| Year |
Citation |
Score |
| 2022 |
Estévez-Gallego J, Álvarez-Bernad B, Pera B, Wullschleger C, Raes O, Menche D, Martínez JC, Lucena-Agell D, Prota AE, Bonato F, Bargsten K, Cornelus J, Giménez-Abián JF, Northcote P, Steinmetz MO, ... ... Paterson I, et al. Chemical modulation of microtubule structure through the laulimalide/peloruside site. Structure (London, England : 1993). PMID 36462501 DOI: 10.1016/j.str.2022.11.006 |
0.493 |
|
| 2022 |
Stockdale TP, Lam NYS, Paterson I. A synthesis-enabled relative configurational assignment of the C31-C46 region of hemicalide. Chemical Communications (Cambridge, England). PMID 35445225 DOI: 10.1039/d2cc01802k |
0.303 |
|
| 2020 |
Ndukwe IE, Wang X, Lam NYS, Ermanis K, Alexander KL, Bertin MJ, Martin GE, Muir G, Paterson I, Britton R, Goodman JM, Helfrich EJN, Piel J, Gerwick WH, Williamson RT. Synergism of anisotropic and computational NMR methods reveals the likely configuration of phormidolide A. Chemical Communications (Cambridge, England). PMID 32520016 DOI: 10.1039/D0Cc03055D |
0.641 |
|
| 2020 |
Pettigrew TR, Porter RJ, Walsh SJ, Housden MP, Lam NYS, Carroll JS, Parker JS, Spring DR, Paterson I. Total synthesis and biological evaluation of simplified aplyronine analogues as synthetically tractable anticancer agents. Chemical Communications (Cambridge, England). PMID 31922172 DOI: 10.1039/C9Cc09050A |
0.8 |
|
| 2019 |
Anketell M, Sharrock T, Paterson I. A Unified Total Synthesis of the Actinoallolides, a Family of Potent Anti-trypanosomal Macrolides. Angewandte Chemie (International Ed. in English). PMID 31743574 DOI: 10.1002/Anie.201914042 |
0.422 |
|
| 2019 |
Lam NYS, Muir G, Challa VR, Britton R, Paterson I. A counterintuitive stereochemical outcome from a chelation-controlled vinylmetal aldehyde addition leads to the configurational reassignment of phormidolide A. Chemical Communications (Cambridge, England). PMID 31353378 DOI: 10.1039/C9Cc05067A |
0.589 |
|
| 2019 |
Lam NYS, Paterson I. Stereocontrolled Synthesis as an Enabling Tool for the Configurational Assignment of Marine Polyketide Natural Products European Journal of Organic Chemistry. 2020: 2310-2320. DOI: 10.1002/Ejoc.201901243 |
0.366 |
|
| 2018 |
Phillips AW, Anketell MJ, Balan T, Lam NYS, Williams S, Paterson I. Toward the total synthesis of patellazole B: synthesis of an advanced C1-C25 fragment corresponding to the macrocyclic skeleton. Organic & Biomolecular Chemistry. PMID 30209471 DOI: 10.1039/C8Ob01621F |
0.491 |
|
| 2018 |
Han BY, Lam NYS, MacGregor CI, Goodman JM, Paterson I. A synthesis-enabled relative stereochemical assignment of the C1-C28 region of hemicalide. Chemical Communications (Cambridge, England). PMID 29536067 DOI: 10.1039/C8Cc00933C |
0.601 |
|
| 2018 |
Anžiček N, Williams S, Housden MP, Paterson I. Toward aplyronine payloads for antibody-drug conjugates: total synthesis of aplyronines A and D. Organic & Biomolecular Chemistry. PMID 29393939 DOI: 10.1039/C7Ob03204H |
0.809 |
|
| 2017 |
Paterson I, Lam NYS. Challenges and discoveries in the total synthesis of complex polyketide natural products. The Journal of Antibiotics. PMID 29066790 DOI: 10.1038/Ja.2017.111 |
0.365 |
|
| 2016 |
Williams S, Jin J, Kan SB, Li M, Gibson LJ, Paterson I. An Expedient Total Synthesis of Chivosazole F: an Actin-Binding Antimitotic Macrolide from the Myxobacterium Sorangium Cellulosum. Angewandte Chemie (International Ed. in English). PMID 27897365 DOI: 10.1002/Anie.201610636 |
0.385 |
|
| 2016 |
MacGregor CI, Han BY, Goodman JM, Paterson I. Toward the stereochemical assignment and synthesis of hemicalide: DP4f GIAO-NMR analysis and synthesis of a reassigned C16-C28 subunit. Chemical Communications (Cambridge, England). PMID 26948938 DOI: 10.1039/C6Cc01074A |
0.594 |
|
| 2016 |
Paterson I, Williams S. Strategy Evolution in the Total Synthesis of (−)-Leiodermatolide Israel Journal of Chemistry. 57: 192-201. DOI: 10.1002/Ijch.201600084 |
0.454 |
|
| 2015 |
Paterson I, Housden MP, Cordier CJ, Burton PM, Mühlthau FA, Loiseleur O. Synthetic studies toward the brasilinolides: controlled assembly of a protected C1-C38 polyol based on fragment union by complex aldol reactions. Organic & Biomolecular Chemistry. 13: 5716-33. PMID 25900249 DOI: 10.1039/C5Ob00498E |
0.818 |
|
| 2014 |
Pereira JH, Petchprayoon C, Hoepker AC, Moriarty NW, Fink SJ, Cecere G, Paterson I, Adams PD, Marriott G. Structural and biochemical studies of actin in complex with synthetic macrolide tail analogues. Chemmedchem. 9: 2286-93. PMID 25047814 DOI: 10.1002/Cmdc.201402150 |
0.561 |
|
| 2014 |
Paterson I, Xuan M, Dalby SM. Total synthesis of jiadifenolide. Angewandte Chemie (International Ed. in English). 53: 7286-9. PMID 24861364 DOI: 10.1002/Anie.201404224 |
0.472 |
|
| 2014 |
Paterson I, Ng KK, Williams S, Millican DC, Dalby SM. Total synthesis of the antimitotic marine macrolide (-)-leiodermatolide. Angewandte Chemie (International Ed. in English). 53: 2692-5. PMID 24481746 DOI: 10.1002/Anie.201310164 |
0.442 |
|
| 2013 |
Kan SB, Ng KK, Paterson I. The impact of the Mukaiyama aldol reaction in total synthesis. Angewandte Chemie (International Ed. in English). 52: 9097-108. PMID 23893491 DOI: 10.1002/Anie.201303914 |
0.386 |
|
| 2013 |
Paterson I, Fink SJ, Lee LY, Atkinson SJ, Blakey SB. Total synthesis of aplyronine C. Organic Letters. 15: 3118-21. PMID 23730909 DOI: 10.1021/Ol401327R |
0.79 |
|
| 2013 |
Dalby SM, Goodwin-Tindall J, Paterson I. Total synthesis of (-)-rhizopodin. Angewandte Chemie (International Ed. in English). 52: 6517-21. PMID 23650089 DOI: 10.1002/Anie.201301978 |
0.308 |
|
| 2013 |
Paterson I, Haslett GW. Synthesis of the C1-C11 western fragment of madeirolide A. Organic Letters. 15: 1338-41. PMID 23451996 DOI: 10.1021/Ol400280B |
0.507 |
|
| 2013 |
Paterson I, Maltas P, Anderson EA. Total synthesis of (+)-spirastrellolide a methyl ester: Challenges and discoveries Pure and Applied Chemistry. 85: 1133-1147. DOI: 10.1351/Pac-Con-13-01-01 |
0.38 |
|
| 2012 |
Xuan M, Paterson I, Dalby SM. Total synthesis of alotaketal A. Organic Letters. 14: 5492-5. PMID 23094646 DOI: 10.1021/Ol302570K |
0.395 |
|
| 2012 |
Paterson I, Anderson EA, Dalby SM, Lim JH, Maltas P. The stereocontrolled total synthesis of spirastrellolide A methyl ester. Fragment coupling studies and completion of the synthesis. Organic & Biomolecular Chemistry. 10: 5873-86. PMID 22504907 DOI: 10.1039/C2Ob25101A |
0.488 |
|
| 2012 |
Paterson I, Anderson EA, Dalby SM, Lim JH, Maltas P, Loiseleur O, Genovino J, Moessner C. The stereocontrolled total synthesis of spirastrellolide A methyl ester. Expedient construction of the key fragments. Organic & Biomolecular Chemistry. 10: 5861-72. PMID 22504866 DOI: 10.1039/C2Ob25100K |
0.472 |
|
| 2012 |
Paterson I, Maltas P, Dalby SM, Lim JH, Anderson EA. A second-generation total synthesis of spirastrellolide A methyl ester. Angewandte Chemie (International Ed. in English). 51: 2749-53. PMID 22311730 DOI: 10.1002/Anie.201108594 |
0.481 |
|
| 2011 |
Paterson I, Paquet T, Dalby SM. Synthesis of the macrocyclic core of leiodermatolide. Organic Letters. 13: 4398-401. PMID 21755949 DOI: 10.1021/Ol2017388 |
0.49 |
|
| 2011 |
Singh AJ, Razzak M, Teesdale-Spittle P, Gaitanos TN, Wilmes A, Paterson I, Goodman JM, Miller JH, Northcote PT. Structure-activity studies of the pelorusides: new congeners and semi-synthetic analogues. Organic & Biomolecular Chemistry. 9: 4456-66. PMID 21512693 DOI: 10.1039/C0Ob01127D |
0.518 |
|
| 2011 |
Paterson I, Naylor GJ, Gardner NM, Guzmán E, Wright AE. Total synthesis and biological evaluation of a series of macrocyclic hybrids and analogues of the antimitotic natural products dictyostatin, discodermolide, and taxol. Chemistry, An Asian Journal. 6: 459-73. PMID 21254424 DOI: 10.1002/Asia.201000541 |
0.439 |
|
| 2011 |
Paterson I, Steadman Neé Doughty VA, McLeod MD, Trieselmann T. Stereocontrolled total synthesis of (+)-concanamycin F: The strategic use of boron-mediated aldol reactions of chiral ketones Tetrahedron. 67: 10119-10128. DOI: 10.1016/J.Tet.2011.09.012 |
0.502 |
|
| 2011 |
Paterson I, Dalby SM, Maltas P. Strategy evolution in the total synthesis of SpirastrellolideA methyl ester Israel Journal of Chemistry. 51: 406-419. DOI: 10.1002/Ijch.201100007 |
0.513 |
|
| 2010 |
Paterson I, Gibson LJ, Kan SB. Synthesis of the C15-C35 northern hemisphere subunit of the chivosazoles. Organic Letters. 12: 5530-3. PMID 21043512 DOI: 10.1021/Ol102425N |
0.4 |
|
| 2010 |
Paterson I, Kan SB, Gibson LJ. Synthesis of the C1-C13 tetraenoate subunit of the chivosazoles. Organic Letters. 12: 3724-7. PMID 20704420 DOI: 10.1021/Ol101630P |
0.434 |
|
| 2010 |
Paterson I, Paquet T. Total synthesis and configurational validation of (+)-phorbaside A. Organic Letters. 12: 2158-61. PMID 20387889 DOI: 10.1021/Ol100693C |
0.455 |
|
| 2010 |
Paterson I, Naylor GJ, Fujita T, Guzmán E, Wright AE. Total synthesis of a library of designed hybrids of the microtubule-stabilising anticancer agents taxol, discodermolide and dictyostatin. Chemical Communications (Cambridge, England). 46: 261-3. PMID 20024345 DOI: 10.1039/B921237J |
0.34 |
|
| 2010 |
