Crimmins, Michael T.- Department of Chemistry, University of North Carolina at Chapel Hill

• J. Am. Chem. Soc. 1986, 108, 3435-3438 Intramolecular Photocycloaddition-Cyclobutane
• Total Synthesis of (-)-Mucocin Michael T. Crimmins,* Yan Zhang, and Frank A. Diaz
• Asymmetric Total Synthesis of (-)-Isolaurallene Michael T. Crimmins* and Kyle A. Emmitte
• An Aldol Approach to the Synthesis of the EF Fragment of Spongistatin 1
• Strategies for the Total Synthesis of C2-C11 Cyclized Cembranoids J. Michael Ellis and Michael T. Crimmins*
• Enantioselective Synthesis of Apoptolidin Sugars
• Tetrahedron 54 (1998) 9229-9272 Tetrahedron report number 461
• Enantioselective Total Synthesis of (+)-SCH 351448
• Asymmetric Aldol Additions with Titanium Enolates of Acyloxazolidinethiones: Dependence of
• Chem.Rev.1988. 88. 1453-1473 1453 Synthetic Applications of Intramolecular Enone-Olefin Photocycloadditions
• Total Synthesis of (+)-Laurencin: An Asymmetric Alkylation-Ring-Closing
• Asymmetric Total Synthesis of Spongistatins 1 and 2 Michael T. Crimmins,* Jason D. Katz, David G. Washburn, Shawn P. Allwein, and Laura F. McAtee
• Formal Total Synthesis of (+)-Trehazolin. Application of an Asymmetric Aldol-Olefin Metathesis Approach to the Synthesis of
• Asymmetric Total Synthesis of Callystatin A: Asymmetric Aldol Additions with Titanium Enolates
• J. Am. Chem. SOC. conformers. When this conformer was excited and its fluorescence
• Solid-Phase Synthesis of Carbocyclic Nucleosides
• DOI: 10.1002/chem.200900777 Enantioselective Total Synthesis of Brevetoxin A: Convergent Coupling
• Enantioselective Synthesis of Apoptolidinone: Exploiting the Versatility of Thiazolidinethione Chiral Auxiliaries
• Convergent, Stereoselective Synthesis of the GHIJ Fragment of Brevetoxin A
• DownloadedBy:[IndianaUniversityLibraries]At:13:5318January2008 SYNTHETIC COMMUNICATIONS, 28(19), 3675-3679 (1998)
• A Highly Convergent Approach toward (-)-Brevenal
• Thus, the spiroketal fragment 2 of avermectin Bth has been prepared in 16 steps in good overall yield from the dial 10. Efforts directed toward connecting the spiroketal and hexahydrobenzofuran fragments and
• Double Diastereoselection in Intramolecular Photocycloadditions: A Radical Rearrangement Approach to the Total Synthesis of the
• Synthesis of the C1-C13 Fragment of Leucascandrolide A
• Titanium Enolates of Thiazolidinethione Chiral Auxiliaries: Versatile Tools for
• The Total Synthesis of (()-Ginkgolide B Michael T. Crimmins,* Jennifer M. Pace, Philippe G. Nantermet, Agnes S. Kim-Meade,
• Temhedmn Lznus. VoL 34. No.2 pp.199-m 1593 oo40-4039/93 s5.00+ .oo RiUttdilIGIOUBriuin PelsamonRcrsL&t
• Total Synthesis of Apoptolidin A Michael T. Crimmins,* Hamish S. Christie, Alan Long, and Kleem Chaudhary
• J.Org. Chem. 1990,55,4235-4237 4235 "umbrella" over the ring. It should also be noted that
• An Intramolecular Diels-Alder Approach to the Eunicellins: Enantioselective Total Syntheses of Ophirin B and
• Tehkdmn L.ef&ers,Vol. 35. NO. 11. pp. 1657-1660. 1994 Elsevia S&me L&I
• Tetrahedron Letters 39 (1998) 7487-7490 TETRAHEDRON
• Tetrahedron Letters,Vol.28,No.32,pp 3651-3654,1987 oo40-4039/87 $3.00 + .OO Printed in Great Britain Pergamon Journals Ltd.
