Donald C. Dittmer - Publications

Affiliations: 
1954-1961 University of Pennsylvania, Philadelphia, PA, United States 
 1962-2001 Chemistry Syracuse University, Syracuse, NY, United States 
Area:
Organic chemistry with tellurium, synthesis of optically active molecules, Zero-solvent reactions

36 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2010 Dittmer DC, Avilov DV, Kandula VS, Purzycki MT, Martens ZJ, Hohn EB, Bacler MW. Tetramic acids and derivatives by telluride-triggered dieckmann cyclizations Arkivoc. 2010: 61-83. DOI: 10.3998/Ark.5550190.0011.608  0.326
2004 Avilov DV, Malusare MG, Arslancan E, Dittmer DC. A telluride-triggered nucleophilic ring opening of monoactivated cyclopropanes. Organic Letters. 6: 2225-8. PMID 15200326 DOI: 10.1021/Ol0492804  0.321
2001 Chao B, Dittmer DC. Tellurium-triggered formation of racemic and non-racemic allylic amines from aziridinemethanol derivatives Tetrahedron Letters. 42: 5789-5791. DOI: 10.1016/S0040-4039(01)01124-8  0.325
2000 Chao B, Dittmer DC. A tellurium-triggered domino reaction for the synthesis of a 1-substituted-3-vinyl-1,3-dihydroisobenzofuran Tetrahedron Letters. 41: 6001-6004. DOI: 10.1016/S0040-4039(00)01047-9  0.362
1999 Xu Q, Dittmer DC. Tellurium: Use in the synthesis of allylic amines from 5-hydroxymethyl- 2-oxazolidinones Tetrahedron Letters. 40: 2255-2258. DOI: 10.1016/S0040-4039(99)00219-1  0.331
1997 Pepito AS, Dittmer DC. Conversion of Aziridinemethanol Sulfonate Esters to Allylic Amines via Tellurium Chemistry(1). The Journal of Organic Chemistry. 62: 7920-7925. PMID 11671893 DOI: 10.1021/Jo962024N  0.365
1995 Chao B, McNulty KC, Dittmer DC. Alkenes from cyclic sulfates and thionocarbonates of 1,2-diols via tellurium chemistry Tetrahedron Letters. 36: 7209-7212. DOI: 10.1016/0040-4039(95)01532-M  0.34
1994 Dittmer DC, Zhang Y, Discordia RP. Concomitant epoxide deoxygenation and deacetylation of glycidyl acetates induced by telluride ion Journal of Organic Chemistry. 59: 1004-1010. DOI: 10.1021/Jo00084A016  0.31
1991 Hoey MD, Dittmer DC. A convenient synthesis of 1,4-dihydro-2,3-benzoxathiin 3-oxide, a useful precursor of o-quinodimethane Journal of Organic Chemistry. 56: 1947-1948. DOI: 10.1021/Jo00005A054  0.383
1988 Jarvis WF, Hoey MD, Finocchio AL, Dittmer DC. Organic reactions of reduced species of sulfur dioxide Journal of Organic Chemistry. 53: 5750-5756. DOI: 10.1021/Jo00259A026  0.314
1986 Poison G, Dittmer DC. Functional group modification via organotellurium chemistry. Synthesis of allyl alcohols from chloromethyloxiranes. Tetrahedron Letters. 27: 5579-5582. DOI: 10.1016/S0040-4039(00)85270-3  0.305
1984 Hartnedy RC, Dittmer DC. Reactions of monothiobenzil and its dimer Journal of Organic Chemistry. 49: 4752-4754. DOI: 10.1002/Chin.198519177  0.325
1984 Sedergran TC, Yokoyama M, Dittmer DC. Reactions of 3-chloro-2H-thiete 1,1-dioxide Journal of Organic Chemistry. 49: 2408-2412. DOI: 10.1002/Chin.198450181  0.31
1979 Dittmer DC, Patwardhan BH, Parker EJ. Synthesis And Properties Of Some New, Stable Thietes (Thiacyclobutenes) Phosphorus Sulfur and Silicon and the Related Elements. 6: 79-80. DOI: 10.1080/03086647908080313  0.313
1979 Patwardhan BH, Parker EJ, Dittmer DC. Synthesis And Properties Of Some Stable, New Thietes (Thiacylobutenes) Phosphorus Sulfur and Silicon and the Related Elements. 10: 5-8. DOI: 10.1080/03086647808069916  0.313
1977 Dittmer DC, McCaskie JE, Babiarz JE, Ruggeri MV. Cycloaddition reactions of vinyl sulfene generated from thiete 1,1-dioxide Journal of Organic Chemistry. 42: 1910-1913. DOI: 10.1021/Jo00431A018  0.347
1973 Dittmer DC, Blidner BB. Models for the pyridine nucleotide coenzymes. Synthesis and properties of bridged dinicotinamide derivatives. Journal of Organic Chemistry. 38: 2873-2882. PMID 4270135 DOI: 10.1002/Chin.197346276  0.304
1972 Dittmer DC, Chang PLF, Davis FA, Stamos IK, Takahashi K. Derivatives of thiacyclobutene (thiete). VII. Reaction of thietes with bases Journal of Organic Chemistry. 37: 1116-1121. DOI: 10.1021/Jo00973A009  0.525
