| Year |
Citation |
Score |
| 2015 |
Puniani E, Cayer C, Kent P, Mullally M, Sánchez-Vindas P, Poveda Álvarez L, Cal V, Merali Z, Arnason JT, Durst T. Ethnopharmacology of Souroubea sympetala and Souroubea gilgii (Marcgraviaceae) and identification of betulinic acid as an anxiolytic principle. Phytochemistry. 113: 73-8. PMID 24641939 DOI: 10.1016/J.Phytochem.2014.02.017 |
0.341 |
|
| 2014 |
Dabrota C, Asim M, Choueiri C, Gargaun A, Korobkov I, Butt A, Carlson KE, Katzenellenbogen JA, Wright JS, Durst T. Synthesis and receptor binding in trans-CD ring-fused A-CD estrogens: comparison with the cis-fused isomers. Bioorganic & Medicinal Chemistry Letters. 24: 3841-4. PMID 25027938 DOI: 10.1016/J.Bmcl.2014.06.066 |
0.453 |
|
| 2013 |
Wright JS, Anderson JM, Shadnia H, Durst T, Katzenellenbogen JA. Experimental versus predicted affinities for ligand binding to estrogen receptor: iterative selection and rescoring of docked poses systematically improves the correlation. Journal of Computer-Aided Molecular Design. 27: 707-21. PMID 23975271 DOI: 10.1007/S10822-013-9670-6 |
0.391 |
|
| 2012 |
Asim M, Klonowska D, Choueiri C, Korobkov I, Carlson KE, Katzenellenbogen JA, Durst T. BC-spiro-estradiols. Synthesis and estrogen receptor binding affinity of four new estradiol isomers. Bioorganic & Medicinal Chemistry Letters. 22: 3713-7. PMID 22546676 DOI: 10.1016/J.Bmcl.2012.04.022 |
0.481 |
|
| 2011 |
Wright JS, Shadnia H, Anderson JM, Durst T, Asim M, El-Salfiti M, Choueiri C, Pratt MA, Ruddy SC, Lau R, Carlson KE, Katzenellenbogen JA, O'Brien PJ, Wan L. A-CD estrogens. I. Substituent effects, hormone potency, and receptor subtype selectivity in a new family of flexible estrogenic compounds. Journal of Medicinal Chemistry. 54: 433-48. PMID 21190382 DOI: 10.1021/Jm100513M |
0.465 |
|
| 2010 |
Guerrero-Analco JA, Martineau L, Saleem A, Madiraju P, Muhammad A, Durst T, Haddad P, Arnason JT. Bioassay-guided isolation of the antidiabetic principle from Sorbus decora (Rosaceae) used traditionally by the Eeyou Istchee Cree First Nations. Journal of Natural Products. 73: 1519-23. PMID 20738101 DOI: 10.1021/Np1003005 |
0.317 |
|
| 2009 |
Asim M, Asim M, El-Salfiti M, Qian Y, Choueiri C, Salari S, Cheng J, Shadnia H, Bal M, Christine Pratt MA, Carlson KE, Katzenellenbogen JA, Wright JS, Durst T. Deconstructing estradiol: removal of B-ring generates compounds which are potent and subtype-selective estrogen receptor agonists. Bioorganic & Medicinal Chemistry Letters. 19: 1250-3. PMID 19167882 DOI: 10.1016/J.Bmcl.2008.12.080 |
0.479 |
|
| 2009 |
Asim M, El-Salfiti M, Qian Y, Choueiri C, Salari S, Cheng J, Shadnia H, Bal M, Christine Pratt MA, Carlson KE, Katzenellenbogen JA, Wright JS, Durst T. Corrigendum to "Deconstructing estradiol: Removal of B-ring generates compounds which are potent and subtype-selective estrogen receptor agonists" [Bioorg. Med. Chem. Lett. 19 (2009) 1250-1253] (DOI:10.1016/j.bmcl.2008.12.080) Bioorganic and Medicinal Chemistry Letters. 19: 2605. DOI: 10.1016/J.Bmcl.2008.12.117 |
0.45 |
|
| 2007 |