Paterson I, Rubenbauer P. Synthetic studies towards iriomoteolide 1a: Stereocontrolled construction of C1-C9 and C11-C23 segments using lactate aldol chemistry Synlett. 571-574. DOI: 10.1055/S-0029-1219347 |
0.406 |
|
| 2010 |
Smith SG, Channon JA, Paterson I, Goodman JM. The stereochemical assignment of acyclic polyols: A computational study of the NMR data of a library of stereopentad sequences from polyketide natural products Tetrahedron. 66: 6437-6444. DOI: 10.1016/J.Tet.2010.06.022 |
0.488 |
|
| 2010 |
Paterson I, Britton R, Delgado O, Gardner NM, Meyer A, Naylor GJ, Poullennec KG. Total synthesis of (-)-dictyostatin, a microtubule-stabilising anticancer macrolide of marine sponge origin Tetrahedron. 66: 6534-6545. DOI: 10.1016/J.Tet.2010.01.083 |
0.644 |
|
| 2010 |
Paterson I, Coster MJ. ChemInform Abstract: Total Synthesis of Altohyrtin A (Spongistatin 1): An Alternative Synthesis of the CD-Spiroacetal Subunit (I). Cheminform. 33: no-no. DOI: 10.1002/CHIN.200234257 |
0.652 |
|
| 2010 |
Paterson I, Florence GJ, Gerlach K, Scott JP, Sereinig N. ChemInform Abstract: A Practical Synthesis of (+)-Discodermolide and Analogues: Fragment Union by Complex Aldol Reactions. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200204240 |
0.308 |
|
| 2010 |
Paterson I, Doughty VA, Florence G, Gerlach K, McLeod MD, Scott JP, Trieselmann T. ChemInform Abstract: Asymmetric Aldol Reactions Using Boron Enolates: Applications to Polyketide Synthesis Cheminform. 32: no-no. DOI: 10.1002/CHIN.200143281 |
0.356 |
|
| 2010 |
Paterson I, Florence GJ, Gerlach K, Scott JP. ChemInform Abstract: Total Synthesis of the Antimicrotubule Agent (+)-Discodermolide Using Boron-Mediated Aldol Reactions of Chiral Ketones. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200013215 |
0.368 |
|
| 2010 |
Paterson I, Doughty VA. ChemInform Abstract: Anti-Aldol Reactions of Lactate-Derived Ketones. Application to the Synthesis of (-)-Tetrahydrolipstatin. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199916252 |
0.342 |
|
| 2010 |
PATERSON I, WALLACE DJ, OBALLA RM. ChemInform Abstract: Studies in Marine Macrolide Synthesis: Synthesis of a Fully Functionalized C1-C28 Subunit of Spongistatin 1 (Altohyrtin A). Cheminform. 30: no-no. DOI: 10.1002/CHIN.199906228 |
0.364 |
|
| 2010 |
PATERSON I, WATSON C, YEUNG K, WARD RA, WALLACE PA. ChemInform Abstract: The Total Synthesis of Scytophycin C. Part 2. Synthesis of Scytophycin C from the Protected Seco Acid. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199903220 |
0.368 |
|
| 2010 |
PATERSON I, YEUNG K, WATSON C, WARD RA, WALLACE PA. ChemInform Abstract: The Total Synthesis of Scytophycin C. Part 1. Stereocontrolled Synthesis of the C1-C32 Protected Seco Acid. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199903219 |
0.347 |
|
| 2010 |
PATERSON I, ARNOTT EA. ChemInform Abstract: Towards the Total Synthesis of Phorboxazoles A and B: Stereocontrolled Synthesis of a C20-C32 Subunit. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199851287 |
0.355 |
|
| 2010 |
PATERSON I, WOODROW MD, COWDEN CJ. ChemInform Abstract: Studies in Marine Macrolide Synthesis: Construction of a 24-Membered Macrocyclic Intermediate for Aplyronine A. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199844262 |
0.348 |
|
| 2010 |
PATERSON I, COWDEN CJ, WOODROW MD. ChemInform Abstract: Studies in Marine Macrolide Synthesis: Stereocontrolled Synthesis of the C1-C11 and C15-C27 Subunits of Aplyronine A. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199844261 |
0.321 |
|
| 2010 |
PATERSON I, WALLACE DJ, COWDEN CJ. ChemInform Abstract: Polyketide Synthesis Using the Boron-Mediated, anti-Aldol Reactions of Lactate-Derived Ketones: Total Synthesis of (-)-ACRL Toxin IIIB. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199830283 |
0.39 |
|
| 2010 |
PATERSON I, WALLACE DJ, GIBSON KR. ChemInform Abstract: Studies in Marine Macrolide Synthesis: Synthesis of a C16-C28 Subunit of Spongistatin 1 (Altohyrtin A) Incorporating the CD-Spiroacetal Moiety. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199812232 |
0.336 |
|
| 2010 |
PATERSON I, OBALLA RM. ChemInform Abstract: Studies in Marine Macrolide Synthesis: Synthesis of the C1-C15 Subunit of Spongistatin 1 (Altohyrtin A) and 15,16-anti Aldol Coupling Reactions. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199808223 |
0.416 |
|
| 2010 |
PATERSON I, MCLEOD MD. ChemInform Abstract: Studies in Macrolide Synthesis: Stereocontrolled Synthesis of a C1-C13 Segment of Concanamycin A. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199738283 |
0.359 |
|
| 2010 |
PATERSON I, WATSON C, YEUNG K, WALLACE PA, WARD RA. ChemInform Abstract: Total Synthesis of Scytophycin C. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199723271 |
0.377 |
|
| 2010 |
PATERSON I, MAN J. ChemInform Abstract: Studies in Macrolide Synthesis: A Novel Cyclodimerization Approach to the Synthesis of Elaiophylin Using a Double Stille Cross-Coupling Reaction. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199717242 |
0.335 |
|
| 2010 |
PATERSON I, OBALLA RM, NORCROSS RD. ChemInform Abstract: Studies in Marine Macrolide Synthesis: Stereocontrolled Synthesis of the AB-Spiroacetal Subunit of Spongistatin 1 (Altohyrtin A). Cheminform. 28: no-no. DOI: 10.1002/CHIN.199712225 |
0.343 |
|
| 2010 |
PATERSON I, NOWAK T. ChemInform Abstract: anti Aldol Reactions of α-Alkoxymethyl Ketones: Application to the Total Synthesis of (+)-Restricticin. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199707278 |
0.313 |
|
| 2010 |
PATERSON I, MCLEOD MD. ChemInform Abstract: Studies in Macrolide Synthesis: A Sequential Aldol/Glycosylation Approach to the Synthesis of Concanamycin A. Cheminform. 27: no-no. DOI: 10.1002/CHIN.199613271 |
0.335 |
|
| 2010 |
NORCROSS RD, PATERSON I. ChemInform Abstract: Total Synthesis of Bioactive Marine Macrolides Cheminform. 27: no-no. DOI: 10.1002/CHIN.199605313 |
0.339 |
|
| 2010 |
PATERSON I, WARD RA, SMITH JD, CUMMING JG, YEUNG K. ChemInform Abstract: The Total Synthesis of Swinholide A. Part 3. A Stereocontrolled Synthesis of (-)-Pre-Swinholide A. Cheminform. 26: no-no. DOI: 10.1002/CHIN.199551287 |
0.355 |
|
| 2010 |
PATERSON I, SMITH JD, WARD RA. ChemInform Abstract: The Total Synthesis of Swinholide A. Part 2. A Stereocontrolled Synthesis of a C1-C15 Segment. Cheminform. 26: no-no. DOI: 10.1002/CHIN.199551286 |
0.358 |
|
| 2010 |
PATERSON I, SCHLAPBACH A. ChemInform Abstract: Studies Towards the Total Synthesis of the Marine-Derived Immunosuppressant Discodermolide: Stereoselective Synthesis of a C9- C24 Subunit. Cheminform. 26: no-no. DOI: 10.1002/CHIN.199539273 |
0.397 |
|
| 2010 |
PATERSON I, NORCROSS RD, WARD RA, ROMEA P, LISTER MA. ChemInform Abstract: Macrolide Synthesis: A Stereocontrolled Synthesis of Oleandolide Employing Reagent- and Substrate-Controlled Aldol Reactions of (S)-1-( Benzyloxy)-2-methylpentan-3-one. Cheminform. 26: no-no. DOI: 10.1002/CHIN.199521283 |
0.355 |
|
| 2010 |
PATERSON I, WALLACE DJ. ChemInform Abstract: anti Aldol Reactions of Lactate-Derived Ketones: Application to the Total Synthesis of (-)-ACRL Toxin IIIB. Cheminform. 26: no-no. DOI: 10.1002/CHIN.199519238 |
0.345 |
|
| 2010 |
PATERSON I, YEUNG K, WARD RA, CUMMING JG, SMITH JD. ChemInform Abstract: Total Synthesis of Swinholide A and Hemiswinholide A. Cheminform. 26: no-no. DOI: 10.1002/CHIN.199517241 |
0.338 |
|
| 2010 |
PATERSON I, WALLACE DJ. ChemInform Abstract: Manipulation of the Aldol Adducts from Lactate-Derived Ketones. A Versatile Chiral Auxiliary for the Asymmetric Synthesis of β- Hydroxy Carbonyl Compounds. Cheminform. 26: no-no. DOI: 10.1002/CHIN.199517032 |
0.305 |
|
| 2010 |
PATERSON I, WALLACE DJ, VELAZQUEZ SM. ChemInform Abstract: Studies in Polypropionate Synthesis: High π-Face Selectivity in syn and anti Aldol Reactions of Chiral Boron Enolates of Lactate-Derived Ketones. Cheminform. 26: no-no. DOI: 10.1002/CHIN.199517031 |
0.354 |
|
| 2010 |
PATERSON I, CUMMING JG, SMITH JD, WARD RA, YEUNG K. ChemInform Abstract: Towards the Synthesis of Swinholide A and Scytophycin C. A Highly Stereocontrolled Synthesis of (-)-Pre-Swinholide A. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199438284 |
0.418 |
|
| 2010 |
PATERSON I, WARD RA, ROMEA P, NORCROSS RD. ChemInform Abstract: Substrate-Controlled Aldol Reactions of Chiral Ethyl Ketones: Application to the Total Synthesis of Oleandomycin. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199434266 |
0.346 |
|
| 2010 |
PATERSON I, WREN SP. ChemInform Abstract: Studies Towards the Total Synthesis of the Marine-Derived Immunosuppressant Discodermolide; Asymmetric Synthesis of a C1-C8 . delta.-Lactone Subunit. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199420297 |
0.398 |
|
| 2010 |
PATERSON I, SMITH JD. ChemInform Abstract: Studies in Marine Macrolide Synthesis: Asymmetric Synthesis of C1-C15/ C16 Subunits of Swinholide A and Scytophycin C. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199402288 |
0.328 |
|
| 2010 |
PATERSON I, YEUNG K. ChemInform Abstract: Studies in Marine Macrolide Synthesis: A Stereocontrolled Synthesis of a C17-C32 Subunit of Scytophycin C. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199402287 |
0.344 |
|
| 2010 |
