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 |
|
Show low-probability matches. |