Year |
Citation |
Score |
2019 |
Anderson JC, Zhang X. A Divergent Synthetic Route to the Vallesamidine, Strempeliopine and Schizozygine Alkaloids: Total Synthesis of (+)-Vallesamidine and (+)-14,15-Dehydrostrempeliopine. Angewandte Chemie (International Ed. in English). PMID 31538685 DOI: 10.1002/anie.201910593 |
0.366 |
|
2016 |
Anderson JC, Campbell IB, Campos S, Reid IH, Rundell CD, Shannon J, Tizzard GJ. Reductive conjugate addition nitro-Mannich route for the stereoselective synthesis of 1,2,3,4-tetrahydroquinoxalines. Organic & Biomolecular Chemistry. PMID 27527672 DOI: 10.1039/c6ob01530a |
0.332 |
|
2016 |
Anderson JC, Rundell CD. Stereoselective Synthesis of Densely Substituted Tetrahydroquinolines by a Conjugate Addition Nitro-Mannich Reaction with Carbon Nucleophiles Synlett. 27: 41-44. DOI: 10.1055/s-0035-1560815 |
0.318 |
|
2016 |
Anderson JC, Barham JP, Rundell CD. ChemInform Abstract: Asymmetric Intramolecular Conjugate Addition Nitro-Mannich Route to cis-2-Aryl-3-nitrotetrahydroquinolines. Cheminform. 47. DOI: 10.1002/chin.201602144 |
0.705 |
|
2015 |
Anderson JC, Barham JP, Rundell CD. Asymmetric Intramolecular Conjugate Addition Nitro-Mannich Route to cis-2-Aryl-3-nitrotetrahydroquinolines. Organic Letters. 17: 4090-3. PMID 26270567 DOI: 10.1021/Acs.Orglett.5B02036 |
0.716 |
|
2015 |
Anderson JC, Campbell IB, Campos S, Shannon J, Tocher DA. Stereoselective synthesis of 1,2-diamine containing indolines by a conjugate addition nitro-Mannich reaction. Organic & Biomolecular Chemistry. 13: 170-7. PMID 25351774 DOI: 10.1039/c4ob01793e |
0.321 |
|
2015 |
Anderson JC, Barham JP, Rundell CD. Asymmetric Intramolecular Conjugate Addition Nitro-Mannich Route to cis-2-Aryl-3-nitrotetrahydroquinolines Organic Letters. 17: 4090-4093. DOI: 10.1021/acs.orglett.5b02036 |
0.7 |
|
2012 |
Anderson JC, Noble A, Tocher DA. Reductive nitro-Mannich route for the synthesis of 1,2-diamine containing indolines and tetrahydroquinolines. The Journal of Organic Chemistry. 77: 6703-27. PMID 22849665 DOI: 10.1021/Jo3010827 |
0.352 |
|
2012 |
Anderson JC, Horsfall LR, Kalogirou AS, Mills MR, Stepney GJ, Tizzard GJ. Stereoselective synthesis of densely functionalized pyrrolidin-2-ones by a conjugate addition/nitro-Mannich/lactamization reaction. The Journal of Organic Chemistry. 77: 6186-98. PMID 22708711 DOI: 10.1021/jo301000r |
0.362 |
|
2012 |
Anderson JC, Noble A, Torres PR. An intramolecular nitro-Mannich route to functionalised tetrahydroquinolines Tetrahedron Letters. 53: 5707-5710. DOI: 10.1016/J.Tetlet.2012.08.062 |
0.345 |
|
2010 |
Anderson JC, Davies EA. Diastereoselective synthesis of substituted prolines via 5-endo-trig cyclisations of aza-[2,3]-Wittig sigmatropic rearrangement products Tetrahedron. 66: 6300-6308. DOI: 10.1016/j.tet.2010.04.095 |
0.378 |
|
2010 |
Anderson JC, Cornell AC, Hodgkinson TJ, Wilkinson JA. ChemInform Abstract: Efficient Diastereoselective Synthesis of Either Form of meso-2,6-Dimethylcyclohexane Carboxaldehyde. Cheminform. 32: no-no. DOI: 10.1002/chin.200135026 |
0.338 |
|
2010 |
Adams H, Anderson JC, Peace S, Pennell AMK. ChemInform Abstract: The Nitro-Mannich Reaction and Its Application to the Stereoselective Synthesis of 1,2-Diamines. Cheminform. 30: no-no. DOI: 10.1002/chin.199925036 |
