Year |
Citation |
Score |
2019 |
Bartko SG, Hamzik PJ, Espindola L, Gomez C, Danheiser RL. Synthesis of Highly Substituted Pyridines via [4 + 2] Cycloadditions of Vinylallenes and Sulfonyl Cyanides. The Journal of Organic Chemistry. PMID 31797669 DOI: 10.1021/Acs.Joc.9B02628 |
0.527 |
|
2018 |
Forneris CC, Wang YP, Mamaliga G, Willumstad TP, Danheiser RL. Furo[2,3- g]thieno[2,3- e]indole: Application of an Ynamide-Based Benzannulation Strategy to the Synthesis of a Tetracyclic Heteroaromatic Compound. Organic Letters. PMID 30256110 DOI: 10.1021/Acs.Orglett.8B02920 |
0.466 |
|
2018 |
Sasaki M, Hamzik PJ, Ikemoto H, Bartko SG, Danheiser RL. Formal Bimolecular [2 + 2 + 2] Cycloaddition Strategy for the Synthesis of Pyridines: Intramolecular Propargylic Ene Reaction/Aza Diels-Alder Reaction Cascades. Organic Letters. 20: 6244-6249. PMID 30247929 DOI: 10.1021/Acs.Orglett.8B02728 |
0.499 |
|
2018 |
Machado VR, Biavatti MW, Danheiser RL. A short and efficient synthesis of the polyacetylene natural product deca-4,6,8-triyn-1-ol Tetrahedron Letters. 59: 3405-3408. DOI: 10.1016/J.Tetlet.2018.07.059 |
0.413 |
|
2017 |
Hamzik PJ, Goutierre AS, Sakai T, Danheiser RL. Aza Diels-Alder Reactions of Nitriles, N,N-Dimethylhydrazones, and Oximino Ethers. Application in Formal [2 + 2 + 2] Cycloadditions for the Synthesis of Pyridines. The Journal of Organic Chemistry. 82: 12975-12991. PMID 29193963 DOI: 10.1021/Acs.Joc.7B02503 |
0.486 |
|
2017 |
Ho T, Fieser M, Danheiser R, Roush W, Fieser L. Tetrakis(triphenylphosphine)nickel(0) Fieser and Fieser's Reagents For Organic Synthesis. DOI: 10.1002/9780471264194.Fos09647 |
0.422 |
|
2017 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W, Smith J. Rhodium(II) carboxylates Fieser and Fieser's Reagents For Organic Synthesis. 0-0. DOI: 10.1002/9780471264194.Fos08768.Pub6 |
0.505 |
|
2017 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W. Phosphorus(V) sulfide Fieser and Fieser's Reagents For Organic Synthesis. DOI: 10.1002/9780471264194.Fos08273.Pub3 |
0.46 |
|
2017 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W. Phenyliodine(III) dichloride Fieser and Fieser's Reagents For Organic Synthesis. 0-0. DOI: 10.1002/9780471264194.Fos07987 |
0.336 |
|
2017 |
Ho T, Fieser M, Danheiser R, Roush W, Fieser L. Palladium(II) acetate Fieser and Fieser's Reagents For Organic Synthesis. 0-0. DOI: 10.1002/9780471264194.Fos07552.Pub6 |
0.511 |
|
2017 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W. Manganese(II) Chloride Fieser and Fieser's Reagents For Organic Synthesis. 368-368. DOI: 10.1002/9780471264194.Fos06703.Pub2 |
0.373 |
|
2017 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W. Magnesium Bromide Etherate Fieser and Fieser's Reagents For Organic Synthesis. 364-364. DOI: 10.1002/9780471264194.Fos06647.Pub2 |
0.431 |
|
2017 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W, Smith J. Lithium 2,2,6,6‐Tetramethylpiperidide, LiTMP Fieser and Fieser's Reagents For Organic Synthesis. 361-362. DOI: 10.1002/9780471264194.Fos06576.Pub4 |
0.554 |
|
2017 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W, Smith J. Lithium diisopropylamide (LDA) Fieser and Fieser's Reagents For Organic Synthesis. 358-359. DOI: 10.1002/9780471264194.Fos06433.Pub6 |
0.479 |
|
2017 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W. Dihydridotetrakis(triphenylphosphine)ruthenium(II) Fieser and Fieser's Reagents For Organic Synthesis. DOI: 10.1002/9780471264194.Fos04013.Pub2 |
0.424 |
|
2017 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W. Copper(II) Chloride Fieser and Fieser's Reagents For Organic Synthesis. DOI: 10.1002/9780471264194.Fos02878.Pub6 |
0.485 |
|
2017 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W. Copper(I) t-Butoxide Fieser and Fieser's Reagents For Organic Synthesis. 225-225. DOI: 10.1002/9780471264194.Fos02868.Pub4 |
0.449 |
|
2017 |
Ho T, Fieser M, Danheiser R, Roush W, Fieser L. Bis(dibenzylideneacetone)palladium(0) Fieser and Fieser's Reagents For Organic Synthesis. 0-0. DOI: 10.1002/9780471264194.Fos01118.Pub3 |
0.484 |
|
2017 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W, Smith J. Copper(I) Chloride Fieser and Fieser's Reagents For Organic Synthesis. 1-4. DOI: 10.1002/047084289X.Rc215.Pub2 |
0.473 |
|
2016 |