1972 Dittmer DC, Chang PLF, Davis FA, Iwanami M, Stamos IK, Takahashi K. Derivatives of thiacyclobutene (thiete). VI. Synthesis and properties of some thietes Journal of Organic Chemistry. 37: 1111-1115. DOI: 10.1021/Jo00973A008  0.493
1972 Dittmer DC, Ikura K, Balquist JM, Takashina N. Derivatives of thiacyclobutene (thiete). V. Molecular reorganization in the reaction of thiete sulfone and tetraphenylcyclopentadienone Journal of Organic Chemistry. 37: 225-230. DOI: 10.1021/Jo00967A011  0.317
1972 DITTMER DC, CHANG PLF, DAVIS FA, IWANAMI M, STAMOS IK, TAKAHASHI K. ChemInform Abstract: DERIVATE VON THIACYCLOBUTEN (THIETE) 6. MITT. SYNTH. UND EIGENSCHAFTEN EINIGER THIACYCLOBUTENE 7. MITT. RK. VON THIACYCLOBUTENEN MIT BASEN Chemischer Informationsdienst. 3: no-no. DOI: 10.1002/Chin.197234251  0.486
1972 DITTMER DC, IKURA K, BALQUIST JM, TAKASHINA N. ChemInform Abstract: DERIVATE DES THIACYCLOBUTENS (THIETES) 5. MITT. MOLEKUELUMLAGERUNG BEI DER RK. VON THIETE-SULFON UND TETRAPHENYLCYCLOPENTADIENON Chemischer Informationsdienst. 3: no-no. DOI: 10.1002/Chin.197218251  0.301
1971 Dittmer DC, Christy ME, Takashina N, Henion RS, Balquist JM. A precautionary note on the synthesis of thiete sulfone Journal of Organic Chemistry. 36: 1324. DOI: 10.1021/Jo00808A043  0.303
1971 Lombardo A, Dittmer DC. Specificity in addition of a halomethyl group to a model for a pyridine nucleotide coenzyme Bioorganic Chemistry. 1: 400-408. DOI: 10.1016/0045-2068(71)90042-3  0.336
1971 DITTMER DC, CHRISTY ME, TAKASHINA N, HENION RS, BALQUIST JM. ChemInform Abstract: VORSICHTSMASSNAHME BEI DER SYNTHESE VON THIET-SULFON Chemischer Informationsdienst. Organische Chemie. 2: no-no. DOI: 10.1002/Chin.197132248  0.312
1970 Bristol DW, Dittmer DC. Reactions of pyridinium salts with alkaline hydrogen peroxide. Formation of pyrrolidinone hydroperoxides from 1-methyl- and 1-benzyl-3-carbamoylpyridinium chloride Journal of Organic Chemistry. 35: 2487-2495. DOI: 10.1021/Jo00833A005  0.331
1970 Dittmer DC, Glassman R. Correction. Diazo Alkane Adducts of Thiete Sulfone (Thiacyclobutene 1,1-Dioxide) in Synthesis of Thiabicyclopentane Dioxides, Pyrazoles, and Tetrahydrothiophene Sulfones Journal of Organic Chemistry. 35: 4005-4006. DOI: 10.1021/Jo00829A030  0.328
1969 Dittmer DC, Whitman ES. Addition of thiobenzophenone to benzenediazonium-2-carboxylate Journal of Organic Chemistry. 34: 2004-2006. DOI: 10.1021/Jo01258A118  0.331
1969 Dittmer DC, Henion RS, Takashina N. Derivatives of thiacyclobutene (thiete). IV. Thermal decomposition of a naphthothiete sulfone. An oxidation-reduction reaction and formation of a cyclic sulfinate ester (sultine) Journal of Organic Chemistry. 34: 1310-1316. DOI: 10.1021/Jo01257A023  0.341
1968 Dittmer DC, Balquist JM. Derivatives of thiacyclobutenes. III. Synthesis of highly unsaturated thiete sulfones Journal of Organic Chemistry. 33: 1364-1367. DOI: 10.1021/Jo01268A013  0.357
1967 Dittmer DC, Davis FA. Derivatives of thiacyclobutene (thiete). II. Reactions of 7-thiabicyclo[4.2.0]oct-1(8)-ene 7,7-dioxide Journal of Organic Chemistry. 32: 3872-3876. DOI: 10.1021/Jo01287A034  0.525
1965 Dittmer DC, Davis FA. Evidence for a Thiete (Thiacyclobutene)1,2 Journal of the American Chemical Society. 87: 2064-2065. DOI: 10.1021/Ja01087A048  0.397
1964 Dittmer DC, Marcantonio AF. Isomerizations of 1-chloro-2-butene and 3-chloro-1-butene Journal of Organic Chemistry. 29: 3473-3475. DOI: 10.1021/Jo01035A007  0.338
1964 Dittmer DC, Davis FA. A new bicyclic thiete sulfone Journal of Organic Chemistry. 29: 3131-3132. DOI: 10.1021/Jo01033A544  0.441
1962 Dittmer DC, Christy ME. Derivatives of thiacyclobutene (thiete) and thiacyclobutane (thietane). I. Reactions of thiete sulfone Journal of the American Chemical Society. 84: 399-402. DOI: 10.1021/Ja00862A018  0.372
1957 Bartlett PD, Dittmer DC. A kinetic study of the Leuchs anhydrides in aqueous solution. II Journal of the American Chemical Society. 79: 2159-2160. DOI: 10.1021/Ja01566A036  0.52
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