0.315 |
|
2010 |
ANDERSON JC, PEARSON DJ. ChemInform Abstract: A Strategy for the Synthesis of Popolohuanone E: Formal Total Synthesis of (.+-.)-Arenarol. Cheminform. 29: no-no. DOI: 10.1002/chin.199849296 |
0.348 |
|
2010 |
ANDERSON JC, SMITH SC, SWARBRICK ME. ChemInform Abstract: Diastereoselective Acyclic Aza-(2,3) Wittig Sigmatropic Rearrangements. Cheminform. 28: no-no. DOI: 10.1002/chin.199742104 |
0.302 |
|
2010 |
DOBLER M, ANDERSON JC, JUCH M, BORSCHBERG H. ChemInform Abstract: Synthesis of Aristotelia-Type Alkaloids. Part 15. Total Synthesis of (+ )-Hobartinol. Cheminform. 26: no-no. DOI: 10.1002/chin.199531217 |
0.352 |
|
2010 |
ANDERSON JC, LEY SV, MARSDEN SP. ChemInform Abstract: Studies Towards the Total Synthesis of Rapamycin: A Convergent and Stereoselective Synthesis of the C22-C32 Carbon Framework Cheminform. 25: no-no. DOI: 10.1002/chin.199429291 |
0.548 |
|
2010 |
LEY SV, ANDERSON JC, BLANEY WM, MORGAN ED, SHEPPARD RN, SIMMONDS MSJ, SLAWIN AMZ, SMITH SC, WILLIAMS DJ, WOOD A. ChemInform Abstract: Chemistry of Insect Antifeedants from Azadirachta indica. Part 11. Characterization and Structure Activity Relationships of Some Novel Rearranged Azadirachtins. Cheminform. 23: no-no. DOI: 10.1002/chin.199209306 |
0.478 |
|
2010 |
ANDERSON JC, LEY SV, SANTAFIANOS D, SHEPPARD RN. ChemInform Abstract: Chemistry of Insect Antifeedants from Azadirachta indica. Part 8. Synthesis of Hydroxydihydrofuran Acetal Fragments for Biological Evaluation and Azadirachtin Total Synthesis Studies. Cheminform. 22: no-no. DOI: 10.1002/chin.199148224 |
0.59 |
|
2010 |
ANDERSON JC, LEY SV. ChemInform Abstract: Chemistry of Insect Antifeedants from Azadirachta indica. Part 7. Preparation of an Optically Pure Hydroxyacetal Epoxide (II) Related to Azadirachtin. Cheminform. 22: no-no. DOI: 10.1002/chin.199118295 |
0.445 |
|
2009 |
Cross WB, Anderson JC, Wilson CS. Nucleophilic reactivity of a d0 molybdenum oxo moiety. Dalton Transactions (Cambridge, England : 2003). 1201-5. PMID 19322492 DOI: 10.1039/B817745G |
0.313 |
|
2009 |
Ley SV, Tackett MN, Maddess ML, Anderson JC, Brennan PE, Cappi MW, Heer JP, Helgen C, Kori M, Kouklovsky C, Marsden SP, Norman J, Osborn DP, Palomero MA, Pavey JB, et al. Total synthesis of rapamycin. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 2874-914. PMID 19204960 DOI: 10.1002/Chem.200801656 |
0.696 |
|
2008 |
Ley SV, Abad-Somovilla A, Anderson JC, Ayats C, Bänteli R, Beckmann E, Boyer A, Brasca MG, Brice A, Broughton HB, Burke BJ, Cleator E, Craig D, Denholm AA, Denton RM, et al. The synthesis of azadirachtin: a potent insect antifeedant. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 10683-704. PMID 18821532 DOI: 10.1002/Chem.200801103 |
0.727 |
|
2008 |
Munday RH, Denton RM, Anderson JC. Asymmetric synthesis of 6'-hydroxyarenarol: the proposed biosynthetic precursor to popolohuanone E. The Journal of Organic Chemistry. 73: 8033-8. PMID 18798670 DOI: 10.1021/Jo801404U |
0.708 |
|
2008 |
Anderson JC, Blake AJ, Mills M, Ratcliffe PD. A general one-step synthesis of beta-nitronitriles. Organic Letters. 10: 4141-3. PMID 18722454 DOI: 10.1021/Ol801691C |
