| Year |
Citation |
Score |
| 2015 |
Burroughs L, Eccleshare L, Ritchie J, Kulkarni O, Lygo B, Woodward S, Lewis W. One-Pot Cannizzaro Cascade Synthesis of ortho-Fused Cycloocta-2,5-dien-1-ones from 2-Bromo(hetero)aryl Aldehydes. Angewandte Chemie (International Ed. in English). 54: 10648-51. PMID 26230528 DOI: 10.1002/Anie.201505347 |
0.54 |
|
| 2014 |
Lygo B, Palframan MJ, Pattenden G. Investigation of transannular cycloaddition reactions involving furanoxonium ions using DFT calculations. Implications for the origin of plumarellide and rameswaralide and related polycyclic metabolites isolated from corals. Organic & Biomolecular Chemistry. 12: 7270-8. PMID 25105757 DOI: 10.1039/C4Ob00734D |
0.323 |
|
| 2012 |
Lygo B, Butt U, Cormack M. Synthesis and evaluation of atropos dihydro-5H-dibenzazepinium halide PTCs derived from α-methylbenzylamine. Organic & Biomolecular Chemistry. 10: 4968-76. PMID 22614161 DOI: 10.1039/C2Ob25437A |
0.447 |
|
| 2011 |
Lucas CL, Lygo B, Blake AJ, Lewis W, Moody CJ. Regioselectivity of the Claisen rearrangement in meta-allyloxy aryl ketones: an experimental and computational study, and application in the synthesis of (R)-(-)-pestalotheol D. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 1972-8. PMID 21274949 DOI: 10.1002/Chem.201002757 |
0.409 |
|
| 2011 |
Lygo B, Davison C, Evans T, Gilks JAR, Leonard J, Roy CE. Highly enantioselective aldol reactions using a tropos dibenz[c,e]azepine organocatalyst Tetrahedron. 67: 10164-10170. DOI: 10.1016/J.Tet.2011.09.101 |
0.547 |
|
| 2010 |
Lygo B, Beynon C, McLeod MC, Roy CE, Wade CE. Application of asymmetric phase-transfer catalysis in the enantioselective synthesis of cis-5-substituted proline esters Tetrahedron. 66: 8832-8836. DOI: 10.1016/J.Tet.2010.09.075 |
0.514 |
|
| 2010 |
LYGO B. ChemInform Abstract: N-Acyl-2-methylaziridines: Synthesis and Utility in the C-Acylation of β-Ketoester Derived Dianions. Cheminform. 27: no-no. DOI: 10.1002/chin.199611287 |
0.3 |
|
| 2010 |
LYGO B. ChemInform Abstract: Reaction of Aziridines with Dianions Derived from β-Keto Esters: Application to the Preparation of Substituted Pyrrolidines. Cheminform. 25: no-no. DOI: 10.1002/chin.199425118 |
0.403 |
|
| 2010 |
LYGO B, O'CONNOR N. ChemInform Abstract: Reaction of Dianions Derived from γ-Substituted β-Keto Esters with Epoxides. Cheminform. 23: no-no. DOI: 10.1002/chin.199249151 |
0.388 |
|
| 2009 |
Sharma P, Lygo B, Lewis W, Moses JE. Biomimetic synthesis and structural reassignment of the tridachiahydropyrones. Journal of the American Chemical Society. 131: 5966-72. PMID 19341238 DOI: 10.1021/Ja900369Z |
0.344 |
|
| 2009 |
Lygo B, Allbutt B, Beaumont DJ, Butt U, Gilks JAR. Synthesis and evaluation of chiral dibenzazepinium halide phase-transfer catalysts Synlett. 675-680. DOI: 10.1055/s-0028-1087810 |
0.315 |
|
| 2009 |
