Similar articles for PMID: 24367411

Year	Number of Results
1997	1
1999	1
2001	5
2002	6
2003	4
2004	4
2005	3
2006	4
2007	3
2008	4
2009	1
2010	5
2011	4
2012	6
2013	8
2014	5
2015	7
2016	3
2017	7
2018	5
2019	7
2020	2
2021	4
2023	1
2024	0

1

Synthesis of the spiroketal core of integramycin.

Prusov EV. Prusov EV. Beilstein J Org Chem. 2013 Nov 12;9:2446-50. doi: 10.3762/bjoc.9.282. eCollection 2013. Beilstein J Org Chem. 2013. PMID: 24367411 Free PMC article.

2

Stereoselective synthesis of a model C(18)-C(35) spiroketal fragment of integramycin.

Sun H, Abbott JR, Roush WR. Sun H, et al. Org Lett. 2011 May 20;13(10):2734-7. doi: 10.1021/ol200834p. Epub 2011 Apr 21. Org Lett. 2011. PMID: 21510632 Free PMC article.

3

Synthesis of the C16-C35 fragment of integramycin using olefin hydroesterification as a linchpin reaction.

Wang L, Floreancig PE. Wang L, et al. Org Lett. 2004 Feb 19;6(4):569-72. doi: 10.1021/ol036339i. Org Lett. 2004. PMID: 14961625

4

NH₄HF₂ as a selective TBS-removal reagent for the synthesis of highly functionalized spiroketal via tandem deprotection/spiroketalization procedure.

Lu H, Zhang FM, Pan JL, Chen T, Li YF. Lu H, et al. J Org Chem. 2014 Jan 17;79(2):546-58. doi: 10.1021/jo402167q. Epub 2013 Dec 24. J Org Chem. 2014. PMID: 24328167

5

Synthesis of the C(2)-C(13) fragment (the A-B spiroketal unit) of spongistatin 1 (altohyrtin A): use of a common intermediate for the synthesis of both spongistatin spiroketals.

Holson EB, Roush WR. Holson EB, et al. Org Lett. 2002 Oct 17;4(21):3723-5. doi: 10.1021/ol026688x. Org Lett. 2002. PMID: 12375928

6

Stereocontrolled Synthesis of Spiroketals: An Engine for Chemical and Biological Discovery.

Verano AL, Tan DS. Verano AL, et al. Isr J Chem. 2017 Apr;57(3-4):279-291. doi: 10.1002/ijch.201600134. Epub 2017 Mar 10. Isr J Chem. 2017. PMID: 29104308 Free PMC article.

7

Asymmetric Synthesis of Spiroketals with Aminothiourea Catalysts.

Yoneda N, Fukata Y, Asano K, Matsubara S. Yoneda N, et al. Angew Chem Int Ed Engl. 2015 Dec 14;54(51):15497-500. doi: 10.1002/anie.201508405. Epub 2015 Oct 29. Angew Chem Int Ed Engl. 2015. PMID: 26510921

8

Computational Evidence of the Incipient Oxocarbenium Ion as a "Hidden Intermediate" During the Cyclization of Hydroxyenol Ether into Spiroketal Under Mild Acidic Condition.

Jindani S, Ganguly B. Jindani S, et al. Chemistry. 2023 Apr 25;29(24):e202203953. doi: 10.1002/chem.202203953. Epub 2023 Mar 17. Chemistry. 2023. PMID: 36757149

9

Access to both anomers of pectenotoxin spiroketals by kinetic spiroketalization.

Pihko PM, Aho JE. Pihko PM, et al. Org Lett. 2004 Oct 14;6(21):3849-52. doi: 10.1021/ol048321t. Org Lett. 2004. PMID: 15469365

10

Concise and Practical Asymmetric Synthesis of a Challenging Atropisomeric HIV Integrase Inhibitor.

Fandrick KR, Li W, Zhang Y, Tang W, Gao J, Rodriguez S, Patel ND, Reeves DC, Wu JP, Sanyal S, Gonnella N, Qu B, Haddad N, Lorenz JC, Sidhu K, Wang J, Ma S, Grinberg N, Lee H, Tsantrizos Y, Poupart MA, Busacca CA, Yee NK, Lu BZ, Senanayake CH. Fandrick KR, et al. Angew Chem Int Ed Engl. 2015 Jun 8;54(24):7144-8. doi: 10.1002/anie.201501575. Epub 2015 May 4. Angew Chem Int Ed Engl. 2015. PMID: 25939331

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