| Year |
Citation |
Score |
| 2020 |
Alhuwaymil ZS, Al-Araj IQM, Al-Dulayymi AR, Jones A, Gates PJ, Valero-Guillén PL, Baird MS, Dulayymi JRA. Mycobacterium alvei (ω-1)-methoxy mycolic acids: absolute stereochemistry and synthesis. Chemistry and Physics of Lipids. 104977. PMID 32961166 DOI: 10.1016/J.Chemphyslip.2020.104977 |
0.372 |
|
| 2020 |
Jones A, Lee OY, Minnikin DE, Baird MS, Al Dulayymi JR. A re-investigation of the mycolic acids of Mycobacterium avium. Chemistry and Physics of Lipids. 104928. PMID 32492381 DOI: 10.1016/J.Chemphyslip.2020.104928 |
0.377 |
|
| 2019 |
Ali OT, Mohammed MO, Dulayymi JRA, Baird MS. Synthesis of a Di-Mycoloyl Tri-Arabinofuranosyl Glycerol Fragment of the Mycobacterial Cell Wall, Based on Synthetic Mycolic Acids. Molecules (Basel, Switzerland). 24. PMID 31590468 DOI: 10.3390/Molecules24193596 |
0.344 |
|
| 2019 |
Ali OT, Mohammed MO, Gates PJ, Baird MS, Al Dulayymi JR. The Synthesis of Mycobacterial Dimycoloyl Diarabinoglycerol Based on Defined Synthetic Mycolic Acids. Chemistry and Physics of Lipids. PMID 30639038 DOI: 10.1016/J.Chemphyslip.2019.01.002 |
0.346 |
|
| 2017 |
Ali OT, Sahb MM, Al Dulayymi JR, Baird MS. Glycerol mycolates from synthetic mycolic acids. Carbohydrate Research. 448: 67-73. PMID 28623736 DOI: 10.1016/J.Carres.2017.04.023 |
0.364 |
|
| 2016 |
Mohammed MO, Al Dulayymi JR, Baird MS. Preparation of the tri-arabino di-mycolate fragment of mycobacterial arabinogalactan from defined synthetic mycolic acids. Carbohydrate Research. 437: 36-42. PMID 27886607 DOI: 10.1016/J.Carres.2016.11.006 |
0.372 |
|
| 2016 |
Ndlandla FL, Ejoh V, Stoltz AC, Naicker B, Cromarty AD, van Wyngaardt S, Khati M, Rotherham LS, Lemmer Y, Niebuhr J, Baumeister CR, Al Dulayymi JR, Swai H, Baird MS, Verschoor JA. Standardization of natural mycolic acid antigen composition and production for use in biomarker antibody detection to diagnose active tuberculosis. Journal of Immunological Methods. PMID 27247168 DOI: 10.1016/J.Jim.2016.05.010 |
0.328 |
|
| 2016 |
Hao P, Alaraj IQ, Dulayymi JR, Baird MS, Liu J, Liu Q. Sterculic Acid and Its Analogues Are Potent Inhibitors of Toxoplasma gondii. The Korean Journal of Parasitology. 54: 139-45. PMID 27180571 DOI: 10.3347/Kjp.2016.54.2.139 |
0.317 |
|
| 2016 |
Ali HM, Koza G, Hameed RT, Rowles R, Davies C, Dulayymi JRA, Gwenin CD, Baird MS. The synthesis of single enantiomers of trans-alkene containing mycolic acids and related sugar esters Tetrahedron. 72: 7143-7158. DOI: 10.1016/J.Tet.2016.08.089 |
0.366 |
|
| 2016 |
Taher SG, Dulayymi JRA, Tima HG, Ali HM, Romano M, Baird MS. Synthesis of wax esters and related trehalose esters from Mycobacterium avium and other mycobacteria Tetrahedron. 72: 3863-3876. DOI: 10.1016/J.Tet.2016.05.004 |
0.38 |
|
| 2015 |
Taher SG, Muzael M, Al Dulayymi JR, Baird MS. Synthetic trehalose esters of cis-alkene and diene α'-mycolic acids of Mycobacteria. Chemistry and Physics of Lipids. 189: 28-38. PMID 26022243 DOI: 10.1016/J.Chemphyslip.2015.05.004 |
0.375 |
|
| 2014 |
Groenewald W, Baird MS, Verschoor JA, Minnikin DE, Croft AK. Differential spontaneous folding of mycolic acids from Mycobacterium tuberculosis. Chemistry and Physics of Lipids. 180: 15-22. PMID 24362064 DOI: 10.1016/J.Chemphyslip.2013.12.004 |
0.324 |
|
| 2014 |
Mohammed MO, Baird MS, Al Dulayymi JR. Mycolyl arabino glycerols from synthetic mycolic acids Tetrahedron Letters. DOI: 10.1016/J.Tetlet.2015.01.070 |
0.348 |
|
| 2014 |
Al Dulayymi JR, Baird MS, Maza-Iglesias M, Hameed RT, Baols KS, Muzael M, Saleh AD. Synthetic trehalose di- and mono-esters of α-, methoxy- and keto-mycolic acids Tetrahedron. 70: 9836-9852. DOI: 10.1016/J.Tet.2014.10.072 |
0.359 |
|
| 2014 |
Al Kremawi DZ, Al Dulayymi JR, Baird MS. Synthetic epoxy-mycolic acids Tetrahedron. DOI: 10.1016/J.Tet.2014.06.089 |
0.413 |
|
| 2014 |