Lygo B, Beynon C, Lumley C, McLeod MC, Wade CE. Co-catalyst enhancement of enantioselective PTC Michael additions involving glycine imines Tetrahedron Letters. 50: 3363-3365. DOI: 10.1016/J.Tetlet.2009.02.123 |
0.395 |
|
| 2009 |
Lygo B. Edited by Keiji Maruoka Asymmetric phase transfer catalysis Wiley-VCH, 2008, 214pp. (hardcover) ISBN 978-3-527-31842-1 Applied Organometallic Chemistry. 24: 65-65. DOI: 10.1002/Aoc.1571 |
0.324 |
|
| 2008 |
Lygo B, Kirton EH, Lumley C. Stereocontrolled synthesis of lepadiformine A. Organic & Biomolecular Chemistry. 6: 3085-90. PMID 18698466 DOI: 10.1039/B805951A |
0.502 |
|
| 2007 |
Lygo B, Gardiner SD, McLeod MC, To DC. Diastereo- and enantioselective synthesis of alpha,beta-epoxyketones using aqueous NaOCl in conjunction with dihydrocinchonidine derived phase-transfer catalysis at room temperature. Scope and limitations. Organic & Biomolecular Chemistry. 5: 2283-90. PMID 17609760 DOI: 10.1039/B706546A |
0.407 |
|
| 2007 |
Lygo B, Beaumont DJ. Two highly effective phase-transfer catalysts for the enantioselective synthesis of α-amino acid derivatives Chimia. 61: 257-262. DOI: 10.2533/Chimia.2007.257 |
0.455 |
|
| 2005 |
Lygo B, Hirst DJ. IMDA reactions of β,δ-diketoester-substituted 1,7,9-undecatrienes: Application in the formal synthesis of solanapyrone D Synthesis. 3257-3262. DOI: 10.1055/S-2005-918445 |
0.471 |
|
| 2005 |
Lygo B, Slack D, Wilson C. Synthesis of neodysiherbaine Tetrahedron Letters. 46: 6629-6632. DOI: 10.1016/J.Tetlet.2005.07.159 |
0.527 |
|
| 2005 |
Lygo B, Allbutt B, Kirton EHM. Asymmetric Michael addition of glycine imines via quaternary ammonium ion catalysis Tetrahedron Letters. 46: 4461-4464. DOI: 10.1016/J.Tetlet.2005.04.096 |
0.445 |
|
| 2004 |
Lygo B, Andrews BI. Asymmetric phase-transfer catalysis utilizing chiral quaternary ammonium salts: asymmetric alkylation of glycine imines. Accounts of Chemical Research. 37: 518-25. PMID 15311950 DOI: 10.1021/ar030058t |
0.351 |
|
| 2004 |
Melville JL, Andrews BI, Lygo B, Hirst JD. Computational screening of combinatorial catalyst libraries. Chemical Communications (Cambridge, England). 1410-1. PMID 15179489 DOI: 10.1039/B402378A |
0.338 |
|
| 2004 |
Lygo B, Humphreys LD. Enantioselective synthesis of renieramide Synlett. 2809-2811. DOI: 10.1055/S-2004-835623 |
0.413 |
|
| 2004 |
Lygo B, Allbutt B. Asymmetric PTC Alkylation of Glycine Imines: Variation of the Imine Ester Moiety Synlett. 326-328. DOI: 10.1055/S-2003-43368 |
0.539 |
|
| 2003 |
Albrow V, Biswas K, Crane A, Chaplin N, Easun T, Gladiali S, Lygo B, Woodward S. Synthesis of an octahydro-1,1′-binaphthyl thioether ligand and comparison with unhydrogenated binaphthyl analogues Tetrahedron Asymmetry. 14: 2813-2819. DOI: 10.1016/S0957-4166(03)00583-4 |
0.321 |
|
| 2003 |
Lygo B, Allbutt B, James SR. Identification of a highly effective asymmetric phase-transfer catalyst derived from α-methylnaphthylamine Tetrahedron Letters. 44: 5629-5632. DOI: 10.1016/S0040-4039(03)01352-2 |
0.457 |
|
| 2003 |
