Publications
Selected publications
- Adding the right (or left) twist to tris-chelate complexes – coordination chemistry of chiral oxazolylphenolates with M3+ ions (M = Al or lanthanide) (Journal article - 2014)
- Supporting lifelong learning: enhancing the value of interactive 3D chemistry (Report - 2010)
- Visible-Light-Controlled Oxidation of Glucose using Titania-Supported Silver Photocatalysts (Journal article - 2016)
- ChemTube3D for iOS (Software / Code - 2017)
- ChemTube3D 2019 responsive version for mobile (Software / Code - 2019)
2021
360° Lab Safety exercises
Gaynor, J., & Greeves, N. (2021). 360° Lab Safety exercises. Retrieved from https://www.chemtube3d.com/chemistry-health-and-safety-360-exercises/
ChemTube3D: Health and Safety section
Gaynor, J., & Greeves, N. (2021). ChemTube3D: Health and Safety section. Retrieved from https://www.chemtube3d.com/category/360/
2020
OBITUARY Stuart Warren (24 Dec 1938-22 Mar 2020)
Aggarwal, V. K., Armstrong, S. K., Caggiano, L., Chibale, K., Clayden, J., Coldham, I., . . . Wyatt, P. (2020). OBITUARY Stuart Warren (24 Dec 1938-22 Mar 2020). ORGANIC & BIOMOLECULAR CHEMISTRY, 18(37), 7236-7237. doi:10.1039/d0ob90121k
2019
ChemTube3D 2019 responsive version for mobile
Greeves, N. (2019). ChemTube3D 2019 responsive version for mobile (Version 3.0) [Computer Software]. Retrieved from https://www.chemtube3d.com/
2018
Recent progress in the synthesis and applications of glycerol carbonate
Christy, S., Noschese, A., Lomeli-Rodriguez, M., Greeves, N., & Lopez-Sanchez, J. A. (2018). Recent progress in the synthesis and applications of glycerol carbonate. CURRENT OPINION IN GREEN AND SUSTAINABLE CHEMISTRY, 14, 99-107. doi:10.1016/j.cogsc.2018.09.003
ChemTube3D for Android
Greeves, N. (2018). ChemTube3D for Android (Version 1.0) [Computer Software]. Retrieved from https://play.google.com/store/apps/details?id=www.chemtube3d.com
2017
ChemTube3D for iOS
Greeves, N. (2017). ChemTube3D for iOS (Version 1.0.1) [Computer Software]. Retrieved from https://itunes.apple.com/gb/app/chemtube3d/id1291952162
2016
Back Cover: Visible‐Light‐Controlled Oxidation of Glucose using Titania‐Supported Silver Photocatalysts (ChemCatChem 22/2016)
Da Vià, L., Recchi, C., Davies, T. E., Greeves, N., & Lopez‐Sanchez, J. A. (2016). Back Cover: Visible‐Light‐Controlled Oxidation of Glucose using Titania‐Supported Silver Photocatalysts (ChemCatChem 22/2016). ChemCatChem, 8(22), 3556. doi:10.1002/cctc.201601429
Visible-Light-Controlled Oxidation of Glucose using Titania-Supported Silver Photocatalysts
Da Via, L., Recchi, C., Davies, T. E., Greeves, N., & Lopez-Sanchez, J. A. (2016). Visible-Light-Controlled Oxidation of Glucose using Titania-Supported Silver Photocatalysts. CHEMCATCHEM, 8(22), 3475-3483. doi:10.1002/cctc.201600775
2015
One-pot visible-light mediated photocatalytic hydrolysis and oxidation of cellobiose to gluconic acid and lower chain carbohydrates
