Improved Synthesis of Cyclic α-Hydrazino Acids of Five- to Nine-Membered Rings and Optical Resolution of 5,6,7-Membered Ring Hydrazino Acids

REFERENCES

• Duttagupta , I. ; Goswami , K. ; Sinha , S. Tetrahedron 2012 , 68 , 8347 – 8357 .
   Web of Science ®Google Scholar
• (a) Hale , K. J. ; Cai , J. ; Delisser , V. ; Manaviazar , S. ; Peak , S. A. ; Bhatia , G. S. ; Collins , T. C. ; Jogiya , N. Tetrahedron 1996, 52, 1047–1068; (b) Coats , R. A. ; Lee , S. L. ; Davis , K. A. ; Patel , K. M. ; Rhoads , E. K. ; Howard , M. H. J. Org. Chem. 2004, 69, 1734–1737; (c) Makino , K. ; Henmi , Y. ; Terasawa , M. ; Harab , O. ; Hamadaa , Y. Tetrahedron Lett. 2005, 46, 555–558; (d) Henmi , Y. ; Makino , K. ; Yoshitomi , Y. ; Hara , O. ; Hamada , Y. Tetrahedron: Asymmetry 2004, 15, 3477–3481; (e) Kennedy , J. P. ; Lindsley , C. W. Tetrahedron Lett. 2010, 51, 2493–2496; (f) Hannachi , J. C. ; Vidal , J. ; Mulatier , J. C. ; Collet , A. J. Org. Chem. 2004, 69, 2367–2373; (g) Li , W. ; Gan , J. ; Ma , D. Org. Lett. 2009, 11, 5694–5697; (h) Chen , M. H. ; Goel , O. P. ; Hyun , J. W. ; Magano , J. ; Rubin , J. R. Bioorg. Med. Chem. Lett. 1999, 9, 1587–1592; (i) Hale , K. J. ; Delisser , V. M. ; Manaviamr , S. Tetrahedron Lett. 1992, 33, 7613–7616; (j) Hassall , C. H. ; Johnson , W. H. ; Theobald , C. J. J. Chem. Soc., Perkin Trans. 1 1979, 1451–1454; (k) Kennedy , J. P. ; Brogan , J. T. ; Lindsley , C. W. Tetrahedron Lett. 2008, 49, 4116–4118; (l) Aoyagi , Y. ; Saitoh , Y. ; Ueno , T. ; Horiguchi , M. ; Takeya , K. J. Org. Chem. 2003, 68, 6899–6904; (m) Küchenthal , C. H. ; Maison , W. Synthesis 2010, 719–740.
   Web of Science ®Google Scholar
• (a) Kim , H. O. ; Lum , C. ; Lee , M. S. Tetrahedron Lett. 1997 , 38 , 4935 – 4938 ; (b) Mish , M. R. ; Guerra , F. M. ; Carreira , E. M. J. Am. Chem. Soc. 1997 , 119 , 8379 – 8380 ; (c) Voss , E. ; Arrault , A. ; Bodiguel , J. ; Jamart-Grégoire , B. Tetrahedron: Asymmetry 2009 , 20 , 1809 – 1812 .
   Web of Science ®Google Scholar
• (a) Guerra , F. M. ; Mish , M. R. ; Carreira , E. M. Org. Lett. 2000 , 2 , 4265 – 4267 ; (b) de los Santos , J. M. ; López , Y. ; Aparicio , D. ; Palacios , F. J. Org. Chem. 2008 , 73 , 550 – 557 .
   PubMed Web of Science ®Google Scholar
• Rutjes , F. P. J. T. ; Teerhuis , N. M. ; Hiemstra , H. ; Speckamp , W. N. Tetrahedron 1993 , 49 , 8605 – 8628 .
   Web of Science ®Google Scholar
• Vougioukalakis , G. C. ; Grubbs , R. H. Chem. Rev. 2010 , 110 , 1746 – 1787 .
   PubMed Web of Science ®Google Scholar
• (a) Brea , R. J. ; Amorin , M. ; Castedo , L. ; Granja , J. R. Angew. Chem., Int. Ed. Engl. 2005 , 44 , 5710 – 5713 ; (b) McKeever , B. ; Pattenden , G. Tetrahedron 2003 , 59 , 2713 – 2727 .
   PubMed Web of Science ®Google Scholar
• X-ray crystallographic data for compounds 22a and 23a have been deposited to the Cambridge Crystallographic Data Centre and assigned the deposition number CCDC 951986 (for 22a) and 951987(for 23a) .
   Google Scholar
• Color versions of one or more of the figures in the article can be found online at www.tandfonline.com/lsyc.
   Google Scholar