Crossref journal-article
American Chemical Society (ACS)
Organic Letters (316)
Authors 7
  1. Giuseppe Bartoli (first)
  2. Marcella Bosco (additional)
  3. Armando Carlone (additional)
  4. Manuela Locatelli (additional)
  5. Massimo Massaccesi (additional)
  6. Paolo Melchiorre (additional)
  7. Letizia Sambri (additional)
References 21 Referenced 114
  1. {'key': 'ol049372tb00001/ol049372tb00001_1', 'first-page': '243', 'volume-title': 'S. C. Tetrahedron', 'author': 'For', 'year': '2000'} / S. C. Tetrahedron by For (2000)
  2. 10.1002/anie.199604511 / Angew. Chem., Int. Ed. Engl. by Li G. (1996)
  3. 10.1002/(SICI)1521-3773(19990201)38:3<326::AID-ANIE326>3.0.CO;2-T / Angew. Chem., Int. Ed. by Review (1999)
  4. 10.1021/ja001923x / J. Am. Chem. Soc. by List B. (2000)
  5. 10.1021/ja017270h / J. Am. Chem. Soc. by Córdova A. (2002)
  6. 10.1021/ja028782e / J. Am. Chem. Soc. by Trost B. M. (2003)
  7. 10.1021/ja973527t / J. Am. Chem. Soc. by Kobayashi S. (1998)
  8. 10.1021/ja034787f / J. Am. Chem. Soc. by Matsunaga S. (2003)
  9. 10.1021/jo00209a047 / J. Org. Chem. by For (1985)
  10. 10.1016/S0957-4166(98)00153-0 / Tetrahedron: Asymmetry by Moderate (1998)
  11. {'volume-title': 'L. E.', 'year': '1995', 'author': 'Highly', 'key': 'ol049372tb00007/ol049372tb00007_1'} / L. E. by Highly (1995)
  12. 10.1002/anie.200352073 / Angew. Chem., Int. Ed. by Bandini M. (2004)
  13. 10.1002/1615-4169(20010129)343:1<5::AID-ADSC5>3.0.CO;2-I / Adv. Synth. Catal. by Keith J. M. (2001)
  14. {'volume-title': 'where ee is the enantiomeric excess of the amino alcohol product and c is the conversion', 'author': 'The', 'key': 'ol049372tb00011/ol049372tb00011_1'} / where ee is the enantiomeric excess of the amino alcohol product and c is the conversion by The
  15. 10.1021/ol026456y / Org. Lett. by Keck G. E. (2002)
  16. 10.1021/jo00135a016 / J. Org. Chem. by Kronenthal D. R. (1982)
  17. 10.1021/jo00236a028 / J. Org. Chem. by It (1988)
  18. {'volume-title': 'only the anti-diastereomer and a single regioisomer was detected by NMR and HPLC analysis. The relative stereochemistry was established through NOE studies on the corresponding cyclic carbamates', 'author': 'In', 'key': 'ol049372tb00014/ol049372tb00014_1'} / only the anti-diastereomer and a single regioisomer was detected by NMR and HPLC analysis. The relative stereochemistry was established through NOE studies on the corresponding cyclic carbamates by In
  19. {'volume-title': 'For products 6 the absolute configuration was assigned by analogy', 'author': 'The', 'key': 'ol049372tb00015/ol049372tb00015_1'} / For products 6 the absolute configuration was assigned by analogy by The
  20. 10.1021/jo990060r / J. Org. Chem. by Thomas A. A. (1999)
  21. 10.1021/ja962600x / J. Am. Chem. Soc. by For (1996)
Dates
Type When
Created 21 years, 2 months ago (June 17, 2004, 12:55 a.m.)
Deposited 3 years, 10 months ago (Oct. 18, 2021, 1:35 a.m.)
Indexed 3 months, 1 week ago (May 9, 2025, 12:47 p.m.)
Issued 21 years, 3 months ago (May 22, 2004)
Published 21 years, 3 months ago (May 22, 2004)
Published Online 21 years, 3 months ago (May 22, 2004)
Published Print 21 years, 2 months ago (June 1, 2004)
Funders 0

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@article{Bartoli_2004, title={Asymmetric Aminolysis of Aromatic Epoxides:  A Facile Catalytic Enantioselective Synthesis of anti-β-Amino Alcohols}, volume={6}, ISSN={1523-7052}, url={http://dx.doi.org/10.1021/ol049372t}, DOI={10.1021/ol049372t}, number={13}, journal={Organic Letters}, publisher={American Chemical Society (ACS)}, author={Bartoli, Giuseppe and Bosco, Marcella and Carlone, Armando and Locatelli, Manuela and Massaccesi, Massimo and Melchiorre, Paolo and Sambri, Letizia}, year={2004}, month=may, pages={2173–2176} }