Bartko SG, Deng J, Danheiser RL. Synthesis of 1‐Iodopropyne Organic Syntheses. 93: 245-262. DOI: 10.1002/0471264229.Os093.18 |
0.476 |
|
2015 |
Willumstad TP, Boudreau PD, Danheiser RL. Synthesis of Highly Substituted Quinolines via a Tandem Ynamide Benzannulation/Iodocyclization Strategy. The Journal of Organic Chemistry. PMID 26259034 DOI: 10.1021/Acs.Joc.5B01648 |
0.522 |
|
2015 |
Deng J, Wang Y, Danheiser RL. Synthesis of 4,4-Dimethoxybut-1-Yne Organic Syntheses. 92: 13-25. DOI: 10.1002/0471264229.Os092.02 |
0.49 |
|
2014 |
Tlais SF, Danheiser RL. N-tosyl-3-azacyclohexyne. Synthesis and chemistry of a strained cyclic ynamide. Journal of the American Chemical Society. 136: 15489-92. PMID 25328003 DOI: 10.1021/Ja509055R |
0.77 |
|
2013 |
Willumstad TP, Haze O, Mak XY, Lam TY, Wang YP, Danheiser RL. Batch and flow photochemical benzannulations based on the reaction of ynamides and diazo ketones. Application to the synthesis of polycyclic aromatic and heteroaromatic compounds. The Journal of Organic Chemistry. 78: 11450-69. PMID 24116731 DOI: 10.1021/Jo402010B |
0.467 |
|
2013 |
Lam TY, Wang YP, Danheiser RL. Benzannulation via the reaction of ynamides and vinylketenes. application to the synthesis of highly substituted indoles. The Journal of Organic Chemistry. 78: 9396-414. PMID 23952525 DOI: 10.1021/jo401635c |
0.459 |
|
2013 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W. Sodium hydrogen sulfide Fieser and Fieser's Reagents For Organic Synthesis. DOI: 10.1002/9780471264194.Fos09217.Pub2 |
0.329 |
|
2013 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W. 4‐Dimethylaminopyridine (DMAP) Fieser and Fieser's Reagents For Organic Synthesis. 254-255. DOI: 10.1002/9780471264194.Fos04311.Pub5 |
0.42 |
|
2013 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W, Smith J. Diisobutylaluminum Hydride, (DIBAL‐H) Fieser and Fieser's Reagents For Organic Synthesis. 253-253. DOI: 10.1002/9780471264194.Fos04085.Pub5 |
0.454 |
|
2013 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W, Smith J. 2,3-Dichloro-5,6-Dicyano-1,4-Benzoquinone (DDQ) Fieser and Fieser's Reagents For Organic Synthesis. 207-209. DOI: 10.1002/9780471264194.Fos03620.Pub5 |
0.351 |
|
2013 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W. t‐Butyl Hydroperoxide Fieser and Fieser's Reagents For Organic Synthesis. DOI: 10.1002/9780471264194.Fos01966.Pub5 |
0.363 |
|
2012 |
Lan Y, Danheiser RL, Houk KN. Why nature eschews the concerted [2 + 2 + 2] cycloaddition of a nonconjugated cyanodiyne. Computational study of a pyridine synthesis involving an ene-Diels-Alder-bimolecular hydrogen-transfer mechanism. The Journal of Organic Chemistry. 77: 1533-8. PMID 22188179 DOI: 10.1021/Jo202424N |
0.386 |
|
2011 |
Robinson JM, Tlais SF, Fong J, Danheiser RL. A [4 + 4] annulation strategy for the synthesis of eight-membered carbocycles based on intramolecular cycloadditions of conjugated enynes. Tetrahedron. 67: 9890-9898. PMID 22267878 DOI: 10.1016/J.Tet.2011.09.031 |
0.798 |
|
2011 |
Wang YP, Danheiser RL. Synthesis of 2-iodoynamides and regioselective [2+2] cycloadditions with ketene. Tetrahedron Letters. 52: 2111-2114. PMID 21479121 DOI: 10.1016/J.Tetlet.2010.11.002 |
0.515 |
|
2011 |
Mak XY, Crombie AL, Danheiser RL. Synthesis of polycyclic benzofused nitrogen heterocycles via a tandem ynamide benzannulation/ring-closing metathesis strategy. Application in a formal total synthesis of (+)-FR900482. The Journal of Organic Chemistry. 76: 1852-73. PMID 21322545 DOI: 10.1021/Jo2000308 |
0.5 |
|
2011 |
Benda K, Knoth T, Danheiser RL, Schaumann E. A New Route to Silyl-substituted Cyclobutenones and Silylketenes. Tetrahedron Letters. 52: 46-48. PMID 21151736 DOI: 10.1016/J.Tetlet.2010.10.130 |
0.373 |
|
2011 |
Ho T, Fieser M, Danheiser R, Roush W, Smith J, Fieser L. Phase‐transfer catalysts Fieser and Fieser's Reagents For Organic Synthesis. 452-452. DOI: 10.1002/9780471264194.Fos07867.Pub4 |
0.532 |
|
2011 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W, Smith J. Mercury(II) Trifluoroacetate Fieser and Fieser's Reagents For Organic Synthesis. DOI: 10.1002/9780471264194.Fos06777.Pub3 |
0.464 |
|
2011 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W. Mercury(II) Acetate Fieser and Fieser's Reagents For Organic Synthesis. 369-369. DOI: 10.1002/9780471264194.Fos06741.Pub2 |