0.311 |
|
2008 |
Veitch GE, Pinto A, Boyer A, Beckmann E, Anderson JC, Ley SV. Synthesis of natural products from the Indian neem tree Azadirachta indica. Organic Letters. 10: 569-72. PMID 18193879 DOI: 10.1021/Ol7027898 |
0.765 |
|
2008 |
Anderson JC, Osborne JD, Woltering TJ. Enantioselective functionalisation of the C-2' position of 1,2,3,4,5-pentamethylazaferrocene via sparteine mediated lithiation: potential new ligands for asymmetric catalysis. Organic & Biomolecular Chemistry. 6: 330-9. PMID 18175002 DOI: 10.1039/B715323F |
0.414 |
|
2008 |
Ley S, Abad-Somovilla A, Anderson J, Ayats C, Bänteli R, Beckmann E, Boyer A, Brasca M, Brice A, Broughton H, Burke B, Cleator E, Craig D, Denholm A, Denton R, et al. Cover Picture: The Synthesis of Azadirachtin: A Potent Insect Antifeedant (Chem. Eur. J. 34/2008) Chemistry - a European Journal. 14: 10503-10503. DOI: 10.1002/Chem.200890139 |
0.767 |
|
2007 |
Anderson JC, Chapman HA. Regiochemical switching of Mitsunobu cyclisation mode of vicinal diamines with pendant hydroxyl group. Organic & Biomolecular Chemistry. 5: 2413-22. PMID 17637961 DOI: 10.1039/B705081J |
0.386 |
|
2006 |
Anderson JC, Chapman HA. Aluminum amalgam for the reduction of sensitive β-nitroamines to 1,2-diamines Synthesis. 3309-3315. DOI: 10.1055/S-2006-950229 |
0.314 |
|
2005 |
Anderson JC, Ford JG, Whiting M. Chirality transfer in the aza-[2,3]-Wittig sigmatropic rearrangement. Organic & Biomolecular Chemistry. 3: 3734-48. PMID 16211110 DOI: 10.1039/B510756C |
0.403 |
|
2005 |
Anderson JC, O'Loughlin JM, Tornos JA. Asymmetric aza-[2,3]-Wittig sigmatropic rearrangements: chiral auxiliary control and formal asymmetric synthesis of (2S, 3R, 4R)-4-hydroxy-3-methylproline and (-)-kainic acid. Organic & Biomolecular Chemistry. 3: 2741-9. PMID 16032352 DOI: 10.1039/B506198A |
0.388 |
|
2005 |
Anderson JC, Howell GP, Lawrence RM, Wilson CS. An asymmetric nitro-Mannich reaction applicable to alkyl, aryl, and heterocyclic imines. The Journal of Organic Chemistry. 70: 5665-70. PMID 15989351 DOI: 10.1021/Jo050762I |
0.381 |
|
2005 |
Anderson JC, Headley C, Stapleton PD, Taylor PW. Synthesis and antibacterial activity of hydrolytically stable (-)-epicatechin gallate analogues for the modulation of beta-lactam resistance in Staphylococcus aureus. Bioorganic & Medicinal Chemistry Letters. 15: 2633-5. PMID 15863332 DOI: 10.1016/J.Bmcl.2005.03.063 |
0.356 |
|
2005 |
Anderson JC, Blake AJ, Howell GP, Wilson C. Scope and limitations of the nitro-Mannich reaction for the stereoselective synthesis of 1,2-diamines. The Journal of Organic Chemistry. 70: 549-55. PMID 15651800 DOI: 10.1021/Jo048304H |
0.387 |
|
2005 |
Anderson JC, Denton RM, Wilson C. A biomimetic strategy for the synthesis of the tricyclic dibenzofuran-1,4-dione core of popolohuanone E. Organic Letters. 7: 123-5. PMID 15624993 DOI: 10.1021/Ol047825O |
0.698 |
|
2005 |
Anderson JC, Osborne J. The Synthesis of New Planar Chiral Heterobidentate Chelate Ligands for Asymmetric Catalysis. Cheminform. 36. DOI: 10.1016/J.Tetasy.2005.01.026 |
0.364 |
|
2005 |