Omar S, Marcotte M, Fields P, Sanchez PE, Poveda L, Mata R, Jimenez A, Durst T, Zhang J, MacKinnon S, Leaman D, Arnason JT, Philogène BJR. Antifeedant activities of terpenoids isolated from tropical Rutales Journal of Stored Products Research. 43: 92-96. DOI: 10.1016/J.Jspr.2005.11.005 |
0.305 |
|
| 2003 |
Hussain HH, Babic G, Durst T, Wright JS, Flueraru M, Chichirau A, Chepelev LL. Development of novel antioxidants: design, synthesis, and reactivity. The Journal of Organic Chemistry. 68: 7023-32. PMID 12946144 DOI: 10.1021/Jo0301090 |
0.319 |
|
| 2003 |
Tripathy S, Reddy R, Durst T. Preparation of benzocyclobutenols by low temperature reaction of ketone enolates with benzynes Canadian Journal of Chemistry. 81: 997-1002. DOI: 10.1139/V03-099 |
0.351 |
|
| 2002 |
Reddy R, Jaquith JB, Neelagiri VR, Saleh-Hanna S, Durst T. Asymmetric synthesis of the highly methylated tryptophan portion of the hemiasterlin tripeptides. Organic Letters. 4: 695-7. PMID 11869104 DOI: 10.1021/Ol016982+ |
0.378 |
|
| 2001 |
Hantos SM, Tripathy S, Alibhai N, Durst T. Synthesis of trichiliasterones A and B 16-Ketosteroids isolated from Trichilia hirta and Trichilia americana Canadian Journal of Chemistry. 79: 1747-1753. DOI: 10.1139/V01-126 |
0.406 |
|
| 2001 |
Hussain H, Kianmehr E, Durst T. Competitive 3+2 and 2+2 cycloadditions of ester stabilized azaallyl anions to benzynes. Ring expansion of initial 3+2 products to isoquinolin-3-ones Tetrahedron Letters. 42: 2245-2248. DOI: 10.1016/S0040-4039(01)00130-7 |
0.41 |
|
| 2000 |
Majerus SL, Alibhai N, Tripathy S, Durst T. New syntheses of dillapiol (4,5-dimethoxy-6-(2- propenyl)-1,3-benzodioxole), its 4-methylthio and other analogs Canadian Journal of Chemistry. 78: 1345-1355. DOI: 10.1139/V00-138 |
0.413 |
|
| 2000 |
Tripathy S, Hussain H, Durst T. Iodine ate complexes and N-lithiobenzocyclobutenamine intermediates in the reactions of α-lithionitriles with benzyne Tetrahedron Letters. 41: 8401-8405. DOI: 10.1016/S0040-4039(00)01493-3 |
0.393 |
|
| 1999 |
Tripathy S, LeBlanc R, Durst T. Formation of 2-Substituted Iodobenzenes from Iodobenzene via Benzyne and Ate Complex Intermediates Organic Letters. 1: 1973-1975. DOI: 10.1021/Ol991129K |
0.325 |
|
| 1999 |
Ben RN, Durst T. Synthesis of Optically Active α-Amino Esters via Dynamic Kinetic Resolution: A Mechanistic Study The Journal of Organic Chemistry. 64: 7700-7706. DOI: 10.1021/Jo9811625 |
0.628 |
|
| 1998 |
O'Meara JA, Gardee N, Jung M, Ben RN, Durst T. Enantioselective Synthesis of β-Dibenzylamino Alcohols via a Dynamic Kinetic Resolution of α-Halo Acids The Journal of Organic Chemistry. 63: 3117-3119. DOI: 10.1021/Jo9712714 |
0.672 |
|
| 1997 |
Lear Y, Durst T. Synthesis Of Regiospecifically Substituted 2-Hydroxybenzocyclobutenones Canadian Journal of Chemistry. 75: 817-824. DOI: 10.1139/V97-098 |
0.385 |
|
| 1997 |
Connolly TJ, Durst T. Metal hydride mediated reduction of 1,3-dimethyl-3(methylthio)oxindole Canadian Journal of Chemistry. 75: 542-546. DOI: 10.1139/V97-064 |
0.319 |
|
| 1997 |
Connolly TJ, Durst T. Metal hydride mediated reduction of 3-(alkylthio)oxindoles containing other potentially reducible groups Canadian Journal of Chemistry. 75: 536-541. DOI: 10.1139/V97-063 |
