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Items: 11


Solvent-dependent divergent functions of Sc(OTf)₃ in stereoselective epoxide-opening spiroketalizations.

Sharma I, Wurst JM, Tan DS.

Org Lett. 2014 May 2;16(9):2474-7. doi: 10.1021/ol500853q. Epub 2014 Apr 17.


Stereoselective synthesis of acortatarins A and B.

Wurst JM, Verano AL, Tan DS.

Org Lett. 2012 Sep 7;14(17):4442-5. doi: 10.1021/ol3019456. Epub 2012 Aug 27.


Stereoelectronic factors in the stereoselective epoxidation of glycals and 4-deoxypentenosides.

Alberch L, Cheng G, Seo SK, Li X, Boulineau FP, Wei A.

J Org Chem. 2011 Apr 15;76(8):2532-47. doi: 10.1021/jo102382r. Epub 2011 Mar 18.


Olefin metathesis-iodoetherification-dehydroiodination strategy for spiroketal subunits of polyether antibiotics.

Tony KA, Dabideen D, Li J, Díaz-Hernández MD, Jiménez-Barbero J, Mootoo DR.

J Org Chem. 2009 Oct 16;74(20):7774-80. doi: 10.1021/jo9014722.


Stereoselective synthesis of benzannulated spiroketals: influence of the aromatic ring on reactivity and conformation.

Liu G, Wurst JM, Tan DS.

Org Lett. 2009 Aug 20;11(16):3670-3. doi: 10.1021/ol901437f.


Natural products as an inspiration in the diversity-oriented synthesis of bioactive compound libraries.

Cordier C, Morton D, Murrison S, Nelson A, O'Leary-Steele C.

Nat Prod Rep. 2008 Aug;25(4):719-37. doi: 10.1039/b706296f. Epub 2008 Apr 14. Review.


An iodoetherification-dehydroiodination strategy for the synthesis of complex spiroketals from dihydroxyalkene precursors.

Tony KA, Li X, Dabideen D, Li J, Mootoo DR.

Org Biomol Chem. 2008 Apr 7;6(7):1165-9. doi: 10.1039/b719247a. Epub 2008 Feb 22.


A unified synthetic approach to polyketides having both skeletal and stereochemical diversity.

Shang S, Iwadare H, Macks DE, Ambrosini LM, Tan DS.

Org Lett. 2007 May 10;9(10):1895-8. Epub 2007 Apr 17.


Diastereoselective synthesis of the pectenotoxin 2 non-anomeric AB spiroacetal.

Vellucci D, Rychnovsky SD.

Org Lett. 2007 Feb 15;9(4):711-4.

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