0.479 |
|
2011 |
Ho T, Fieser M, Danheiser R, Roush W, Fieser L. Lithium Naphthalenide, LN Fieser and Fieser's Reagents For Organic Synthesis. DOI: 10.1002/9780471264194.Fos06537.Pub3 |
0.522 |
|
2011 |
Ho T, Fieser M, Danheiser R, Roush W, Fieser L. Cerium(III) Chloride Fieser and Fieser's Reagents For Organic Synthesis. 119-120. DOI: 10.1002/9780471264194.Fos02299.Pub3 |
0.504 |
|
2011 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W. 9-Borabicyclo[3.3.1]nonane Fieser and Fieser's Reagents For Organic Synthesis. 98-98. DOI: 10.1002/9780471264194.Fos01498.Pub3 |
0.548 |
|
2010 |
Sakai T, Danheiser RL. Cyano Diels-Alder and cyano ene reactions. Applications in a formal [2 + 2 + 2] cycloaddition strategy for the synthesis of pyridines. Journal of the American Chemical Society. 132: 13203-5. PMID 20815385 DOI: 10.1021/Ja106901U |
0.461 |
|
2010 |
Robinson JM, Sakai T, Okano K, Kitawaki T, Danheiser RL. Formal [2 + 2 + 2] cycloaddition strategy based on an intramolecular propargylic ene reaction/Diels-Alder cycloaddition cascade. Journal of the American Chemical Society. 132: 11039-41. PMID 20698669 DOI: 10.1021/Ja1053829 |
0.472 |
|
2010 |
Lawlor MD, Lee TW, Danheiser RL. ChemInform Abstract: Rhodium-Catalyzed Rearrangement of α-Diazo Thiol Esters to Thio-Substituted Ketenes. Application in the Synthesis of Cyclobutanones, Cyclobutenones, and β-Lactams. Cheminform. 31: no-no. DOI: 10.1002/chin.200046086 |
0.565 |
|
2010 |
Bennett DM, Okamoto I, Danheiser RL. ChemInform Abstract: Hetero [4 + 2] Cycloadditions of (Trialkylsilyl)vinylketenes. Synthesis of α,β-Unsaturated δ-Valerolactones and -lactams. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199949127 |
0.306 |
|
2010 |
DANHEISER RL, LEE TW, MENICHINCHERI M, BRUNELLI S, NISHIUCHI M. ChemInform Abstract: Synthesis of Alkylidenecyclopropanes via Thermal Cycloreversion of . alpha.-Spirocyclopropyl-β-lactones. Cheminform. 28: no-no. DOI: 10.1002/chin.199742093 |
0.468 |
|
2010 |
DANHEISER RL, TROVA MP. ChemInform Abstract: Synthesis of Linear Furocoumarins via a Photochemical Aromatic Annulation Strategy. An Efficient Total Synthesis of Bergapten. Cheminform. 26: no-no. DOI: 10.1002/CHIN.199539262 |
0.364 |
|
2010 |
BRONK BS, LIPPARD SJ, DANHEISER RL. ChemInform Abstract: Intramolecular Conjugate Addition Reactions via Organozinc Compounds. Cheminform. 24: no-no. DOI: 10.1002/chin.199350095 |
0.32 |
|
2010 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W, Smith J. Silver(I) trifluoromethanesulfonate (triflate) Fieser and Fieser's Reagents For Organic Synthesis. DOI: 10.1002/9780471264194.Fos08967.Pub3 |
0.435 |
|
2010 |
Ho T, Fieser M, Danheiser R, Roush W, Fieser L. 4-Phenyl-1,2,4-triazoline-3,5-dione (PTAD) Fieser and Fieser's Reagents For Organic Synthesis. 0-0. DOI: 10.1002/9780471264194.Fos08190 |
0.504 |
|
2009 |
Mak XY, Ciccolini RP, Robinson JM, Tester JW, Danheiser RL. Synthesis of amides and lactams in supercritical carbon dioxide. The Journal of Organic Chemistry. 74: 9381-7. PMID 19921799 DOI: 10.1021/Jo9021875 |
0.383 |
|
2009 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W, Smith J. Tetrabutylammonium Fluoride, TBAF Fieser and Fieser's Reagents For Organic Synthesis. 0-0. DOI: 10.1002/9780471264194.Fos09497.Pub2 |
0.518 |
|
2009 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W. Sodium bis(2‐methoxyethoxy)aluminum hydride (SMEAH, Red‐AlÒ) Fieser and Fieser's Reagents For Organic Synthesis. DOI: 10.1002/9780471264194.Fos09016.Pub2 |
0.377 |
|
2009 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W. Potassium t‐amyloxide Fieser and Fieser's Reagents For Organic Synthesis. DOI: 10.1002/9780471264194.Fos08377.Pub2 |
0.428 |
|
2009 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W, Smith J. Phosphoryl chloride (Phosphorus oxychloride) Fieser and Fieser's Reagents For Organic Synthesis. 0-0. DOI: 10.1002/9780471264194.Fos08277.Pub2 |
0.406 |
|
2009 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W. Ethylenebis(triphenylphosphine)platinum(0) Fieser and Fieser's Reagents For Organic Synthesis. 0-0. DOI: 10.1002/9780471264194.Fos05108 |
0.368 |
|