0.336 |
|
| 1997 |
MacKinnon SL, Bensimon C, Arnason JT, Sanchez-Vindas PE, Durst T. Spirocaracolitones, CD-spiro-triterpenoids from Ruptiliocarpon caracolito Journal of Organic Chemistry. 62: 840-845. DOI: 10.1021/Jo9611531 |
0.342 |
|
| 1997 |
Connolly TJ, Durst T. The synthesis of sultines from δ-hydroxy sulfoxides revisited Tetrahedron Letters. 38: 1337-1340. DOI: 10.1016/S0040-4039(97)00093-2 |
0.391 |
|
| 1997 |
Connolly TJ, Durst T. Photochemically generated bicyclic ortho-quinodimethanes: Photo- enolization of bicyclic aldehydes and ketones Tetrahedron. 53: 15969-15982. DOI: 10.1016/S0040-4020(97)10068-0 |
0.416 |
|
| 1997 |
Connolly TJ, Durst T. The synthesis of bicyclic ortho-quinodimethanes from tricyclic sulfones Tetrahedron. 53: 15957-15968. DOI: 10.1016/S0040-4020(97)10066-7 |
0.386 |
|
| 1996 |
Lear Y, Durst T. Synthesis and biological evaluation of carbon-substituted C-4 derivatives of podophyllotoxin Canadian Journal of Chemistry. 74: 1704-1708. DOI: 10.1139/V96-187 |
0.307 |
|
| 1995 |
O'Meara JA, Jung M, Durst T. Dynamic kinetic resolution of racemic α-halo acids via a chiral imidazolidinone auxiliary Tetrahedron Letters. 36: 2559-2562. DOI: 10.1016/0040-4039(95)00339-E |
0.531 |
|
| 1994 |
Koh K, Durst T. Stereoselective SN2 Reactions of the (R)-Pantolactone Ester of Racemic .alpha.-Halo Carboxylic Acids with Aryl Oxides. A Synthesis of (S)-2-Aryloxy and (S)-2-Hydroxy Acids Journal of Organic Chemistry. 59: 4683-4686. DOI: 10.1021/Jo00095A053 |
0.35 |
|
| 1994 |
Ben RN, Breau L, Bensimon C, Durst T. Unusual stereochemical results in the reaction of alpha-lithio derivatives of bicyclic sulfoxides Tetrahedron. 50: 6061-6076. DOI: 10.1016/S0040-4020(01)90458-2 |
0.621 |
|
| 1994 |
Durst T, Ben R, Jung M. FC43 the synthesis of α-amino acid esters using α-hydroxy amides as chiral auxiliaries European Journal of Pharmaceutical Sciences. 2: 111. DOI: 10.1016/0928-0987(94)90152-X |
0.672 |
|
| 1994 |
Boch R, Bradley JC, Durst T, Scaiano JC. Z E photoisomerization of benzylidenebenzocyclobutenones via ketene-allene intermediates. A laser flash photolysis study Tetrahedron Letters. 35: 19-22. DOI: 10.1016/0040-4039(94)88151-0 |
0.629 |
|
| 1994 |
Koh K, Ben RN, Durst T. A facile synthesis of optically active C2-symmetric 2,5-disubstituted pyrrolidines and other β,β′-dihydroxyamines Tetrahedron Letters. 35: 375-378. DOI: 10.1016/0040-4039(94)85057-7 |
0.637 |
|
| 1993 |
Durst T, Breau L, Ben RN. Sulfonium Ylides. Application to the Synthesis of Optically Active Epoxides Phosphorus, Sulfur, and Silicon and the Related Elements. 74: 215-232. DOI: 10.1080/10426509308038109 |
0.608 |
|
| 1993 |
Koh K, Ben RN, Durst T. Reaction of (R)-pantolactone esters of alpha-bromoacids with amines a remarkable synthesis of optically active alpha-amino esters Tetrahedron Letters. 34: 4473-4476. DOI: 10.1016/0040-4039(93)88062-N |
0.643 |
|
| 1992 |
Shakya S, Durst T. Anionic 4+2 Cyclization Route to 3-Sulfur Substituted Isocephem Analogs Heterocycles. 34: 67-83. DOI: 10.3987/Com-91-5882 |
0.389 |
|
| 1992 |