Lygo B, Andrews BI. Enantioselective synthesis of aroylalanine derivatives Tetrahedron Letters. 44: 4499-4502. DOI: 10.1016/S0040-4039(03)01017-7 |
0.518 |
|
| 2003 |
Lygo B, Bhatia M, Cooke JWB, Hirst DJ. Synthesis of (±)-solanapyrones A and B Tetrahedron Letters. 44: 2529-2532. DOI: 10.1016/S0040-4039(03)00288-0 |
0.36 |
|
| 2003 |
Lygo B, Andrews BI, Slack D. Stereoselective approach to C-glycosylasparagines Tetrahedron Letters. 44: 9039-9041. DOI: 10.1016/J.Tetlet.2003.09.212 |
0.45 |
|
| 2002 |
Lygo B, To DC. Asymmetric epoxidation via phase-transfer catalysis: direct conversion of allylic alcohols into alpha,beta-epoxyketones. Chemical Communications (Cambridge, England). 2360-1. PMID 12430440 DOI: 10.1039/B206530D |
0.376 |
|
| 2002 |
Lygo B, Andrews BI, Crosby J, Peterson JA. Asymmetric alkylation of glycine imines using in situ generated phase-transfer catalysts Tetrahedron Letters. 43: 8015-8018. DOI: 10.1016/S0040-4039(02)01982-2 |
0.443 |
|
| 2002 |
Lygo B, Humphreys LD. Enantioselective synthesis of α-carbon deuterium-labelled L-α-amino acids Tetrahedron Letters. 43: 6677-6679. DOI: 10.1016/S0040-4039(02)01251-0 |
0.451 |
|
| 2001 |
Lygo B, To DCM. Improved procedure for the room temperature asymmetric phase-transfer mediated epoxidation of α,β-unsaturated ketones Tetrahedron Letters. 42: 1343-1346. DOI: 10.1016/S0040-4039(00)02208-5 |
0.444 |
|
| 2001 |
Lygo B, Crosby J, Peterson JA. An enantioselective approach to bis-α-amino acids Tetrahedron. 57: 6447-6453. DOI: 10.1016/S0040-4020(01)00536-1 |
0.465 |
|
| 2001 |
Lygo B, Crosby J, Lowdon TR, Peterson JA, Wainwright PG. Studies on the enantioselective synthesis of α-amino acids via asymmetric phase-transfer catalysis Tetrahedron. 57: 2403-2409. DOI: 10.1016/S0040-4020(01)00094-1 |
0.5 |
|
| 2001 |
Lygo B, Crosby J, Lowdon TR, Wainwright PG. Structure-selectivity studies on catalysts for the phase-transfer catalysed asymmetric alkylation of glycine imine esters Tetrahedron. 57: 2391-2402. DOI: 10.1016/S0040-4020(01)00093-X |
0.427 |
|
| 1999 |
Lygo B. Enantioselective synthesis of dityrosine and isodityrosine via asymmetric phase-transfer catalysis Tetrahedron Letters. 40: 1389-1392. DOI: 10.1016/S0040-4039(98)02616-1 |
0.344 |
|
| 1999 |
Lygo B, Crosby J, Peterson JA. Enantioselective synthesis of bis-α-amino acid esters via asymmetric phase-transfer catalysis Tetrahedron Letters. 40: 1385-1388. DOI: 10.1016/S0040-4039(98)02615-X |
0.383 |
|
| 1998 |
Lygo B, Wainwright PG. Asymmetric phase-transfer mediated epoxidation of α,β-unsaturated ketones using catalysts derived from Cinchona alkaloids Tetrahedron Letters. 39: 1599-1602. DOI: 10.1016/S0040-4039(97)10779-1 |
0.309 |
|
| 1997 |
Lygo B, Wainwright PG. A new class of asymmetric phase-transfer catalysts derived from Cinchona alkaloids - Application in the enantioselective synthesis of α-amino acids Tetrahedron Letters. 38: 8595-8598. DOI: 10.1016/S0040-4039(97)10293-3 |
0.372 |
|