• An Efficient Asymmetric Approach to Carbocyclic Nucleosides: Asymmetric
• Regioselectivity in the Palladium-Catalyzed Addition of Carbon Nucleophiles to Carbocyclic Derivatives
• Total Synthesis of the Proposed Structure of Briarellin J
• Enantioselective Total Synthesis of FD-891 Michael T. Crimmins* and Franck Caussanel
• 652 J.Org.Chem. 1988,53,652-657 Total Synthesis of Milbemycin &
• Total Synthesis of (+)-Prelaureatin and (+)-Laurallene Michael T. Crimmins* and Elie A. Tabet
• Organic Syntheses, Coll. Vol. 10, p.355 (2004); Vol. 77, p.114 (2000). THE SYNTHESIS OF 2-ALKYL-4-PYRONES FROM MELDRUM'S
• Highly Selective Acetate Aldol Additions Using Mesityl-Substituted Chiral
• An Efficient, General Asymmetric Synthesis of Carbocyclic Nucleosides: Application of an Asymmetric Aldol/Ring-Closing
• Synthetic approaches to the microtubule stabilizing agent (-)-laulimalide Michael T Crimmins
• Tetrahedron Letters 39 (1998) 3439-3442 TETRAHEDRON
• Total Synthesis of Brevetoxin A Michael T. Crimmins,* J. Lucas Zuccarello, J. Michael Ellis, Patrick J. McDougall,
• Synthesis of Crossed [2 + 2] Photocycloadducts: A Novel Approach
• Tetrahedron Letters,Vo1.30,No.44,pp 5997-6000,1989 0040-4039/89 $3.00 + .oo Printed in Great Britain Pergamon Press plc
• Enantioselective Total Synthesis of Spirofungins A and B
• Total Synthesis of Irciniastatin A (Psymberin)
• DOI: 10.1002/chem.200900776 Enantioselective Total Synthesis of Brevetoxin A: Unified Strategy for the B,
• Enantioselective Total Synthesis of (-)-Pironetin: Iterative Aldol Reactions
• An Intramolecular Diels-Alder Strategy for the Asbestinins: Enantioselective Total Syntheses of 11-Acetoxy-4-deoxyasbestinin D
• Synthesis of the C29-C37 Bicyclic Ether Core of (+)-Sorangicin A
• Improved Synthesis of the ABCDE Fragment of Brevetoxin A
• Enantioselective Total Synthesis of Bistramide A Michael T. Crimmins* and Amy C. DeBaillie
• Establishing the Absolute Configuration of the Asbestinins: Enantioselective Total Synthesis of 11-Acetoxy-4-deoxyasbestinin D
• A Convergent Coupling Strategy for the Formation of Polycyclic Ethers
• Enantioselective Total Synthesis of (+)-Gigantecin: Exploiting the Asymmetric Glycolate Aldol Reaction
• An Intramolecular Diels-Alder Approach to the Eunicelins: Enantioselective Total Synthesis of Ophirin B
• LETTER 1371 An Improved Procedure for Asymmetric Aldol Additions with N-Acyl
• Enantioselective Total Synthesis of (+)-Obtusenyne Michael T. Crimmins* and Mark T. Powell
• Asymmetric Total Synthesis of (-)-Laulimalide: Exploiting the Asymmetric Glycolate Alkylation Reaction
• Ring closing metathesis for the formation of medium ring ethers: the total synthesis of (2)-isolaurallene
• Asymmetric Aldol Additions: Use of Titanium Tetrachloride and (-)-Sparteine for the Soft Enolization of N-Acyl Oxazolidinones,