Mustafa HH, Baird MS, Al Dulayymi JR, Tverezovskiy VV. Tandem rearrangements of a cyclic bis-allene This paper is dedicated to the late Ivan Bolesov, scholar, supervisor and friend Tetrahedron. 70: 1502-1507. DOI: 10.1016/J.Tet.2013.12.058 |
0.337 |
|
| 2013 |
Bolesov IG, Solov'eva VA, Baird MS. Functionalized α-bromocyclopropylmagnesium bromides: Generation and some reactions Russian Journal of Organic Chemistry. 49: 1580-1589. DOI: 10.1134/S1070428013110043 |
0.425 |
|
| 2013 |
Koza G, Muzael M, Schubert-Rowles RR, Theunissen C, Al Dulayymi JR, Baird MS. The synthesis of methoxy and keto mycolic acids containing methyl-trans-cyclopropanes Tetrahedron. 69: 6285-6296. DOI: 10.1016/J.Tet.2013.04.134 |
0.389 |
|
| 2012 |
Verschoor JA, Baird MS, Grooten J. Towards understanding the functional diversity of cell wall mycolic acids of Mycobacterium tuberculosis. Progress in Lipid Research. 51: 325-39. PMID 22659327 DOI: 10.1016/J.Plipres.2012.05.002 |
0.309 |
|
| 2011 |
Vander Beken S, Al Dulayymi JR, Naessens T, Koza G, Maza-Iglesias M, Rowles R, Theunissen C, De Medts J, Lanckacker E, Baird MS, Grooten J. Molecular structure of the Mycobacterium tuberculosis virulence factor, mycolic acid, determines the elicited inflammatory pattern. European Journal of Immunology. 41: 450-60. PMID 21268014 DOI: 10.1002/Eji.201040719 |
0.312 |
|
| 2010 |
Beukes M, Lemmer Y, Deysel M, Al Dulayymi JR, Juma'a RA, Baird MS, Mark SB, Koza G, Iglesias MM, Maximiliano MI, Rowles RR, Richard RR, Theunissen C, Grooten J, Toschi G, et al. Structure-function relationships of the antigenicity of mycolic acids in tuberculosis patients. Chemistry and Physics of Lipids. 163: 800-8. PMID 20875402 DOI: 10.1016/J.Chemphyslip.2010.09.006 |
0.314 |
|
| 2010 |
Muzael M, Koza G, Al Dulayymi JJ, Baird MS. The synthesis of a major alpha'-mycolic acid of Mycobacterium smegmatis. Chemistry and Physics of Lipids. 163: 678-84. PMID 20573597 DOI: 10.1016/J.Chemphyslip.2010.05.203 |
0.319 |
|
| 2010 |
Al Kremawi DZ, Al Dulayymi JR, Baird MS. The first synthesis of epoxy-mycolic acids Tetrahedron Letters. 51: 1698-1701. DOI: 10.1016/J.Tetlet.2010.01.078 |
0.398 |
|
| 2010 |
Driver CHS, Balogun MO, Toschi G, Verschoor JA, Baird MS, Pilcher LA. A biomimetic approach to the synthesis of a mycolic acid motif Tetrahedron Letters. 51: 1185-1186. DOI: 10.1016/J.Tetlet.2009.12.105 |
0.395 |
|
| 2009 |
Gratraud P, Huws E, Falkard B, Adjalley S, Fidock DA, Berry L, Jacobs WR, Baird MS, Vial H, Kremer L. Oleic acid biosynthesis in Plasmodium falciparum: characterization of the stearoyl-CoA desaturase and investigation as a potential therapeutic target. Plos One. 4: e6889. PMID 19707292 DOI: 10.1371/Journal.Pone.0006889 |
0.316 |
|
| 2009 |
Koza G, Rowles R, Theunissen C, Al-Dulayymi JR, Baird MS. The synthesis of single enantiomers of trans-alkene-containing mycolic acids Tetrahedron Letters. 50: 7259-7262. DOI: 10.1016/J.Tetlet.2009.10.009 |
0.403 |
|
| 2009 |
Al Dulayymi JR, Baird MS, Maza-Iglesias M, Beken SV, Grooten J. The first unique synthetic mycobacterial cord factors Tetrahedron Letters. 50: 3702-3705. DOI: 10.1016/J.Tetlet.2009.03.213 |
0.308 |
|
| 2009 |
Sheshenev AE, Baird MS, Bolesov IG, Shashkov AS. Stereo- and regiocontrol in ene-dimerisation and trimerisation of 1-trimethylsilyl-3-phenylcyclopropene Tetrahedron. 65: 10552-10564. DOI: 10.1016/J.Tet.2009.10.077 |
0.318 |
|
| 2009 |
Koza G, Theunissen C, Al Dulayymi JR, Baird MS. The synthesis of single enantiomers of mycobacterial ketomycolic acids containing cis-cyclopropanes Tetrahedron. 65: 10214-10229. DOI: 10.1016/J.Tet.2009.09.099 |
0.384 |
|
| 2009 |
Sheshenev AE, Baird MS, Croft AK, Bolesov IG. Generation and stereoselective transformations of 3-phenylcyclopropene Tetrahedron. 65: 10036-10046. DOI: 10.1016/J.Tet.2009.09.098 |
0.356 |
|
| 2008 |