Anderson JC, Denton RM, Wilson C. A Biomimetric Strategy for the Synthesis of the Tricyclic Dibenzofuran-1,4-dione Core (I) of Popolohuanone E (II). Cheminform. 36. DOI: 10.1002/chin.200520224 |
0.641 |
|
2004 |
Anderson JC, Munday RH. Vinyldimethylphenylsilanes as safety catch silanols in fluoride-free palladium-catalyzed cross-coupling reactions. The Journal of Organic Chemistry. 69: 8971-4. PMID 15575787 DOI: 10.1021/Jo048746T |
0.374 |
|
2004 |
Anderson JC, Denton RM, Hickin HG, Wilson C. Synthesis of dibenzofuran-1,4-diones using the Dötz benzannulation Tetrahedron. 60: 2327-2335. DOI: 10.1016/j.tet.2004.01.021 |
0.708 |
|
2004 |
Anderson JC, Denton RM, Hickin HG, Wilson C. Synthesis of Dibenzofuran-1,4-diones Using the Doetz Benzannulation. Cheminform. 35. DOI: 10.1016/J.Tet.2004.01.021 |
0.706 |
|
2004 |
Anderson JC, Cran JW, King NP. Studies into Diastereoselective Doetz Benzannulations for the Synthesis of Axially Chiral Biaryls. Cheminform. 35. DOI: 10.1002/chin.200404080 |
0.335 |
|
2003 |
Anderson JC, Blake AJ, Arnall-Culliford JC. Synthesis of planar chiral ferrocenyl 1,3-diamines and 1,3-amino ethers. Organic & Biomolecular Chemistry. 1: 3586-91. PMID 14599022 DOI: 10.1039/B307014J |
0.364 |
|
2003 |
Anderson JC, Blake AJ, Graham JP, Wilson C. Investigation of the asymmetric ionic Diels-Alder reaction for the synthesis of cis-decalins. Organic & Biomolecular Chemistry. 1: 2877-85. PMID 12968338 DOI: 10.1039/B305116A |
0.439 |
|
2003 |
Anderson JC, Whiting M. Total synthesis of (+/-)-kainic Acid with an aza-[2,3]-Wittig sigmatropic rearrangement as the key stereochemical determining step. The Journal of Organic Chemistry. 68: 6160-3. PMID 12895045 DOI: 10.1021/Jo030101Q |
0.401 |
|
2003 |
Anderson JC, Blake AJ, Graham JP, Wilson C. Investigation of the asymmetric ionic Diels-Alder reaction for the synthesis of cis-decalins Organic and Biomolecular Chemistry. 1: 2877-2885. DOI: 10.1039/b305116a |
0.334 |
|
2003 |
Anderson JC, Skerratt S. Synthesis of α,α-Disubstituted Unnatural Amino Acid Derivatives Using the Aza[2,3]Wittig Sigmatropic Rearrangement. Cheminform. 34. DOI: 10.1039/B207295E |
0.358 |
|
2003 |
Anderson JC, Cran JW, King NP. Studies into diastereoselective Dötz benzannulations for the synthesis of axially chiral biaryls Tetrahedron Letters. 44: 7771-7774. DOI: 10.1016/J.Tetlet.2003.08.096 |
0.401 |
|
2002 |
Anderson JC, Anguille S, Bailey R. The direct use of phenyldimethylsilanes in silicon assisted palladium catalysed cross coupling. Chemical Communications (Cambridge, England). 2018-9. PMID 12357758 DOI: 10.1039/B205765D |
0.342 |
|
2002 |
Anderson JC, Cran JW, King NP. Steric and electronic limitations for the Dötz benzannulation of aromatic alkynes Tetrahedron Letters. 43: 3849-3852. DOI: 10.1016/S0040-4039(02)00680-9 |
0.398 |
|
2001 |
Anderson JC, Cornell AC, Hodgkinson TJ, Wilkinson JA. Efficient diastereoselective synthesis of either form of meso-2,6-dimethylcyclo-hexane carboxaldehyde Synthetic Communications. 31: 939-946. DOI: 10.1081/Scc-100103331 |
0.392 |
|
2001 |
Anderson JC, Flaherty A. Stereocontrolled synthesis of (2S*,3R*,4R*)-4-hydroxy-3-methylproline using a silicon assisted aza-[2,3]-Wittig sigmatropic rearrangement Journal of the Chemical Society-Perkin Transactions 1. 267-269. DOI: 10.1039/B007586H |
