Year |
Citation |
Score |
2020 |
Aggarwal VK, Armstrong SK, Caggiano L, Chibale K, Clayden J, Coldham I, Greeves N, Hartley RC, Knight JG, Kuhnert N, Mitchell HJ, Nelson A, O'Brien P, Thomas SP, Wyatt P. Stuart Warren (24 Dec 1938-22 Mar 2020). Organic & Biomolecular Chemistry. PMID 32936190 DOI: 10.1039/D0Ob90121K |
0.619 |
|
2016 |
Da Vià L, Recchi C, Davies TE, Greeves N, Lopez-Sanchez JA. Visible-Light-Controlled Oxidation of Glucose using Titania-Supported Silver Photocatalysts. Chemcatchem. 8: 3475-3483. PMID 28450968 DOI: 10.1002/Cctc.201600775 |
0.348 |
|
2011 |
Holden DL, Goulding HV, Bacsa J, Berry NG, Greeves N, Stephenson RA, Harrington RW, Clegg W, Fogg AM. Unusual hybrid materials prepared by the oxidation of a ketone Crystal Growth and Design. 11: 3013-3019. DOI: 10.1021/Cg200286T |
0.379 |
|
2011 |
Aspinall HC, Beckingham O, Farrar MD, Greeves N, Thomas CD. A general and convenient route to oxazolyl ligands Tetrahedron Letters. 52: 5120-5123. DOI: 10.1016/J.Tetlet.2011.07.070 |
0.332 |
|
2010 |
Aspinall HC, Greeves N, Hin SLF. A new Yb3+-catalyzed pinacol and imine-coupling reaction Tetrahedron Letters. 51: 1558-1561. DOI: 10.1016/J.Tetlet.2010.01.057 |
0.404 |
|
2010 |
GREEVES N, LEE W, BARKLEY JV. ChemInform Abstract: Synthetic Applications of the Tandem (2,3)-Wittig-Anionic Oxy-Cope Rearrangement. Part 2. Stereoselective Trisubstituted δ-Lactone and Tetrahydropyran Synthesis. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199749155 |
0.307 |
|
2010 |
GREEVES N, LEE W. ChemInform Abstract: Synthetic Applications of the Tandem (2,3)-Wittig-Anionic Oxy-Cope Rearrangement. Part 1. Stereoselective Disubstituted Tetrahydropyran Synthesis by Electrophile Initiated Cyclization. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199749154 |
0.324 |
|
2010 |
TROST BM, GREENSPAN PD, GEISSLER H, KIM JH, GREEVES N. ChemInform Abstract: Total Synthesis of (+)-(2′S,3′R)-Zoapatanol. Cheminform. 26: no-no. DOI: 10.1002/chin.199517183 |
0.393 |
|
2010 |
GREEVES N, VINES KJ. ChemInform Abstract: Stereoconvergent ′One-Pot′ Tandem (2,3)-Wittig-Anionic Oxy-Cope Rearrangement of Acyclic Bis-Allylic Ethers in the Diastereoselective Synthesis of Substituted Tetrahydropyrans. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199443160 |
0.354 |
|
2010 |
GREEVES N, TORODE JS. ChemInform Abstract: Synthesis of Phenylthiomethyl Substituted Furans by Lewis Acid Catalyzed Substitution. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199415153 |
0.326 |
|
2005 |
Aspinall HC, Greeves N, Valla C. Samarium diiodide-catalyzed diastereoselective pinacol couplings. Organic Letters. 7: 1919-22. PMID 15876019 DOI: 10.1021/Ol050256F |
0.365 |
|
2005 |
Aspinall HC, Bickley JF, Greeves N, Kelly RV, Smith PM. Lanthanide Pybox Complexes as Catalysts for Enantioselective Silylcyanation of Aldehydes Organometallics. 24: 3458-3467. DOI: 10.1021/Om050197+ |
0.361 |
|
2003 |
Greeves N, Lee W, McLachlan SP, Oakes GH, Purdie M, Bickley JF. Short synthesis of a tetrasubstituted tetrahydropyran with five stereogenic centres—stereoselective double tandem rearrangements and cyclisation Tetrahedron Letters. 44: 9035-9038. DOI: 10.1016/J.Tetlet.2003.09.209 |
0.463 |
|
2003 |
Aspinall HC, Greeves N, McIver EG. Modular chiral polyether podands and their lanthanide complexes Tetrahedron. 59: 10453-10463. DOI: 10.1016/J.Tet.2003.06.008 |
0.351 |
|
2002 |
Aspinall HC, Bissett JS, Greeves N, Levin D. Three component synthesis of homoallylic amines. Efficient catalysis by lanthanum triflate/benzoic acid Tetrahedron Letters. 43: 323-325. DOI: 10.1016/S0040-4039(01)02116-5 |
