinone Methides with 4-Cyanopyridines Enabled by Pyridine-Boryl Radicals: Access to Pyridylated Diarylmethanes with Anti-Cancer Activity. Chemistry 2022;28:e202200264. [PMID: 35301762 DOI: 10.1002/chem.202200264] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Qu C, Song G, Huang J, Huang R, Chen Y, Liu T, Tang D, Xu Z, Chen Z. Tandem isonitrile insertion/azacyclopropylidene-annulated cyclohexenone–tropone rearrangement of p -QMs and TosMIC: de novo synthesis of pyrrolotropones with anti-cancer activity. Org Chem Front 2021;8:6515-21. [DOI: 10.1039/d1qo01256h] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Asahara H, Bonkohara A, Takagi M, Iwai K, Ito A, Yoshioka K, Tani S, Umezu K, Nishiwaki N. Development of a synthetic equivalent of α,α-dicationic acetic acid leading to unnatural amino acid derivatives via tetrafunctionalized methanes. Org Biomol Chem 2022;20:2282-92. [PMID: 35234775 DOI: 10.1039/d1ob02482e] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Yu KY, Deng YH, Ge XM, An XT, Shu PF, Cao YX, Zhao XH, Fan CA. Tandem (2 + 2) Annulation/Retro-4π Electrocyclization/Imino-Nazarov Cyclization Reaction of p-Quinone Methides with Ynamides: Expeditious Construction of Functionalized Aminoindenes. Org Lett 2021;23:5885-90. [PMID: 34279973 DOI: 10.1021/acs.orglett.1c02003] [Reference Citation Analysis]
14 Singh G, Pandey R, Pankhade YA, Fatma S, Anand RV. Construction of Oxygen- and Nitrogen-based Heterocycles from p-Quinone Methides. Chem Rec 2021. [PMID: 34369640 DOI: 10.1002/tcr.202100137] [Reference Citation Analysis]
15 Luo C, Zhou T, Wang W, Han P, Jing L. An Efficient Approach to Access 2,2‐Diarylanilines via Visible‐Light‐Promoted Decarboxylative Cross‐Coupling Reactions. Asian J Org Chem 2021;10:2342-6. [DOI: 10.1002/ajoc.202100458] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
16 Qu C, Huang R, Li Y, Liu T, Chen Y, Song G. Selective sulfonylation and isonitrilation of para-quinone methides employing TosMIC as a source of sulfonyl group or isonitrile group. Beilstein J Org Chem 2021;17:2822-31. [PMID: 34925621 DOI: 10.3762/bjoc.17.193] [Reference Citation Analysis]
17 Pan HP, Zhu ZQ, Qiu ZW, Liu HF, Ma JD, Li BQ, Feng N, Ma AJ, Peng JB, Zhang XZ. Dearomatization of 2,3-Disubstituted Indoles via 1,8-Addition of Propargylic (Aza)-para-Quinone Methides. J Org Chem 2021;86:16518-34. [PMID: 34714074 DOI: 10.1021/acs.joc.1c01857] [Reference Citation Analysis]