Benadie Y, Deysel M, Siko DG, Roberts VV, Van Wyngaardt S, Thanyani ST, Sekanka G, Ten Bokum AM, Collett LA, Grooten J, Baird MS, Verschoor JA. Cholesteroid nature of free mycolic acids from M. tuberculosis. Chemistry and Physics of Lipids. 152: 95-103. PMID 18312856 DOI: 10.1016/J.Chemphyslip.2008.01.004 |
0.321 |
|
| 2007 |
Sekanka G, Baird M, Minnikin D, Grooten J. Mycolic acids for the control of tuberculosis Expert Opinion On Therapeutic Patents. 17: 315-331. DOI: 10.1517/13543776.17.3.315 |
0.318 |
|
| 2007 |
Koza G, Baird MS. The first synthesis of single enantiomers of ketomycolic acids Tetrahedron Letters. 48: 2165-2169. DOI: 10.1016/J.Tetlet.2007.01.100 |
0.406 |
|
| 2007 |
Baird MS, Boitsov VM, Stepakov AV, Molchanov AP, Kopf J, Rajaratnam M, Kostikov RR. Preparation and reactions of some 2,2-difunctional 1,1-dibromocyclopropanes Tetrahedron. 63: 7717-7726. DOI: 10.1016/J.Tet.2007.04.104 |
0.418 |
|
| 2007 |
Al Dulayymi JR, Baird MS, Roberts E, Deysel M, Verschoor J. The first syntheses of single enantiomers of the major methoxymycolic acid of Mycobacterium tuberculosis Tetrahedron. 63: 2571-2592. DOI: 10.1016/J.Tet.2007.01.007 |
0.329 |
|
| 2006 |
Roberts IO, Baird MS. A new short synthesis of 10R-tuberculostearic acid and its enantiomer. Chemistry and Physics of Lipids. 142: 111-7. PMID 16690044 DOI: 10.1016/J.Chemphyslip.2006.03.006 |
0.343 |
|
| 2006 |
Al Dulayymi JR, Baird MS, Roberts E, Minnikin DE. The synthesis of single enantiomers of meromycolic acids from mycobacterial wax esters Tetrahedron. 62: 11867-11880. DOI: 10.1016/J.Tet.2006.09.019 |
0.401 |
|
| 2006 |
Al-Dulayymi JR, Baird MS, Mohammed H, Roberts E, Clegg W. The synthesis of one enantiomer of the α-methyl-trans-cyclopropane unit of mycolic acids Tetrahedron. 62: 4851-4862. DOI: 10.1016/J.Tet.2006.03.007 |
0.382 |
|
| 2006 |
Toschi G, Baird MS. An improved procedure for the preparation of the β-hydroxy-α- alkyl fatty acid fragment of mycolic acids Tetrahedron. 62: 3221-3227. DOI: 10.1016/J.Tet.2006.01.070 |
0.353 |
|
| 2005 |
Al Dulayymi JR, Baird MS, Roberts E. The synthesis of a single enantiomer of a major α-mycolic acid of M. tuberculosis Tetrahedron. 61: 11939-11951. DOI: 10.1016/J.Tet.2005.09.056 |
0.365 |
|
| 2005 |
Sheshenev AE, Baird MS, Bolesov IG. Synthesis of 1-bromosubstituted analogs of cis-deltamethrinic and cis-permethrinic acids Russian Journal of Organic Chemistry. 41: 1601-1609. DOI: 10.1007/S11178-006-0005-0 |
0.369 |
|
| 2004 |
Coxon GD, Al Dulayymi JR, Morehouse C, Brennan PJ, Besra GS, Baird MS, Minnikin DE. Synthesis and properties of methyl 5-(1'R,2'S)-(2-octadecylcycloprop-1-yl)pentanoate and other omega-19 chiral cyclopropane fatty acids and esters related to mycobacterial mycolic acids. Chemistry and Physics of Lipids. 127: 35-46. PMID 14706739 DOI: 10.1016/J.Chemphyslip.2003.09.001 |
0.367 |
|
| 2004 |
Sun XF, Sun R, Fowler P, Baird MS. Physicochemical characterization of lignin isolated with high yield and purity from wheat straw International Journal of Polymer Analysis and Characterization. 9: 317-337. DOI: 10.1080/10236660490935727 |
0.323 |
|
| 2004 |
Sheshenev AE, Baird MS, Croft AK, Bolesov IG. Generation and stereocontrolled trapping of 3-phenylcyclopropene and its derivatives Mendeleev Communications. 14: 299-301. DOI: 10.1070/Mc2004V014N06Abeh002061 |
0.31 |
|
| 2004 |
Sun XF, Sun RC, Tomkinson J, Baird MS. Degradation of wheat straw lignin and hemicellulosic polymers by a totally chlorine-free method Polymer Degradation and Stability. 83: 47-57. DOI: 10.1016/S0141-3910(03)00205-2 |
0.339 |
|
| 2004 |
Roberts IO, Baird MS, Liu Y. The absolute stereochemistry of cascarillic acid Tetrahedron Letters. 45: 8685-8686. DOI: 10.1016/J.Tetlet.2004.09.141 |
0.348 |
|
| 2004 |
Al Dulayymi JR, Baird MS, Jones K. The absolute stereochemistry of grenadamide Tetrahedron. 60: 341-345. DOI: 10.1016/J.Tet.2003.11.006 |
