Diastereoselective Synthesis of Cyclopropyl Boronic Esters

Synlett

Volumn 1997, Issue 8, 1997, Pages 977-979

  Pietruszka, Jörg ^a   Widenmeyer, Markus ^a  

^a UNIVERSITY OF STUTTGART   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0002803025     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1997-5790     Document Type: Article

References (38)

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13. For applications of this method in polycyclopropane synthesis, see for instance: (c) McDonald, W. S.; Verbicky, C. A.; Zercher, C. K. J. Org. Chem. 1997, 62, 1215; (d) Charette, A. B.; Lebel, H. J. Am. Chem. Soc. 1996, 118, 10327; (e) Barrett, A. G. M.; Kasdorf, K. J. Am. Chem. Soc. 1996, 118, 11030; (f) Barrett, A. G. M.; Hamprecht, D.; White, A. J. P.; Williams, D. J. J. Am. Chem. Soc. 1996, 118, 7863.
14. For applications of this method in polycyclopropane synthesis, see for instance: (c) McDonald, W. S.; Verbicky, C. A.; Zercher, C. K. J. Org. Chem. 1997, 62, 1215; (d) Charette, A. B.; Lebel, H. J. Am. Chem. Soc. 1996, 118, 10327; (e) Barrett, A. G. M.; Kasdorf, K. J. Am. Chem. Soc. 1996, 118, 11030; (f) Barrett, A. G. M.; Hamprecht, D.; White, A. J. P.; Williams, D. J. J. Am. Chem. Soc. 1996, 118, 7863.
15. For applications of this method in polycyclopropane synthesis, see for instance: (c) McDonald, W. S.; Verbicky, C. A.; Zercher, C. K. J. Org. Chem. 1997, 62, 1215; (d) Charette, A. B.; Lebel, H. J. Am. Chem. Soc. 1996, 118, 10327; (e) Barrett, A. G. M.; Kasdorf, K. J. Am. Chem. Soc. 1996, 118, 11030; (f) Barrett, A. G. M.; Hamprecht, D.; White, A. J. P.; Williams, D. J. J. Am. Chem. Soc. 1996, 118, 7863.
16. For applications of this method in polycyclopropane synthesis, see for instance: (c) McDonald, W. S.; Verbicky, C. A.; Zercher, C. K. J. Org. Chem. 1997, 62, 1215; (d) Charette, A. B.; Lebel, H. J. Am. Chem. Soc. 1996, 118, 10327; (e) Barrett, A. G. M.; Kasdorf, K. J. Am. Chem. Soc. 1996, 118, 11030; (f) Barrett, A. G. M.; Hamprecht, D.; White, A. J. P.; Williams, D. J. J. Am. Chem. Soc. 1996, 118, 7863.
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35. Note that the same selectivity (∼ 25% ee) was obtained when adding Pd(II)-acetate to the reaction mixture after the addition of diazomethane under standard conditions.
36. 16O requires 128.1201).
37. Caution: The generation and the handling with diazomethane requires special precautions: Lombardi, P. Chem. Ind. (London) Nov. 5, 1990, 708; Moss, S. ibid. Feb. 21, 1994, 122.
38. Caution: The generation and the handling with diazomethane requires special precautions: Lombardi, P. Chem. Ind. (London) Nov. 5, 1990, 708; Moss, S. ibid. Feb. 21, 1994, 122.