These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
164 related articles for article (PubMed ID: 28272609)
1. Stevens rearrangement of thioethers with arynes: a facile access to multi-substituted β-keto thioethers. Xu XB; Lin ZH; Liu Y; Guo J; He Y Org Biomol Chem; 2017 Mar; 15(13):2716-2720. PubMed ID: 28272609 [TBL] [Abstract][Full Text] [Related]
2. Synthesis of Functionalized β-Keto Arylthioethers by the Aryne Induced [2,3] Stevens Rearrangement of Allylthioethers. Thangaraj M; Gaykar RN; Roy T; Biju AT J Org Chem; 2017 Apr; 82(8):4470-4476. PubMed ID: 28349686 [TBL] [Abstract][Full Text] [Related]
3. Aryne triggered [2,3]-sigmatropic rearrangement of allyl and propargyl thioethers. Tan J; Zheng T; Xu K; Liu C Org Biomol Chem; 2017 Jun; 15(23):4946-4950. PubMed ID: 28569310 [TBL] [Abstract][Full Text] [Related]
4. An Umpolung Oxa-[2,3] Sigmatropic Rearrangement Employing Arynes for the Synthesis of Functionalized Enol Ethers. Gaykar RN; George M; Guin A; Bhattacharjee S; Biju AT Org Lett; 2021 May; 23(9):3447-3452. PubMed ID: 33830779 [TBL] [Abstract][Full Text] [Related]
5. Transition-metal-free cross-coupling of thioethers with aryl(cyano)iodonium triflates: a facile and efficient method for the one-pot synthesis of thiocyanates. Zhu D; Chang D; Shi L Chem Commun (Camb); 2015 Apr; 51(33):7180-3. PubMed ID: 25811416 [TBL] [Abstract][Full Text] [Related]
6. Insertion of Arynes into P-O Bonds: One-Step Simultaneous Construction of C-P and C-O Bonds. Qi N; Zhang N; Allu SR; Gao J; Guo J; He Y Org Lett; 2016 Dec; 18(23):6204-6207. PubMed ID: 27934369 [TBL] [Abstract][Full Text] [Related]
7. Application of Sulfur Ylides in 1,2-Difunctionalization of Arynes via Insertion into a C-S σ-Bond. Ahire MM; Thoke MB; Mhaske SB Org Lett; 2018 Feb; 20(3):848-851. PubMed ID: 29350042 [TBL] [Abstract][Full Text] [Related]
8. The Aryne [2,3] Stevens Rearrangement. Roy T; Thangaraj M; Kaicharla T; Kamath RV; Gonnade RG; Biju AT Org Lett; 2016 Oct; 18(20):5428-5431. PubMed ID: 27736088 [TBL] [Abstract][Full Text] [Related]
9. A concise synthesis of (E)-3-aryl-2,3,4,5-tetrahydro-1H-3-benzazonines by aryne induced [2,3] Stevens rearrangement of 1,2,3,4-tetrahydroisoquinolines. Pan X; Ma Y; Liu Z Org Biomol Chem; 2018 Oct; 16(40):7393-7399. PubMed ID: 30259034 [TBL] [Abstract][Full Text] [Related]
10. Transition-metal-free C-S bond formation: a facile access to aryl sulfones from sodium sulfinates via arynes. Pandya VG; Mhaske SB Org Lett; 2014 Jul; 16(14):3836-9. PubMed ID: 25003211 [TBL] [Abstract][Full Text] [Related]
11. Straightforward access to α-carbonyloxy esters and β-keto thioethers from aryldiazoacetates. Kumar N; Gola AK; Pandey SK Org Biomol Chem; 2024 Feb; 22(8):1624-1628. PubMed ID: 38318863 [TBL] [Abstract][Full Text] [Related]
12. Facile Synthesis of β-trifluoromethyl thioethers via DBN-catalyzed Hydrothiolation of α-(Trifluoromethyl)styrenes with Thiols. Deng Y; Huang J; Qian Y; Sun Z; Huang Q; Cao S Chem Asian J; 2024 Oct; 19(20):e202400698. PubMed ID: 39039023 [TBL] [Abstract][Full Text] [Related]
13. Oxidative β-Csp(3) -H Functionalization of tBuOH: A Selective Radical/Radical Cross-Coupling Access to β-Hydroxy Thioethers. Li Y; Liu D; Liu C; Lei A Chem Asian J; 2016 Aug; 11(16):2246-9. PubMed ID: 27378452 [TBL] [Abstract][Full Text] [Related]
14. Synthesis of difluoromethyl and deuterium-labeled difluoromethyl thioethers from aliphatic electrophiles. Ding T; Jiang L; Yi W Chem Commun (Camb); 2020 Apr; 56(28):3995-3998. PubMed ID: 32154520 [TBL] [Abstract][Full Text] [Related]
15. Transition-metal-free α-arylation of β-keto amides via an interrupted insertion reaction of arynes. Mohanan K; Coquerel Y; Rodriguez J Org Lett; 2012 Sep; 14(17):4686-9. PubMed ID: 22928933 [TBL] [Abstract][Full Text] [Related]
16. Supported Cu(II)-Schiff base: novel heterogeneous catalyst with extremely high activity for eco-friendly, one-pot and multi-component C-S bond-forming reaction toward a wide range of thioethers as biologically active cores. Shiri P; Amani AM; Aboonajmi J Mol Divers; 2022 Apr; 26(2):1249-1258. PubMed ID: 33978897 [TBL] [Abstract][Full Text] [Related]