0.322 |
|
| 2004 |
Sun XF, Sun RC, Fowler P, Baird MS. Isolation and characterisation of cellulose obtained by a two-stage treatment with organosolv and cyanamide activated hydrogen peroxide from wheat straw Carbohydrate Polymers. 55: 379-391. DOI: 10.1016/J.Carbpol.2003.10.004 |
0.333 |
|
| 2004 |
Boitsov VM, Kostikov RR, Molchanov AP, Stepakov AV, Baird MS. Dehydrohalogenation of substituted diethyl halocyclopropane-1,1- dicarboxylates Russian Journal of Organic Chemistry. 40: 1760-1763. DOI: 10.1007/S11178-005-0095-0 |
0.344 |
|
| 2003 |
Phetsuksiri B, Jackson M, Scherman H, McNeil M, Besra GS, Baulard AR, Slayden RA, DeBarber AE, Barry CE, Baird MS, Crick DC, Brennan PJ. Unique mechanism of action of the thiourea drug isoxyl on Mycobacterium tuberculosis. The Journal of Biological Chemistry. 278: 53123-30. PMID 14559907 DOI: 10.1074/Jbc.M311209200 |
0.311 |
|
| 2003 |
Al Dulayymi JR, Baird MS, Roberts E. The synthesis of a single enantiomer of a major alpha-mycolic acid of Mycobacterium tuberculosis. Chemical Communications (Cambridge, England). 228-9. PMID 12585404 DOI: 10.1039/B209876H |
0.329 |
|
| 2003 |
Nizovtsev AV, Al Dulayymi JR, Baird MS, Bolesov IG, Tverezovskii VV. Effective and selective mild catalytic hydrodehalogenation of halocyclopropanes: Preparative capabilities and mechanistic aspects Kinetics and Catalysis. 44: 151-164. DOI: 10.1023/A:1023340109395 |
0.316 |
|
| 2003 |
Coxon GD, Al-Dulayymi JR, Baird MS, Knobl S, Roberts E, Minnikin DE. The synthesis of (11R,12S)-lactobacillic acid and its enantiomer Tetrahedron Asymmetry. 14: 1211-1222. DOI: 10.1016/S0957-4166(03)00165-4 |
0.358 |
|
| 2003 |
Sun XF, Sun RC, Tomkinson J, Baird MS. Preparation of sugarcane bagasse hemicellulosic succinates using NBS as a catalyst Carbohydrate Polymers. 53: 483-495. DOI: 10.1016/S0144-8617(03)00150-4 |
0.307 |
|
| 2002 |
Baird MS, Nizovtsev AV, Bolesov IG. Bromine-magnesium exchange in gem-dibromocyclopropanes using Grignard reagents Tetrahedron. 58: 1581-1593. DOI: 10.1016/S0040-4020(02)00018-2 |
0.353 |
|
| 2001 |
Baird MS, Huber FAM, Clegg W. Stereocontrolled approaches to 2-(2-aminoalkyl)-1-hydroxycyclopropanes Tetrahedron. 57: 9849-9858. DOI: 10.1016/S0040-4020(01)00996-6 |
0.312 |
|
| 2001 |
Baird MS, Huber FAM, Tverezovsky VV, Bolesov IG. Intramolecular trapping of amides by 1-lithio-1-bromocyclopropanes Tetrahedron. 57: 1593-1600. DOI: 10.1016/S0040-4020(00)00385-9 |
0.344 |
|
| 2000 |
Potter DM, Baird MS. Carcinogenic effects of ptaquiloside in bracken fern and related compounds. British Journal of Cancer. 83: 914-20. PMID 10970694 DOI: 10.1054/Bjoc.2000.1368 |
0.304 |
|
| 2000 |
Al Dulayymi JR, Baird MS, Bolesov IG, Nizovtsev AV, Tverezovsky VV. Hydrodehalogenation of 1,1-dibromocyclopropanes by Grignard reagents promoted by titanium compounds Journal of the Chemical Society. Perkin Transactions 2. 1603-1617. DOI: 10.1039/A910317L |
0.376 |
|
| 2000 |
Al Dulayymi JR, Baird MS, Roberts E. The synthesis of single enantiomers of a meromycolic acid Tetrahedron Letters. 41: 7107-7110. DOI: 10.1016/S0040-4039(00)01147-3 |
0.37 |
|
| 2000 |
Al Dulayymi JR, Baird MS, Hussain HH, Alhourani BJ, Alhabashna AMY, Coles SJ, Hursthouse MB. The cycloaddition of cyclopropenes to enones Tetrahedron Letters. 41: 4205-4208. DOI: 10.1016/S0040-4039(00)00566-9 |
0.37 |
|
| 2000 |
Al Dulayymi AR, Al Dulayymi JR, Baird MS. A flexible route to [4.1.1]Propellanes Tetrahedron. 56: 1115-1125. DOI: 10.1016/S0040-4020(99)01069-8 |
0.383 |
|
| 1999 |
Pavlov V, Gazizova V, Shamov G, Moskva V, Winsel H, Meijere AD, Baird M, Kulinkovich O. The Development of a New Approaches to the Synthesis of Polyfunctional Phosphorylated Cyclopropanes Phosphorus Sulfur and Silicon and the Related Elements. 147: 311-311. DOI: 10.1080/10426509908053636 |
0.308 |