PATERSON I, TILLYER RD. ChemInform Abstract: High π-Face Selectivity in Anti-Aldol Reactions of E-Enol Borinates from Chiral Alkoxymethyl Ketones: Stereocontrolled Synthesis of a C24- C32 Polyol Subunit (I) of Rapamycin. Cheminform. 24: no-no. DOI: 10.1002/CHIN.199349063 |
0.388 |
|
| 2010 |
GOODMAN JM, PATERSON I. ChemInform Abstract: Enolization of Ketones by Dialkylboron Chlorides and Triflates: A Model for the Effect of Reagent Leaving Group, Substrate Structure, and Amine Base. Cheminform. 24: no-no. DOI: 10.1002/CHIN.199316065 |
0.489 |
|
| 2010 |
GENNARI C, HEWKIN CT, MOLINARI F, BERNARDI A, COMOTTI A, GOODMAN JM, PATERSON I. ChemInform Abstract: The Rational Design of Highly Stereoselective Boron Enolates Using Transition-State Computer Modeling: A Novel, Asymmetric Anti Aldol Reaction for Ketones. Cheminform. 24: no-no. DOI: 10.1002/CHIN.199302068 |
0.524 |
|
| 2010 |
PATERSON I, HULME AN, WALLACE DJ. ChemInform Abstract: Stereocontrolled, Two-Directional, Chain Synthesis Using the Boron Aldol Reaction and Double Ireland-Claisen Rearrangement. Cheminform. 23: no-no. DOI: 10.1002/CHIN.199231092 |
0.331 |
|
| 2010 |
PATERSON I, LISTER MA, RYAN GR. ChemInform Abstract: Asymmetric Aldol Reactions Using Chiral Boron Reagents: Application to the Synthesis of Tirandamycin A. Cheminform. 23: no-no. DOI: 10.1002/CHIN.199203087 |
0.367 |
|
| 2010 |
PATERSON I, OSBORNE S. ChemInform Abstract: Stereoselective Aldol Reactions of β-Chlorovinyl Ketones Using Dienol Borinate: A New Synthesis of Dihydropyrones. Cheminform. 22: no-no. DOI: 10.1002/CHIN.199111180 |
0.304 |
|
| 2009 |
Paterson I, Florence GJ. The chemical synthesis of discodermolide. Topics in Current Chemistry. 286: 73-119. PMID 23563611 DOI: 10.1007/128_2008_7 |
0.371 |
|
| 2009 |
Paterson I, Dalby SM. Synthesis and stereochemical determination of the spirastrellolides. Natural Product Reports. 26: 865-73. PMID 19554238 DOI: 10.1039/B906991G |
0.44 |
|
| 2009 |
Paterson I, Findlay AD, Noti C. Total synthesis of (-)-spirangien A, an antimitotic polyketide isolated from the myxobacterium Sorangium cellulosum. Chemistry, An Asian Journal. 4: 594-611. PMID 19173216 DOI: 10.1002/Asia.200800445 |
0.487 |
|
| 2009 |
Paterson I, Burton PM, Cordier CJ, Housden MP, Mühlthau FA, Loiseleur O. Toward the total synthesis of the brasilinolides: construction of a differentially protected C20-C38 segment. Organic Letters. 11: 693-6. PMID 19123806 DOI: 10.1021/Ol802769E |
0.81 |
|
| 2009 |
Paterson I, Mühlthau FA, Cordier CJ, Housden MP, Burton PM, Loiseleur O. Toward the total synthesis of the brasilinolides: stereocontrolled assembly of a C1-C19 polyol segment. Organic Letters. 11: 353-6. PMID 19072327 DOI: 10.1021/Ol802562B |
0.8 |
|
| 2009 |
Paterson I, Gardner NM, Guzmán E, Wright AE. Total synthesis and biological evaluation of novel C2-C6 region analogues of dictyostatin. Bioorganic & Medicinal Chemistry. 17: 2282-9. PMID 19022679 DOI: 10.1016/J.Bmc.2008.10.084 |
0.407 |
|
| 2009 |
Paterson I, Gardner NM, Naylor GJ. Total synthesis of novel dictyostatin analogs and hybrids as microtubule-stabilizing anticancer agents Pure and Applied Chemistry. 81: 169-180. DOI: 10.1351/Pac-Con-08-09-17 |
0.439 |
|
| 2009 |
Paterson I, Findlay AD. Recent advances in the total synthesis of polyketide natural products as promising anticancer agents Australian Journal of Chemistry. 62: 624-638. DOI: 10.1071/Ch09104 |
0.396 |
|
| 2009 |
Paterson I, Razzak M, Anderson EA. Synthesis of Saliniketal B Synfacts. 2009: 123-123. DOI: 10.1055/S-0028-1087610 |
0.338 |
|
| 2008 |
Paterson I, Findlay AD, Noti C. Total synthesis of (-)-spirangien A and its methyl ester. Chemical Communications (Cambridge, England). 6408-10. PMID 19048171 DOI: 10.1039/B816229H |
0.41 |
|
| 2008 |
Paterson I, Gardner NM, Guzmán E, Wright AE. Total synthesis and biological evaluation of potent analogues of dictyostatin: modification of the C2-C6 dienoate region. Bioorganic & Medicinal Chemistry Letters. 18: 6268-72. PMID 18951787 DOI: 10.1016/J.Bmcl.2008.09.109 |
0.39 |
|
| 2008 |
Paterson I, Miller NA. Total synthesis of the marine macrolide (+)-neopeltolide. Chemical Communications (Cambridge, England). 4708-10. PMID 18830467 DOI: 10.1039/B812914B |
0.483 |
|
| 2008 |
Paterson I, Razzak M, Anderson EA. Total synthesis of (-)-saliniketals A and B. Organic Letters. 10: 3295-8. PMID 18578531 DOI: 10.1021/Ol801148D |
0.417 |
|
| 2008 |
Florence GJ, Gardner NM, Paterson I. Development of practical syntheses of the marine anticancer agents discodermolide and dictyostatin Natural Product Reports. 25: 342-375. PMID 18389141 DOI: 10.1039/B705661N |
0.373 |
|
| 2008 |
Paterson I, Anderson EA, Dalby SM, Lim JH, Genovino J, Maltas P, Moessner C. Total synthesis of spirastrellolide A methyl ester--part 2: Subunit union and completion of the synthesis. Angewandte Chemie (International Ed. in English). 47: 3021-5. PMID 18307179 DOI: 10.1002/Anie.200705566 |
0.426 |
|
| 2008 |
Paterson I, Anderson EA, Dalby SM, Lim JH, Genovino J, Maltas P, Moessner C. Total synthesis of spirastrellolide A methyl ester--part 1: Synthesis of an advanced C17-C40 bis-spiroacetal subunit. Angewandte Chemie (International Ed. in English). 47: 3016-20. PMID 18307178 DOI: 10.1002/Anie.200705565 |
0.479 |
|
| 2008 |
Paterson I, Ashton K, Britton R, Cecere G, Chouraqui G, Florence GJ, Knust H, Stafford J. Total synthesis of (-)-reidispongiolide A, an actin-targeting macrolide isolated from the marine sponge Reidispongia coerulea. Chemistry, An Asian Journal. 3: 367-87. PMID 18181126 DOI: 10.1002/Asia.200700357 |
0.802 |
|
| 2008 |
Paterson I, Gardner NM, Poullennec KG, Wright AE. Synthesis and biological evaluation of 10,11-dihydrodictyostatin, a potent analogue of the marine anticancer agent dictyostatin. Journal of Natural Products. 71: 364-9. PMID 18081257 DOI: 10.1021/Np070547S |
0.346 |
|
| 2008 |
Paterson I, Findlay AD. Total synthesis of cytotoxic marine macrolides: Callipeltoside A, aurisides A and B, and dolastatin 19 Pure and Applied Chemistry. 80: 1773-1782. DOI: 10.1351/Pac200880081773 |
0.4 |
|
| 2008 |
Paterson I, Anderson EA, Dalby SM, Lim JH, Genovino J, Maltas P, Moessner C. Synthesis of Spirastrellolide A Methyl Ester Synfacts. 2008: 901-901. DOI: 10.1055/S-2008-1077983 |
0.377 |
|
| 2008 |
Paterson I, Anderson EA, Findlay AD, Knappy CS. Total synthesis of pteridic acids A and B Tetrahedron. 64: 4768-4777. DOI: 10.1016/J.Tet.2008.01.132 |
0.362 |
|
| 2008 |
Paterson I. ChemInform Abstract: Total Synthesis of Polyketides Using Asymmetric Aldol Reactions Cheminform. 39. DOI: 10.1002/CHIN.200802253 |
0.366 |
|
| 2008 |
Paterson I, Berrisford DJ. Epoxides in asymmetric synthesis: Enantioselective opening by nucleophiles promoted by chiral transition metal complexes Organic Synthesis Highlights Iii. 62-66. DOI: 10.1002/9783527620784.Ch11B |
0.379 |
|
| 2008 |
Paterson I, Berrisford DJ. Epoxides in Asymmetric Synthesis: Enantioselective Opening by Nucleophiles Promoted by Chiral Transition Metal Complexes Organic Synthesis Set. 62-66. DOI: 10.1002/9783527620784.ch11b |
0.737 |
|
| 2007 |
Paterson I, Findlay AD, Anderson EA. Synthesis of an advanced C10-C32 spiroacetal fragment and assignment of the absolute configuration of spirangien A. Angewandte Chemie (International Ed. in English). 46: 6699-702. PMID 17665392 DOI: 10.1002/Anie.200702735 |
0.434 |
|
| 2007 |
Paterson I, Ashton K, Britton R, Cecere G, Chouraqui G, Florence GJ, Stafford J. Total synthesis of (-)-reidispongiolide A, an actin-targeting marine macrolide. Angewandte Chemie (International Ed. in English). 46: 6167-71. PMID 17615611 DOI: 10.1002/Anie.200702178 |
0.789 |
|
| 2007 |
Paterson I, Anderson EA, Dalby SM, Genovino J, Lim JH, Moessner C. Synthesis of two diastereomeric C1-C22 fragments of spirastrellolide A. Chemical Communications (Cambridge, England). 1852-4. PMID 17476409 DOI: 10.1039/B700827A |
0.435 |
|
| 2007 |
Paterson I, Gardner NM, Poullennec KG, Wright AE. Synthesis and biological evaluation of novel analogues of dictyostatin. Bioorganic & Medicinal Chemistry Letters. 17: 2443-7. PMID 17336522 DOI: 10.1016/J.Bmcl.2007.02.031 |
0.328 |
|
| 2007 |
Paterson I, Florence GJ, Heimann AC, Mackay AC. Stereocontrolled total synthesis of (-)-aurisides A and B. Angewandte Chemie (International Ed. in English). 44: 1130-3. PMID 15666414 DOI: 10.1002/Anie.200462267 |
0.35 |
|
| 2007 |
Paterson I, Anderson EA, Dalby SM, Lim JH, Loiseleur O, Maltas P, Moessner C. Progress toward a total synthesis of spirastrellolide A Pure and Applied Chemistry. 79: 667-676. DOI: 10.1351/Pac200779040667 |
0.474 |
|
| 2007 |
Paterson I, Findlay AD, Florence GJ. Total synthesis and stereochemical reassignment of (+)-dolastatin 19, a cytotoxic marine macrolide isolated from Dolabella auricularia Tetrahedron. 63: 5806-5819. DOI: 10.1016/J.Tet.2007.01.048 |
0.501 |
|
| 2006 |
Paterson I, Anderson EA, Dalby SM, Lim JH, Maltas P, Moessner C. Synthesis of the DEF-bis-spiroacetal of spirastrellolide A exploiting a double asymmetric dihydroxylation/spiroacetalisation strategy. Chemical Communications (Cambridge, England). 4186-8. PMID 17031426 DOI: 10.1039/B612697A |
0.484 |
|
| 2006 |
Paterson I, Findlay AD, Florence GJ. Total synthesis and stereochemical reassignment of (+)-dolastatin 19. Organic Letters. 8: 2131-4. PMID 16671799 DOI: 10.1021/Ol060609Q |