| 1997 |
Lygo B, Crosby J, Lowdon TR, Wainwright PG. Enantio- and diastereoselective synthesis of all four possible stereoisomers of 2-(phenylhydroxymethyl)quinuclidine Tetrahedron Letters. 38: 2343-2346. DOI: 10.1016/S0040-4039(97)00310-9 |
0.392 |
|
| 1993 |
Lygo B. Reaction of Aziridines with Dianions Derived from β-Ketoesters: Application to the Preparation of Substituted Pyrrolidines Synlett. 1993: 764-766. DOI: 10.1055/s-1993-22601 |
0.364 |
|
| 1992 |
Lygo B, O'Connor N. Reaction of Dianions Derived from γ-Substituted β-Keto Esters with Epoxides Synlett. 1992: 529-530. DOI: 10.1055/s-1992-21404 |
0.373 |
|
| 1990 |
LEY SV, ANTHONY NJ, ARMSTRONG A, BRASCA MG, CLARKE T, CULSHAW D, GRECK C, GRICE P, JONES AB, LYGO B, MADIN A, SHEPPARD RN, SLAWIN AMZ, WILLIAMS DJ. ChemInform Abstract: A Highly Convergent Total Synthesis of the Spiroacetal Macrolide (+)-Milbemycin β1. Cheminform. 21. DOI: 10.1002/chin.199011329 |
0.411 |
|
| 1989 |
Ley SV, Anthony NJ, Armstrong A, Brasca MG, Clarke T, Culshaw D, Greck C, Grice P, Jones AB, Lygo B, Madin A, Sheppard RN, Slawin AMZ, Williams DJ. A highly convergent total synthesis of the spiroacetal macrolide (+)-milbemycinβ1 Tetrahedron. 45: 7161-7194. DOI: 10.1016/S0040-4020(01)89182-1 |
0.573 |
|
| 1988 |
Lygo B, O'connor N, Wilson PR. Reaction of dianions derived from β-ketoesters with epoxides-utility in the preparation of synthetically useful tetrahydrofurans Tetrahedron. 44: 6881-6888. DOI: 10.1016/S0040-4020(01)86217-7 |
0.361 |
|
| 1986 |
Ley SV, Lygo B, Sternfeld F, Wonnacott A. Alkylation reactions of anions derived from 2-benzenesulphonyl tetrahydropyran and their application to spiroketal syntiesis Tetrahedron. 42: 4333-4342. DOI: 10.1016/S0040-4020(01)87660-2 |
0.525 |
|
| 1986 |
LEY SV, LYGO B, STERNFELD F, WONNACOTT A. ChemInform Abstract: Alkylation Reactions of Anions Derived from 2-Benzenesulphonyl Tetrahydropyran and Their Application to Spiroketal Synthesis. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198652180 |
0.571 |
|
| 1985 |
Ley SV, Lygo B, Organ HM, Wonnacott A. Wittig and horner-wittig coupling reactions of 2-substituted cyclic ethers and their application to spiroketal synthesis Tetrahedron. 41: 3825-3836. DOI: 10.1016/S0040-4020(01)91403-6 |
0.561 |
|
| 1985 |
LEY SV, LYGO B, ORGAN HM, WONNACOTT A. ChemInform Abstract: Wittig and Horner-Wittig Coupling Reactions of 2-Substituted Cyclic Ethers and Their Application to Spiroketal Synthesis. Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198552214 |
0.549 |
|
| 1985 |
LEY SV, LYGO B, WONNACOTT A. ChemInform Abstract: PREPARATION AND REACTIONS OF 2-BENZENESULFONYLTETRAHYDROPYRAN Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198523189 |
0.495 |
|
| 1985 |
Ley SV, Lygo B, Wonnacott A. Preparation and reactions of 2-benzenesulphonyltetrahydropyran Tetrahedron Letters. 26: 535-538. DOI: 10.1002/Chin.198523189 |
0.471 |
|
| 1985 |