Durst T, Behnia LD. Synthesis of non-enolizable α- and β-peltatins Canadian Journal of Chemistry. 70: 1082-1086. DOI: 10.1139/V92-142 |
0.389 |
|
| 1992 |
Bradley JC, Durst T, Williams AJ. Thermolysis of 2-benzylidenebenzocyclobutenols The Journal of Organic Chemistry. 57: 6575-6579. DOI: 10.1021/Jo00050A038 |
0.681 |
|
| 1992 |
Durst T, Koh K. Asymmetric synthesis of alpha-halo esters Tetrahedron Letters. 33: 6799-6802. DOI: 10.1016/S0040-4039(00)61779-3 |
0.356 |
|
| 1992 |
Connors R, Durst T. Acyl cyanides as carbonyl heterodienophiles Tetrahedron Letters. 33: 7277-7280. DOI: 10.1016/S0040-4039(00)60164-8 |
0.331 |
|
| 1992 |
Bradley J, Durst T. Visualization of column chromatography Tetrahedron Letters. 33: 7733-7734. DOI: 10.1016/0040-4039(93)88031-D |
0.597 |
|
| 1991 |
Breau L, Sharma NK, Butler IR, Durst T. Synthesis and X-ray crystal structure determination of 3,4-diphenyl-6-(diphenylmethyl)-1,5-dioxa-2-thiane-2-oxide Canadian Journal of Chemistry. 69: 185-188. DOI: 10.1139/V91-029 |
0.395 |
|
| 1991 |
Bradley JC, Durst T. Synthesis of 2-benzylidenebenzocyclobutenones via an intramolecular Stille coupling reaction The Journal of Organic Chemistry. 56: 5459-5462. DOI: 10.1021/Jo00018A050 |
0.653 |
|
| 1990 |
Durst T, Sharma MK, Gabe EJ, Lee FL. Carbanions derived from 3-methoxyazetidinones: precursors for the preparation of 3,3-disubstituted azetidinones Journal of Organic Chemistry. 55: 5525-5528. DOI: 10.1021/Jo00307A027 |
0.343 |
|
| 1990 |
Etkin N, Babu SD, Fooks CJ, Durst T. Preparation of 3-acetyl-2-hydroxyindoles via rhodium carbenoid aromatic carbon-hydrogen insertion The Journal of Organic Chemistry. 55: 1093-1096. DOI: 10.1021/Jo00290A052 |
0.35 |
|
| 1990 |
Breau L, Ogilvie W, Durst T. Preparation of optically active stilbene oxides via sulfonium salts derived from C2 symmetric thiolanes. Tetrahedron Letters. 31: 35-38. DOI: 10.1016/S0040-4039(00)94327-2 |
0.337 |
|
| 1989 |
Babu SD, Hrytsak MD, Durst T. Intramolecular rhodium carbenoid insertions into aromatic C—H bonds. Preparation of 1,3-dihydrothiophene 2,2-dioxides fused onto aromatic rings Canadian Journal of Chemistry. 67: 1071-1076. DOI: 10.1139/V89-162 |
0.425 |
|
| 1988 |
Ogilvie WW, Durst T. Oxidation of 3-alkylidene-β-lactams. A preparation of 3-alkenyl-3-hydroxy-β-lactams Canadian Journal of Chemistry. 66: 304-309. DOI: 10.1139/V88-053 |
0.409 |
|
| 1988 |
Macdonald DI, Durst T. A highly stereoselective synthesis of podophyllotoxin and analogues based on an intramolecular Diels-Alder reaction The Journal of Organic Chemistry. 53: 3663-3669. DOI: 10.1021/Jo00251A003 |
0.315 |
|
| 1987 |
Khan Z, Durst T. Preparation of 1-thio and 1-amino substituted 1,3-dihydrobenzo[c]thiophene 2,2-dioxides Canadian Journal of Chemistry. 65: 482-486. DOI: 10.1139/V87-083 |
0.386 |
|
| 1987 |
Glinski MB, Freed JC, Durst T. Preparation of 2-substituted podophyllotoxin derivatives The Journal of Organic Chemistry. 52: 2749-2753. DOI: 10.1021/Jo00389A020 |
0.356 |
|
| 1986 |
Durst T, Charlton JL, Mount DB. Reactions of 1-hydroxy-1,3-dihydrobenzo[c]thiophen-2,2-dioxides. Preparation of benz-fused δ-sultines Canadian Journal of Chemistry. 64: 246-249. DOI: 10.1139/V86-042 |
