260 related articles for article (PubMed ID: 11421792)
1. Stereoselectivity and regioselectivity in the segment-coupling Prins cyclization.
Jaber JJ; Mitsui K; Rychnovsky SD
J Org Chem; 2001 Jun; 66(13):4679-86. PubMed ID: 11421792
[TBL] [Abstract][Full Text] [Related]
2. 1,4-Hydroiodination of dienyl alcohols with TMSI to form homoallylic alcohols containing a multisubstituted Z-alkene and application to Prins cyclization.
Xu Y; Yin Z; Lin X; Gan Z; He Y; Gao L; Song Z
Org Lett; 2015 Apr; 17(8):1846-9. PubMed ID: 25825952
[TBL] [Abstract][Full Text] [Related]
3. Axial-selective prins cyclizations by solvolysis of alpha-bromo ethers.
Jasti R; Vitale J; Rychnovsky SD
J Am Chem Soc; 2004 Aug; 126(32):9904-5. PubMed ID: 15303848
[TBL] [Abstract][Full Text] [Related]
4. Tetrahydropyran rings from a Mukaiyama-Michael cascade reaction.
Bolla ML; Patterson B; Rychnovsky SD
J Am Chem Soc; 2005 Nov; 127(46):16044-5. PubMed ID: 16287289
[TBL] [Abstract][Full Text] [Related]
5. Synthesis of (-)-centrolobine by Prins cyclizations that avoid racemization.
Marumoto S; Jaber JJ; Vitale JP; Rychnovsky SD
Org Lett; 2002 Oct; 4(22):3919-22. PubMed ID: 12599492
[TBL] [Abstract][Full Text] [Related]
6. Oxonia-cope prins cyclizations: a facile method for the synthesis of tetrahydropyranones bearing quaternary centers.
Dalgard JE; Rychnovsky SD
J Am Chem Soc; 2004 Dec; 126(48):15662-3. PubMed ID: 15571386
[TBL] [Abstract][Full Text] [Related]
7. A novel Prins cyclization through benzylic/allylic C-H activation.
Yu B; Jiang T; Li J; Su Y; Pan X; She X
Org Lett; 2009 Aug; 11(15):3442-5. PubMed ID: 19603799
[TBL] [Abstract][Full Text] [Related]
8. Stereoselectivity of intramolecular SN' cyclizations of alkyllithium reagents on methoxy alkenes.
La Cruz TE; Rychnovsky SD
J Org Chem; 2006 Feb; 71(3):1068-73. PubMed ID: 16438522
[TBL] [Abstract][Full Text] [Related]
9. Prins Cyclization Catalyzed by a Fe(III) /Trimethylsilyl Halide System: The Oxocarbenium Ion Pathway versus the [2+2] Cycloaddition.
Pérez SJ; Purino M; Miranda PO; Martín VS; Fernández I; Padrón JI
Chemistry; 2015 Oct; 21(43):15211-7. PubMed ID: 26471437
[TBL] [Abstract][Full Text] [Related]
10. Silyl enol ether Prins cyclization: diastereoselective formation of substituted tetrahydropyran-4-ones.
Tay GC; Huang CY; Rychnovsky SD
J Org Chem; 2014 Sep; 79(18):8733-49. PubMed ID: 25200563
[TBL] [Abstract][Full Text] [Related]
11. Stereoselective synthesis of spirocyclic oxindoles via Prins cyclizations.
Castaldi MP; Troast DM; Porco JA
Org Lett; 2009 Aug; 11(15):3362-5. PubMed ID: 19719184
[TBL] [Abstract][Full Text] [Related]
12. Solvolysis of a tetrahydropyranyl mesylate: mechanistic implications for the Prins cyclization, 2-oxonia-cope rearrangement, and Grob fragmentation.
Jasti R; Rychnovsky SD
Org Lett; 2006 May; 8(10):2175-8. PubMed ID: 16671810
[TBL] [Abstract][Full Text] [Related]
13. Acid-promoted Prins cyclizations of enol ethers to form tetrahydropyrans.
Hart DJ; Bennett CE
Org Lett; 2003 May; 5(9):1499-502. PubMed ID: 12713308
[TBL] [Abstract][Full Text] [Related]
14. Utilization of an oxonia-Cope rearrangement as a mechanistic probe for Prins cyclizations.
Jasti R; Anderson CD; Rychnovsky SD
J Am Chem Soc; 2005 Jul; 127(27):9939-45. PubMed ID: 15998101
[TBL] [Abstract][Full Text] [Related]
15. Diastereoselective synthesis of dihydropyrans via Prins cyclization of enol ethers: total asymmetric synthesis of (+)-civet cat compound.
Sultana S; Indukuri K; Deka MJ; Saikia AK
J Org Chem; 2013 Dec; 78(23):12182-8. PubMed ID: 24245586
[TBL] [Abstract][Full Text] [Related]
16. Factors controlling the alkyne prins cyclization: the stability of dihydropyranyl cations.
Miranda PO; Ramírez MA; Martín VS; Padrón JI
Chemistry; 2008; 14(20):6260-8. PubMed ID: 18512867
[TBL] [Abstract][Full Text] [Related]
17. Cu(II)-catalyzed olefin migration and Prins cyclization: highly diastereoselective synthesis of substituted tetrahydropyrans.
Ghosh AK; Nicponski DR
Org Lett; 2011 Aug; 13(16):4328-31. PubMed ID: 21797234
[TBL] [Abstract][Full Text] [Related]
18. Chirality transfer in Au-catalyzed cyclization reactions of monoallylic diols: selective access to specific enantiomers based on olefin geometry.
Aponick A; Biannic B
Org Lett; 2011 Mar; 13(6):1330-3. PubMed ID: 21314106
[TBL] [Abstract][Full Text] [Related]
19. Synergistic effects between Lewis and Brønsted acids: application to the Prins cyclization.
Breugst M; Grée R; Houk KN
J Org Chem; 2013 Oct; 78(19):9892-7. PubMed ID: 23984760
[TBL] [Abstract][Full Text] [Related]
20. Mechanistic and computational studies of exocyclic stereocontrol in the synthesis of bryostatin-like cis-2,6-disubstituted 4-alkylidenetetrahydropyrans by Prins cyclization.
Ogawa Y; Painter PP; Tantillo DJ; Wender PA
J Org Chem; 2013 Jan; 78(1):104-15. PubMed ID: 23121542
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
