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.
3. Prins cyclization of bis(silyl) homoallylic alcohols to form 2,6-cis-tetrahydropyrans containing a geometrically defined exocyclic vinylsilane: efficient synthesis of ring B of the bryostatins. Lu J; Song Z; Zhang Y; Gan Z; Li H Angew Chem Int Ed Engl; 2012 May; 51(22):5367-70. PubMed ID: 22504783 [No Abstract] [Full Text] [Related]
4. Diastereoselective synthesis of substituted tetrahydrofurans via Prins cyclization of enol ethers. Gogoi P; Das VK; Saikia AK J Org Chem; 2014 Sep; 79(18):8592-8. PubMed ID: 25185033 [TBL] [Abstract][Full Text] [Related]
5. An environmentally benign synthesis of cis-2,6-disubstituted tetrahydropyrans via indium-mediated tandem allylation/Prins cyclization reaction. Pham M; Allatabakhsh A; Minehan TG J Org Chem; 2008 Jan; 73(2):741-4. PubMed ID: 18095701 [TBL] [Abstract][Full Text] [Related]
6. Green chemistry: solvent- and metal-free Prins cyclization. Application to sequential reactions. Clarisse D; Pelotier B; Piva O; Fache F Chem Commun (Camb); 2012 Jan; 48(1):157-9. PubMed ID: 22068454 [TBL] [Abstract][Full Text] [Related]
7. A diastereoselective ring contraction of 1,3-dioxepins to 2,3,4-trisubstituted and tetrasubstituted tetrahydrofurans. Nasveschuk CG; Rovis T J Org Chem; 2008 Jan; 73(2):612-7. PubMed ID: 18088144 [TBL] [Abstract][Full Text] [Related]
8. Formal [4 + 2] cycloaddition of donor-acceptor cyclobutanes and aldehydes: stereoselective access to substituted tetrahydropyrans. Parsons AT; Johnson JS J Am Chem Soc; 2009 Oct; 131(40):14202-3. PubMed ID: 19764759 [TBL] [Abstract][Full Text] [Related]
9. Stereoselective synthesis of highly O-functionalized enantiopure 2,3,4-trisubstituted tetrahydrofurans by tandem debenzylative cyclization of glycal derived 2,3-epoxy alcohols. Reddy LV; Roy AD; Roy R; Shaw AK Chem Commun (Camb); 2006 Aug; (32):3444-6. PubMed ID: 16896489 [TBL] [Abstract][Full Text] [Related]
10. Completely OH-selective FeCl3-catalyzed Prins cyclization: highly stereoselective synthesis of 4-OH-tetrahydropyrans. Zheng K; Liu X; Qin S; Xie M; Lin L; Hu C; Feng X J Am Chem Soc; 2012 Oct; 134(42):17564-73. PubMed ID: 23030638 [TBL] [Abstract][Full Text] [Related]
11. InCl3 catalyzed highly diastereoselective [3 + 2] cycloaddition of 1,2-cyclopropanated sugars with aldehydes: a straightforward synthesis of persubstituted bis-tetrahydrofurans and perhydrofuro[2,3-b]pyrans. Ma X; Tang Q; Ke J; Yang X; Zhang J; Shao H Org Lett; 2013 Oct; 15(20):5170-3. PubMed ID: 24093645 [TBL] [Abstract][Full Text] [Related]
12. Prins cyclizations in silyl additives with suppression of epimerization: versatile tool in the synthesis of the tetrahydropyran backbone of natural products. Chan KP; Loh TP Org Lett; 2005 Sep; 7(20):4491-4. PubMed ID: 16178566 [TBL] [Abstract][Full Text] [Related]
13. TMSBr/InBr3-promoted Prins cyclization/homobromination of dienyl alcohol with aldehyde to construct cis-THP containing an exocyclic E-alkene. Li L; Sun X; He Y; Gao L; Song Z Chem Commun (Camb); 2015 Oct; 51(80):14925-8. PubMed ID: 26303284 [TBL] [Abstract][Full Text] [Related]
14. One-pot synthesis and SAR study of cis-2,6-dialkyl-4-chloro-tetrahydropyrans. Miranda PO; León LG; Martín VS; Padrón JI; Padrón JM Bioorg Med Chem Lett; 2006 Jun; 16(12):3135-8. PubMed ID: 16603350 [TBL] [Abstract][Full Text] [Related]
15. Stereoselective synthesis of 2,4,6-trisubstituted tetrahydropyrans by the use of cyclopropanols as homoenols. Lee HG; Lysenko IL; Cha JK Angew Chem Int Ed Engl; 2007; 46(18):3326-8. PubMed ID: 17385770 [No Abstract] [Full Text] [Related]
16. Highly stereoselective prins cyclization of silylmethyl-substituted cyclopropyl carbinols to 2,4,6-trisubstituted tetrahydropyrans. Yadav VK; Kumar NV J Am Chem Soc; 2004 Jul; 126(28):8652-3. PubMed ID: 15250708 [TBL] [Abstract][Full Text] [Related]
17. 2-Arylcyclopropylmethanol as a substitute for homoallyl aryl alcohol in the construction of cis-2,6-disubstituted tetrahydropyran: synthesis of (±)-centrolobine. Yadav VK; Verma AK; Kumar P; Hulikal V Chem Commun (Camb); 2014 Dec; 50(97):15457-60. PubMed ID: 25354489 [TBL] [Abstract][Full Text] [Related]