GODOY J, LEY SV, LYGO B. ChemInform Abstract: SYNTHESIS OF THE SPIROACETAL UNIT RELATED TO THE AVERMECTINS AND MILBEMYCINS Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198507204 |
0.43 |
|
| 1985 |
LEY SV, LYGO B, MOLINES H. ChemInform Abstract: SYNTHESIS OF (.+-.)-CIS-6-METHYLTETRAHYDROPYRAN-2-YLACETIC ACID, A NATURAL PRODUCT FROM VIVERRA CIVETTA, USING ORGANOSELENIUM-MEDIATED CYCLIZATION REACTIONS Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198504341 |
0.527 |
|
| 1984 |
Ley SV, Lygo B, Molines H. Synthesis of (±)-cis-6-methyltetrahydropyran-2-ylacetic acid, a natural product from viverra civetta, using organoselenium-mediated cyclisation reactions Journal of the Chemical Society, Perkin Transactions 1. 2403-2405. DOI: 10.1039/P19840002403 |
0.52 |
|
| 1984 |
Ley SV, Lygo B. A new route to spiro-ketals using the Horner-Wittig reaction of 2-diphenylphosphinoxy cyclic ethers Tetrahedron Letters. 25: 113-116. DOI: 10.1016/S0040-4039(01)91163-3 |
0.53 |
|
| 1984 |
DOHERTY AM, LEY SV, LYGO B, WILLIAMS DJ. ChemInform Abstract: SYNTHESIS OF SPIROACETALS USING ORGANOSELENIUM-MEDIATED CYCLIZATION REACTIONS. X-RAY MOLECULAR STRUCTURE O (2S,8R)-8-METHYL-2-PHENYL-1,7-DIOXASPIRO(5.5)UNDECAN-4(R)-OL Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198438356 |
0.403 |
|
| 1984 |
LEY SV, LYGO B. ChemInform Abstract: A NEW ROUTE TO SPIRO-KETALS USING THE HORNER-WITTIG REACTION OF 2-DIPHENYLPHOSPHINOXY CYCLIC ETHERS Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198417241 |
0.51 |
|
| 1983 |
LEY SV, LYGO B, MOLINES H, MORTON JA. ChemInform Abstract: SYNTHESIS OF (CIS-6-METHYLTETRAHYDROPYRAN-2-YL)ACETIC ACID INVOLVING THE USE OF AN ORGANOSELENIUM-MEDIATED CYCLIZATION REACTION Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198315227 |
0.532 |
|
| 1983 |
LEY SV, LYGO B. ChemInform Abstract: SYNTHESIS OF METHYL-1,6-DIOXASPIRO(4,5)DECANES USING ORGANOSELENIUM-MEDIATED CYCLIZATION REACTIONS Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198309201 |
0.54 |
|
| 1982 |
Ley SV, Lygo B. Synthesis of methyl-1,6-dioxaspiro[4,5]decanes using organoselenium mediated cyclization reactions Tetrahedron Letters. 23: 4625-4628. DOI: 10.1016/S0040-4039(00)85671-3 |
0.531 |
|
| 1982 |
Ley SV, Lygo B, Molines H, Morton JA. Synthesis of (cis-6-methyltetrahydropyran-2-yl)acetic acid involving the use of an organoselenium-mediated cyclization reaction Journal of the Chemical Society, Chemical Communications. 1251-1252. DOI: 10.1002/Chin.198315227 |
0.519 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 1999 |
Lygo B, Crosby J, Peterson JA. Enantioselective alkylation of alanine-derived imines using quaternary ammonium catalysts. Tetrahedron Letters. 40: 8671-8674. DOI: 10.1016/S0040-4039(99)01836-5 |
0.3 |
|
| 2002 |
Lygo B. Buchbesprechung: Quaternary Ammonium Salts. Their Use in Phase-Transfer Catalysis. Von R. Allen Jones Angewandte Chemie. 114: 1114-1115. DOI: 10.1002/1521-3757(20020315)114:6<1114::Aid-Ange1114>3.0.Co;2-J |
