Year |
Citation |
Score |
2022 |
He Q, Cao L, Wei Y, Dake G. Utility of 2-Diphenylphosphoryloxy-1,3-Dienes in Multicomponent Hetero-Diels-Alder Reactions to Construct Functionalized Six-Membered Nitrogen Heterocycles. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 35522607 DOI: 10.1002/chem.202201328 |
0.365 |
|
2020 |
Voth CN, Dake GR. Nickel-Catalyzed Arylative Additions on 2-Alkynyl-N
-Arylsulfonylanilides to Construct Functionalized Indoles European Journal of Organic Chemistry. 2020: 744-748. DOI: 10.1002/Ejoc.201901835 |
0.361 |
|
2014 |
Castillo-Contreras EB, Stahl AM, Dake GR. Annulated isoxazoles via [3 + 2] cycloaddition of alkenyl bromides and oximoyl chlorides and Ag(I) promoted elimination. The Journal of Organic Chemistry. 79: 7250-5. PMID 25050466 DOI: 10.1021/Jo501376Q |
0.362 |
|
2014 |
Castillo-Contreras EB, Dake GR. DMAP promoted tandem addition reactions forming substituted tetrahydroxanthones Organic Letters. 16: 1642-1645. PMID 24621113 DOI: 10.1021/Ol5002945 |
0.462 |
|
2014 |
Serin SC, Patrick BO, Dake GR, Gates DP. Reaction of an enantiomerically pure phosphaalkene-oxazoline with MeM nucleophiles (M = Li and MgBr): Stereoselectivity and noninnocence of the P-mesityl substituent Organometallics. 33: 7215-7222. DOI: 10.1021/Om501008M |
0.391 |
|
2013 |
Loosley BC, Andersen RJ, Dake GR. Total synthesis of cladoniamide G. Organic Letters. 15: 1152-4. PMID 23413919 DOI: 10.1021/Ol400055V |
0.335 |
|
2012 |
Dake GR. Enamides and related functional groups as nucleophilic components in ring-forming processes catalyzed by electrophilic metal salts Synlett. 23: 814-824. DOI: 10.1055/S-0031-1290351 |
0.322 |
|
2010 |
Kozak JA, Patrick BO, Dake GR. Gold(I)-catalyzed intramolecular tandem addition/Friedel-Crafts reactions between acyclic enamides and 1-arylalkynes. The Journal of Organic Chemistry. 75: 8585-90. PMID 21087043 DOI: 10.1021/Jo102036N |
0.399 |
|
2010 |
Dugal-Tessier J, Dake GR, Gates DP. Chiral phosphaalkene-oxazoline ligands for the palladium-catalyzed asymmetric allylic alkylation. Organic Letters. 12: 4667-9. PMID 20863121 DOI: 10.1021/Ol1020652 |
0.408 |
|
2010 |
Dugal-Tessier J, Kuhn PS, Dake GR, Gates DP. Synthesis of functional phosphines with ortho-substituted aryl groups: 2-RC6H4PH2 and 2-RC6H 4P(SiMe3)2 (R = 2-/-Pr- or 2-f-Bu-) Heteroatom Chemistry. 21: 265-270. DOI: 10.1002/Hc.20606 |
0.321 |
|
2010 |
TROST BM, DAKE GR. ChemInform Abstract: Nitrogen Pronucleophiles in the Phosphine-Catalyzed γ-Addition Reaction. Cheminform. 29: no-no. DOI: 10.1002/chin.199801059 |
0.467 |
|
2010 |
TROST BM, DAKE GR. ChemInform Abstract: Nucleophilic α-Addition to Alkynoates. A Synthesis of Dehydroamino Acids. Cheminform. 28: no-no. DOI: 10.1002/chin.199750097 |
0.407 |
|
2009 |
Kozak JA, Dodd JM, Harrison TJ, Jardine KJ, Patrick BO, Dake GR. Enamides and enesulfonamides as nucleophiles: formation of complex ring systems through a platinum(II)-catalyzed addition/Friedel-Crafts pathway. The Journal of Organic Chemistry. 74: 6929-35. PMID 19689099 DOI: 10.1021/Jo901512M |
0.396 |
|
2008 |
Dake GR, Fenster EE, Patrick BO. A synthetic approach to the fusicoccane A-B ring fragment based on a Pauson-Khand cycloaddition/Norrish type 1 fragmentation Journal of Organic Chemistry. 73: 6711-6715. PMID 18652507 DOI: 10.1021/Jo800933F |
0.373 |
|
2008 |
Hurley PB, Dake GR. Synthetic studies toward halichlorine: Complex azaspirocycle formation with use of an NBS-promoted semipinacol reaction Journal of Organic Chemistry. 73: 4131-4138. PMID 18444680 DOI: 10.1021/Jo800336K |
0.451 |
|
2008 |
Kozak JA, Dake GR. Total synthesis of (+)-fawcettidine. Angewandte Chemie (International Ed. in English). 47: 4221-3. PMID 18431724 DOI: 10.1002/Anie.200800522 |
0.427 |
|
2007 |
Harrison TJ, Patrick BO, Dake GR. Platinum(II)-catalyzed cyclizations forming quaternary carbon centers, using enesulfonamides, enecarbamates, or enamides as nucleophiles Organic Letters. 9: 367-370. PMID 17217306 DOI: 10.1021/Ol062939G |
0.436 |
|
2006 |
Harrison TJ, Kozak JA, Corbella-Pané M, Dake GR. Pyrrole synthesis catalyzed by AgOTf or cationic Au(I) complexes. The Journal of Organic Chemistry. 71: 4525-9. PMID 16749784 DOI: 10.1021/Jo060382C |
0.412 |
|
2006 |