2009 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W, Smith J. Diisobutylaluminum Hydride (DIBAH, DIBAL) Fieser and Fieser's Reagents For Organic Synthesis. 0-0. DOI: 10.1002/9780471264194.Fos04085.Pub2 |
0.448 |
|
2009 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W. Chlorotris(triphenylphosphine)rhodium(I) (Wilkinson's catalyst) Fieser and Fieser's Reagents For Organic Synthesis. 0-0. DOI: 10.1002/9780471264194.Fos02718.Pub2 |
0.463 |
|
2009 |
Ho T, Fieser M, Fieser L, Danheiser R, Roush W, Smith J. Chloromethyl methyl ether Fieser and Fieser's Reagents For Organic Synthesis. DOI: 10.1002/9780471264194.Fos02563.Pub2 |
0.355 |
|
2009 |
Ho T, Fieser M, Danheiser R, Roush W, Smith J, Fieser L. N,N′‐Carbonyldiimidazole Fieser and Fieser's Reagents For Organic Synthesis. 0-0. DOI: 10.1002/9780471264194.Fos02244.Pub2 |
0.493 |
|
2009 |
Hwang S, Kang HR, Kim S, Haze O, Danheiser RL. Synthesis of polyynes by in situ desilylative bromination and palladium-catalyzed coupling: (7-(Benzyloxy)Hepta-1,3,5-Triynyl) triisopropylsilane Organic Syntheses. 86: 225-235. |
0.364 |
|
2008 |
Austin WF, Zhang Y, Danheiser RL. A benzannulation strategy for the synthesis of phenols and heteroaromatic compounds based on the reaction of (trialkylsilyl)vinylketenes with lithium ynolates. Tetrahedron. 64: 915-925. PMID 19180173 DOI: 10.1016/j.tet.2007.10.113 |
0.364 |
|
2006 |
Kohnen AL, Mak XY, Lam TY, Dunetz JR, Danheiser RL. [2+2] Cycloaddition of ketenes with ynamides. A general method for the synthesis of 3-aminocyclobutenone derivatives. Tetrahedron. 62: 3815-3822. PMID 21394235 DOI: 10.1016/J.Tet.2005.11.088 |
0.519 |
|
2005 |
Smith CJ, Tsang MW, Holmes AB, Danheiser RL, Tester JW. Palladium catalysed aryl amination reactions in supercritical carbon dioxide. Organic & Biomolecular Chemistry. 3: 3767-81. PMID 16211113 DOI: 10.1039/B509345G |
0.361 |
|
2005 |
Dunetz JR, Ciccolini RP, Fröling M, Paap SM, Allen AJ, Holmes AB, Tester JW, Danheiser RL. Pictet-Spengler reactions in multiphasic supercritical carbon dioxide/CO2-expanded liquid media. In situ generation of carbamates as a strategy for reactions of amines in supercritical carbon dioxide. Chemical Communications (Cambridge, England). 4465-7. PMID 16136252 DOI: 10.1039/B508151C |
0.328 |
|
2005 |
Hayes ME, Shinokubo H, Danheiser RL. Intramolecular [4 + 2] cycloadditions of benzynes with conjugated enynes, arenynes, and dienes. Organic Letters. 7: 3917-20. PMID 16119931 DOI: 10.1021/ol051372l |
0.757 |
|
2005 |
Austin WF, Zhang Y, Danheiser RL. Reactions of (trialkylsilyl)vinylketenes with lithium ynolates: a new benzannulation strategy. Organic Letters. 7: 3905-8. PMID 16119928 DOI: 10.1021/ol051307b |
0.345 |
|
2005 |
Davie CP, Danheiser RL. Stereoselective synthesis of highly substituted cyclopentenones through [4+1] annulations of trialkylsilyl vinyl ketenes with alpha-benzotriazolyl organolithium compounds. Angewandte Chemie (International Ed. in English). 44: 5867-70. PMID 16086353 DOI: 10.1002/anie.200501579 |
0.301 |
|
2005 |
Maloney KM, Danheiser RL. Total synthesis of quinolizidine alkaloid (-)-217A. Application of iminoacetonitrile cycloadditions in organic synthesis. Organic Letters. 7: 3115-8. PMID 15987219 DOI: 10.1021/ol051185n |
0.332 |
|
2005 |
Dunetz JR, Danheiser RL. Synthesis of highly substituted indolines and indoles via intramolecular [4 + 2] cycloaddition of ynamides and conjugated enynes. Journal of the American Chemical Society. 127: 5776-7. PMID 15839661 DOI: 10.1021/ja051180l |
0.343 |
|
2005 |
Thongsornkleeb C, Danheiser RL. A practical method for the synthesis of 2-alkynylpropenals. The Journal of Organic Chemistry. 70: 2364-7. PMID 15760233 DOI: 10.1021/jo047869a |
0.347 |
|
2004 |
Crombie AL, Kane JL, Shea KM, Danheiser RL. Ring expansion-annulation strategy for the synthesis of substituted azulenes and oligoazulenes. 2. Synthesis of azulenyl halides, sulfonates, and azulenylmetal compounds and their application in transition-metal-mediated coupling reactions. The Journal of Organic Chemistry. 69: 8652-67. PMID 15575741 DOI: 10.1021/Jo048698C |
0.725 |
|
2004 |
Nakanishi K, Danheiser RL. Saturo Masamune (1928–2003): Natural Products and Small Rings Angewandte Chemie International Edition. 43: 922-922. DOI: 10.1002/Anie.200490020 |
0.357 |
|
2004 |