|
| 1999 |
Coxon GD, Knobl S, Roberts E, Baird MS, Al Dulayymi JR, Besra GS, Brennan PJ, Minnikin DE. The synthesis of both enantiomers of lactobacillic acid and mycolic acid analogues Tetrahedron Letters. 40: 6689-6692. DOI: 10.1016/S0040-4039(99)01378-7 |
0.357 |
|
| 1999 |
Baird MS, Licence P, Tverezovsky VV, Bolesov IG, Clegg W. Enantiomerically pure 2,2-dibromocyclopropanecarboxylic acids, simple chiral building blocks Tetrahedron. 55: 2773-2784. DOI: 10.1016/S0040-4020(99)00048-4 |
0.584 |
|
| 1998 |
Baird MS, Huber FAM, Tverezovzky VV, Bolesov IG. Intramolecular trapping of esters and amides by 1-lithio-1- bromocyclopropanes Tetrahedron Letters. 39: 9081-9084. DOI: 10.1016/S0040-4039(98)01999-6 |
0.372 |
|
| 1998 |
Al Dulayymi AR, Baird MS. Pyridazines by addition of diazoalkanes to 1-bromo- and 1,2- dibromocyclopropenes Tetrahedron. 54: 12897-12906. DOI: 10.1016/S0040-4020(98)00781-9 |
0.359 |
|
| 1997 |
Ai Dulayymi AR, Baird MS, Clegg W. An unusual rearrangement of isoxazoles to 2-alkenoylpyrroles or 1- azafulvenes Tetrahedron Letters. 38: 8271-8274. DOI: 10.1016/S0040-4039(97)10165-4 |
0.318 |
|
| 1997 |
Tverezovsky VV, Baird MS, Bolesov IG. Synthesis of (2S,3R,4S)-3,4-methanoproline and analogues by cyclopropylidene insertion Tetrahedron. 53: 14773-14792. DOI: 10.1016/S0040-4020(97)00988-5 |
0.31 |
|
| 1997 |
Al Dulayymi JR, Baird MS, Dale CM, Grehan BJ, Shortt MF. Synthesis of putative Δ6-, Δ12- and Δ15-desaturase inhibitors Tetrahedron. 53: 1099-1110. DOI: 10.1016/S0040-4020(96)01033-2 |
0.31 |
|
| 1996 |
Pavlov VA, Kurdjukov AI, Moskva VV, Baird MS. Synthesis of functionalized heterocycles bearing phosphonate moiety via phosphorylnitrile oxides. Stereochemistry and unusual cycloadditions Phosphorus, Sulfur and Silicon and Related Elements. 109: 509-512. DOI: 10.1080/10426509608545202 |
0.324 |
|
| 1996 |
Dulayymi JRA, Baird MS, Bolesov IG, Tveresovsky V, Rubin M. A simple and efficient hydrodehalogenation of 1,1-dihalocyclopropanes Tetrahedron Letters. 37: 8933-8936. DOI: 10.1016/S0040-4039(96)02051-5 |
0.376 |
|
| 1996 |
Al Dulayymi AR, Baird MS. 2-Vinyl-1,1,2-trihalocyclopropanes - Valuable five carbon cyclopropane and cyclopropene synthetic intermediates Tetrahedron. 52: 10955-10968. DOI: 10.1016/0040-4020(96)00592-3 |
0.351 |
|
| 1996 |
Al Dulayymi AR, Al Dulayymi JR, Baird MS, Gerrard ME, Koza G, Harkins SD, Roberts E. 1,2,2-Tribromocyclopropanecarboxylic acid and derivatives - Valuable intermediates for four carbon cyclopropane and cyclopropene synthons Tetrahedron. 52: 3409-3424. DOI: 10.1016/0040-4020(95)01123-4 |
0.364 |
|
| 1995 |
Al Dulayymi JR, Baird MS. A direct and a formal trapping of propa-1,2-dienylidene Tetrahedron Letters. 36: 3393-3396. DOI: 10.1016/0040-4039(95)00490-4 |
0.363 |
|
| 1995 |
Al Dulayymi AR, Al Dulayymi JR, Baird MS, Rajaram L. The generation and trapping of 1,2-Dibromo-3-methylbut-2-en-1-ylidenes Tetrahedron. 51: 8371-8382. DOI: 10.1016/0040-4020(95)00448-H |
0.381 |
|
| 1994 |
Hartmann S, Minnikin DE, Römming HJ, Baird MS, Ratledge C, Wheeler PR. Synthesis of methyl 3-(2-octadecylcyclopropen-1-yl)propanoate and methyl 3-(2-octadecylcyclopropen-1-yl)pentanoate and cyclopropane fatty acids as possible inhibitors of mycolic acid biosynthesis. Chemistry and Physics of Lipids. 71: 99-108. PMID 8039261 DOI: 10.1016/0009-3084(94)02315-8 |
0.358 |
|
| 1994 |
Dulayymi JRA, Baird MS, Fitton HL, Rajaram L. 1,2-Dibromoalk-2-enylidenes by ring-opening of 1,2-dibromo-3-alkylcyclopropenes at ambient temperature Journal of the Chemical Society, Perkin Transactions 1. 1633-1641. DOI: 10.1039/P19940001633 |
0.332 |
|
| 1994 |
Al Dulayymi AR, Baird MS. A flexible route to 1-bromo-2-alkylcyclopropenes Journal of the Chemical Society, Perkin Transactions 1. 1547-1548. DOI: 10.1039/P19940001547 |
0.318 |
|
| 1993 |
