Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 116

1.

Synthesis of 2,6-trans- and 3,3,6-trisubstituted tetrahydropyran-4-ones from Maitland-Japp derived 2H-dihydropyran-4-ones: a total synthesis of diospongin B.

Clarke PA, Nasir NM, Sellars PB, Peter AM, Lawson CA, Burroughs JL.

Org Biomol Chem. 2016 Jul 12;14(28):6840-52. doi: 10.1039/c6ob01182a.

PMID:
27340028
2.

A Maitland-Japp inspired synthesis of dihydropyran-4-ones and their stereoselective conversion to functionalised tetrahydropyran-4-ones.

Clarke PA, Sellars PB, Nasir NM.

Org Biomol Chem. 2015 Apr 28;13(16):4743-50. doi: 10.1039/c5ob00292c.

PMID:
25804802
3.
4.

Silyl enol ether Prins cyclization: diastereoselective formation of substituted tetrahydropyran-4-ones.

Tay GC, Huang CY, Rychnovsky SD.

J Org Chem. 2014 Sep 19;79(18):8733-49. doi: 10.1021/jo501580p. Epub 2014 Sep 9.

6.
7.

Synthesis of the bis-tetrahydropyran core of amphidinol 3.

Crimmins MT, Martin TJ, Martinot TA.

Org Lett. 2010 Sep 3;12(17):3890-3. doi: 10.1021/ol1015898.

8.

The asymmetric Maitland-Japp reaction and its application to the construction of the C1-C19 bis-pyran unit of phorboxazole B.

Clarke PA, Santos S, Mistry N, Burroughs L, Humphries AC.

Org Lett. 2011 Feb 18;13(4):624-7. doi: 10.1021/ol102860r. Epub 2011 Jan 19.

PMID:
21247215
9.

A general strategy for construction of both 2,6-cis- and 2,6-trans-disubstituted tetrahydropyrans: substrate-controlled asymmetric total synthesis of (+)-scanlonenyne.

Lee H, Kim KW, Park J, Kim H, Kim S, Kim D, Hu X, Yang W, Hong J.

Angew Chem Int Ed Engl. 2008;47(22):4200-3. doi: 10.1002/anie.200705663. No abstract available.

PMID:
18435525
10.

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 6;78(23):12182-8. doi: 10.1021/jo4015547. Epub 2013 Nov 20.

PMID:
24245586
11.

Synthesis of 2,4,5-trisubstituted tetrahydropyrans as peptidomimetic scaffolds for melanocortin receptor ligands.

Kulesza A, Ebetino FH, Mishra RK, Cross-Doersen D, Mazur AW.

Org Lett. 2003 Apr 17;5(8):1163-6.

PMID:
12688709
12.

Pyranone natural products as inspirations for catalytic reaction discovery and development.

McDonald BR, Scheidt KA.

Acc Chem Res. 2015 Apr 21;48(4):1172-83. doi: 10.1021/ar5004576. Epub 2015 Mar 6.

13.

Strategies for the construction of tetrahydropyran rings in the synthesis of natural products.

Nasir NM, Ermanis K, Clarke PA.

Org Biomol Chem. 2014 Jun 7;12(21):3323-35. doi: 10.1039/c4ob00423j. Epub 2014 Apr 17. Review.

PMID:
24744139
14.

Prins-type macrocyclizations as an efficient ring-closing strategy in natural product synthesis.

Crane EA, Scheidt KA.

Angew Chem Int Ed Engl. 2010 Nov 2;49(45):8316-26. doi: 10.1002/anie.201002809. Review.

15.

The one-pot, multi-component construction of highly substituted tetrahydropyran-4-ones using the Maitland-Japp reaction.

Clarke PA, Martin WH, Hargreaves JM, Wilson C, Blake AJ.

Org Biomol Chem. 2005 Oct 7;3(19):3551-63. Epub 2005 Aug 26.

PMID:
16172694
16.

ent-Kaurane-based regio- and stereoselective inverse electron demand hetero-Diels-Alder reactions: synthesis of dihydropyran-fused diterpenoids.

Ding C, Wang L, Chen H, Wild C, Ye N, Ding Y, Wang T, White MA, Shen Q, Zhou J.

Org Biomol Chem. 2014 Nov 14;12(42):8442-52. doi: 10.1039/c4ob01040j.

17.

Total synthesis of jerangolid A.

Hanessian S, Focken T, Oza R.

Org Lett. 2010 Jul 16;12(14):3172-5. doi: 10.1021/ol101103q.

PMID:
20565089
18.

5- And 6-exocyclic products, cis-2,3,5-trisubstituted tetrahydrofurans, and cis-2,3,6-trisubstituted tetrahydropyrans via Prins-type cyclization.

Chavre SN, Choo H, Lee JK, Pae AN, Kim Y, Cho YS.

J Org Chem. 2008 Oct 3;73(19):7467-71. doi: 10.1021/jo800967p. Epub 2008 Aug 29. Erratum in: J Org Chem. 2008 Nov 7;73(21):8682.

PMID:
18761436
20.

Stereoselective synthesis of 2,6-cis-substituted tetrahydropyrans: Brønsted acid-catalyzed intramolecular oxa-conjugate cyclization of α,β-unsaturated ester surrogates.

Fuwa H, Ichinokawa N, Noto K, Sasaki M.

J Org Chem. 2012 Mar 16;77(6):2588-607. doi: 10.1021/jo202179s. Epub 2011 Dec 28.

PMID:
22148171

Supplemental Content

Support Center