0.485 |
|
| 2006 |
Paterson I, Lyothier I. Total synthesis of (+)-discodermolide: an improved endgame exploiting a Still-Gennari-type olefination with a C1-C8 beta-ketophosphonate fragment. Organic Letters. 6: 4933-6. PMID 15606103 DOI: 10.1021/Ol0478842 |
0.446 |
|
| 2006 |
Paterson I, Anderson EA, Dalby SM, Loiseleur O. Toward the Synthesis of Spirastrellolide A: Construction of Two C1—C25 Diastereomers Containing the BC—Spiroacetal. Cheminform. 37. DOI: 10.1002/CHIN.200601211 |
0.312 |
|
| 2005 |
Yeung KS, Paterson I. Advances in the total synthesis of biologically important marine macrolides. Chemical Reviews. 105: 4237-313. PMID 16351045 DOI: 10.1021/Cr040614C |
0.395 |
|
| 2005 |
Paterson I, Anderson EA, Dalby SM, Loiseleur O. Toward the synthesis of spirastrellolide A: construction of two C1-C25 diastereomers containing the BC-spiroacetal. Organic Letters. 7: 4125-8. PMID 16146368 DOI: 10.1021/Ol051405X |
0.47 |
|
| 2005 |
Paterson I, Anderson EA, Dalby SM, Loiseleur O. Toward the synthesis of spirastrellolide a: construction of a tetracyclic C26-C40 subunit containing the DEF-bis-spiroacetal. Organic Letters. 7: 4121-4. PMID 16146367 DOI: 10.1021/Ol051403C |
0.48 |
|
| 2005 |
Paterson I, Gottschling D, Menche D. Towards the combinatorial synthesis of spongistatin fragment libraries by using asymmetric aldol reactions on solid support. Chemical Communications (Cambridge, England). 3568-70. PMID 16010326 DOI: 10.1039/B505746A |
0.674 |
|
| 2005 |
Paterson I, Lyothier I. Development of a third-generation total synthesis of (+)-discodermolide: an expedient Still-Gennari-type fragment coupling utilizing an advanced beta-ketophosphonate. The Journal of Organic Chemistry. 70: 5494-507. PMID 15989331 DOI: 10.1021/JO050481A |
0.377 |
|
| 2005 |
Paterson I, Chen DY, Coster MJ, Aceña JL, Bach J, Wallace DJ. The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: fragment couplings, completion of the synthesis, analogue generation and biological evaluation. Organic & Biomolecular Chemistry. 3: 2431-40. PMID 15976860 DOI: 10.1039/B504151A |
0.74 |
|
| 2005 |
Paterson I, Coster MJ, Chen DY, Aceña JL, Bach J, Keown LE, Trieselmann T. The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: the southern hemisphere EF segment. Organic & Biomolecular Chemistry. 3: 2420-30. PMID 15976859 DOI: 10.1039/B504149J |
0.721 |
|
| 2005 |
Paterson I, Coster MJ, Chen DY, Gibson KR, Wallace DJ. The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: the CD-spiroacetal segment. Organic & Biomolecular Chemistry. 3: 2410-9. PMID 15976858 DOI: 10.1039/b504148a |
0.682 |
|
| 2005 |
Paterson I, Coster MJ, Chen DY, Oballa RM, Wallace DJ, Norcross RD. The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: the AB-spiroacetal segment. Organic & Biomolecular Chemistry. 3: 2399-409. PMID 15976857 DOI: 10.1039/B504146E |
0.754 |
|
| 2005 |
Paterson I, Menche D, Håkansson AE, Longstaff A, Wong D, Barasoain I, Buey RM, Díaz JF. Design, synthesis and biological evaluation of novel, simplified analogues of laulimalide: modification of the side chain. Bioorganic & Medicinal Chemistry Letters. 15: 2243-7. PMID 15837302 DOI: 10.1016/J.Bmcl.2005.03.018 |
0.579 |
|
| 2005 |
Paterson I, Delgado O, Florence GJ, Lyothier I, O'Brien M, Scott JP, Sereinig N. A second-generation total synthesis of (+)-discodermolide: the development of a practical route using solely substrate-based stereocontrol. The Journal of Organic Chemistry. 70: 150-60. PMID 15624917 DOI: 10.1021/Jo048534W |
0.527 |
|
| 2005 |
Paterson I, Chen D, Coster M, Aceña J, Bach J, Wallace D. Synthesis of Spongistatin 1 Synfacts. 2006: 0002-0002. DOI: 10.1055/S-2005-921666 |
0.718 |
|
| 2005 |
Paterson I, Anderson EA, Dalby SM. Synthesis of the C1-C21 southern hemisphere of the originally proposed structure of spirastrellolide A Synthesis. 3225-3228. DOI: 10.1055/S-2005-918449 |
0.446 |
|
| 2005 |
Paterson I, Delgado O, Florence GJ, Lyothier I, O’Brien M, Scott JP, Sereinig N. Synthesis of Discodermolide Using Solely Substrate-Based Stereocontrol Synfacts. 2005: 101-101. DOI: 10.1055/S-2005-872154 |
0.388 |
|
| 2005 |
Paterson I, Florence GJ, Heimann AC, MacKay AC. Total Synthesis of (-)-Aurisides A and B Synfacts. 2005: 6-6. DOI: 10.1055/S-2005-865342 |
0.343 |
|
| 2005 |
Paterson I, Menche D, Britton R, Håkansson AE, Silva-Martínez MA. Conformational studies and solution structure of laulimalide and simplified analogues using NMR spectroscopy and molecular modelling Tetrahedron Letters. 46: 3677-3682. DOI: 10.1016/J.Tetlet.2005.03.149 |
0.645 |
|
| 2005 |
Paterson I, Lyothier I. Total Synthesis of (+)-Discodermolide: An Improved Endgame Exploiting a Still?Gennari-Type Olefination with a C1?C8 ?-Ketophosphonate Fragment. Cheminform. 36. DOI: 10.1002/CHIN.200519227 |
0.307 |
|
| 2004 |
Paterson I, Steven A, Luckhurst CA. Phorboxazole B synthetic studies: construction of C(1-32) and C(33-46) subtargets. Organic & Biomolecular Chemistry. 2: 3026-38. PMID 15480468 DOI: 10.1039/B407240E |
0.484 |
|
| 2004 |
Paterson I, Britton R, Delgado O, Meyer A, Poullennec KG. Total synthesis and configurational assignment of (-)-dictyostatin, a microtubule-stabilizing macrolide of marine sponge origin. Angewandte Chemie (International Ed. in English). 43: 4629-33. PMID 15317000 DOI: 10.1002/Anie.200460589 |
0.567 |
|
| 2004 |
Paterson I, Britton R, Ashton K, Knust H, Stafford J. Synthesis of antimicrofilament marine macrolides: Synthesis and configurational assignment of a C5-C16 degradation fragment of reidispongiolide A Proceedings of the National Academy of Sciences of the United States of America. 101: 11986-11991. PMID 15201432 DOI: 10.1073/Pnas.0401548101 |
0.628 |
|
| 2004 |
Paterson I, Bergmann H, Menche D, Berkessel A. Synthesis of novel 11-desmethyl analogues of laulimalide by Nozaki-Kishi coupling. Organic Letters. 6: 1293-5. PMID 15070320 DOI: 10.1021/Ol049791Q |
0.739 |
|
| 2004 |
Paterson I, Britton R, Delgado O, Wright AE. Stereochemical determination of dictyostatin, a novel microtubule-stabilising macrolide from the marine sponge Corallistidae sp. Chemical Communications (Cambridge, England). 632-3. PMID 15010754 DOI: 10.1039/B316390C |
0.528 |
|
| 2004 |
Paterson I, Mackay AC. Studies Towards the Synthesis of Superstolide A: An Aldol-Based Construction of an Advanced C1-C5/C20-C26 Segment Synlett. 2004: 1359-1362. DOI: 10.1055/S-2004-825619 |
0.449 |
|
| 2004 |
Mickel SJ, Niederer D, Daeffler R, Osmani A, Kuesters E, Schmid E, Schaer K, Gamboni R, Chen W, Loeser E, Kinder FR, Konigsberger K, Prasad K, Ramsey TM, Repič O, ... ... Paterson I, et al. Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 5: Linkage of Fragments C1-6and C7-24and Finale Organic Process Research & Development. 8: 122-130. DOI: 10.1021/Op034134J |
0.451 |
|
| 2004 |
Mickel SJ, Sedelmeier GH, Niederer D, Schuerch F, Seger M, Schreiner K, Daeffler R, Osmani A, Bixel D, Loiseleur O, Cercus J, Stettler H, Schaer K, Gamboni R, Bach A, ... ... Paterson I, et al. Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 4: Preparation of Fragment C7-24 Organic Process Research & Development. 8: 113-121. DOI: 10.1021/Op034133R |
0.439 |
|
| 2004 |
Paterson I, Davies RDM, Heimann AC, Marquez R, Meyer A. Stereocontrolled Total Synthesis of (-)-Callipeltoside A. Cheminform. 35. DOI: 10.1002/CHIN.200413183 |
0.339 |
|
| 2004 |
Paterson I, Britton R, Delgado O, Meyer A, Poullennec KG, Shin Y, Fournier J, Fukui Y, Brückner AM, Curran DP. Cover Picture: Total Synthesis and Configurational Assignment of (−)-Dictyostatin, a Microtubule-Stabilizing Macrolide of Marine Sponge Origin / Total Synthesis of (−)-Dictyostatin: Confirmation of Relative and Absolute Configurations (Angew. Chem. Int. Ed. 35/2004) Angewandte Chemie International Edition. 43: 4537-4537. DOI: 10.1002/Anie.200490122 |
0.393 |
|
| 2004 |
Cowden CJ, Paterson I. Asymmetric Aldol Reactions Using Boron Enolates Organic Reactions. 1-200. DOI: 10.1002/0471264180.Or051.01 |
0.465 |
|
| 2003 |
Paterson I, Davies RD, Heimann AC, Marquez R, Meyer A. Stereocontrolled total synthesis of (-)-callipeltoside A. Organic Letters. 5: 4477-80. PMID 14602029 DOI: 10.1021/Ol0357853 |
0.515 |
|
| 2003 |
Paterson I, Ashton K, Britton R, Knust H. Toward the synthesis of reidispongiolide A: Stereocontrolled synthesis of the C17-C22 and C23-C35 degradation fragments Organic Letters. 5: 1963-1966. PMID 12762697 DOI: 10.1021/Ol034558Y |
0.621 |
|
| 2003 |
Toomes C, Jackson A, Maguire K, Wood J, Gollin S, Ishwad C, Paterson I, Prime S, Parkinson K, Bell S, Woods G, Markham A, Oliver R, Woodward R, Sloan P, et al. The presence of multiple regions of homozygous deletion at the CSMD1 locus in oral squamous cell carcinoma question the role of CSMD1 in head and neck carcinogenesis. Genes, Chromosomes & Cancer. 37: 132-40. PMID 12696061 DOI: 10.1002/Gcc.10191 |
0.406 |
|
| 2003 |
Paterson I, Aceña JL, Bach J, Chen DY, Coster MJ. Synthesis and biological evaluation of spongistatin/altohyrtin analogues: E-ring dehydration and C46 side-chain truncation. Chemical Communications (Cambridge, England). 462-3. PMID 12638950 |
0.66 |
|
| 2003 |