• Diastereoselective Alkylations of Oxazolidinone Glycolates: A Useful
• SPECIALTOPIC 899 Synthesis 2000, No. 6, 899903 ISSN 0039-7881 Thieme Stuttgart New York
• Synthesis of the C16-C28 Spiroketal Subunit of Spongistatin 1
• Total Synthesis of (()-Ginkgolide B Michael T. Crimmins,* Jennifer M. Pace,
• An Asymmetric Aldol-Ring-Closing Metathesis Strategy for the Enantioselective Construction of Oxygen Heterocycles: An Efficient
• TETRAHEDRON Pergamon Tetrahedron Letters 39 (1998) 7005-7008
• Asymmetric Aldol-Ring-Closing Metathesis Strategy for the Enantioselective
• Solvent Effects on Diastereoselective Intramolecular [2 + 2] Photocycloadditions: Reversal of Selectivity
• Asymmetric Total Synthesis of (+)-Milbemycin D Michael T. Crimmins,* Rima S. Al-awar, Isabelle M. Vallin, W. Gary Hollis, Jr.,
• 3146 J. Am. Chem. SOC.1993, 115, 3146-3 155 Synthetic Studies on the Ginkgolides: Total Synthesis of
• J. Am. Chem. SOC.1992,114, 5445-5447 5445 all mutants as indicated by linear plots of peak current vs (scan
• TeuahedmnLetters.Vol.33. No.2, pp. 181-184.1992 Printed in Great Britain
• 5894 J. Org. Chem. 1990,55,5894-5900 synthetic route for triazole preparation.
• J.Org. Chem. 1989,54, 1157-1161 1157 nitrogen. The residual solid was then dissolved in 1mL of 0.2
• Tetrahedron Letters,Vo1.28,No.43,pp 5063-5066,1987 0040-4039/!87 $3.00 + .OO Printed in Great Britain Perqaraon Journals Ltd.
• Tetrahedron Letters,Vo1.28,No.32,pp 3647-3650,1987 0040-4039/87 $3.00 + .OO Printed in Great Britain Pergamon Journals Ltd.
• 800 J. Am. Chem. SOC.1986, 108, 800-806 Approach of a 1,3-diene (in a parallel plane orthogonal to the
• Tetrahedron Letters,Vol.26,No.8,Dp 997-1000,1985 0040-4039/85 $3.00 + .OO Printed in Great Britain 01985 Perqamon Press Ltd.
• J.Org. Chem. 1984,49, 3033-3035 3033 Proposed SequentialConversion of Coal's
• Tetrahedron Letters,Vo1.24,No.48,pp 5303-5304,1983 oo4o-4039/83 $3.00 + .OO Printed in Great Britain 01983 Pergamon Press Ltd.
• Tetrahedron Letters,Vo1.24,No.42,pp 4551-4554,1983 0040-4039/83 $3.00 + .OO Printed in Great Britain 01983 Pergamon Press Ltd.
• 1038 J.Org. Chem. 1993,58,1038-1047 Addition of Zinc Homoenolates to Acetylenic Esters and Amides: A
• Asymmetric Total Synthesis of Pyranicin Michael T. Crimmins* and Danielle L. Jacobs
• Formal Synthesis of 6-Deoxyerythronolide B
• Synthesis of the Bis-tetrahydropyran Core of Amphidinol 3
• Tetrahedron Letters, vo1.27, No.3, pp 291-294, 1986 0040-4039/86 $3.00 + .OO Printed in Great Britain 01986 Pergamon Press Ltd.
• A Hetero-Diels-Alder Approach to Complex Pyrones: An Improved
• Enantioselective Total Synthesis of (+)-Leucascandrolide A Macrolactone
• Anti-Selective Aldol Reactions with Titanium Enolates of
• 2076 J.Org. Chem. 1984,49, 2076-2077 90046-38-1; 9, 90046-39-2; 10, 30494-12-3; 11, 90046-40-5; 12,
• Enantioselective Total Synthesis of (+)-Rogioloxepane A