Da Via, L., Davies, T., Greeves, N., & Lopez-Sanchez, J. (2015). One-pot visible-light mediated photocatalytic hydrolysis and oxidation of cellobiose to gluconic acid and lower chain carbohydrates. In ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY Vol. 250. Retrieved from https://www.webofscience.com/
2014
Adding the right (or left) twist to tris-chelate complexes – coordination chemistry of chiral oxazolylphenolates with M3+ ions (M = Al or lanthanide)
Aspinall, H., Bacsa, J., Beckingham, O., Eden, E. G. B., Greeves, N., Hobbs, M. D., . . . Thomas, C. D. (2014). Adding the right (or left) twist to tris-chelate complexes – coordination chemistry of chiral oxazolylphenolates with M3+ ions (M = Al or lanthanide). Dalton Transactions, 43(3), 1434-1442. doi:10.1039/C3DT52366G
2011
A general and convenient route to oxazolyl ligands
Aspinall, H. C., Beckingham, O., Farrar, M. D., Greeves, N., & Thomas, C. D. (2011). A general and convenient route to oxazolyl ligands. TETRAHEDRON LETTERS, 52(40), 5120-5123. doi:10.1016/j.tetlet.2011.07.070
Unusual Hybrid Materials Prepared by the Oxidation of a Ketone
Holden, D. L., Goulding, H. V., Bacsa, J., Berry, N. G., Greeves, N., Stephenson, R. A., . . . Fogg, A. M. (2011). Unusual Hybrid Materials Prepared by the Oxidation of a Ketone. CRYSTAL GROWTH & DESIGN, 11(7), 3013-3019. doi:10.1021/cg200286t
ChemPreLab
Sedghi, G., Berry, N., & Greeves, N. (2011). ChemPreLab. Wavelength, 7(1), 42-43.
ChemPreLab: Chemistry pre-lab virtual experiments
Sedghi, G., Berry, N., Greeves, N., & Barnes, K. (2011). ChemPreLab: Chemistry pre-lab virtual experiments. In Variety Conference. York.
Providing Recordings of Chemistry Teaching
Berry, N., Greeves, N., Aspinall, H., Bunyan, N., Barnes, K., Bradford, M., & Chin, P. (2011). Providing Recordings of Chemistry Teaching. Wavelength, 7(1), 6-9.
2010
A new Yb<SUP>3+</SUP>-catalyzed pinacol and imine-coupling reaction
Aspinall, H. C., Greeves, N., & Hin, S. L. F. (2010). A new Yb<SUP>3+</SUP>-catalyzed pinacol and imine-coupling reaction. TETRAHEDRON LETTERS, 51(12), 1558-1561. doi:10.1016/j.tetlet.2010.01.057
ChemTube3D Interactive 3D Organic Reaction Mechanisms
Greeves, N., & Berry, N. G. (2010). ChemTube3D Interactive 3D Organic Reaction Mechanisms (Version 2.0) [Internet (free access)]. Liverpool. Retrieved from http://www.chemtube3d.com/
Supporting lifelong learning: enhancing the value of interactive 3D chemistry
Barnes, K., Greeves, N., Berry, N., Bunyan, N., & Strivens, J. (2010). Supporting lifelong learning: enhancing the value of interactive 3D chemistry. Bristol: JISC. Retrieved from http://www.jisc.ac.uk/whatwedo/programmes/elearning/ltig/ichem3d.aspx
2009
ChemTube3D - Polymers
Greeves, N., & Vernon, L. M. (2009). ChemTube3D - Polymers (Version 1.0) [Internet (free access)]. Liverpool. Retrieved from http://www.chemtube3d.com/polymer
Working with the Physical Sciences Centre
Greeves, N. (2009). Working with the Physical Sciences Centre. Wavelength, 5(2), 4-5.