Berkessel A, Menche D, Sklorz CA, Schröder M, Paterson I. A highly enantioselective catalyst for the asymmetric Nozaki-Hiyama-Kishi reaction of allylic and vinylic halides. Angewandte Chemie (International Ed. in English). 42: 1032-5. PMID 12616559 DOI: 10.1002/Anie.200390265 |
0.696 |
|
| 2003 |
Paterson I, Di Francesco ME, Kühn T. Toward the synthesis of peloruside a: fragment synthesis and coupling studies. Organic Letters. 5: 599-602. PMID 12583779 DOI: 10.1021/Ol034035Q |
0.474 |
|
| 2003 |
Paterson I, Tudge M. Stereocontrolled total synthesis of (+)-leucascandrolide A. Angewandte Chemie (International Ed. in English). 42: 343-7. PMID 12548695 DOI: 10.1002/Anie.200390112 |
0.448 |
|
| 2003 |
Paterson I, Delgado O, Florence GJ, Lyothier I, Scott JP, Sereinig N. 1,6-asymmetric induction in boron-mediated aldol reactions: application to a practical total synthesis of (+)-discodermolide. Organic Letters. 5: 35-8. PMID 12509884 DOI: 10.1021/Ol0270780 |
0.476 |
|
| 2003 |
Paterson I, Temal-Laïb T. Toward the combinatorial synthesis of polyketide libraries: asymmetric aldol reactions with alpha-chiral aldehydes on solid support. Organic Letters. 4: 2473-6. PMID 12123354 DOI: 10.1021/Ol026046+ |
0.413 |
|
| 2003 |
Paterson I, Acena JL, Bach J, Chen DY, Coster MJ. Synthesis and Biological Evaluation of Spongistatin/Altohyrtin Analogues: E-Ring Dehydration and C46 Side-Chain Truncation. Cheminform. 34. DOI: 10.1039/B212651F |
0.686 |
|
| 2003 |
Paterson I, Luckhurst CA. Toward the Total Synthesis of Phorboxazole A: Synthesis of an Advanced C4—C32 Subunit Using the Jacobsen Hetero Diels—-Alder Reaction. Cheminform. 34. DOI: 10.1016/S0040-4039(03)00754-8 |
0.45 |
|
| 2003 |
Paterson I, Luckhurst CA. Toward the total synthesis of phorboxazole A: synthesis of an advanced C4–C32 subunit using the Jacobsen hetero Diels–Alder reaction Tetrahedron Letters. 44: 3749-3754. DOI: 10.1016/S0040-4039(03)00754-8 |
0.363 |
|
| 2003 |
Paterson I, Tudge M. A fully stereocontrolled total synthesis of (+)-leucascandrolide A Tetrahedron. 59: 6833-6849. DOI: 10.1016/S0040-4020(03)00814-7 |
0.503 |
|
| 2003 |
Paterson I, Delgado O. Synthesis of novel discodermolide analogues with modified hydrogen-bonding donor/acceptor sites Tetrahedron Letters. 44: 8877-8882. DOI: 10.1016/J.Tetlet.2003.09.172 |
0.327 |
|
| 2003 |
Paterson I, Florence G. The Development of a Practical Total Synthesis of Discodermolide, a Promising Microtubule-Stabilizing Anticancer Agent European Journal of Organic Chemistry. 2003: 2193-2208. DOI: 10.1002/Ejoc.200300061 |
0.353 |
|
| 2003 |
Paterson I, Tudge M. A Fully Stereocontrolled Total Synthesis of (+)-Leucascandrolide A. Cheminform. 34. DOI: 10.1002/CHIN.200351193 |
0.344 |
|
| 2003 |
Paterson I, Tudge M. Stereocontrolled Total Synthesis of (+)-Leucascandrolide A Cheminform. 34. DOI: 10.1002/CHIN.200319196 |
0.339 |
|
| 2002 |
Yeung KS, Paterson I. Actin-binding marine macrolides: total synthesis and biological importance. Angewandte Chemie (International Ed. in English). 41: 4632-53. PMID 12481316 DOI: 10.1002/Anie.200290057 |
0.395 |
|
| 2002 |
Paterson I, Chen DY, Franklin AS. Total synthesis of siphonarin B and dihydrosiphonarin B. Organic Letters. 4: 391-4. PMID 11820887 DOI: 10.1021/Ol017082W |
0.385 |
|
| 2002 |
Paterson I, Blakey SB, Cowden CJ. Studies in marine macrolide synthesis: stereocontrolled synthesis of a C21–C34 subunit of the aplyronines Tetrahedron Letters. 43: 6005-6008. DOI: 10.1016/S0040-4039(02)01217-0 |
0.662 |
|
| 2002 |
Paterson I, Coster MJ. Total synthesis of altohyrtin A (spongistatin 1): an alternative synthesis of the CD-spiroacetal subunit Tetrahedron Letters. 43: 3285-3289. DOI: 10.1016/S0040-4039(02)00527-0 |
0.682 |
|
| 2001 |
Paterson I, Chen DY, Coster MJ, Aceña JL, Bach J, Gibson KR, Keown LE, Oballa RM, Trieselmann T, Wallace DJ, Hodgson AP, Norcross RD. Stereocontrolled Total Synthesis of (+)-Altohyrtin A/Spongistatin 1. Angewandte Chemie (International Ed. in English). 40: 4055-4060. PMID 29712249 DOI: 10.1002/1521-3773(20011105)40:21<4055::Aid-Anie4055>3.0.Co;2-H |
0.695 |
|
| 2001 |
Paterson I, Davies RDM, Marquez R. Total Synthesis of the Callipeltoside Aglycon. Angewandte Chemie (International Ed. in English). 40: 603-607. PMID 29712021 DOI: 10.1002/1521-3773(20010202)40:3<603::Aid-Anie603>3.0.Co;2-O |
0.441 |
|
| 2001 |
Paterson I, Chen DY, Coster MJ, Aceña JL, Bach J, Gibson KR, Keown LE, Oballa RM, Trieselmann T, Wallace DJ, Hodgson AP, Norcross RD. Stereocontrolled Total Synthesis of (+)-Altohyrtin A/Spongistatin 1 Financial support was provided by the EPSRC (GR/L41646), Cambridge Commonwealth Trust (Scholarship to M.J.C.), EC (Marie Curie Postdoctoral Fellowship to J.L.A.), DFG (Postdoctoral Fellowship to T.T.), NSERC-Canada (Postdoctoral Fellowship to R.M.O.), Churchill College (Research Fellowship to D.J.W.), Kingapos;s College and Sims Fund, Cambridge (Scholarship to D.Y.K.C.). We also thank Merck and AstraZeneca Pharmaceuticals for generous support, and Dr. Anne Butlin (AZ) and Dr. Nick Bampos (Cambridge) for valuable assistance. Angewandte Chemie (International Ed. in English). 40: 4055-4060. PMID 12404491 DOI: 10.1002/1521-3773(20011105)40:21<4055::AID-ANIE4055>3.0.CO;2-H |
0.604 |
|
| 2001 |
Paterson I, De Savi C, Tudge M. Total synthesis of the microtubule-stabilizing agent (-)-laulimalide. Organic Letters. 3: 3149-52. PMID 11574017 DOI: 10.1021/Ol010150U |
0.458 |
|
| 2001 |
Paterson I, Florence GJ, Gerlach K, Scott JP, Sereinig N. A practical synthesis of (+)-discodermolide and analogues: fragment union by complex aldol reactions. Journal of the American Chemical Society. 123: 9535-44. PMID 11572673 DOI: 10.1021/Ja011211M |
0.528 |
|
| 2001 |
Paterson I, De Savi C, Tudge M. Synthesis of the macrocyclic core of laulimalide. Organic Letters. 3: 213-6. PMID 11430037 DOI: 10.1021/Ol000342+ |
0.463 |
|
| 2001 |
Paterson I, Mackay AC. Boron-mediated aldol reactions of ethyl α-(N,N)-dibenzylamino ketones: control of enolisation geometry and aldehyde π-facial selectivity Tetrahedron Letters. 42: 9269-9272. DOI: 10.1016/S0040-4039(01)01982-7 |
0.387 |
|
| 2001 |
Paterson I, Collett LA. Remote 1,5-stereoinduction in boron aldol reactions of methyl ketones: application to the convergent assembly of the 1,3-polyol sequence of (+)-roxaticin Tetrahedron Letters. 42: 1187-1191. DOI: 10.1016/S0040-4039(00)02205-X |
0.443 |
|
| 2000 |
Paterson I, Donghi M, Gerlach K. A Combinatorial Approach to Polyketide‐Type Libraries by Iterative Asymmetric Aldol Reactions Performed on Solid Support Angewandte Chemie. 39: 3315-3319. PMID 11028089 DOI: 10.1002/1521-3773(20000915)39:18<3315::Aid-Anie3315>3.0.Co;2-9 |
0.341 |
|
| 2000 |
Paterson I, Chen DY, Aceña JL, Franklin AS. Studies in marine polypropionate synthesis: total synthesis of (-)-baconipyrone C. Organic Letters. 2: 1513-6. PMID 10841467 DOI: 10.1021/Ol000027N |
0.52 |
|
| 2000 |
Paterson I, Florence GJ, Gerlach K, Scott JP. Total Synthesis of the Antimicrotubule Agent (+)-Discodermolide Using Boron-Mediated Aldol Reactions of Chiral Ketones. Angewandte Chemie (International Ed. in English). 39: 377-380. PMID 10649416 DOI: 10.1002/(Sici)1521-3773(20000117)39:2<377::Aid-Anie377>3.0.Co;2-E |
0.457 |
|
| 2000 |
Paterson I, Florence GJ. Synthesis of (+)-discodermolide and analogues by control of asymmetric induction in aldol reactions of γ-chiral (Z)-enals Tetrahedron Letters. 41: 6935-6939. DOI: 10.1016/S0040-4039(00)01165-5 |
0.442 |
|
| 2000 |
Paterson I, Chen DY, Acena JL, Franklin AS. ChemInform Abstract: Marine Polypropionate Synthesis: Total Synthesis of (-)-Baconipyrone C. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200037232 |
0.408 |
|
| 1999 |
Paterson I, Scott JP. Laboratory emulation of polyketide biosynthesis: an iterative, aldol-based, synthetic entry to polyketide libraries using (R)- and (S)-1-(benzyloxy)-2-methylpentan-3-one, and conformational aspects of extended polypropionates Journal of the Chemical Society-Perkin Transactions 1. 1003-1014. DOI: 10.1039/A809818B |
0.356 |
|
| 1999 |
Paterson I, Lombart H, Allerton C. Total Synthesis of Elaiolide Using a Copper(I)-Promoted Stille Cyclodimerization Reaction Organic Letters. 1: 19-22. DOI: 10.1021/Ol990004C |
0.501 |
|
| 1999 |
Paterson I, Brown RE, Urch CJ. Studies towards the synthesis of lophotoxin and pukalide: Synthesis of the 14-membered macrocyclic core and some acyclic structural analogues Tetrahedron Letters. 40: 5807-5810. DOI: 10.1016/S0040-4039(99)01119-3 |
0.464 |
|
| 1999 |
Paterson I, Doughty VA. anti-Aldol reactions of lactate-derived ketones. Application to the synthesis of (−)-tetrahydrolipstatin Tetrahedron Letters. 40: 393-394. DOI: 10.1016/S0040-4039(98)02321-1 |
0.429 |
|
| 1998 |
Paterson I. Polyketide Synthesis Using the Boron-Mediated, anti-Aldol Reactions of Lactate-Derived Ketones: Total Synthesis of (-)-ACRL Toxin IIIB Synthesis. 1998: 639-652. DOI: 10.1055/S-1998-5929 |
0.481 |
|
| 1998 |
Paterson I, Cowden CJ, Rahn VS, Woodrow MD. A Facile Oxidation/Deprotection of Electron Rich Silyl Ethers Using DDQ Synlett. 1998: 915-917. DOI: 10.1055/S-1998-1810 |
0.328 |
|
| 1998 |
Paterson I, Wallace DJ, Oballa RM. Studies in marine macrolide synthesis: Synthesis of a fully functionalised C1C28 subunit of spongistatin 1 (altohyrtin A) Tetrahedron Letters. 39: 8545-8548. DOI: 10.1016/S0040-4039(98)01908-X |
