| Year |
Citation |
Score |
| 2022 |
Williams MB, Wells RJ, Boyer A. Synthesis and reactivity of 1-sulfonylcyclooctatriazoles. Chemical Communications (Cambridge, England). PMID 36278837 DOI: 10.1039/d2cc03648g |
0.337 |
|
| 2022 |
Williams MB, Boyer A. Modular Synthesis of Highly Substituted 3-Azapyrroles by Rh(II)-Catalyzed N-H Bond Insertion and Cyclodehydration. The Journal of Organic Chemistry. PMID 35503987 DOI: 10.1021/acs.joc.2c00434 |
0.368 |
|
| 2015 |
Boyer A. Enantioselective synthesis of (+)-petromyroxol, enabled by rhodium-catalyzed denitrogenation and rearrangement of a 1-sulfonyl-1,2,3-triazole. The Journal of Organic Chemistry. 80: 4771-5. PMID 25891197 DOI: 10.1021/acs.joc.5b00399 |
0.376 |
|
| 2015 |
Clark JS, Romiti F, Hogg KF, Hamid MH, Richter SC, Boyer A, Redman JC, Farrugia LJ. Synthesis of cyclopropyl-substituted furans by brønsted Acid promoted cascade reactions. Angewandte Chemie (International Ed. in English). 54: 5744-7. PMID 25782604 DOI: 10.1002/Anie.201500625 |
0.563 |
|
| 2014 |
Boyer A. Rhodium(II)-catalyzed stereocontrolled synthesis of 2-tetrasubstituted saturated heterocycles from 1-sulfonyl-1,2,3-triazoles. Organic Letters. 16: 5878-81. PMID 25364826 DOI: 10.1021/ol5028267 |
0.363 |
|
| 2014 |
Boyer A. Rhodium(II)-catalyzed stereocontrolled synthesis of dihydrofuran-3-imines from 1-tosyl-1,2,3-triazoles. Organic Letters. 16: 1660-3. PMID 24575756 DOI: 10.1021/ol500309x |
0.366 |
|
| 2012 |
Clark JS, Boyer A, Aimon A, Engel García P, Lindsay DM, Symington AD, Danoy Y. Organocatalytic synthesis of highly substituted furfuryl alcohols and amines. Angewandte Chemie (International Ed. in English). 51: 12128-31. PMID 23097350 DOI: 10.1002/Anie.201207300 |
0.58 |
|
| 2011 |
Boyer A, Lautens M. Rhodium-catalyzed domino enantioselective synthesis of bicyclo[2.2.2]lactones. Angewandte Chemie (International Ed. in English). 50: 7346-9. PMID 21698727 DOI: 10.1002/Anie.201101773 |
0.482 |
|
| 2010 |
Webster R, Boyer A, Fleming MJ, Lautens M. Practical asymmetric synthesis of bioactive aminotetralins from a racemic precursor using a regiodivergent resolution Organic Letters. 12: 5418-5421. PMID 21043435 DOI: 10.1021/Ol1022239 |
0.485 |
|
| 2009 |
Boyer A, Veitch GE, Beckmann E, Ley SV. Second-generation synthesis of azadirachtin: a concise preparation of the propargylic mesylate fragment. Angewandte Chemie (International Ed. in English). 48: 1317-20. PMID 19140148 DOI: 10.1002/Anie.200805395 |
0.542 |
|
| 2008 |
Veitch GE, Boyer A, Ley SV. The azadirachtin story. Angewandte Chemie (International Ed. in English). 47: 9402-29. PMID 19031481 DOI: 10.1002/Anie.200802675 |
0.407 |
|
| 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 |
0.493 |
|
| 2008 |
Fuchter MJ, Smith CJ, Tsang MW, Boyer A, Saubern S, Ryan JH, Holmes AB. Clean and efficient synthesis of O-silylcarbamates and ureas in supercritical carbon dioxide. Chemical Communications (Cambridge, England). 2152-4. PMID 18438499 DOI: 10.1039/B801537F |
0.482 |
|
| 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 |
0.585 |
|
| 2007 |
Veitch GE, Beckmann E, Burke BJ, Boyer A, Maslen SL, Ley SV. Synthesis of azadirachtin: a long but successful journey. Angewandte Chemie (International Ed. in English). 46: 7629-32. PMID 17665403 DOI: 10.1002/Anie.200703027 |
0.434 |
|
| 2007 |
Veitch GE, Beckmann E, Burke BJ, Boyer A, Ayats C, Ley SV. A relay route for the synthesis of azadirachtin. Angewandte Chemie (International Ed. in English). 46: 7633-5. PMID 17665383 DOI: 10.1002/Anie.200703028 |
0.472 |
|
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