Al Dulayymi JR, Baird MS, Byard SJ, Carr G, Ellames GJ, Firth JW, Herbert JM, Donald MA, Vojvodic PR, Wrench LM. Degradation studies under neutral and basic conditions on ciprofibrate, an orally active hypolipidemic agent containing a (4-alkoxyaryl)-1,1- dichlorocyclopropane unit Journal of the Chemical Society, Perkin Transactions 2. 43-48. DOI: 10.1039/P29930000043 |
0.354 |
|
| 1993 |
Baird MS, Li X, Al Dulayymi JR, Kurdjukov AI, Pavlov VA. Unusual chemo- and stereo-selectivities in the reactions of 1,2-dichlorocyclopropenes with nitrile oxides Journal of the Chemical Society, Perkin Transactions 1. 2507-2508. DOI: 10.1039/P19930002507 |
0.335 |
|
| 1993 |
Baird MS, Shortt MF, Hussain HH, Al Dulayymi JR. Highly functionalised methylenecyclopropanes from cyclopropenes Journal of the Chemical Society, Perkin Transactions 1. 1945-1946. DOI: 10.1039/P19930001945 |
0.312 |
|
| 1993 |
Baird MS, Grehan B. A new approach to cyclopropene fatty acids involving 1,2-deiodination Journal of the Chemical Society, Perkin Transactions 1. 1547-1548. DOI: 10.1039/P19930001547 |
0.34 |
|
| 1993 |
Besra GS, Minnikin DE, Simpson MJ, Baird MS, Wheeler PR, Ratledge C. The synthesis of methyl 4-(2-octadecylcyclopropen-l-yl)butanoate: a possible inhibitor in mycolic acid biosynthesis Chemistry and Physics of Lipids. 66: 35-40. DOI: 10.1016/0009-3084(93)90028-2 |
0.369 |
|
| 1992 |
Baird MS, Buxton SR, Mitra MM, Norin T, Spielbüchler P, Pedersen JB, Krogsgaard-Larsen P. 1-trimethylsilylbuta-1,3-dienes and 1-trimethylsilylbicyclo[1.1.0]-butanes from 1,1,1-tribromobut-3-enes Acta Chemica Scandinavica. 46: 669-677. DOI: 10.3891/Acta.Chem.Scand.46-0669 |
0.317 |
|
| 1992 |
Baird MS, Dacre R, Tomkinson J. A tandem silica-induced ring-opening and cyclisation of 1-aryl-1-chlorocyclopropanes leading to indenes Journal of the Chemical Society-Perkin Transactions 1. 535-536. DOI: 10.1039/P19920000535 |
0.381 |
|
| 1992 |
Baird MS, Dale CM, Lytollis W, Simpson MJ. A new approach to cyclopropene fatty acids Tetrahedron Letters. 33: 1521-1522. DOI: 10.1016/S0040-4039(00)91664-2 |
0.341 |
|
| 1992 |
Al-Dulayymi JR, Baird MS. An unusual anion-promoted hydrogen shift Tetrahedron Letters. 33: 835-838. DOI: 10.1016/S0040-4039(00)77728-8 |
0.323 |
|
| 1992 |
Dulayymi JRA, Baird MS, Fitton HL. The stereochemistry of ring-opening of 3-alkyl-1,1-dihalocyclopropenes to vinylcarbenes at ambient temperature Tetrahedron Letters. 33: 4803-4806. DOI: 10.1016/S0040-4039(00)61290-X |
0.356 |
|
| 1991 |
Baird MS, Baxter AGW, Hoorfar A, Jefferies I. Ring-size and substituent effects in intramolecular reactions of alkylidenecarbenes (carbenoids) Journal of the Chemical Society-Perkin Transactions 1. 2575-2581. DOI: 10.1039/P19910002575 |
0.321 |
|
| 1990 |
Baird MS, Mahli BS, Sheppard L. A regio- and stereo-selective route to 1,1,3- and 1,2,3-trihalogenobutadienes by dehydrohalogenation of alkyl-substituted 1,1,2,3-tetrahalogenocyclopropanes Journal of the Chemical Society-Perkin Transactions 1. 1881-1886. DOI: 10.1039/P19900001881 |
0.328 |
|
| 1990 |
Al-Dulayymi JR, Baird MS. Optically active dihydropyrans and 3-methylenetetrahydrofurans from cyclopropenylethanol derivatives Tetrahedron. 46: 5703-5714. DOI: 10.1016/S0040-4020(01)87769-3 |
0.342 |
|
| 1989 |
Al-Dulayymi JR, Baird MS, Clegg W. A highly stereoselective generation and trapping of 1,2-dichloro-3-methyl-4-phenylbut-2-enylidene Journal of the Chemical Society-Perkin Transactions 1. 1799-1803. DOI: 10.1039/P19890001799 |
0.343 |
|
| 1989 |
Al-Dulayymi J, Baird MS. A novel route to optically active dihydropyrans and 3-methylenetetrahydrofurans Tetrahedron Letters. 30: 253-256. DOI: 10.1016/S0040-4039(00)95174-8 |
0.342 |
|
| 1989 |
Dulayymi JRA, Baird MS. Generation and trapping of vinylcarbenes at ambient temperature: a route to functionalised vinyl- and allylidene-cyclopropanes Tetrahedron. 45: 7601-7614. DOI: 10.1016/S0040-4020(01)89222-X |
