Marcus Tius to Cyclopentanes
This is a "connection" page, showing publications Marcus Tius has written about Cyclopentanes.
Connection Strength
3.313
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Miller CM, Benneche T, Tius MA. First total synthesis of the marine natural products clavulolactones II and III. Org Biomol Chem. 2015 Apr 07; 13(13):4051-8.
Score: 0.511
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Kitamura K, Shimada N, Stewart C, Atesin AC, Atesin TA, Tius MA. Enantioselective palladium(0)-catalyzed Nazarov-type cyclization. Angew Chem Int Ed Engl. 2015 May 18; 54(21):6288-91.
Score: 0.510
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Jolit A, Vazquez-Rodriguez S, Yap GP, Tius MA. Diastereospecific nazarov cyclization of fully substituted dienones: generation of vicinal all-carbon-atom quaternary stereocenters. Angew Chem Int Ed Engl. 2013 Oct 11; 52(42):11102-5.
Score: 0.457
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Berger GO, Tius MA. Terpestacin core structure. control of stereochemistry. Org Lett. 2005 Oct 27; 7(22):5011-3.
Score: 0.265
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Batson WA, Sethumadhavan D, Tius MA. Alpha-hydroxy cyclopentenones from alpha-diketones. Org Lett. 2005 Jun 23; 7(13):2771-4.
Score: 0.259
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Forest J, Bee C, Cordaro F, Tius MA. Isomerization-cyclization approach to the synthesis of 2-hydroxy-5-alkylidene-cyclopent-2-enones. Org Lett. 2003 Oct 30; 5(22):4069-72.
Score: 0.231
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Bee C, Tius MA. Convergent cyclopentannelation process. Org Lett. 2003 May 15; 5(10):1681-4.
Score: 0.224
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Leclerc E, Tius MA. The first example of Nazarov reactions of vinyl cumulenyl ketones. Org Lett. 2003 Apr 17; 5(8):1171-4.
Score: 0.223
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Tius MA. Cationic cyclopentannelation of allene ethers. Acc Chem Res. 2003 Apr; 36(4):284-90.
Score: 0.222
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Harrington PE, Murai T, Chu C, Tius MA. Asymmetric cyclopentannelation: camphor-derived auxiliary. J Am Chem Soc. 2002 Aug 28; 124(34):10091-100.
Score: 0.213
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Tius MA. Allene ether Nazarov cyclization. Chem Soc Rev. 2014 May 07; 43(9):2979-3002.
Score: 0.116
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Banaag AR, Tius MA. Traceless chiral auxiliaries for the allene ether Nazarov cyclization. J Org Chem. 2008 Nov 07; 73(21):8133-41.
Score: 0.081