Wilson MS, Woo JCS, Dake GR. A synthetic approach toward nitiol: Construction of two 1,22-dihydroxynitianes Journal of Organic Chemistry. 71: 4237-4245. PMID 16709067 DOI: 10.1021/Jo0604585 |
0.495 |
|
2006 |
Dake G, Harrison T, Kozak J, Corbella-Pané M. Silver- and Gold-Catalyzed Pyrrole Synthesis Synfacts. 2006: 0989-0989. DOI: 10.1055/s-2006-949350 |
0.325 |
|
2005 |
Harrison TJ, Dake GR. An expeditious, high-yielding construction of the food aroma compounds 6-acetyl-1,2,3,4-tetrahydropyridine and 2-acetyl-1-pyrroline Journal of Organic Chemistry. 70: 10872-10874. PMID 16356012 DOI: 10.1021/Jo051940A |
0.368 |
|
2005 |
Fenster MDB, Dake GR. An asymmetric formal synthesis of fasicularin Chemistry - a European Journal. 11: 639-649. PMID 15565724 DOI: 10.1002/Chem.200400749 |
0.474 |
|
2004 |
Harrison TJ, Dake GR. Pt(II) or Ag(I) salt catalyzed cycloisomerizations and tandem cycloadditions forming functionalized azacyclic arrays Organic Letters. 6: 5023-5026. PMID 15606126 DOI: 10.1021/Ol047696B |
0.436 |
|
2004 |
Woo JCS, Fenster E, Dake GR. A convenient method for the conversion of hindered carboxylic acids to N-methoxy-N-methyl (Weinreb) amides Journal of Organic Chemistry. 69: 8984-8986. PMID 15575791 DOI: 10.1021/Jo048385H |
0.31 |
|
2004 |
Dake GR, Fenster MD, Fleury M, Patrick BO. Investigations of alpha-siloxy-epoxide ring expansions forming 1-azaspirocyclic ketones. The Journal of Organic Chemistry. 69: 5676-83. PMID 15307739 DOI: 10.1021/Jo049356+ |
0.442 |
|
2004 |
Dake GR, Fenster MD, Hurley PB, Patrick BO. Synthesis of functionalized 1-azaspirocyclic cyclopentanones using bronsted acid or N-bromosuccinimide promoted ring expansions. The Journal of Organic Chemistry. 69: 5668-75. PMID 15307738 DOI: 10.1021/Jo0493572 |
0.453 |
|
2004 |
Easton LP, Dake GR. Nucleophilic additions of lactam-derived enol triflates to aldehydes mediated by nickel(II) and chromium(II) salts Canadian Journal of Chemistry. 82: 139-144. DOI: 10.1139/V03-164 |
0.32 |
|
2003 |
Fenster MDB, Dake GR. A Formal Construction of Fasicularin Organic Letters. 5: 4313-4316. PMID 14601988 DOI: 10.1021/Ol035566H |
0.441 |
|
2003 |
Hurley PB, Dake GR. N-Bromosuccinimide Promoted Ring Expansion Reactions: Diastereoselective Formation of Functionalized Azaspirocyclic Cyclopentanones Synlett. 2131-2134. DOI: 10.1055/S-2003-42068 |
0.435 |
|
2002 |
Stork G, Niu D, Fujimoto RA, Koft ER, Balkovec JM, Tata JR, Dake GR, Appendino G, Zanardi F, Casiraghi G. The first stereoselective total synthesis of quinine Chemtracts. 15: 175-182. |
0.541 |
|
2001 |
Stork G, Niu D, Fujimoto RA, Koft ER, Balkovec JM, Tata JR, Dake GR, Fujimoto A. The first stereoselective total synthesis of quinine. Journal of the American Chemical Society. 123: 3239-42. PMID 11457058 DOI: 10.1021/Ja004325R |
0.534 |
|
2001 |
Fenster MDB, Patrick BO, Dake GR. Construction of Azaspirocyclic Ketones through α-Hydroxyiminium Ion or α-Siloxy Epoxide Semipinacol Rearrangements Organic Letters. 3: 2109-2112. PMID 11418061 DOI: 10.1021/Ol0160708 |
0.431 |
|
2001 |
Wilson MS, Dake GR. Stereocontrolled Construction of the A-Ring of Nitiol Using a Pauson-Khand Cycloaddition-Ring Fragmentation Strategy Organic Letters. 3: 2041-2044. PMID 11418044 DOI: 10.1021/Ol016002L |
0.412 |
|
2001 |
Stork G, Niu D, Fujimoto RA, Koft ER, Balkovec JM, Tata JR, Dake GR. The First Stereoselective Total Synthesis of Quinine [J.Am. Chem. Soc.2001,123(14), 3239−3242]. Journal of the American Chemical Society. 123: 8644-8644. DOI: 10.1021/Ja015138B |
0.52 |
|
1997 |
Trost BM, Dake GR. Nitrogen Pronucleophiles in the Phosphine-Catalyzed γ-Addition Reaction The Journal of Organic Chemistry. 62: 5670-5671. DOI: 10.1021/Jo970848E |
0.51 |
|
1997 |
Trost BM, Dake GR. Nucleophilic α-addition to alkynoates. A synthesis of dehydroamino acids Journal of the American Chemical Society. 119: 7595-7596. DOI: 10.1021/Ja971238Z |
0.459 |
|
1997 |
Trost BM, Dake GR. Nitrogen Pronucleophiles in the Phosphine-Catalyzed γ-Addition Reaction Journal of Organic Chemistry. 62: 5670-5671. |
0.352 |
|
1997 |
Trost BM, Dake GR. Nitrogen Pronucleophiles in the Phosphine-Catalyzed γ-Addition Reaction Journal of Organic Chemistry. 62: 5670-5671. |
0.352 |
|
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