0.449 |
|
| 1998 |
Paterson I, Arnott EA. Towards the total synthesis of phorboxazoles A and B: Stereocontrolled synthesis of a C20C32 subunit Tetrahedron Letters. 39: 7185-7188. DOI: 10.1016/S0040-4039(98)01539-1 |
0.511 |
|
| 1998 |
Paterson I, Woodrow MD, Cowden CJ. Studies in marine macrolide synthesis: Construction of a 24-membered macrocyclic intermediate for aplyronine A Tetrahedron Letters. 39: 6041-6044. DOI: 10.1016/S0040-4039(98)01192-7 |
0.419 |
|
| 1998 |
Paterson I, Cowden CJ, Woodrow MD. Studies in marine macrolide synthesis: Stereocontrolled synthesis of the C1C11 and C15C27 subunits of aplyronine A Tetrahedron Letters. 39: 6037-6040. DOI: 10.1016/S0040-4039(98)01191-5 |
0.428 |
|
| 1998 |
Paterson I, Watson C, Yeung KS, Ward RA, Wallace PA. The total synthesis of scytophycin C. Part 2: Synthesis of scytophycin C from the protected seco acid Tetrahedron. 54: 11955-11970. DOI: 10.1016/S0040-4020(98)83051-2 |
0.488 |
|
| 1998 |
Paterson I, Yeung KS, Watson C, Ward RA, Wallace PA. The total synthesis of scytophycin C. Part 1: Stereocontrolled synthesis of the C1-C32 protected seco acid Tetrahedron. 54: 11935-11954. DOI: 10.1016/S0040-4020(98)83050-0 |
0.493 |
|
| 1998 |
Gennari C, Ceccarelli S, Piarulli U, Aboutayab K, Donghi M, Paterson I. Stereocontrolled synthesis of polyketide libraries: Boron-mediated aldol reactions with aldehydes on solid support Tetrahedron. 54: 14999-15016. DOI: 10.1016/S0040-4020(98)00940-5 |
0.485 |
|
| 1997 |
Paterson I, Watson C, Yeung KS, Wallace PA, Ward RA. Total Synthesis of Scytophycin C. The Journal of Organic Chemistry. 62: 452-453. PMID 11671432 DOI: 10.1021/Jo962189W |
0.468 |
|
| 1997 |
Paterson I, Wallace DJ, Gibson KR. Studies in marine macrolide synthesis: Synthesis of a C16-C28 subunit of spongistatin 1 (altohyrtin A) incorporating the CD-spisoacetal moiety Tetrahedron Letters. 38: 8911-8914. DOI: 10.1016/S0040-4039(97)10483-X |
0.395 |
|
| 1997 |
Paterson I, Oballa RM. Studies in marine macrolide synthesis: Synthesis of the C1C15 subunit of spongistatin 1 (altohyrtin A) and 15,16-anti aldol coupling reactions Tetrahedron Letters. 38: 8241-8244. DOI: 10.1016/S0040-4039(97)10126-5 |
0.507 |
|
| 1997 |
Paterson I, Scott JP. Polyketide library synthesis: Iterative assembly of extended polypropionates using (R)- and (S)-1-(benzyloxy)-2-methylpentan-3-one Tetrahedron Letters. 38: 7441-7444. DOI: 10.1016/S0040-4039(97)01751-6 |
0.394 |
|
| 1997 |
Paterson I, Keown LE. Studies in marine macrolide synthesis: Stereocontrolled synthesis of the F-ring subunit of spongistatin 1 (altohyrtin A) Tetrahedron Letters. 38: 5727-5730. DOI: 10.1016/S0040-4039(97)01257-4 |
0.406 |
|
| 1997 |
Paterson I, Feßner K, Finlay MV. Studies towards the synthesis of the zaragozic acids: Synthesis of the bicyclic acetal core of zaragozic acid C Tetrahedron Letters. 38: 4301-4304. DOI: 10.1016/S0040-4039(97)00885-X |
0.418 |
|
| 1997 |
Paterson I, McLeod MD. Studies in macrolide synthesis: Stereocontrolled synthesis of a C1C13 segment of concanamycin A Tetrahedron Letters. 38: 4183-4186. DOI: 10.1016/S0040-4039(97)00816-2 |
0.495 |
|
| 1997 |
Paterson I, Man J. Studies in macrolide synthesis: A novel cyclodimerisation approach to the synthesis of elaiophylin using a double Stille cross-coupling reaction Tetrahedron Letters. 38: 695-698. DOI: 10.1016/S0040-4039(96)02395-7 |
0.456 |
|
| 1996 |
Paterson I, Feßner K, Finlay MV, Jacobs MF. Studies towards the synthesis of the zaragozic acids: A novel epoxide cyclisation approach to the formation of the bicyclic acetal core Tetrahedron Letters. 37: 8803-8806. DOI: 10.1016/S0040-4039(96)02083-7 |
0.418 |
|
| 1996 |
Paterson I, Gibson KR, Oballa RM. Remote, 1,5-anti stereoinduction in the boron-mediated aldol reactions of β-oxygenated methyl ketones Tetrahedron Letters. 37: 8585-8588. DOI: 10.1016/0040-4039(96)01962-4 |
0.368 |
|
| 1996 |
Paterson I, Nowak T. Anti Aldol reactions of α-alkoxymethyl ketones: Application to the total synthesis of (+)-restricticin Tetrahedron Letters. 37: 8243-8246. DOI: 10.1016/0040-4039(96)01879-5 |
0.428 |
|
| 1996 |
Paterson I, Perkins MV. Total Synthesis of (−)-Denticulatins A and B Using Efficient Methods of Acyclic Stereocontrol. Tetrahedron. 52: 1811-1834. DOI: 10.1016/0040-4020(95)01015-7 |
0.436 |
|
| 1995 |
Paterson I, Schlapbach A. Studies Towards the Total Synthesis of the Marine-Derived Immunosuppressant Discodermolide: Stereoselective Synthesis of a C9-C24 Subunit Synlett. 1995: 498-500. DOI: 10.1055/S-1995-5276 |
0.489 |
|
| 1995 |
Paterson I, Hulme AN. Total Synthesis of (-)-Ebelactone A and B The Journal of Organic Chemistry. 60: 3288-3300. DOI: 10.1021/Jo00116A010 |
0.343 |
|
| 1995 |
Norcross RD, Paterson I. Total Synthesis of Bioactive Marine Macrolides Chemical Reviews. 95: 2041-2114. DOI: 10.1021/Cr00038A012 |
0.441 |
|
| 1995 |
Bernardi A, Gennari C, Goodman JM, Paterson I. The rational design and systematic analysis of asymmetric aldol reactions using enol borinates: Applications of transition state computer modelling Tetrahedron-Asymmetry. 6: 2613-2636. DOI: 10.1016/0957-4166(95)00343-N |
0.53 |
|
| 1995 |
Paterson I, McLeod MD. Studies in macrolide synthesis: A sequential aldol/glycosylation approach to the synthesis of concanamycin A Tetrahedron Letters. 36: 9065-9068. DOI: 10.1016/0040-4039(95)01913-3 |
0.508 |
|
| 1995 |
Paterson I, Bower S, McLeod MD. Stereocontrolled aldol additions to α-methylene-β-alkoxy aldehydes: Application to the synthesis of a C13C25 segment of bafilomycin A1 Tetrahedron Letters. 36: 175-178. DOI: 10.1016/0040-4039(94)02205-P |
0.422 |
|
| 1995 |
Paterson I, Yeung KS, Ward RA, Smith JD, Cuimming JG, Lamboley S. The total synthesis of swinholide A. Part 4: Synthesis of swinholide A and isoswinholide A from the protected monomeric seco acid, pre-swinholide A Tetrahedron. 51: 9467-9486. DOI: 10.1016/0040-4020(95)00549-N |
0.428 |
|
| 1995 |
Paterson I, Ward RA, Smith JD, Cumming JG, Yeung KS. The total synthesis of swinholide A. Part 3: A stereocontrolled synthesis of (-)-pre-swinholide A Tetrahedron. 51: 9437-9466. DOI: 10.1016/0040-4020(95)00548-M |
0.499 |
|
| 1995 |
Paterson I, Cumming JG, Ward RA, Lamboley S. The total synthesis of swinholide A. Part 1: A stereocontrolled synthesis of a C19-C32 segment Tetrahedron. 51: 9393-9412. DOI: 10.1016/0040-4020(95)00546-K |
0.468 |
|
| 1995 |
Bernardi A, Gennari C, Goodman JM, Leue V, Paterson I. Mechanistic insights from ab initio calculations on a nitrogen analogue of the boron-mediated aldol reaction Tetrahedron. 51: 4853-4866. DOI: 10.1016/0040-4020(95)00170-D |
0.552 |
|
| 1994 |
Paterson I. Recent Progress in the Chemical Synthesis of Antibiotics and Related Microbial Products Synthesis. 1994: 223-223. DOI: 10.1055/S-1994-25442 |
0.326 |
|
| 1994 |
Franklin AS, Paterson I. Recent developments in asymmetric aldol methodology Contemporary Organic Synthesis. 1: 317. DOI: 10.1039/Co9940100317 |
0.314 |
|
| 1994 |
Paterson I, Norcross RD, Ward RA, Romea P, Lister MA. Studies in Macrolide Synthesis: A Stereocontrolled Synthesis of Oleandolide Employing Reagent- and Substrate-Controlled Aldol Reactions of (S)-1-(Benzyloxy)-2-methylpentan-3-one Journal of the American Chemical Society. 116: 11287-11314. DOI: 10.1021/Ja00104A010 |
0.452 |
|
| 1994 |
Paterson I, Yeung KS, Ward RA, Cumming JG, Smith JD. Total synthesis of swinholide A and hemiswinholide A Journal of the American Chemical Society. 116: 9391-9392. DOI: 10.1021/Ja00099A091 |
0.441 |
|
| 1994 |
Paterson I, Ward RA, Romea P, Norcross RD. Substrate-Controlled Aldol Reactions of Chiral Ethyl Ketones: Application to the Total Synthesis of Oleandomycin Journal of the American Chemical Society. 116: 3623-3624. DOI: 10.1021/Ja00087A068 |
0.445 |
|
| 1994 |
Paterson I, Smith JD, Ward RA, Cumming JG. Total Synthesis of (-)-Preswinholide A Journal of the American Chemical Society. 116: 2615-2616. DOI: 10.1021/Ja00085A050 |
0.441 |
|
| 1994 |
Paterson I, Wallace DJ. Anti aldol reactions of lactate-derived ketones: Application to the total synthesis of (-)-ACRL toxin IIIB Tetrahedron Letters. 35: 9477-9480. DOI: 10.1016/S0040-4039(00)78576-5 |
0.505 |
|
| 1994 |
Paterson I, Cumming JG, Smith JD, Ward RA, Yeung KS. Towards the synthesis of swinholide A and scytophycin C. A highly stereocontrolled synthesis of (-)-pre-swinholide A Tetrahedron Letters. 35: 3405-3408. DOI: 10.1016/S0040-4039(00)76920-6 |
0.534 |
|
| 1994 |
Bernardi A, Comotti A, Gennari C, Hewkin CT, Goodman JM, Schlapbach A, Paterson I. Computer-assisted design of chiral boron enolates: The role of ate complexes in determining aldol stereoselectivity. Tetrahedron. 50: 1227-1242. DOI: 10.1016/S0040-4020(01)80834-6 |
0.551 |
|
| 1994 |
Paterson I, Wallace DJ. Manipulation of the aldol adducts from lactate-derived ketones. A versatile chiral auxiliary for the asymmetric synthesis of β-hydroxy carbonyl compounds Tetrahedron Letters. 35: 9087-9090. DOI: 10.1016/0040-4039(94)88435-8 |
0.393 |
|
| 1994 |
Paterson I, Wallace DJ, Velázquez SM. Studies in polypropionate synthesis: High π-face selectivity in syn and anti aldol reactions of chiral boron enolates of lactate-derived ketones Tetrahedron Letters. 35: 9083-9086. DOI: 10.1016/0040-4039(94)88434-X |