2008
ChemTube3D - Interactive 3D Solid State Structures
Greeves, N., & Ho, S. K. (2008). ChemTube3D - Interactive 3D Solid State Structures (Version 1.0) [Internet (free access)]. Liverpool. Retrieved from http://www.chemtube3d.com/solidstate
ChemTube3D Interactive 3D Organic Reaction Mechanisms
Greeves, N., Lawrenson, A., & Barnes, K. (2008). ChemTube3D Interactive 3D Organic Reaction Mechanisms (Version 1.0) [Internet (free access)]. Liverpool. Retrieved from http://www.chemtube3d.com/
2005
doi:10.1021/om050197
Lanthanide pybox complexes as catalysts for enantioselective silylcyanation of aldehydes
Aspinall, H. C., Bickley, J. F., Greeves, N., Kelly, R. V., & Smith, P. M. (2005). Lanthanide pybox complexes as catalysts for enantioselective silylcyanation of aldehydes. ORGANOMETALLICS, 24(14), 3458-3467. doi:10.1021/om050197+
Samarium diiodide-catalyzed diastereoselective pinacol couplings
Aspinall, H. C., Greeves, N., & Valla, C. (2005). Samarium diiodide-catalyzed diastereoselective pinacol couplings. ORGANIC LETTERS, 7(10), 1919-1922. doi:10.1021/ol050256f
2003
Modular chiral polyether podands and their lanthanide complexes
Aspinall, H. C., Greeves, N., & McIver, E. G. (2003). Modular chiral polyether podands and their lanthanide complexes. TETRAHEDRON, 59(52), 10453-10463. doi:10.1016/j.tet.2003.06.008
Short synthesis of a tetrasubstituted tetrahydropyran with five stereogenic centres-stereoselective double tandem rearrangements and cyclisation
Greeves, N., Lee, W. M., McLachlan, S. P., Oakes, G. H., Purdie, M., & Bickley, J. F. (2003). Short synthesis of a tetrasubstituted tetrahydropyran with five stereogenic centres-stereoselective double tandem rearrangements and cyclisation. TETRAHEDRON LETTERS, 44(50), 9035-9038. doi:10.1016/j.tetlet.2003.09.209
2002
Defining effective chiral binding sites at lanthanides - highly enantioselective reagents and catalysts from binaphtholate and pybox ligands
Aspinall, H. C., & Greeves, N. (2002). Defining effective chiral binding sites at lanthanides - highly enantioselective reagents and catalysts from binaphtholate and pybox ligands. JOURNAL OF ORGANOMETALLIC CHEMISTRY, 647(1-2), 151-157. doi:10.1016/S0022-328X(01)01370-5
Lanthanum triflate-catalysed allylation of aldehydes: crucial activation by benzoic acid
Aspinall, H. C., Bissett, J. S., Greeves, N., & Levin, D. (2002). Lanthanum triflate-catalysed allylation of aldehydes: crucial activation by benzoic acid. TETRAHEDRON LETTERS, 43(2), 319-321. doi:10.1016/S0040-4039(01)02115-3
Three component synthesis of homoallylic amines. Efficient catalysis by lanthanum triflate/benzoic acid
Aspinall, H. C., Bissett, J. S., Greeves, N., & Levin, D. (2002). Three component synthesis of homoallylic amines. Efficient catalysis by lanthanum triflate/benzoic acid. TETRAHEDRON LETTERS, 43(2), 323-325. doi:10.1016/S0040-4039(01)02116-5
2001
Chemistry in Britain review [6]
Greeves, N. (2001). Chemistry in Britain review [6]. Chemistry in Britain, 37(9), 25.
2000
Pinwheel-shaped heterobimetallic lanthanide alkali metal binaphtholates: Ionic size matters!
Aspinall, H. C., Bickley, J. F., Dwyer, J. L. M., Greeves, N., Kelly, R. V., & Steiner, A. (2000). Pinwheel-shaped heterobimetallic lanthanide alkali metal binaphtholates: Ionic size matters!. ORGANOMETALLICS, 19(25), 5416-5423. doi:10.1021/om0006256
