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Cagle, Phillip C., Meyer, Oliver, Weickhardt, Konrad, Arif, Atta M., Gladysz, J. A. (1995) Enantioselective Synthesis of Organosulfur Compounds via [2,3] Rearrangements of Ylides Derived from Di(allyl) and Di(propargyl) Sulfide Complexes. Control of Carbon Configuration by an Easily Resolved and Recycled Chiral Transition Metal Auxiliary. Journal Of The American Chemical Society, 117 (47) 11730-11744 doi:10.1021/ja00152a014

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Reference TypeJournal (article/letter/editorial)
TitleEnantioselective Synthesis of Organosulfur Compounds via [2,3] Rearrangements of Ylides Derived from Di(allyl) and Di(propargyl) Sulfide Complexes. Control of Carbon Configuration by an Easily Resolved and Recycled Chiral Transition Metal Auxiliary
JournalJournal Of The American Chemical Society
AuthorsCagle, Phillip C.Author
Meyer, OliverAuthor
Weickhardt, KonradAuthor
Arif, Atta M.Author
Gladysz, J. A.Author
Year1995 (November)Volume117
Issue47
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja00152a014Search in ResearchGate
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Mindat Ref. ID1497366Long-form Identifiermindat:1:5:1497366:4
GUID0
Full ReferenceCagle, Phillip C., Meyer, Oliver, Weickhardt, Konrad, Arif, Atta M., Gladysz, J. A. (1995) Enantioselective Synthesis of Organosulfur Compounds via [2,3] Rearrangements of Ylides Derived from Di(allyl) and Di(propargyl) Sulfide Complexes. Control of Carbon Configuration by an Easily Resolved and Recycled Chiral Transition Metal Auxiliary. Journal Of The American Chemical Society, 117 (47) 11730-11744 doi:10.1021/ja00152a014
Plain TextCagle, Phillip C., Meyer, Oliver, Weickhardt, Konrad, Arif, Atta M., Gladysz, J. A. (1995) Enantioselective Synthesis of Organosulfur Compounds via [2,3] Rearrangements of Ylides Derived from Di(allyl) and Di(propargyl) Sulfide Complexes. Control of Carbon Configuration by an Easily Resolved and Recycled Chiral Transition Metal Auxiliary. Journal Of The American Chemical Society, 117 (47) 11730-11744 doi:10.1021/ja00152a014
In(1995, November) Journal Of The American Chemical Society Vol. 117 (47) American Chemical Society (ACS)

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Meyer, O., Cagle, P. C., Weickhardt, K., Vichard, D., Gladysz, John A. (1996) Enantioselective syntheses of organosulfur compounds via [2,3] sigmatropic rearrangements of ylides derived from di(allyl), di(propargyl), and di(benzyl) sulfide complexes; Control of carbon configuration by an easily resolved and recycled rhenium auxiliary. Pure and Applied Chemistry, 68 (1) 79-88 doi:10.1351/pac199668010079
Cagle, Phillip C., Arif, Atta M., Gladysz, J. A. (1994) Enantioselective Syntheses of Organosulfur Compounds via [2,3] Sigmatropic Rearrangements of Ylides of Diallyl and Dipropargyl Sulfonium Salts. Control of Carbon Configuration by an Easily Resolved and Recycled Chiral Transition-Metal Auxiliary. Journal Of The American Chemical Society, 116 (8) 3655-3656 doi:10.1021/ja00087a084
Cagle, Phillip C., Meyer, Oliver, Vichard, Dominique, Weickhardt, Konrad, Arif, Atta M., Gladysz, J. A. (1996) Reactions oft-BuOK and Dibenzyl, Benzyl Allyl, and Allyl β-Keto Sulfide Complexes of the Chiral Rhenium Lewis Acid [(η5-C5H5)Re(NO)(PPh3)]+:  Highly Diastereoselective or Chemoselective [2,3]-Sigmatropic Rearrangements. Organometallics, 15. 194-204 doi:10.1021/om950701i
Richter-Addo, George B., Knight, D. Andrew, Dewey, Michael A., Arif, Atta M., Gladysz, J. A. (1993) New strategies for enantioselective syntheses of 1-alkyl- and 1,4-dialkyl-1,2,3,4-tetrahydroisoquinolines: diastereoselective additions of nucleophiles and electrophiles to isoquinoline mediated by an easily resolved and recycled chiral transition metal auxiliary. Journal Of The American Chemical Society, 115 (25) 11863-11873 doi:10.1021/ja00078a026
Bell, Peter T., Cagle, Phillip C., Vichard, Dominique, Gladysz, J. A. (1996) Diallyl Sulfide Complexes of Chiral Iron and Ruthenium Lewis Acids:  Ylide Generation and Diastereoselective [2,3] Sigmatropic Rearrangements To Give Thiolate Complexes with New Carbon Stereocenters. Organometallics, 15. 4695-4701 doi:10.1021/om960541q
Meyer, Oliver, Arif, Atta M., Gladysz, J. A. (1995) A New Reaction of Coordinated Sulfoxides: Facile and Highly Diastereoselective Deprotonation of a Chiral, Cationic Rhenium DMSO Complex to an Ylide and Subsequent [1,2] Migration of Rhenium from Sulfur to Carbon. Organometallics, 14. 1844-1849 doi:10.1021/om00004a043
Johnson, Todd J., Alvey, Luke J., Brady, Monika, Mayne, Charles L., Arif, Atta M., Gladysz, J. A. (1995) Synthesis, Structure, and Reactivity of Chiral RheniumN-Pyrrolyl Complexes Regiochemistry of Electrophilic Addition and Unprecedented Rearrangements to Carbon-Ligated Species. Chemistry - A European Journal, 1 (5). 294-303 doi:10.1002/chem.19950010506
Dalton, Dennis M., Fernandez, Jesus M., Emerson, Kenneth, Larsen, Raymond D., Arif, Atta M., Gladysz, J. A. (1990) Selective activation of one methyl ketone enantioface via .sigma.-binding to a chiral transition-metal template: synthesis, structure, and reactivity of rhenium ketone complexes [(.eta.5-C5H5)Re(NO)(PPh3)(.eta.1-O:C(CH3)R)]+X-. Journal Of The American Chemical Society, 112 (25) 9198-9212 doi:10.1021/ja00181a024
Weng, Weiqing, Ramsden, James A., Arif, Atta M., Gladysz, J. A. (1993) A new form of coordinated carbon: an unsupported linear C3 chain spanning two different transition metals. Journal Of The American Chemical Society, 115 (9) 3824-3825 doi:10.1021/ja00062a078
Bodner, Gerardo S., Fernandez, Jesus M., Arif, Atta M., Gladysz, J. A. (1988) Selective binding of one enantioface of monosubstituted alkenes to the chiral transition metal Lewis acid [(.eta.5-C5H5)Re(NO)(PPh3)]+. Journal Of The American Chemical Society, 110 (12) 4082-4084 doi:10.1021/ja00220a082
Weng, Weiqing, Bartik, Tamas, Brady, Monika, Bartik, Berit, Ramsden, James A., Arif, Atta M., Gladysz, J. A. (1995) Synthesis, Structure, and Redox Chemistry of Heteropolymetallic Carbon Complexes with MC2M', MC4M', and MC4M'C4M Linkages. Transmetalations of Lithiocarbon Complexes (.eta.5-C5Me5)Re(NO)(PPh3)(C.tplbond.CLi) and (.eta.5-C5Me5)Re(NO)(PPh3)(C.tplbond.CC.tplbond.CLi) Journal Of The American Chemical Society, 117 (48) 11922-11931 doi:10.1021/ja00153a014
 
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