0.461 |
|
| 1994 |
Paterson I, Cumming JG, Smith JD, Ward RA. Studies in marine macrolide synthesis: Boron and silicon-mediated coupling strategies for Swinholide A Tetrahedron Letters. 35: 441-444. DOI: 10.1016/0040-4039(94)85075-5 |
0.406 |
|
| 1994 |
Garson MJ, Goodman JM, Paterson I. A configurational model for siphonariid polypropionates derived from structural and biosynthetic considerations Tetrahedron Letters. 35: 6929-6932. DOI: 10.1016/0040-4039(94)85044-5 |
0.519 |
|
| 1994 |
Paterson I, Franklin AS. Assignment of the absolute configuration of the siphonarins and baconipyrones. Enantiocontrolled synthesis of a γ-pyrone subunit Tetrahedron Letters. 35: 6925-6928. DOI: 10.1016/0040-4039(94)85043-7 |
0.413 |
|
| 1993 |
Paterson I, Yeung K, Smaill JB. The Horner-Wadsworth-Emmons Reaction in Natural Products Synthesis: Expedient Construction of Complex (E)-Enones Using Barium Hydroxide Synlett. 1993: 774-776. DOI: 10.1055/S-1993-22605 |
0.389 |
|
| 1993 |
Paterson I, Tillyer RD. High π-face selectivity in anti aldol reactions of E-enol borinates from chiral alkoxymethyl ketones: stereocontrolled synthesis of a C24-C32 polyol subunit of rapamycin The Journal of Organic Chemistry. 58: 4182-4184. DOI: 10.1021/Jo00068A002 |
0.496 |
|
| 1993 |
Vulpetti A, Gardner M, Gennari C, Bernardi A, Goodman JM, Paterson I. Origins of stereoselectivity in the addition of chiral allyl- and crotylboranes to aldehydes: the development and application of a force field model of the transition state Journal of Organic Chemistry. 58: 1711-1718. DOI: 10.1021/Jo00059A019 |
0.494 |
|
| 1993 |
Paterson I, Perkins MV. Total synthesis of the marine polypropionate (+)-muamvatin. A configurational model for siphonariid metabolites Journal of the American Chemical Society. 115: 1608-1610. DOI: 10.1021/Ja00057A074 |
0.381 |
|
| 1993 |
Paterson I, Bower S, Tillyer RD. 13-Asymmetric induction in the aldol reactions of α-methylene-β-alkoxy aldehydes Tetrahedron Letters. 34: 4393-4396. DOI: 10.1016/S0040-4039(00)79361-0 |
0.337 |
|
| 1993 |
Paterson I, Tillyer RD, Ryan GR. Studies in biomimetic polyether synthesis: Synthesis of an A-ring subunit of etheromycin Tetrahedron Letters. 34: 4389-4392. DOI: 10.1016/S0040-4039(00)79360-9 |
0.434 |
|
| 1993 |
Paterson I, Smith JD. Studies in marine macrolide synthesis: Asymmetric synthesis of C1-C15/C16 subunits of swinholide A and scytophycin C. Tetrahedron Letters. 34: 5351-5354. DOI: 10.1016/S0040-4039(00)73995-5 |
0.442 |
|
| 1993 |
Paterson I, Kap-Sun Y. Studies in marine macrolide synthesis: A stereocontrolled synthesis of a C17-C32 subunit of scytophycin C. Tetrahedron Letters. 34: 5347-5350. DOI: 10.1016/S0040-4039(00)73994-3 |
0.464 |
|
| 1993 |
Paterson I, Tillyer RD, Smaill JB. Studies in biomimetic polyether synthesis: Construction of an ABCD-ring subunit of etheromycin using polyepoxide cascade cyclisations. Tetrahedron Letters. 34: 7137-7140. DOI: 10.1016/S0040-4039(00)61619-2 |
0.444 |
|
| 1993 |
Vulpetti A, Bernardi A, Gennari C, Goodman JM, Paterson I. Origins of π-face selectivity in the aldol reactions of chiral E-enol borinates: a computational study using transition state modelling. Tetrahedron. 49: 685-696. DOI: 10.1016/S0040-4020(01)86270-0 |
0.547 |
|
| 1992 |
Paterson I. New methods and strategies for the stereocontrolled synthesis of polypropionate-derived natural products Pure and Applied Chemistry. 64: 1821-1830. DOI: 10.1351/Pac199264121821 |
0.48 |
|
| 1992 |
Gennari C, Hewkin CT, Molinari F, Bernardi A, Comotti A, Goodman JM, Paterson I. The rational design of highly stereoselective boron enolates using transition-state computer modeling: a novel, asymmetric anti aldol reaction for ketones The Journal of Organic Chemistry. 57: 5173-5177. DOI: 10.1021/Jo00045A033 |
0.556 |
|
| 1992 |
Paterson I, Smith JD. Stereocontrolled synthesis of a C(1)-C(15) segment for the marine macrolides swinholide A and scytophycin C: use of a vinylogous Mukaiyama aldol reaction The Journal of Organic Chemistry. 57: 3261-3264. DOI: 10.1021/Jo00038A002 |
0.418 |
|
| 1992 |
Paterson I, Lister M, Norcross RD. Studies in macrolide synthesis: A stereocontrolled synthesis of a (9S)-macrolide intermediate for oleandomycin using chiral boron reagents. Tetrahedron Letters. 33: 1767-1770. DOI: 10.1016/S0040-4039(00)91728-3 |
0.496 |
|
| 1992 |
Paterson I, Cumming JG. A stereocontrolled synthesis of a C19-C32 / C17-C30 Segment for swinholide A and misakinolide A, Cytotoxic dimeric macrolides from theonella swinhoei. Tetrahedron Letters. 33: 2847-2850. DOI: 10.1016/S0040-4039(00)78876-9 |
0.415 |
|
| 1992 |
Paterson I, Perkins MV. Studies in polypropionate synthesis: stereoselective synthesis of (−)-denticulatins A and B Tetrahedron Letters. 33: 801-804. DOI: 10.1016/S0040-4039(00)77719-7 |
0.461 |
|
| 1992 |
Paterson I, Tillyer RD. Studies in polypropionate synthesis: high π-face selectivity in syn aldol reactions of tin(II) enolates from (R)- and (S)-1-benzyloxy-2-methylpentan-3-one. Tetrahedron Letters. 33: 4233-4236. DOI: 10.1016/S0040-4039(00)74697-1 |
0.387 |
|
| 1992 |
Goodman JM, Paterson I. Enolisation of ketones by dialkylboron chlorides and trifiates: A model for the effect of reagent leaving group substrate structure and amine base Tetrahedron Letters. 33: 7223-7226. DOI: 10.1016/S0040-4039(00)60878-X |
0.59 |
|
| 1992 |
Bernardi A, Cassinari A, Comotti A, Gardner M, Gennari C, Goodman JM, Paterson I. Developing a force field for the transition state of the aldol reaction of enolborinates: Evaluation of the use of fixed point charges. Tetrahedron. 48: 4183-4192. DOI: 10.1016/S0040-4020(01)92196-9 |
0.49 |
|
| 1992 |
Gennari C, Vieth S, Comotti A, Vulpetti A, Goodman JM, Paterson I. Diastereofacial selectivity in the aldol reactions of chiral α-methyl aldehydes: a computer modelling approach. Tetrahedron. 48: 4439-4458. DOI: 10.1016/S0040-4020(01)80452-X |
0.585 |
|
| 1992 |
PATERSON I, BERRISFORD DJ. ChemInform Abstract: meso-Epoxides in Asymmetric Synthesis. Enantioselective Opening by Nucleophiles in the Presence of Chiral Lewis Acids. Cheminform. 23: no-no. DOI: 10.1002/CHIN.199251339 |
0.334 |
|
| 1992 |
Paterson I, Berrisford DJ. Meso epoxides in asymmetric synthesis: Enantioselective opening by nucleophiles in the presence of chiral lewis acids Angewandte Chemie (International Edition in English). 31: 1179-1180. DOI: 10.1002/Anie.199211791 |
0.773 |
|
| 1992 |
Paterson I, Berrisford DJ. meso-Epoxide in der asymmetrischen Synthese: enantioselektive öffnung durch Nucleophile in Gegenwart von chiralen Lewis-Säuren Angewandte Chemie. 104: 1204-1205. DOI: 10.1002/Ange.19921040907 |
0.771 |
|
| 1991 |
Paterson I, Osborne S. Enol Borinates in Organic Synthesis: Regioselective α-Sulphenylation and α-Selenenylation of Ketones Synlett. 1991: 145-146. DOI: 10.1055/S-1991-20656 |
0.324 |
|
| 1991 |
Paterson I, Lister M, Ryan GR. Asymmetric aldol reactions using chiral boron reagents: Application to the synthesis of tirandamycin A Tetrahedron Letters. 32: 1749-1752. DOI: 10.1016/S0040-4039(00)74320-6 |
0.467 |
|
| 1991 |
Bernardi A, Capelli AM, Comotti A, Gennari C, Gardner M, Goodman JM, Paterson I. Origins of stereoselectivity in chiral boron enolate aldol reactions: A computational study using transition state modellings Tetrahedron. 47: 3471-3484. DOI: 10.1016/S0040-4020(01)86409-7 |
0.582 |
|
| 1991 |
Paterson I, N. Hulme A, J. Wallace D. Stereocontrolled, two-directional, chain synthesis using the Boron Aldol reaction and double Ireland-Claisen rearrangement. Tetrahedron Letters. 32: 7601-7604. DOI: 10.1016/0040-4039(91)80545-H |
0.408 |
|
| 1990 |
Bernardi A, Capelli AM, Gennari C, Goodman JM, Paterson I. Transition-state modeling of the aldol reaction of boron enolates: a force field approach The Journal of Organic Chemistry. 55: 3576-3581. DOI: 10.1021/Jo00298A038 |
0.574 |
|
| 1990 |
Goodman JM, Kahn SD, Paterson I. Theoretical studies of aldol stereoselectivity: the development of a force field model for enol borinates and the investigation of chiral enolate .pi.-face selectivity The Journal of Organic Chemistry. 55: 3295-3303. DOI: 10.1021/Jo00297A058 |
0.542 |
|
| 1990 |
Paterson I, Hulme AN. Total synthesis of the esterase inhibitor (±)-ebelactone a using an aldol-claisen strategy Tetrahedron Letters. 31: 7513-7516. DOI: 10.1016/S0040-4039(00)88532-9 |
0.396 |
|
| 1990 |
Paterson I, Goodman JM, Anne Lister M, Schumann RC, McClure CK, Norcross RD. Enantio- and diastereoselective aldol reactions of achiral ethyl and methyl ketones with aldehydes: the use of enol diisopinocampheylborinates Tetrahedron. 46: 4663-4684. DOI: 10.1016/S0040-4020(01)85588-5 |
0.723 |
|
| 1990 |
Paterson I, Osborne S. Stereoselective aldol reactions of β-chlorovinyl ketones using dienol borinates: A new synthesis of dihydropyrones. Tetrahedron Letters. 31: 2213-2216. DOI: 10.1016/0040-4039(90)80112-Y |
0.431 |
|
| 1990 |
PATERSON I, GOODMAN JM, LISTER MA, SCHUMANN RC, MCCLURE CK, NORCROSS RD. ChemInform Abstract: Enantio- and Diastereoselective Aldol Reactions of Achiral Ethyl and Methyl Ketones with Aldehydes: The Use of Enol Diisopinocampheylborinates. Cheminform. 21. DOI: 10.1002/CHIN.199044102 |