0.399 |
|
2002 |
Aspinall HC, Bissett JS, Greeves N, Levin D. Lanthanum triflate-catalysed allylation of aldehydes: crucial activation by benzoic acid Tetrahedron Letters. 43: 319-321. DOI: 10.1016/S0040-4039(01)02115-3 |
0.337 |
|
2002 |
Aspinall HC, Greeves N. Defining effective chiral binding sites at lanthanides—highly enantioselective reagents and catalysts from binaphtholate and pybox ligands Journal of Organometallic Chemistry. 647: 151-157. DOI: 10.1016/S0022-328X(01)01370-5 |
0.34 |
|
2000 |
Aspinall HC, Dwyer JLM, Greeves N, Smith PM. Lanthanide complexes with C2 symmetric ligands for use in enantioselective organic synthesis Journal of Alloys and Compounds. 303: 173-177. DOI: 10.1016/S0925-8388(00)00661-7 |
0.396 |
|
1999 |
Aspinall HC, Dwyer JLM, Greeves N, Steiner A. Li3[Ln(binol)3]·6THF: New Anhydrous Lithium Lanthanide Binaphtholates and Their Use in Enantioselective Alkyl Addition to Aldehydes Organometallics. 18: 1366-1368. DOI: 10.1021/Om981011S |
0.365 |
|
1999 |
Aspinall HC, Greeves N, Smith PM. Catalytic, asymmetric cyanohydrin synthesis mediated by lanthanide(III) chloride pybox complexes Tetrahedron Letters. 40: 1763-1766. DOI: 10.1016/S0040-4039(98)02685-9 |
0.38 |
|
1998 |
Aspinall HC, Dwyer JLM, Greeves N, McIver aEG, Woolley JC. Solubilized Lanthanide Triflates: Lewis Acid Catalysis by Polyether and Poly(ethylene glycol) Complexes of Ln(OTf)3 Organometallics. 17: 1884-1888. DOI: 10.1021/Om9709087 |
0.329 |
|
1998 |
Aspinall HC, Greeves N, McIver EG. Ytterbium Triflate Catalysed Allylation Of Aldehydes : An Unusual Benzoic Acid Induced Acceleration Tetrahedron Letters. 39: 9283-9286. DOI: 10.1016/S0040-4039(98)02086-3 |
0.399 |
|
1997 |
Greeves N, Lee W, Barkley JV. Synthetic Applications (II) of the Tandem [2,3]-Wittig-Anionic Oxy-Cope Rearrangement: Stereoselective Trisubstituted δ-Lactone and Tetrahydropyran Synthesis Tetrahedron Letters. 38: 6453-6456. DOI: 10.1016/S0040-4039(97)01475-5 |
0.445 |
|
1997 |
Greeves N, Lee W. Synthetic Applications (I) of the Tandem [2,3]-Wittig-Anionic Oxy-Cope Rearrangement: Stereoselective Disubstituted Tetrahydropyran Synthesis by Electrophile Initiated Cyclisation Tetrahedron Letters. 38: 6449-6452. DOI: 10.1016/S0040-4039(97)01474-3 |
0.453 |
|
1997 |
Greeves N, Lee W. Stereoselective [2,3]-Wittig and Tandem [2,3]-Wittig-Anionic Oxy-Cope Rearrangements of Bis-allylic Ethers : Effect of Substituents Tetrahedron Letters. 38: 6445-6448. DOI: 10.1016/S0040-4039(97)01473-1 |
0.457 |
|
1997 |
Aspinall HC, Greeves N, Lee W, McIver EG, Smith PM. An improved Williamson etherification of hindered alcohols promoted by 15-crown-5 and sodium hydride Tetrahedron Letters. 38: 4679-4682. DOI: 10.1016/S0040-4039(97)00965-9 |
0.426 |
|
1996 |
Greeves N, Pease JE. Enantioselective addition of tris(TADDOL) organocerium reagents to aldehydes Tetrahedron Letters. 37: 5821-5824. DOI: 10.1016/0040-4039(96)01236-1 |
0.423 |
|
1996 |
Greeves N, Pease JE, Bowden MC, Brown SM. Enantioselective addition of organocerium reagents to aldehydes — Effects of TADDOL ligand structure Tetrahedron Letters. 37: 2675-2678. DOI: 10.1016/0040-4039(96)00358-9 |
0.353 |
|
1994 |
Greeves N, Torode JS. Regio- and Stereoselective Palladium(0) Catalysed Hydrostannation of Disubstituted Propargyl Alcohols Synlett. 1994: 537-538. DOI: 10.1055/S-1994-22920 |
0.361 |
|
1994 |
Greeves N, Vines KJ. Stereoconvergent ‘one-pot’ tandem [2,3]-Wittig-anionic oxy-Cope rearrangement of acyclic bis-allylic ethers in the diastereoselective synthesis of substituted tetrahydropyrans Journal of the Chemical Society, Chemical Communications. 1469-1470. DOI: 10.1039/C39940001469 |