Nakanishi K, Danheiser RL. Saturo Masamune (1928–2003): Naturstoffe und kleine Ringe Angewandte Chemie. 116: 940-940. DOI: 10.1002/Ange.200490020 |
0.306 |
|
2003 |
Dunetz JR, Danheiser RL. Copper-mediated N-alkynylation of carbamates, ureas, and sulfonamides. A general method for the synthesis of ynamides. Organic Letters. 5: 4011-4. PMID 14535766 DOI: 10.1021/ol035647d |
0.392 |
|
2003 |
Amos DT, Renslo AR, Danheiser RL. Intramolecular [4 + 2] cycloadditions of iminoacetonitriles: a new class of azadienophiles for hetero Diels-Alder reactions. Journal of the American Chemical Society. 125: 4970-1. PMID 12708834 DOI: 10.1021/ja034629o |
0.652 |
|
2003 |
Danheiser RL, Okamoto I, Lawlor MD, Lee TW, Denmark SE, Ober MH. Generation and [2+2] cycloadditions of thio-substituted ketenes: trans-1-(4-methoxyphenyl)-4-phenyl-3-(phenylthio)azetidin-2-one [(2-azetidinone, 1-(4-methoxyphenyl)-4-phenyl-3-(phenylthio)-, trans-)] Organic Syntheses. 80: 160-171. DOI: 10.15227/Orgsyn.080.0160 |
0.429 |
|
2003 |
Danheiser RL, Okamoto I, Lawlor MD, Lee TW. Generation and [2 + 2] Cycloadditions of Thio‐Substituted Ketenes: trans‐1‐(4‐Methoxyphenyl)‐4‐Phenyl‐3‐(Phenylthio)Azetidin‐2‐One Organic Syntheses. 80: 160-171. DOI: 10.1002/0471264180.Os080.18 |
0.361 |
|
2003 |
Danheiser RL, Renslo AR, Amos DT, Wright GT. Preparation of Substituted Pyridines Via Regiocontrolled [4 + 2] Cycloadditions of Oximinosulfonates: Methyl 5‐Methylpyridine‐2‐Carboxylate Organic Syntheses. 80: 133-143. DOI: 10.1002/0471264180.Os080.16 |
0.672 |
|
2003 |
Danheiser RL, Miller RF, Brisbois RG. Detrifluoroacetylative Diazo Group Transfer: (E)‐1‐Diazo‐4‐Phenyl‐3‐Buten‐2‐One Organic Syntheses. 134-134. DOI: 10.1002/0471264180.Os073.14 |
0.315 |
|
2003 |
Danheiser RL, Nowick JS, Lee JH, Miller RF, Huboux AH. Synthesis of β‐Lactones and Alkenes via Thiol Esters: (E)‐2,3‐Dimethyl‐3‐Dodecene Organic Syntheses. 73: 61-61. DOI: 10.1002/0471264180.Os073.07 |
0.675 |
|
2003 |
Danheiser RL, Fink DM, Okano K, Tsai Y, Szczepanski SW. (1‐oxo‐2‐propenyl)trimethylsilane Organic Syntheses. 14-14. DOI: 10.1002/0471264180.Os066.03 |
0.388 |
|
2003 |
Danheiser RL, Tsai Y, Fink DM. A General Method for the Synthesis of Allenylsilanes: 1-Methyl-1-(Trimethylsilyl)Allene Organic Syntheses. 1-1. DOI: 10.1002/0471264180.Os066.01 |
0.417 |
|
2003 |
Danheiser RL, Okamoto I, Lawlor MD, Lee TW. Generation and [2+2] cycloadditions of thio-substituted ketenes: Trans-1-(4-methoxyphenyl)-4-phenyl-3-(phenylthio)azetidin-2-one (2-azetidinone, 1-(4-methoxyphenyl)-4-phenyl-3-(phenylthio)-, trans-) Organic Syntheses. 80: 160-171. |
0.521 |
|
2003 |
Danheiser RL, Renslo AR, Amos DT, Wright GT. Preparation of substituted pyridines via regiocontrolled [4 + 2] cycloadditions of oximinosulfonates: Methyl 5-methylpyridine-2-carboxylate. (2-Pyridinecarboxylic acid, 5-methyl-, methyl ester) Organic Syntheses. 80: 133-143. |
0.567 |
|
2002 |
Dalton AM, Zhang Y, Davie CP, Danheiser RL. Synthesis of 2-indanones via [4 + 1] annulation reactions of (trialkylsilyl)arylketenes. Organic Letters. 4: 2465-8. PMID 12123352 DOI: 10.1021/Ol026014M |
0.485 |
|
2001 |
Kane JL, Shea KM, Crombie AL, Danheiser RL. A ring expansion-annulation strategy for the synthesis of substituted azulenes. Preparation and Suzuki coupling reactions of 1-azulenyl triflates. Organic Letters. 3: 1081-4. PMID 11277800 DOI: 10.1021/Ol0156897 |
0.685 |
|
2000 |
Dudley GB, Takaki KS, Cha DD, Danheiser RL. Total synthesis of (-)-ascochlorin via a cyclobutenone-based benzannulation strategy. Organic Letters. 2: 3407-10. PMID 11029223 DOI: 10.1021/Ol006561C |
0.66 |
|
2000 |
Shea KM, Lee KL, Danheiser RL. Synthesis and properties of 9-alkyl- and 9-Arylcyclopenta Organic Letters. 2: 2353-6. PMID 10930282 DOI: 10.1021/Ol0061283 |
0.668 |
|
2000 |
Lawlor MD, Lee TW, Danheiser RL. Rhodium-catalyzed rearrangement of alpha-diazo thiol esters to thio-substituted ketenes. Application in the synthesis of cyclobutanones, cyclobutenones, and beta-lactams. The Journal of Organic Chemistry. 65: 4375-84. PMID 10891141 DOI: 10.1021/jo000227c |
0.513 |
|
2000 |
Shea KM, Lee KL, Danheiser RL. ChemInform Abstract: Synthesis and Properties of 9-Alkyl- and 9-Arylcyclopenta[a]phenalenes. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200045116 |