0.676 |
|
| 1990 |
PATERSON I, GOODMAN JM, ISAKA M. ChemInform Abstract: Aldol Reactions in Polypropionate Synthesis: High π-Face Selectivity of Enol Borinates from α-Chiral Methyl and Ethyl Ketones Under Substrate Control. Cheminform. 21. DOI: 10.1002/chin.199031063 |
0.561 |
|
| 1989 |
Paterson I, Goodman JM, Isaka M. Aldol reactions in polypropionate synthesis: High π-face selectivity of enol borinates from α-chiral methyl and ethyl ketones under substrate control Tetrahedron Letters. 30: 7121-7124. DOI: 10.1016/S0040-4039(01)93440-9 |
0.609 |
|
| 1989 |
Paterson I, Goodman JM. Aldol reactions of methylketones using chiral boron reagents: A reversal in aldehyde enantioface selectivity Tetrahedron Letters. 30: 997-1000. DOI: 10.1016/S0040-4039(00)95300-0 |
0.598 |
|
| 1989 |
Paterson I, McClure CK, Schumann RC. A short asymmetric synthesis of a C19–C27 segment of rifamycin S. Kinetic resolution in the aldol reactions of ethylketones using chiral boron reagents Tetrahedron Letters. 30: 1293-1296. DOI: 10.1016/S0040-4039(00)72740-7 |
0.64 |
|
| 1989 |
Paterson I, Rawson DJ. Studies in macrolide synthesis: A highly stereoselective synthesis of (+)-(9S)-dihydroerythronolide a using macrocyclic stereocontrol Tetrahedron Letters. 30: 7463-7466. DOI: 10.1016/S0040-4039(00)70726-X |
0.46 |
|
| 1989 |
Paterson I, Mark G, Banks BJ. Studies in marine cembranolide synthesis: A synthesis of 2,3,5-trisubstituted furan intermediates for lophotoxin and pukalide Tetrahedron. 45: 5283-5292. DOI: 10.1016/S0040-4020(01)81102-9 |
0.419 |
|
| 1989 |
PATERSON I, GARDNER M, BANKS BJ. ChemInform Abstract: Marine Cembranolide Synthesis: A Synthesis of 2,3,5-Trisubstituted Furan Intermediates for Lophotoxin and Pukalide. Cheminform. 20. DOI: 10.1002/CHIN.198952296 |
0.377 |
|
| 1989 |
PATERSON I, GOODMAN JM. ChemInform Abstract: Aldol Reactions of Methyl Ketones Using Chiral Boron Reagents: A Reversal in Aldehyde Enantioface Selectivity. Cheminform. 20. DOI: 10.1002/CHIN.198940136 |
0.553 |
|
| 1989 |
PATERSON I, MCCLURE CK, SCHUMANN RC. ChemInform Abstract: A Short Asymmetric Synthesis of a C19-C27 Segment (V) of Rifamycin S. Kinetic Resolution in the Aldol Reactions of Ethyl Ketones (.+-.)-(I) Using Chiral Boron Reagents. Cheminform. 20. DOI: 10.1002/CHIN.198938090 |
0.632 |
|
| 1989 |
PATERSON I, BODDY I. ChemInform Abstract: Studies in Polyether Synthesis: Spiroacetal Formation by Directed Bisepoxide Cyclization. Cheminform. 20. DOI: 10.1002/CHIN.198916208 |
0.345 |
|
| 1988 |
Paterson I, Boddy I. Studies in polyether synthesis: Spiroacetal formation by directed bisepoxide cyclisation. Tetrahedron Letters. 29: 5301-5304. DOI: 10.1016/S0040-4039(00)80743-1 |
0.442 |
|
| 1988 |
Paterson I, Laffan DD, Rawson DJ. Studies in macrolide synthesis: A concise asymmetric synthesis of a macrolide intermediate for the erythronolides. Tetrahedron Letters. 29: 1461-1464. DOI: 10.1016/S0040-4039(00)80325-1 |
0.499 |
|
| 1988 |
Paterson I, Anne Lister M. Aldol condensations of chiral ethylketones: Control by chiral boron reagents. Tetrahedron Letters. 29: 585-588. DOI: 10.1016/S0040-4039(00)80157-4 |
0.415 |
|
| 1988 |
Paterson I. α-alkylation and α-alkylidenation of carbonyl compounds by o-silylated enolate phenylthioalkylation Tetrahedron. 44: 4207-4219. DOI: 10.1016/S0040-4020(01)86667-9 |
0.41 |
|
| 1988 |
Paterson I, Arya P. Degradation of oleandomycin: controlled removal of sugars to give oleandonolide c3,c5-acetonide Tetrahedron. 44: 253-260. DOI: 10.1016/S0040-4020(01)85115-2 |
0.398 |
|
| 1987 |
Goodman JM, Paterson I, Kahn SS. A force field model for boron enolates Tetrahedron Letters. 28: 5209-5212. DOI: 10.1016/S0040-4039(00)95631-4 |
0.472 |
|
| 1987 |
Paterson I, Boddy I, Mason I. Studies in polyether synthesis using polyepoxide cyclisations. Tetrahedron Letters. 28: 5205-5208. DOI: 10.1016/S0040-4039(00)95630-2 |
0.46 |
|
| 1987 |
Paterson I, McClure CK. Studies in macrolide synthesis: aldol condensations of chiral ethylketones via boron enolates Tetrahedron Letters. 28: 1229-1232. DOI: 10.1016/S0040-4039(00)95333-4 |
0.642 |
|
| 1987 |
PATERSON I, MCCLURE CK. ChemInform Abstract: Studies in Macrolide Synthesis: Aldol Condensations of Chiral Ethylketones via Boron Enolates. Cheminform. 18. DOI: 10.1002/CHIN.198735099 |
0.622 |
|
| 1987 |
PATERSON I, LISTER MA, MCCLURE CK. ChemInform Abstract: Enantioselective Aldol Condensations: The Use of Ketone Boron Enolates with Chiral Ligands Attached to Boron. Cheminform. 18. DOI: 10.1002/CHIN.198710132 |
0.559 |
|
| 1986 |
Paterson I, Lister M, McClure CK. Enantioselective aldol condensations: The use of ketone boron enolates with chiral ligands attached to boron. Tetrahedron Letters. 27: 4787-4790. DOI: 10.1016/S0040-4039(00)85065-0 |
0.607 |
|
| 1985 |
Alexander RP, Paterson I. Asymmetric alkylation and sulphenylation of chiral O-silylated imide enolates Tetrahedron Letters. 26: 5339-5340. DOI: 10.1016/S0040-4039(00)95033-0 |
0.356 |
|
| 1985 |
PATERSON I, MANSURI MM. ChemInform Abstract: RECENT DEVELOPMENTS IN THE TOTAL SYNTHESIS OF MACROLIDE ANTIBIOTICS Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198551354 |
0.393 |
|
| 1983 |
Paterson I, Patel SK, Porter JR. Studies in macrolide synthesis: an efficient synthesis of two chiral fragments of erythronolide a Tetrahedron Letters. 24: 3395-3396. DOI: 10.1016/S0040-4039(00)86280-2 |
0.489 |
|
| 1983 |
Patel SK, Paterson I. O-silylated enolates in organic synthesis: sulphur-mediated alkylation of esters with alkenes Tetrahedron Letters. 24: 1315-1318. DOI: 10.1016/S0040-4039(00)81644-5 |
0.402 |
|
| 1983 |
PATERSON I, PATEL SK, PORTER JR. ChemInform Abstract: STUDIES IN MACROLIDE SYNTHESIS: AN EFFICIENT SYNTHESIS OF TWO CHIRAL FRAGMENTS OF ERYTHRONOLIDE A Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198349215 |
0.359 |
|
| 1983 |
PATERSON I. ChemInform Abstract: STUDIES IN MACROLIDE SYNTHESIS: A SYNTHESIS OF TWO CHIRAL FRAGMENTS OF OLEANDOMYCIN AND LANKAMYCIN Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198326349 |
0.368 |
|
| 1982 |
Stork G, Paterson I, Lee FKC. Stereoselective synthesis of the chiral sequence of erythronolide A Journal of the American Chemical Society. 104: 4686-4688. DOI: 10.1021/Ja00381A035 |
0.58 |
|
| 1982 |
Khan HA, Paterson I. O-silylated enolate phenylthioalkylation: a new synthesis of unsaturated 1,5-dicarbonyl compounds. Tetrahedron Letters. 23: 2399-2402. DOI: 10.1016/S0040-4039(00)87352-9 |
0.355 |
|
| 1982 |
Khan HA, Paterson I. O-silylated enolate phenylthialkylation: A synthesis of α,β-unsaturated 5- and 6-membered lactones. Tetrahedron Letters. 23: 5083-5084. DOI: 10.1016/S0040-4039(00)85578-1 |
0.349 |
|
| 1981 |
Paterson I, Price LG. O-Silylated dienolates in organic synthesis: γ-Selective alkylation of unsaturated carbonyl compounds by 1,5-dithienium fluoroborate. Tetrahedron Letters. 22: 2833-2836. DOI: 10.1016/S0040-4039(01)90565-9 |
0.357 |
|
| 1981 |
Paterson I, Price LG. O-Silylated enolates in organic synthesis: α-Alkylation of carbonyl compounds by 1,3-dithienium fluoroborate. Tetrahedron Letters. 22: 2829-2832. DOI: 10.1016/S0040-4039(01)90564-7 |
0.361 |
|
| 1979 |
Fleming I, Paterson I. A Simple Synthesis of Carvone Using Silyl Enol Ethers Synthesis. 1979: 736-738. DOI: 10.1055/S-1979-28821 |
0.633 |
|
| 1979 |
Fleming I, Paterson I. Allylsilanes in Organic Synthesis: A Method for the Introduction of Two Carbon Substituents in Place of Carbonyl Oxygen Synthesis. 1979: 446-448. DOI: 10.1055/S-1979-28713 |
0.504 |
|
| 1979 |
Fleming I, Goldhill J, Paterson I. γ-Alkylation of unsaturated ketones and esters: zinc bromide-catalysed alkylation of O-silylated dienolates Tetrahedron Letters. 20: 3209-3212. DOI: 10.1016/S0040-4039(01)95364-X |
0.56 |
|
| 1979 |
Fleming I, Goldhill J, Paterson I. γ-Sulphenylation of αβ-unsaturated aldehydes, ketones, and esters: the use of O-silylated dienolates Tetrahedron Letters. 20: 3205-3208. DOI: 10.1016/S0040-4039(01)95363-8 |
0.532 |
|
| 1979 |
Paterson I, Fleming I. α-Alkylation and α-alkylidenation of carbonyl compounds: Lewis acid-promoted phenylthioalkylation of o-silylated enolates Tetrahedron Letters. 20: 2179-2182. DOI: 10.1016/S0040-4039(01)86295-X |
0.532 |
|
| 1979 |
Paterson I. α-Alkylation of ketones, esters, and lactones: zinc bromide-catalysed alkylation of o-silylated enolates, a synthesis of (±)-ar-turmerone Tetrahedron Letters. 20: 1519-1520. DOI: 10.1016/S0040-4039(01)86195-5 |
0.375 |
|
| 1979 |
Paterson I, Fleming I. α-methylenation of lactones and esters zinc bromide-catalysed phenylthiomethylation of o-silylated enolates Tetrahedron Letters. 20: 993-994. DOI: 10.1016/S0040-4039(01)86071-8 |
0.509 |
|
| 1979 |
FLEMING I, PATERSON I. ChemInform Abstract: A SIMPLE SYNTHESIS OF CARVONE USING SILYL ENOL ETHERS Chemischer Informationsdienst. 10. DOI: 10.1002/chin.197952143 |
0.377 |
|
| 1979 |
PATERSON I. ChemInform Abstract: α-ALKYLATION OF KETONES, ESTERS, AND LACTONES: ZINC BROMIDE-CATALYZED ALKYLATION OF O-SILYLATED ENOLATES, A SYNTHESIS OF (.+-.)-AR-TURMERONE Chemischer Informationsdienst. 10. DOI: 10.1002/chin.197933130 |
0.304 |
|
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