0.34 |
|
| 1989 |
Baird MS, Hussain HH. 1, 2-Dichloro-3,3-dimethylcyclopropene as a source of 1,2-dichlo-3-methylbut-2-enzylidene at ambient temperature Tetrahedron. 45: 6221-6238. DOI: 10.1016/S0040-4020(01)85133-4 |
0.339 |
|
| 1988 |
Al-Dulayymi J, Baird MS, Clegg W. The stereoselectivity of ring-opening of 3-substituted cyclopropenes and intermolecular trapping of derived vinylcarbenes Tetrahedron Letters. 29: 6149-6152. DOI: 10.1016/S0040-4039(00)82291-1 |
0.343 |
|
| 1987 |
Baird MS, Hussain HH, Clegg W. Regioselective ring-opening and dimerisation of methyl 3,3-dimethylcyclopropenecarboxylate Journal of the Chemical Society-Perkin Transactions 1. 1609-1612. DOI: 10.1039/P19870001609 |
0.332 |
|
| 1987 |
Baird MS, Hussain HH. The preparation and decomposition of alkyl 2-diazopent-4-enoates and 1-trimethylsilyl-1-diazobut-3-enes Tetrahedron. 43: 215-224. DOI: 10.1016/S0040-4020(01)89947-6 |
0.364 |
|
| 1986 |
Baird MS, Hussain HH, Nethercott W. The preparation and lithiation of 1-halogenocyclopropenes Journal of the Chemical Society-Perkin Transactions 1. 1845-1853. DOI: 10.1039/P19860001845 |
0.305 |
|
| 1985 |
Baird MS, Gerrard ME, Searle RJG. Trapping of the tribromomethylanion by electron poor alkenes Tetrahedron Letters. 26: 6353-6356. DOI: 10.1016/S0040-4039(01)84597-4 |
0.305 |
|
| 1984 |
Nilsen NO, Skattebøl L, Baird MS, Buxton SR, Slowey PD. A simple route to 1-bromobicyclo[1.1.0]butanes by intramolecular trapping of 1-bromo-1-lithiocyclopropanes Tetrahedron Letters. 25: 2887-2890. DOI: 10.1016/S0040-4039(01)81317-4 |
0.37 |
|
| 1984 |
Baird MS, Buxton SR, Whitley JS. Cyclopropene-carbene rearrangements at low temperatures. Generation and trapping of 1,2-dichloro-3-methylbut-2-en-1-ylidene Tetrahedron Letters. 25: 1509-1512. DOI: 10.1016/S0040-4039(01)80199-4 |
0.32 |
|
| 1983 |
Baird MS, Nethercott W. 1-halocyclopropenes and propargylic halides from the reaction of trihalocyclopropanes with methyl lithium Tetrahedron Letters. 24: 605-608. DOI: 10.1016/S0040-4039(00)81476-8 |
0.349 |
|
| 1982 |
Baird MS, Nethercott W, Reese CB. A simple entry to the cis-bicyclo[3.3.0]octa-2,6-diene system Journal of the Chemical Society, Chemical Communications. 224-225. DOI: 10.1039/C39820000224 |
0.513 |
|
| 1982 |
Baird MS, Nethercott W, Reese CB. A Simple Entry To The Cis-Bicyclo(3.3.0)Octa-2,6-Diene System Cheminform. 13. DOI: 10.1002/Chin.198224173 |
0.511 |
|
| 1979 |
Baird MS, Baxter AGW. The reaction of 1,1-dibromocyclopropanecarboxamides with methyllithium Journal of the Chemical Society-Perkin Transactions 1. 11: 2317-2325. DOI: 10.1039/P19790002317 |
0.33 |
|
| 1979 |
Baird MS. The chemistry of cyclopropylidenes. Part 1. Reaction of 7,7-dibromo-3-vinylbicyclo[4.1.0]heptanes with methyl-lithium Journal of the Chemical Society-Perkin Transactions 1. 10: 1020-1028. DOI: 10.1039/P19790001020 |
0.361 |
|
| 1979 |
Baird MS, Sadler P, Hatem J, Zahra J, Waegell B. Efficient pathway to the tetracyclo[4.2.0.02,8.04,7]octane (bishomoprismane) system by carbenoid insertion†; Journal of the Chemical Society, Chemical Communications. 452-453. DOI: 10.1039/C39790000452 |
0.344 |
|
| 1976 |
Baird MS. Iodocyclopropanes. Part I. Di-iodocarbene adducts of some cyclic olefins Journal of the Chemical Society-Perkin Transactions 1. 54-56. DOI: 10.1039/P19760000054 |
0.343 |
|
| 1976 |
Baird MS, Kaura AC. Intramolecular insertion of cyclopropylidenes into N–H bonds and into C–H bonds adjacent to nitrogen Journal of the Chemical Society, Chemical Communications. 356-357. DOI: 10.1039/C39760000356 |
0.346 |
|
| 1976 |
Baird MS, Reese CB. Carbene-carbene rearrangements. A simple route to III- and tetrahydropentalenes Tetrahedron Letters. 17: 2895-2898. DOI: 10.1016/S0040-4039(01)85531-3 |
0.499 |
|
| 1976 |