0.298 |
|
| 2002 |
Lygo B. Book Review: Quaternary Ammonium Salts. Their Use in Phase-Transfer Catalysis. By R. Allen Jones Angewandte Chemie International Edition. 41: 1074-1074. DOI: 10.1002/1521-3773(20020315)41:6<1074::Aid-Anie1074>3.0.Co;2-V |
0.296 |
|
| 1995 |
Lygo B. N-Acyl-2-methylaziridines: Synthesis and utility in the C-acylation of β-ketoester derived dianions Tetrahedron. 51: 12859-12868. DOI: 10.1016/0040-4020(95)00820-X |
0.279 |
|
| 2008 |
Lygo B. Phase-transfer reactions Second Supplements to the 2nd Edition of Rodd's Chemistry of Carbon Compounds: a Modern Comprehensive Treatise. 5: 101-149. DOI: 10.1016/B978-044453347-0.50420-1 |
0.275 |
|
| 1990 |
LYGO B, O'CONNOR N. ChemInform Abstract: Epoxide Ring Opening by Dianions Derived from β-Keto Sulfones. Synthetic Studies on the 7-Hydroxy-4-oxo-2,3-alkenoate System and Medium-Ring Lactones. Cheminform. 21. DOI: 10.1002/chin.199039209 |
0.273 |
|
| 1984 |
Godoy J, Ley SV, Lygo B. Synthesis of the spiroacetal unit related to the avermectins and milbemycins Journal of the Chemical Society, Chemical Communications. 1381-1382. |
0.257 |
|
| 1999 |
Lygo B, Wainwright PG. Phase-transfer catalysed asymmetric epoxidation of enones using N- anthracenylmethyl-substituted cinchona alkaloids Tetrahedron. 55: 6289-6300. DOI: 10.1016/S0040-4020(99)00205-7 |
0.256 |
|
| 1989 |
LYGO B. ChemInform Abstract: Stereoselective Synthesis of (.+-.)-Methyl Homononactate (VII) and (.+-.)-Methyl 8-epi-Homononactate (VIII). Cheminform. 20. DOI: 10.1002/chin.198912321 |
0.254 |
|
| 1988 |
LYGO B, O'CONNOR N. ChemInform Abstract: Stereoselective Synthesis of (.+-.)-Methyl Nonactate and (.+-.)-Methyl 8-epi- Nonactate. Cheminform. 19. DOI: 10.1002/chin.198803144 |
0.254 |
|
| 2010 |
LYGO B. ChemInform Abstract: Use of an Alanine-Derived β-Keto Sulfone in the Synthesis of Peptide Isosteres. Cheminform. 24: no-no. DOI: 10.1002/chin.199322178 |
0.242 |
|
| 1984 |
Doherty AM, Ley SV, Lygo B, Williams DJ. Synthesis of spiroacetals using organoselenium-mediated cyclisation reactions. X-Ray molecular structure of (2S,8R)-8-methyl-2-phenyl-1,7- dioxaspiro-[5.5]undecan-4(R)-ol Journal of the Chemical Society, Perkin Transactions 1. 1371-1377. |
0.242 |
|
| 1990 |
Lygo B, O'Connor N. Epoxide Ring Opening by Dianions Derived from β-Ketosulphones. Synthetic Studies on the 7-Hydroxy-4-oxopropenoate System and Medium-Ring Lactones Synlett. 1990: 282-284. DOI: 10.1055/s-1990-21066 |
0.241 |
|
| 2004 |
Lygo B, Andrews BI, Hirst JD, Melville JL, Peterson JA, Slack D. Rapid screening of cinchona alkaloid derived phase-transfer catalysts. Application in the optimization of a glycine imine alkylation Chimica Oggi. 22: 8-10. |
0.239 |
|
| 2002 |
Lygo B, To DCM. Asymmetric epoxidation via phase-transfer catalysis: Direct conversion of allylic alcohols into α,β-epoxyketones Chemical Communications. 2360-2361. |
0.228 |
|
| 2003 |