0.389 |
|
| 1986 |
Macdonald DI, Durst T. A highly stereoselective Diels-Alder based synthesis of (.+-.)-podophyllotoxin The Journal of Organic Chemistry. 51: 4749-4750. DOI: 10.1021/Jo00374A056 |
0.312 |
|
| 1986 |
Hrytsak M, Etkin N, Durst T. Intramolecular rhodium carbenoid insertions into aromatic CH bonds. Preparation of 1-carboalkoxy-1,3-dihydrobenzo[C]thiophene 2,2-dioxides Tetrahedron Letters. 27: 5679-5682. DOI: 10.1016/S0040-4039(00)85299-5 |
0.421 |
|
| 1986 |
Macdonald DI, Durst T. A synthesis of -2-arylbenzocyclobuten-1-ols Tetrahedron Letters. 27: 2235-2238. DOI: 10.1016/S0040-4039(00)84495-0 |
0.374 |
|
| 1984 |
Charlton JL, Durst T. o-quinodimethanes from 3,6-dihydrobenzo[b]-1,2-oxathiin-2-oxides Tetrahedron Letters. 25: 5287-5290. DOI: 10.1016/S0040-4039(01)81585-9 |
0.353 |
|
| 1984 |
Charlton JL, Durst T. Photochemical synthesis of α-oxygenated benzothiophenedioxides Tetrahedron Letters. 25: 2663-2666. DOI: 10.1016/S0040-4039(01)81257-0 |
0.344 |
|
| 1983 |
Glinski MB, Durst T. Synthesis of (±)-epiisopodophyllotoxin Canadian Journal of Chemistry. 61: 573-575. DOI: 10.1139/V83-101 |
0.361 |
|
| 1983 |
Hamlet AB, Durst T. 1-(Dialkylaminomethyl)-azetidin-2-ones. Intermediates in a highly stereoselective preparation of trans-3,4-disubstituted azetidin-2-ones Canadian Journal of Chemistry. 61: 411-415. DOI: 10.1139/V83-073 |
0.426 |
|
| 1983 |
Martel A, Daris J, Bachand C, Ménard M, Durst T, Belleau B. Nuclear analogs of β-lactam antibiotics. XVII. Stereospecific synthesis of penem and carbapenem precursors Canadian Journal of Chemistry. 61: 1899-1901. DOI: 10.1002/Chin.198348339 |
0.321 |
|
| 1983 |
Georg G, Durst T. Reaction of 4-(iodomethyl)azetidin-2-ones with tetracarbonylferrate(II) The Journal of Organic Chemistry. 48: 2092-2095. DOI: 10.1002/Chin.198346162 |
0.474 |
|
| 1983 |
Glinski MB, Durst T. Synthesis Of (.+-.)-Epiisopodophyllotoxin Cheminform. 14. DOI: 10.1002/Chin.198332351 |
0.324 |
|
| 1981 |
Decesare JM, Corbel B, Durst T, Blount JF. γ- and δ-epoxy sulfones. Formation of different ring-sized products upon reaction with CH3MgI or LiN[CH(CH3)2]2 Canadian Journal of Chemistry. 59: 1415-1424. DOI: 10.1139/V81-208 |
0.362 |
|
| 1981 |
Venugopalan B, Hamlet AB, Durst T. A short synthesis of the Δ-carbopenem ring system☆ Tetrahedron Letters. 22: 191-194. DOI: 10.1016/0040-4039(81)80052-4 |
0.398 |
|
| 1981 |
DECESARE JM, CORBEL B, DURST T, BLOUNT JF. ChemInform Abstract: Γ- AND Δ-EPOXY SULFONES. FORMATION OF DIFFERENT RING-SIZED PRODUCTS UPON REACTION WITH METHYLMAGNESIUM IODIDE OR LITHIUM DIISOPROPYLAMIDE Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198139106 |
0.357 |
|
| 1981 |
VENUGOPALAN B, HAMLET AB, DURST T. ChemInform Abstract: A SHORT SYNTHESIS OF THE Δ1-CARBOPENEM RING SYSTEM Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198117211 |
0.351 |
|
| 1979 |
Aida T, Legault R, Dugat D, Durst T. Cyclization reactions of 4-(3′-butenyl)azetidin-2-one a route to the carbopenam ring system Tetrahedron Letters. 20: 4993-4994. DOI: 10.1016/S0040-4039(01)86770-8 |