Allan AR, Baird MS. Homo-1,4-addition to cyclo-octa-1,4-diene and cyclohepta-1,4-diene Tetrahedron Letters. 17: 3831-3832. DOI: 10.1016/S0040-4039(00)93122-8 |
0.372 |
|
| 1976 |
Baird MS, Reese CB. Preparation of cyclonona-1,2,5-triene, cyclonona-1,2,5,7-tetraene and cyclodeca-1,2,5,6-tetraene Tetrahedron. 32: 2153-2156. DOI: 10.1016/0040-4020(76)85127-7 |
0.505 |
|
| 1976 |
Baird MS. Iodocyclopropanes. I. Diiodocarbene Adducts Of Cyclic Olefins Cheminform. 7. DOI: 10.1002/Chin.197612096 |
0.327 |
|
| 1975 |
Allan AR, Baird MS. A carbenoid route to the 6-oxatricyclo[3,2,1,02,7]octane ring system Journal of the Chemical Society, Chemical Communications. 172-173. DOI: 10.1039/C39750000172 |
0.322 |
|
| 1974 |
Baird MS. Tetracyclo[3,3,1,02,4,02,8]nonane. A strained spiro-compound Journal of the Chemical Society, Chemical Communications. 197-198. DOI: 10.1039/C39740000197 |
0.347 |
|
| 1974 |
Baird MS. Sterespecific reduction and methylation of two 1-iodo-trans-cycloalkenes Journal of the Chemical Society, Chemical Communications. 196-197. DOI: 10.1039/C39740000196 |
0.357 |
|
| 1972 |
Baird MS, Reese CB, Stebles MRD. Die Rk. Von Magnesium Mit Dibromcyclo‐Octanen Und ‐Nonanen, Eine Neue Transannulare Eliminierungsrk. Cheminform. 3. DOI: 10.1002/Chin.197207141 |
0.444 |
|
| 1971 |
Baird MS, Reese CB, Stebles MRD. Action of magnesium on dibromocyclo-octanes and -nonanes. A novel transannular elimination reaction Journal of the Chemical Society D: Chemical Communications. DOI: 10.1039/C2971001340B |
0.522 |
|
| 1971 |
Baird MS. Preparation of 3-oxabicyclo[3,1,0]hexanes; a useful carbenoid insertion reaction Journal of the Chemical Society D: Chemical Communications. 1145-1146. DOI: 10.1039/C29710001145 |
0.334 |
|
| 1971 |
Baird M, Reese C. Ag+-assisted methanolysis of halogenocarbene adducts of cyclohepta-1,3-diene Tetrahedron Letters. 12: 4637-4640. DOI: 10.1016/S0040-4039(01)97550-1 |
0.457 |
|
| 1971 |
Baird MS, Reese CB, Shaw A. The addition of bromine to cyclonona-1,2-diene Tetrahedron. 27: 231-236. DOI: 10.1016/S0040-4020(01)92413-5 |
0.535 |
|
| 1970 |
Baird MS, Reese CB. Preparation of some derivatives of cis,trans-cyclo-octa-1,4-diene Journal of the Chemical Society D: Chemical Communications. 1644-1645. DOI: 10.1039/C29700001644 |
0.551 |
|
| 1969 |
Baird MS, Reese CB. Thermal rearrangement of 9,9-dibromobicyclo[6,1,0]non-4-ene and related compounds Journal of the Chemical Society C: Organic. 1808-1813. DOI: 10.1039/J39690001808 |
0.543 |
|
| 1969 |
Baird MS, Reese CB. Action of heat on halogenocarbene adducts of cycloheptene and cis-cyclo-octene Journal of the Chemical Society C: Organic. 1803-1807. DOI: 10.1039/J39690001803 |
0.508 |
|
| 1969 |
Baird MS, Lindsay DG, Reese CB. Thermal rearrangement of halogenocarbene adducts of cyclic olefins Journal of the Chemical Society C: Organic. 1173-1178. DOI: 10.1039/J39690001173 |
0.513 |
|
| 1969 |
Wasserman H, Cochoy R, Baird M. Additions and Corrections - Cyclopropanone Reactions . Cyclobutanone Derivatives from Vinylic and Acetylenic Cyclopropanols. Journal of the American Chemical Society. 91: 4943-4943. DOI: 10.1021/Ja01045A607 |
0.329 |
|
| 1969 |
Wasserman HH, Cochoy RE, Baird MS. Cyclopropanone reactions. Cyclobutanone derivatives from vinylic and acetylenic cyclopropanols Journal of the American Chemical Society. 91: 2375-2376. DOI: 10.1021/Ja01037A034 |
0.326 |
|
| 1969 |
Baird M, Reese C. Pyrolytic and electron impact studies on 1-bromo- and 1, 1-dibromo-2, 3-dimethylcyclopropanes Tetrahedron Letters. 10: 2117-2120. DOI: 10.1016/S0040-4039(01)88100-4 |
0.445 |
|
| 1968 |
Baird MS, Lindsay DG, Reese CB. Thermal rearrangements of 9,9-dibromobicyclo[6,1,0]non-2-ene and related compounds Chemical Communications (London). 784-785. DOI: 10.1039/C19680000784 |
0.484 |
|
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