0.31 |
|
2001 |
Anderson JC, Cubbon RJ, Harling JD. Investigation of the importance of nitrogen substituents in a N–P chiral ligand for enantioselective allylic alkylation Tetrahedron: Asymmetry. 12: 923-935. DOI: 10.1016/S0957-4166(01)00137-9 |
0.384 |
|
2000 |
Anderson JC, Flaherty A. Strategies for protodesilylation of C-2 trialkylsilyl terminal alkenes Journal of the Chemical Society-Perkin Transactions 1. 3025-3027. DOI: 10.1039/B006049F |
0.322 |
|
2000 |
Anderson JC, McDermott BP, Griffin EJ. Asymmetric Epoxide Cyclisation Route to the F-pyran Fragment of the Altohyrtins and Key Aldol Studies Tetrahedron. 56: 8747-8767. DOI: 10.1016/S0040-4020(00)00804-8 |
0.37 |
|
1999 |
Anderson JC, Cubbon RJ, Harling JD. Dramatic reversal of enantioselection in a palladium catalysed allylic substitution by choice of nitrogen substituents in a N–P chiral ligand Tetrahedron: Asymmetry. 10: 2829-2832. DOI: 10.1016/S0957-4166(99)00298-0 |
0.374 |
|
1999 |
Anderson JC, McDermott BP. Asymmetric synthesis of the F-pyran fragment of the altohyrtins Tetrahedron Letters. 40: 7135-7138. DOI: 10.1016/S0040-4039(99)01481-1 |
0.396 |
|
1998 |
Anderson JC, Pearson DJ. A strategy for the synthesis of popolohuanone E: formal total synthesis of (±)-arenarol Journal of the Chemical Society-Perkin Transactions 1. 2023-2030. DOI: 10.1039/A802413H |
0.434 |
|
1998 |
Anderson JC. The importance of nitrogen substituents in chiral amino thiol ligands for the asymmetric addition of diethylzinc to aromatic aldehydes Chemical Communications. 393-394. DOI: 10.1039/A707937K |
0.343 |
|
1998 |
Anderson JC, Dupau P, Craig Siddons D, Smith SC, Swarbrick ME. The aza-[2,3]-Wittig sigmatropic rearrangement of Z(C)-alkenes Tetrahedron Letters. 39: 2649-2650. DOI: 10.1016/S0040-4039(98)00229-9 |
0.389 |
|
1998 |
Anderson JC, Roberts CA. The tri-n-butyltin group as a novel stereocontrol element and synthetic handle in the aza-[2,3]-Wittig sigmatropic rearrangement Tetrahedron Letters. 39: 159-162. DOI: 10.1016/S0040-4039(97)10477-4 |
0.424 |
|
1995 |
Simmonds MSJ, Blaney WM, Ley SV, Anderson JC, Banteli R, Denholm AA, Green PCW, Grossman RB, Gutteridge C, Jennens L, Smith SC, Toogood PL, Wood A. Behavioural and neurophysiological responses of Spodoptera littoralis to azadirachtin and a range of synthetic analogues Entomologia Experimentalis Et Applicata. 77: 69-80. DOI: 10.1111/J.1570-7458.1995.Tb01987.X |
0.639 |
|
1995 |
Dobler M, Anderson JC, Juch M, Borschberg H. Synthesis ofAristotelia-Type Alkaloids. Part XV. Total synthesis of (+)-hobartinol Helvetica Chimica Acta. 78: 292-300. DOI: 10.1002/hlca.19950780204 |
0.334 |
|
1994 |
Anderson JC, Ley SV, Marsden SP. Studies towards the total synthesis of rapamycin: A convergent and stereoselective synthesis of the C22C32 carbon framework Tetrahedron Letters. 35: 2087-2090. DOI: 10.1016/S0040-4039(00)73057-7 |
0.646 |
|
1994 |
Blaney WM, Simmonds MSJ, Ley SV, Anderson JC, Smith SC, Wood A. Effect of azadirachtin-derived decalin (perhydronaphthalene) and dihydrofuranacetal (furo[2, 3-fo]pyran) fragments on the feeding behaviour of Spodoptera littoralis Pesticide Science. 40: 169-173. DOI: 10.1002/Ps.2780400212 |