Lygo B, Bhatia M, Cooke JWB, Hirst DJ. Synthesis of (.+-.)-Solanapyrones A and B. Cheminform. 34. DOI: 10.1002/chin.200326231 |
0.201 |
|
| 2002 |
Lygo B. Use of an Alanine Derived ß-Ketosulfone in the Synthesis of Peptide Isosteres Synlett. 1992: 793-795. DOI: 10.1055/s-1992-21492 |
0.193 |
|
| 2006 |
Lygo B, Gardiner SD, To DCM. Stereoselective synthesis of the epoxysuccinyl peptide E-64c Synlett. 2063-2066. DOI: 10.1055/s-2006-948191 |
0.192 |
|
| 2010 |
LYGO B. ChemInform Abstract: N-Acyl Aziridines - C-Acylating Agents for the Preparation of Polyketides. Cheminform. 25: no-no. DOI: 10.1002/chin.199447129 |
0.191 |
|
| 1995 |
Lygo B, Rudd CN. Synthesis of Xaa-Gly-Xaa′ keto-methylene tri-peptide isosteres incorporating phenylalanine, tyrosine and valine units Tetrahedron Letters. 36: 3577-3580. DOI: 10.1016/0040-4039(95)00564-S |
0.185 |
|
| 1994 |
Lygo B, Swiatyj M, Trabsa H, Voyle M. Synthesis of (+)-Gabosines C and E from D-ribose Tetrahedron Letters. 35: 4197-4200. DOI: 10.1016/S0040-4039(00)73150-9 |
0.183 |
|
| 2010 |
ALOUI M, LYGO B, TRABSA H. ChemInform Abstract: Observations on the Modified Fujimoto-Belleau Approach to Mannose- Derived Carbocyclic Sugars. Cheminform. 25: no-no. DOI: 10.1002/chin.199429240 |
0.173 |
|
| 1999 |
Lygo B, Crosby J, Lowdon T, Wainwright PG. Asymmetric approaches to 2-hydroxymethylquinuclidine derivatives Tetrahedron. 55: 2795-2810. DOI: 10.1016/S0040-4020(99)00050-2 |
0.163 |
|
| 1994 |
Lygo B. N-acyl aziridines - C-acylating agents for the preparation of polyketides Tetrahedron Letters. 35: 5073-5074. DOI: 10.1016/S0040-4039(00)73323-5 |
0.159 |
|
| 1988 |
Lygo B. Stereoselective synthesis of (±)-methyl homononactate and (±)-methyl 8-epi-homononactate Tetrahedron. 44: 6889-6896. DOI: 10.1016/S0040-4020(01)86218-9 |
0.159 |
|
| 1987 |
Lygo B, O'Connor N. Stereoselective synthesis of (±)-methyl nonactate and (±)-methyl 8-epi-nonactate. Tetrahedron Letters. 28: 3597-3600. DOI: 10.1016/S0040-4039(00)95545-X |
0.159 |
|
| 2005 |
Melville JL, Lovelock KR, Wilson C, Allbutt B, Burke EK, Lygo B, Hirst JD. Exploring phase-transfer catalysis with molecular dynamics and 3D/4D quantitative structure-selectivity relationships. Journal of Chemical Information and Modeling. 45: 971-81. PMID 16045291 DOI: 10.1021/Ci050051L |
0.142 |
|
| 2010 |
Lygo B, Beaumont DJ, Cooke JWB, Hirst DJ. Synthesis of brombyins II and III, cyclostachines A and B, and cyclopiperstachine, plant-derived octahydronaphthalenes Synlett. 618-622. DOI: 10.1055/S-0029-1219158 |
0.13 |
|
| 1994 |
Aloui M, Lygo B, Trabsa H. Observations on the Modified Fujimoto-Belleau Approach to Mannose-Derived Carbocyclic Sugars Synlett. 1994: 115-116. DOI: 10.1055/s-1994-22759 |
0.118 |
|
| 1993 |
Balmer E, Germain A, Jackson WP, Lygo B. Larger scale preparation of optically-active allylic alcohols Journal of the Chemical Society, Perkin Transactions 1. 399-400. |
0.081 |
|
| Hide low-probability matches. |