Lithium binaphtholates: Chiral chains and clusters
Aspinall, H. C., Bickley, J. F., Dwyer, J. L. M., Greeves, N., & Steiner, A. (2000). Lithium binaphtholates: Chiral chains and clusters. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 39(16), 2858-2861. doi:3.0.CO;2-T">10.1002/1521-3773(20000818)39:16<2858::AID-ANIE2858>3.0.CO;2-T
Lanthanide complexes with C<sub>2</sub> symmetric ligands for use in enantioselective organic synthesis
Aspinall, H. C., Dwyer, J. L. M., Greeves, N., & Smith, P. M. (2000). Lanthanide complexes with C<sub>2</sub> symmetric ligands for use in enantioselective organic synthesis. JOURNAL OF ALLOYS AND COMPOUNDS, 303, 173-177. doi:10.1016/S0925-8388(00)00661-7
1999
Li<sub>3</sub>[Ln(binol)<sub>3</sub>]•6THF:: New anhydrous lithium lanthanide binaphtholates and their use in enantioselective alkyl addition to aldehydes
Aspinall, H. C., Dwyer, J. L. M., Greeves, N., & Steiner, A. (1999). Li<sub>3</sub>[Ln(binol)<sub>3</sub>]•6THF:: New anhydrous lithium lanthanide binaphtholates and their use in enantioselective alkyl addition to aldehydes. ORGANOMETALLICS, 18(8), 1366-1368. doi:10.1021/om981011s
Catalytic, asymmetric cyanohydrin synthesis mediated by lanthanide(III) chloride pybox complexes
Aspinall, H. C., Greeves, N., & Smith, P. M. (1999). Catalytic, asymmetric cyanohydrin synthesis mediated by lanthanide(III) chloride pybox complexes. TETRAHEDRON LETTERS, 40(9), 1763-1766. doi:10.1016/S0040-4039(98)02685-9
1998
Ytterbium triflate catalysed allylation of aldehydes: An unusual benzoic acid induced acceleration
Aspinall, H. C., Greeves, N., & McIver, E. G. (1998). Ytterbium triflate catalysed allylation of aldehydes: An unusual benzoic acid induced acceleration. TETRAHEDRON LETTERS, 39(50), 9283-9286. doi:10.1016/S0040-4039(98)02086-3
New homochiral lanthanide(III) triflates in Lewis acid catalysis
Aspinall, H. C., Greeves, N., & McIver, E. G. (1998). New homochiral lanthanide(III) triflates in Lewis acid catalysis. JOURNAL OF ALLOYS AND COMPOUNDS, 275, 773-776. doi:10.1016/S0925-8388(98)00438-1
Solubilized lanthanide triflates:: Lewis acid catalysis by polyether and poly(ethylene glycol) complexes of Ln(OTf)<sub>3</sub>
Aspinall, H. C., Dwyer, J. L. M., Greeves, N., McIver, E. G., & Woolley, J. C. (1998). Solubilized lanthanide triflates:: Lewis acid catalysis by polyether and poly(ethylene glycol) complexes of Ln(OTf)<sub>3</sub>. ORGANOMETALLICS, 17(9), 1884-1888. doi:10.1021/om9709087
1997
Stereoselective [2,3]-Wittig and tandem [2,3]-Wittig-anionic oxy-cope rearrangements of bis-allylic ethers: Effect of substituents
Greeves, N., & Lee, W. M. (1997). Stereoselective [2,3]-Wittig and tandem [2,3]-Wittig-anionic oxy-cope rearrangements of bis-allylic ethers: Effect of substituents. TETRAHEDRON LETTERS, 38(36), 6445-6448. doi:10.1016/S0040-4039(97)01473-1
Synthetic applications .1. of the tandem [2,3]-Wittig-anionic oxy-cope rearrangement: Stereoselective disubstituted tetrahydropyran synthesis by electrophile initiated cyclisation