0.474 |
|
1994 |
Greeves N, Lyford L, Pease JE. Ligand effects on diastereoselective addition of organocerium reagents to aldehydes and cyclic ketones Tetrahedron Letters. 35: 285-288. DOI: 10.1016/S0040-4039(00)76533-6 |
0.43 |
|
1994 |
Aspinall HC, Browning AF, Greeves N, Ravenscroft P. Ytterbium trifluoromethanesulfonate [Yb(OTf)3] as a novel catalyst for the allylation of aldehydes Tetrahedron Letters. 35: 4639-4640. DOI: 10.1016/S0040-4039(00)60750-5 |
0.377 |
|
1994 |
Greeves N, Vines KJ. Acyclic stereocontrol via sequential and tandem [2,3]-Wittig-anionic oxy-Cope rearrangements Tetrahedron Letters. 35: 7077-7080. DOI: 10.1016/0040-4039(94)88230-4 |
0.426 |
|
1994 |
Trost BM, Greenspan PD, Geissler H, Kim JH, Greeves N. A Total Synthesis of(+)-2′S, 3′R-Zoapatanol Angewandte Chemie International Edition in English. 33: 2182-2184. DOI: 10.1002/Anie.199421821 |
0.456 |
|
1994 |
Trost BM, Greenspan PD, Geissler H, Kim JH, Greeves N. Totalsynthese von ( + )−2′S,3′R-Zoapatanol Angewandte Chemie. 106: 2296-2298. DOI: 10.1002/Ange.19941062122 |
0.319 |
|
1993 |
Greeves N, Torode JS. Synthesis of Phenylthiomethyl Substitution Furans by Lewis Acid Catalysed Substitution Synthesis. 1993: 1109-1112. DOI: 10.1055/S-1993-26011 |
0.4 |
|
1993 |
Chibale K, Greeves N, Lyford L, Pease JE. New homochiral binaphthol-modified organolanthanide reagents for the enantioselective addition to aldehydes Tetrahedron: Asymmetry. 4: 2407-2410. DOI: 10.1016/S0957-4166(00)82211-9 |
0.623 |
|
1992 |
Ayrey PM, Bolton MA, Buss AD, Greeves N, Levin D, Wallace P, Warren S. Stereochemically controlled synthesis of unsaturated alcohols by the Horner–Wittig reaction Journal of the Chemical Society-Perkin Transactions 1. 3407-3417. DOI: 10.1039/P19920003407 |
0.66 |
|
1992 |
Greeves N, Lyford L. Ultrasound assisted preparation of organocerium reagents Tetrahedron Letters. 33: 4759-4760. DOI: 10.1016/S0040-4039(00)61278-9 |
0.349 |
|
1991 |
Brown PS, Greeves N, McElroy AB, Warren S. The synthesis of (Z)-penta-2,4-dien-1 -ol and substituted (E)-pentadienols by the stereochemically controlled Horner–Wittig reaction Journal of the Chemical Society, Perkin Transactions 1. 1485-1492. DOI: 10.1039/P19910001485 |
0.649 |
|
1988 |
BUSS AD, GREEVES N, MASON R, WARREN S. ChemInform Abstract: Applications of the Stereochemically-Controlled Horner-Wittig Reaction: Synthesis of Feniculin, (E)-Non-6-en-1-ol, a Pheromone of the Mediterranean Fruit Fly, (E)- and (Z)-Dec-5-en-1-ol, Trisubstituted Alkenes, and (Z)-α-Bisabolene. Cheminform. 19. DOI: 10.1002/CHIN.198813363 |
0.312 |
|
1987 |
Buss AD, Greeves N, Mason RP, Warren S. Applications of the stereochemically-controlled Horner-Wittig reaction: synthesis of feniculin, (E)-non-6-en-1-ol, a pheromone of the mediterranean fruit fly, (E)- and (Z)-dec-5-en-1-ol, tri-substituted alkenes, and (Z)-α-bisabolene Journal of the Chemical Society-Perkin Transactions 1. 2569-2577. DOI: 10.1039/P19870002569 |
0.626 |
|
1986 |
Greeves N, Warren S. Stereochemically controlled synthesis of unsaturated hydroxy-acids by the horner-wittig reaction Tetrahedron Letters. 27: 259-262. DOI: 10.1016/S0040-4039(00)83991-X |
0.646 |
|
1984 |
Buss AD, Greeves N, Levin D, Wallace P, Warren S. Synthesis of single isomers (E or Z) of unsaturated alcohols by the horner-wittig reaction Tetrahedron Letters. 25: 357-360. DOI: 10.1016/S0040-4039(00)99882-4 |
0.637 |
|
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