0.352 |
|
2000 |
Shea KM, Lee KL, Danheiser RL. Synthesis and properties of 9-alkyl- and 9-arylcyclopenta[a]phenalenes Organic Letters. 2: 2353-2356. |
0.642 |
|
1999 |
Bennett DM, Okamoto I, Danheiser RL. Hetero [4 + 2] cycloadditions of (trialkylsilyl)vinylketenes. Synthesis of alpha,beta-unsaturated delta-valerolactones and -lactams. Organic Letters. 1: 641-4. PMID 10823193 DOI: 10.1021/Ol9907217 |
0.419 |
|
1999 |
Weinstein RD, Renslo AR, Danheiser RL, Tester JW. Silica-Promoted Diels-Alder Reactions in Carbon Dioxide from Gaseous to Supercritical Conditions Journal of Physical Chemistry B. 103: 2878-2887. DOI: 10.1021/Jp984227G |
0.578 |
|
1998 |
Loebach JL, Bennett DM, Danheiser RL. (Trialkylsilyl)vinylketenes: Synthesis and application as diene components in Diels-Alder cycloadditions Journal of Organic Chemistry. 63: 8380-8389. DOI: 10.1021/Jo981289U |
0.563 |
|
1998 |
Renslo AR, Danheiser RL. Synthesis of substituted pyridines via regiocontrolled [4 + 2] cycloadditions of oximinosulfonates Journal of Organic Chemistry. 63: 7840-7850. DOI: 10.1021/Jo981014E |
0.656 |
|
1998 |
Loebach JL, Bennett DM, Danheiser RL. The reaction of (Trialkylsilyl)vinylketens with carbenoid reagents: A new [4+] annulation route to cyclopentenones [6] Journal of the American Chemical Society. 120: 9690-9691. DOI: 10.1021/Ja982101R |
0.427 |
|
1998 |
Wills MSB, Danheiser RL. Intramolecular [4 + 2] cycloaddition reactions of conjugated ynones. Formation of polycyclic furans via the generation and rearrangement of strained heterocyclic allenes [9] Journal of the American Chemical Society. 120: 9378-9379. DOI: 10.1021/ja9819209 |
0.326 |
|
1997 |
Renslo AR, Weinstein RD, Tester JW, Danheiser RL. Concerning the Regiochemical Course of the Diels-Alder Reaction in Supercritical Carbon Dioxide. The Journal of Organic Chemistry. 62: 4530-4533. PMID 11671790 DOI: 10.1021/Jo9704523 |
0.551 |
|
1997 |
Danheiser RL, Lee TW, Menichincheri M, Brunelli S, Nishiuchi M. Synthesis of alkylidenecyclopropanes via thermal cycloreversion of α-spirocyclopropyl-β-lactones Synlett. 469-470. DOI: 10.1055/S-1997-6134 |
0.533 |
|
1996 |
Weinstein RD, Renslo AR, Danheiser RL, Harris JG, Tester JW. Inetic correlation of Diels-Alder reactions in supercritical carbon dioxide The Journal of Physical Chemistry. 100: 12337-12341. DOI: 10.1021/Jp960180S |
0.579 |
|
1996 |
Danheiser RL, Nowick JS, Lee JH, Miller RF, Huboux AH. Synthesis of β-lactones and alkenes via thiol esters: (E)-2,3-dimethyl-3-dodecene Organic Syntheses. 73: 61-70. |
0.604 |
|
1995 |
Danheiser RL, Trova MP. Synthesis of Linear Furocoumarins via a Photochemical Aromatic Annulation Strategy. An Efficient Total Synthesis of Bergapten Synlett. 1995: 573-574. DOI: 10.1055/S-1995-5297 |
0.351 |
|
1994 |
Danheiser RL, Gould AE, Fer?andez De La Pradilla R, Helgason AL. Intramolecular [4 + 2] cycloaddition reactions of conjugated enynes Journal of Organic Chemistry. 59: 5514-5515. DOI: 10.1021/Jo00098A002 |
0.477 |
|
1994 |
Danheiser RL, Helgason AL. Total synthesis of the phenalenone diterpene salvilenone Journal of the American Chemical Society. 116: 9471-9479. DOI: 10.1021/ja00100a009 |
0.363 |
|
1993 |
Bronk BS, Lippard SJ, Danheiser RL. Intramolecular conjugate addition reactions via organozinc compounds Organometallics. 12: 3340-3349. DOI: 10.1021/Om00032A065 |
0.302 |
|
1993 |
Danheiser RL, Choi YM, Menichincheri M, Stoner EJ. Synthesis of allenes via thermal cycloreversion of .alpha.-alkylidene-.beta.-lactones The Journal of Organic Chemistry. 58: 322-327. DOI: 10.1021/Jo00054A011 |
0.423 |
|
1993 |
Bronk BS, Lippard SJ, Danheiser RL. Intramolecular conjugate addition reactions via organozinc compounds Organometallics. 12: 3340-3349. |
0.302 |
|
1992 |
Danheiser RL, Casebier DS, Loebach JL. Total synthesis of dan shen diterpenoid quinones Tetrahedron Letters. 33: 1149-1152. DOI: 10.1016/S0040-4039(00)91882-3 |
0.398 |
|
1991 |
Danheiser RL, Nowick JS. A practical and efficient method for the synthesis of .beta.-lactones The Journal of Organic Chemistry. 56: 1176-1185. DOI: 10.1021/Jo00003A047 |
0.687 |
|
1991 |
Danheiser RL, Nowick JS. A practical and efficient method for the synthesis of β-lactones Journal of Organic Chemistry. 56: 1176-1185. |