Greeves, N., & Lee, W. M. (1997). Synthetic applications .1. of the tandem [2,3]-Wittig-anionic oxy-cope rearrangement: Stereoselective disubstituted tetrahydropyran synthesis by electrophile initiated cyclisation. TETRAHEDRON LETTERS, 38(36), 6449-6452. doi:10.1016/S0040-4039(97)01474-3
Synthetic applications .2. of the tandem [2,3]-Wittig-anionic oxy-cope rearrangement: Stereoselective trisubstituted delta-lactone and tetrahydropyran synthesis
Greeves, N., Lee, W. M., & Barkley, J. V. (1997). Synthetic applications .2. of the tandem [2,3]-Wittig-anionic oxy-cope rearrangement: Stereoselective trisubstituted delta-lactone and tetrahydropyran synthesis. TETRAHEDRON LETTERS, 38(36), 6453-6456. doi:10.1016/S0040-4039(97)01475-5
An improved Williamson etherification of hindered alcohols promoted by 15-crown-5 and sodium hydride
Aspinall, H. C., Greeves, N., Lee, W. M., McIver, E. G., & Smith, P. M. (1997). An improved Williamson etherification of hindered alcohols promoted by 15-crown-5 and sodium hydride. TETRAHEDRON LETTERS, 38(26), 4679-4682. doi:10.1016/S0040-4039(97)00965-9
1996
Enantioselective addition of tris(TADDOL) organocerium reagents to aldehydes
Greeves, N., & Pease, J. E. (1996). Enantioselective addition of tris(TADDOL) organocerium reagents to aldehydes. TETRAHEDRON LETTERS, 37(32), 5821-5824. doi:10.1016/0040-4039(96)01236-1
Enantioselective addition of organocerium reagents to aldehydes - Effects of TADDOL ligand structure
Greeves, N., Pease, J. E., Bowden, M. C., & Brown, S. M. (1996). Enantioselective addition of organocerium reagents to aldehydes - Effects of TADDOL ligand structure. TETRAHEDRON LETTERS, 37(15), 2675-2678. doi:10.1016/0040-4039(96)00358-9
1995
1-Lithio-3-trimethylsilyl-1-propyne
Greeves, N. (n.d.). 1-Lithio-3-trimethylsilyl-1-propyne. doi:10.1002/047084289x.rl033
Propynyllithium
Greeves, N. (n.d.). Propynyllithium. doi:10.1002/047084289x.rp277
Propynylmagnesium Bromide
Greeves, N. (n.d.). Propynylmagnesium Bromide. doi:10.1002/047084289x.rp278
1994
STEREOCONVERGENT ONE-POT TANDEM [2,3]-WITTIG-ANIONIC OXY-COPE REARRANGEMENT OF ACYCLIC BIS-ALLYLIC ETHERS IN THE DIASTEREOSELECTIVE SYNTHESIS OF SUBSTITUTED TETRAHYDROPYRANS
GREEVES, N., & VINES, K. J. (1994). 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, (12), 1469-1470. doi:10.1039/c39940001469
A TOTAL SYNTHESIS OF (+)2'S,3'R-ZOAPATANOL
TROST, B. M., GREENSPAN, P. D., GEISSLER, H., KIM, J. H., & GREEVES, N. (1994). A TOTAL SYNTHESIS OF (+)2'S,3'R-ZOAPATANOL. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 33(21), 2182-2184. doi:10.1002/anie.199421821
ACYCLIC STEREOCONTROL VIA SEQUENTIAL AND TANDEM [2,3]-WITTIG-ANIONIC OXY-COPE REARRANGEMENTS
GREEVES, N., & VINES, K. J. (1994). ACYCLIC STEREOCONTROL VIA SEQUENTIAL AND TANDEM [2,3]-WITTIG-ANIONIC OXY-COPE REARRANGEMENTS. TETRAHEDRON LETTERS, 35(38), 7077-7080. doi:10.1016/0040-4039(94)88230-4
Regio- and Stereoselective Palladium(0) Catalysed Hydrostannation of Disubstituted Propargyl Alcohols
Greeves, N., & Torode, J. S. (1994). Regio- and Stereoselective Palladium(0) Catalysed Hydrostannation of Disubstituted Propargyl Alcohols. Synlett, 1994(07), 537-538. doi:10.1055/s-1994-22920
YTTERBIUM TRIFLUOROMETHANESULFONATE [YB(OTF)(3)] AS A NOVEL CATALYST FOR THE ALLYLATION OF ALDEHYDES