0.405 |
|
| 1979 |
Gowland BD, Durst T. Benzocyclobutyl phenyl sulfone. An evaluation of its potential as a precursor to substituted benzocyclobutenes and ortho-quinodimethanes Canadian Journal of Chemistry. 57: 1462-1467. DOI: 10.1002/Chin.197945189 |
0.386 |
|
| 1979 |
Durst T, Tin K, Reinach-Hirtzbach FD, Decesare JM, Ryan MD. α,β-Epoxy sulfoxides and sulfones. Synthesis and some reactions Canadian Journal of Chemistry. 57: 258-266. DOI: 10.1002/Chin.197924201 |
0.411 |
|
| 1978 |
Durst T, Huang JC, Sharma NK, Smith DJH. Photochemical extrusion of sulfur dioxide from sultines Canadian Journal of Chemistry. 56: 512-516. DOI: 10.1002/Chin.197829146 |
0.358 |
|
| 1978 |
Corbel B, Decesare JM, Durst T. Preparation of cyclobutenones and cyclopent-2-enones via epoxy sulfone cyclizations Canadian Journal of Chemistry. 56: 505-511. DOI: 10.1002/Chin.197829129 |
0.339 |
|
| 1977 |
Sharma NK, Reinach‐Hirtzbach FD, Durst T. Synthesis Of Sultines Via Tert‐Butyl Hydroxyalkyl Sulfoxides Cheminform. 8. DOI: 10.1002/Chin.197704199 |
0.335 |
|
| 1977 |
DE REINACH-HIRTZBACH F, DURST T. ChemInform Abstract: REACTION OF α,β-EPOXYSULFONES WITH MAGNESIUM BROMIDE. PREPARATION OF α-BROMO ALDEHYDES AND KETONES Chemischer Informationsdienst. 8: no-no. DOI: 10.1002/Chin.197701192 |
0.378 |
|
| 1976 |
Sharma NK, Reinach-Hirtzbach Fd, Durst T. Synthesis of sultines via tert-butyl hydroxyalkyl sulfoxides Canadian Journal of Chemistry. 54: 3012-3025. DOI: 10.1139/V76-427 |
0.39 |
|
| 1976 |
Alper H, Des Roches D, Durst T, Legault R. Molybdenum hexacarbonyl catalyzed rearrangement of epoxides The Journal of Organic Chemistry. 41: 3611-3613. DOI: 10.1021/Jo00884A029 |
0.379 |
|
| 1976 |
de Reinach-Hirtzbach F, Durst T. Reaction of α,β-epoxysulfones with MgBr2, preparation of α-bromo aldehydes and ketones. Tetrahedron Letters. 17: 3677-3680. DOI: 10.1016/S0040-4039(00)93079-X |
0.369 |
|
| 1975 |
Durst T, Molin M. Effect of salts on the stereoselectivity of reactions of α-lithio sulfoxides Tetrahedron Letters. 16: 63-66. DOI: 10.1016/S0040-4039(00)71778-3 |
0.375 |
|
| 1973 |
Sharma N, Jung F, Durst T. Synthesis of cyclic sulfinate esters (sultines) via -butyl hydroxyalkyl sulfoxides Tetrahedron Letters. 14: 2863-2866. DOI: 10.1016/S0040-4039(01)96072-1 |
0.383 |
|
| 1971 |
Durst T. α-Lithio-δ-sultones: high preference for equatorial vs. axial lithium Tetrahedron Letters. 12: 4171-4174. DOI: 10.1016/S0040-4039(01)97491-X |
0.312 |
|
| 1970 |
Durst T, Tin K. Thermal and acid-catalyzed rearrangement of α-epoxy sulfoxides and sulfones Tetrahedron Letters. 11: 2369-2372. DOI: 10.1016/S0040-4039(01)98231-0 |
0.339 |
|
| 1968 |
Corey EJ, Durst T. Synthesis of olefins and ketones from carbonyl compounds and sulfinamides Journal of the American Chemical Society. 90: 5548-5552. DOI: 10.1021/Ja01022A041 |
0.422 |
|
| 1963 |
King J, Durst T. Rearrangement of benzylsulphonyl chloride with tertiary amines: a route to a little-known class of sulphur compounds Tetrahedron Letters. 4: 585-589. DOI: 10.1016/S0040-4039(01)90678-1 |
0.525 |
|
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