0.526 |
|
1991 |
Ley SV, Anderson JC, Blaney WM, Morgan E, Sheppard RN, Simmonds MS, Slawin AM, Smith SC, Williams DJ, Wood A. Chemistry of insect antifeedants from Azadirachta indica (part 11): Characterisation and structure activity relationships of some novel rearranged azadirachtins. Tetrahedron. 47: 9231-9246. DOI: 10.1016/S0040-4020(01)96211-8 |
0.554 |
|
1990 |
Simmonds MSJ, Blaney WM, Ley SV, Anderson JC, Toogood PL. Azadirachtin: structural requirements for reducing growth and increasing mortality in lepidopterous larvae Entomologia Experimentalis Et Applicata. 55: 169-181. DOI: 10.1111/J.1570-7458.1990.Tb01360.X |
0.497 |
|
1990 |
Blaney WM, Simmonds MSJ, Ley SV, Anderson JC, Toogood PL. Antifeedant effects of azadirachtin and structurally related compounds on lepidopterous larvae Entomologia Experimentalis Et Applicata. 55: 149-160. DOI: 10.1111/J.1570-7458.1990.Tb01358.X |
0.501 |
|
1990 |
Anderson JC, Ley SV. Chemistry of insect antifeedants from azadirachta indica (part 7): Preparation of an optically pure hydroxyacetal epoxide related to azadirachtin. Tetrahedron Letters. 31: 3437-3440. DOI: 10.1016/S0040-4039(00)97416-1 |
0.522 |
|
1990 |
Anderson JC, Ley SV. Chemistry of insect antifeedants from azadirachta indica (part 6): Synthesis of an optically pure acetal intermediate for potential use in the synthesis of azadirachtin and novel antifeedants. Tetrahedron Letters. 31: 431-432. DOI: 10.1016/S0040-4039(00)94574-X |
0.595 |
|
1990 |
Cole MD, Anderson JC, Blaney WM, Fellows LE, Ley SV, Sheppard RN, Simmonds MS. Neo-clerodane insect antifeedants from Scutellaria galericulata Phytochemistry. 29: 1793-1796. DOI: 10.1016/0031-9422(90)85018-B |
0.491 |
|
1989 |
Anderson JC, Blaney WM, Cole MD, Fellows LL, Ley SV, Sheppard RN, Simmonds MS. The structure of two new clerodane diterpenoid potent insect antifeedants from Scutellaria woronowii (Juz); jodrellin A & B Tetrahedron Letters. 30: 4737-4740. DOI: 10.1016/S0040-4039(01)80789-9 |
0.486 |
|
1989 |
Ley SV, Anderson JC, Blaney WM, Jones PS, Lidert Z, Morgan E, Robinson NG, Santafianos D, Simmonds MS, Toogood PL. Insect antifeedants from azadirachta indica (part 5): Chemical modification and structure-activity relationships of azadirachtin and some related limonoids Tetrahedron. 45: 5175-5192. DOI: 10.1016/S0040-4020(01)81095-4 |
0.509 |
|
1989 |
LEY SV, ANDERSON JC, BLANEY WM, JONES PS, LIDERT Z, MORGAN ED, ROBINSON NG, SANTAFIANOS D, SIMMONDS MSJ, TOOGOOD PL. ChemInform Abstract: Insect Antifeedants from Azadirachta indica. Part 5. Chemical Modification and Structure-Activity Relationships of Azadirachtin and Some Related Limonoids. Cheminform. 20. DOI: 10.1002/chin.198951310 |
0.439 |
|
1988 |
Ley SV, Anderson JC, Blaney WM, Lidert Z, Morgan E, Robinson NG, Simmonds MS. Chemistry of insect antifeedants from azadirachta indica (part 3): reactions on the C-22,23 enol ether double bond of azadirachtin and conversion to 22,23-dihydro-23-β-methoxyazadirachtin. Tetrahedron Letters. 29: 5433-5436. DOI: 10.1016/S0040-4039(00)82888-9 |
0.569 |
|
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