0.574 |
|
1990 |
Danheiser RL, Miller RF, Brisbois RG, Park SZ. An improved method for the synthesis of .alpha.-diazo ketones Journal of Organic Chemistry. 55: 1959-1964. DOI: 10.1021/Jo00293A053 |
0.347 |
|
1990 |
Danheiser RL, Brisbois RG, Kowalczyk JJ, Miller RF. An annulation method for the synthesis of highly substituted polycyclic aromatic and heteroaromatic compounds Journal of the American Chemical Society. 112: 3093-3100. DOI: 10.1021/Ja00164A033 |
0.538 |
|
1990 |
Danheiser RL, Cha DD. Total synthesis of the host defense stimulant maesanin Tetrahedron Letters. 31: 1527-1530. DOI: 10.1016/0040-4039(90)80007-9 |
0.368 |
|
1989 |
Nowick JS, Danheiser RL. Application of (.alpha.-phosphonoacyl)silane reagents to the synthesis of .alpha.,.beta.-unsaturated acylsilanes The Journal of Organic Chemistry. 54: 2798-2802. DOI: 10.1021/Jo00273A007 |
0.583 |
|
1989 |
Danheiser RL, Stoner EJ, Koyama H, Yamashita DS, Klade CA. A new synthesis of substituted furans Journal of the American Chemical Society. 111: 4407-4413. |
0.378 |
|
1989 |
Becker DA, Danheiser RL. A new synthesis of substituted azulenes Journal of the American Chemical Society. 111: 389-391. |
0.366 |
|
1989 |
Nowick JS, Danheiser RL. Application of (α-phosphonoacyl)silane reagents to the synthesis of α,β-unsaturated acylsilanes Journal of Organic Chemistry. 54: 2798-2802. |
0.566 |
|
1988 |
Danheiser RL, Nishida ], Savariar S, Trova MP. Trialkylsilyloxyalkynes: Synthesis and aromatic annulation reactions Tetrahedron Letters. 29: 4917-4920. DOI: 10.1016/S0040-4039(00)80640-1 |
0.425 |
|
1988 |
Nowick JS, Danheiser RL. Chemistry of cyclopropylacylsilanes I. α-functionalized acylsilane reagents for the cyclopropanation of electrophilic alkenes Tetrahedron. 44: 4113-4134. DOI: 10.1016/S0040-4020(01)86660-6 |
0.645 |
|
1986 |
Danheiser RL, Carini DJ, Kwasigroch CA. Scope and stereochemical course of the addition of (trimethylsilyl)allenes to ketones and aldehydes. A regiocontrolled synthesis of homopropargylic alcohols Journal of Organic Chemistry. 51: 3870-3878. DOI: 10.1021/Jo00370A023 |
0.371 |
|
1986 |
Danheiser RL, Gee SK, Perez JJ. Total synthesis of mycophenolic acid Journal of the American Chemical Society. 108: 806-810. DOI: 10.1002/Chin.198625332 |
0.443 |
|
1985 |
Danheiser RL, Fink DM, Okano K, Tsai YM, Szczepanski SW. A practical and efficient synthesis of .alpha.,.beta.-unsaturated acylsilanes The Journal of Organic Chemistry. 50: 5393-5396. DOI: 10.1021/Jo00225A083 |
0.323 |
|
1985 |
Danheiser RL, Morin JM, Salaski EJ. Efficient total synthesis of (.+-.)-anatoxin a Journal of the American Chemical Society. 107: 8066-8073. DOI: 10.1021/Ja00312A045 |
0.422 |
|
1985 |
Danheiser RL, Fink DM. The reaction of allenylsilanes with α,β-unsaturated acylsilanes: new annulation approaches to five and six-membered carbocyclic compounds Tetrahedron Letters. 26: 2513-2516. DOI: 10.1016/S0040-4039(00)98824-5 |
0.423 |
|
1985 |
Danheiser RL, Fink DM. Conjugate addition of allylsilanes to α,β-unsaturated acylsilanes Tetrahedron Letters. 26: 2509-2512. DOI: 10.1016/S0040-4039(00)98823-3 |
0.435 |
|
1985 |
Danheiser RL, Fink DM, Okano K, Tsai YM, Szczepanski SW. A practical and efficient synthesis of α,β-unsaturated acylsilanes Journal of Organic Chemistry. 50: 5393-5396. DOI: 10.1002/Chin.198622238 |
0.395 |
|
1985 |
Danheiser RL, Bronson JJ, Okano K. Carbanion-accelerated vinylcyclopropane rearrangement. Application in a general, stereocontrolled annulation approach to cyclopentene derivatives Journal of the American Chemical Society. 107: 4579-4581. DOI: 10.1002/Chin.198545128 |
0.31 |
|
1985 |
Danheiser RL, Savoca AC. Applications of cyclopropylboranes in organic synthesis. 1. A stereocontrolled route to substituted cyclopropanol derivatives Journal of Organic Chemistry. 50: 2401-2403. DOI: 10.1002/Chin.198543191 |
0.424 |
|
1984 |
Danheiser RL. The Total Synthesis of Gibberellic Acid Strategies and Tactics in Organic Synthesis. 1: 21-70. DOI: 10.1016/B978-0-12-450280-2.50006-5 |
0.443 |
|
1984 |
Danheiser RL, Gee SK. A regiocontrolled annulation approach to highly substituted aromatic compounds Journal of Organic Chemistry. 49: 1672-1674. DOI: 10.1002/Chin.198440138 |
0.336 |
|
1983 |