ASPINALL, H. C., BROWNING, A. F., GREEVES, N., & RAVENSCROFT, P. (1994). YTTERBIUM TRIFLUOROMETHANESULFONATE [YB(OTF)(3)] AS A NOVEL CATALYST FOR THE ALLYLATION OF ALDEHYDES. TETRAHEDRON LETTERS, 35(26), 4639-4640. doi:10.1016/S0040-4039(00)60750-5
LIGAND EFFECTS ON DIASTEREOSELECTIVE ADDITION OF ORGANOCERIUM REAGENTS TO ALDEHYDES AND CYCLIC-KETONES
GREEVES, N., LYFORD, L., & PEASE, J. E. (1994). LIGAND EFFECTS ON DIASTEREOSELECTIVE ADDITION OF ORGANOCERIUM REAGENTS TO ALDEHYDES AND CYCLIC-KETONES. TETRAHEDRON LETTERS, 35(2), 285-288. doi:10.1016/S0040-4039(00)76533-6
1993
NEW HOMOCHIRAL BINAPHTHOL-MODIFIED ORGANOLANTHANIDE REAGENTS FOR THE ENANTIOSELECTIVE ADDITION TO ALDEHYDES
CHIBALE, K., GREEVES, N., LYFORD, L., & PEASE, J. E. (1993). NEW HOMOCHIRAL BINAPHTHOL-MODIFIED ORGANOLANTHANIDE REAGENTS FOR THE ENANTIOSELECTIVE ADDITION TO ALDEHYDES. TETRAHEDRON-ASYMMETRY, 4(12), 2407-2410. doi:10.1016/S0957-4166(00)82211-9
SYNTHESIS OF PHENYLTHIOMETHYL SUBSTITUTED FURANS BY LEWIS-ACID CATALYZED SUBSTITUTION
GREEVES, N., & TORODE, J. S. (1993). SYNTHESIS OF PHENYLTHIOMETHYL SUBSTITUTED FURANS BY LEWIS-ACID CATALYZED SUBSTITUTION. SYNTHESIS-STUTTGART, (11), 1109-1112. Retrieved from https://www.webofscience.com/
1992
ULTRASOUND ASSISTED PREPARATION OF ORGANOCERIUM REAGENTS
GREEVES, N., & LYFORD, L. (1992). ULTRASOUND ASSISTED PREPARATION OF ORGANOCERIUM REAGENTS. TETRAHEDRON LETTERS, 33(33), 4759-4760. doi:10.1016/S0040-4039(00)61278-9
STEREOCHEMICALLY CONTROLLED SYNTHESIS OF UNSATURATED ALCOHOLS BY THE HORNER-WITTIG REACTION
AYREY, P. M., BOLTON, M. A., BUSS, A. D., GREEVES, N., LEVIN, D., WALLACE, P., & WARREN, S. (1992). STEREOCHEMICALLY CONTROLLED SYNTHESIS OF UNSATURATED ALCOHOLS BY THE HORNER-WITTIG REACTION. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, (24), 3407-3417. doi:10.1039/p19920003407
1991
THE SYNTHESIS OF (Z)-PENTA-2,4-DIEN-1-OL AND SUBSTITUTED (E)-PENTADIENOLS BY THE STEREOCHEMICALLY CONTROLLED HORNER-WITTIG REACTION
BROWN, P. S., GREEVES, N., MCELROY, A. B., & WARREN, S. (1991). 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, (6), 1485-1492. doi:10.1039/p19910001485
1987
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)-DEC-5-EN-1-OL, AND (Z)-DEC-5-EN-1-OL, TRI-SUBSTITUTED ALKENES, AND (Z)-ALPHA-BISABOLENE
BUSS, A. D., GREEVES, N., MASON, R., & WARREN, S. (1987). 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)-DEC-5-EN-1-OL, AND (Z)-DEC-5-EN-1-OL, TRI-SUBSTITUTED ALKENES, AND (Z)-ALPHA-BISABOLENE. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, (12), 2569-2577. doi:10.1039/p19870002569
1986
STEREOCHEMICALLY CONTROLLED SYNTHESIS OF UNSATURATED HYDROXY-ACIDS BY THE HORNER-WITTIG REACTION
GREEVES, N., & WARREN, S. (1986). STEREOCHEMICALLY CONTROLLED SYNTHESIS OF UNSATURATED HYDROXY-ACIDS BY THE HORNER-WITTIG REACTION. TETRAHEDRON LETTERS, 27(2), 259-262. doi:10.1016/S0040-4039(00)83991-X
1984
SYNTHESIS OF SINGLE ISOMERS (E OR Z) OF UNSATURATED ALCOHOLS BY THE HORNER-WITTIG REACTION
BUSS, A. D., GREEVES, N., LEVIN, D., WALLACE, P., & WARREN, S. (1984). SYNTHESIS OF SINGLE ISOMERS (E OR Z) OF UNSATURATED ALCOHOLS BY THE HORNER-WITTIG REACTION. TETRAHEDRON LETTERS, 25(3), 357-360. doi:10.1016/S0040-4039(00)99882-4