Danheiser RL, Sard H. The regiochemical course of [2+2] cycloadditions of dichloroketene with vinyl- and alkynylsilanes Tetrahedron Letters. 24: 23-26. DOI: 10.1016/S0040-4039(00)81316-7 |
0.407 |
|
1981 |
Danheiser RL, Morin JM, Yu M, Basak A. Cationic cyclizations initiated by electrocyclic cleavage of cyclopropanes. Synthesis of lactones, tetrahydropyrans, and tetrahydrofurans Tetrahedron Letters. 22: 4205-4208. DOI: 10.1016/S0040-4039(01)82105-5 |
0.489 |
|
1981 |
Danheiser RL, Martinez-Davila C, Sard H. Cyclohexenol annulation via the alkoxy-accelerated rearrangement of vinylcyclobutanes Tetrahedron. 37: 3943-3950. DOI: 10.1016/S0040-4020(01)93268-5 |
0.48 |
|
1981 |
Danheiser RL, Martinez-Davila C, Auchus RJ, Kadonaga JT. A stereoselective synthesis of cyclopentene derivatives from 1,3-dienes Journal of the American Chemical Society. 103: 2443-2446. DOI: 10.1002/Chin.198134170 |
0.515 |
|
1981 |
Danheiser RL, Carini DJ, Basak A. (Trimethylsilyl)cyclopentene annulation: A regiocontrolled approach to the synthesis of five-membered rings Journal of the American Chemical Society. 103: 1604-1606. |
0.302 |
|
1980 |
Danheiser RL, Sard H. (Trimethylsilyl)vinylketene: A stable vinylketene and reactive enophile in [4 + 2] cycloadditions Journal of Organic Chemistry. 45: 4810-4812. DOI: 10.1021/Jo01311A065 |
0.361 |
|
1980 |
Danheiser RL, Martinez-Davila C, Morin JM. Synthesis of 3-cyclopentenols by alkoxy-accelerated vinylcyclopropane rearrangement Journal of Organic Chemistry. 45: 1340-1341. |
0.397 |
|
1979 |
COREY EJ, DANHEISER RL, CHANDRASEKARAN S, KECK GE, GOPALAN B, LARSEN SD, SIRET P, GRAS J. ChemInform Abstract: STEREOSPECIFIC TOTAL SYNTHESIS OF GIBBERELLIC ACID Chemischer Informationsdienst. 10. DOI: 10.1002/chin.197912390 |
0.63 |
|
1979 |
Corey EJ, Danheiser RL, Chandrasekaran S, Siret P, Keck GE, Gras J-. Stereospecific Total Synthesis Of Gibberellic Acid. A Key Tricyclic Intermediate Cheminform. 10. DOI: 10.1002/Chin.197912389 |
0.692 |
|
1978 |
Corey EJ, Danheiser RL, Chandrasekaran S, Keck GE, Gopalan B, Larsen SD, Siret P, Gras JL. Stereospecific total synthesis of gibberellic acid Journal of the American Chemical Society. 100: 8034-8036. DOI: 10.1021/Ja00493A056 |
0.743 |
|
1978 |
Corey EJ, Danheiser RL, Chandrasekaran S, Siret P, Keck GE, Gras JL. Stereospecific total synthesis of gibberellic acid. A key tricyclic intermediate Journal of the American Chemical Society. 100: 8031-8034. DOI: 10.1021/Ja00493A055 |
0.692 |
|
1978 |
Corey EJ, Danheiser RL, Chandrasekaran S, Keck GE, Gopalan B, Larsen SD, Siret P, Gras JL. Stereospecific total synthesis of gibberellic acid [24] Journal of the American Chemical Society. 100: 8034-8036. |
0.621 |
|
1978 |
Corey EJ, Danheiser RL, Chandrasekaran S, Siret P, Keck GE, Gras JL. Stereospecific total synthesis of gibberellic acid. A key tricyclic intermediate [23] Journal of the American Chemical Society. 100: 8031-8034. |
0.644 |
|
1976 |
Corey EJ, Danheiser RL, Chandrasekaran S. New reagents for the intermolecular and intramolecular pinacolic coupling of ketones and aldehydes The Journal of Organic Chemistry. 41: 260-265. DOI: 10.1021/Jo00864A016 |
0.652 |
|
1973 |
Stork G, Danheiser RL. Regiospecific alkylation of cyclic .beta.-diketone enol ethers. General synthesis of 4-alkylcyclohexenones The Journal of Organic Chemistry. 38: 1775-1776. DOI: 10.1021/Jo00949A048 |
0.389 |
|
1973 |
Stork G, Danheiser RL, Ganem B. Spiroannelation of enol ethers of cyclic 1,3-diketones. Simple stereospecific synthesis of .beta.-vetivone Journal of the American Chemical Society. 95: 3414-3415. DOI: 10.1021/Ja00791A074 |
0.366 |
|
1973 |
Corey EJ, Danheiser RL. A method for the stereospecific synthesis of the A and B rings of gibberellic acid Tetrahedron Letters. 14: 4477-4480. DOI: 10.1016/S0040-4039(01)87253-1 |
0.524 |
|
1973 |
Stork G, Danheiser RL, Ganem B. Spiroannelation of enol ethers of cyclic 1,3-diketones. A simple stereospecific synthesis of β-vetivone [25] Journal of the American Chemical Society. 95: 3414-3415. |
0.344 |
|
1973 |
Stork G, Danheiser RL. The regiospecific alkylation of cyclic β diketone enol ethers. A general synthesis of 4-alkylcyclohexenones Journal of Organic Chemistry. 38: 1775-1776. |
0.367 |
|
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