Organocatalytic stereoselective synthesis of passifloricin A

Organic and Biomolecular Chemistry

Volumn 10, Issue 9, 2012, Pages 1820-1825

  Kumar, Pradeep ^a   Pandey, Menaka ^a   Gupta, Priti ^a   Dhavale, Dilip D ^b  

^a NATIONAL CHEMICAL LABORATORY   (India)

^b UNIVERSITY OF PUNE   (India)

Author keywords

[No Author keywords available]

Indexed keywords

DIASTEREOMERIC EXCESS; ENANTIOSELECTIVE SYNTHESIS; LACTONE MOIETY; OLEFINATION; ORGANOCATALYTIC; RING CLOSING METATHESIS; STEREOSELECTIVE SYNTHESIS;

ALDEHYDES; AMINO ACIDS; STEREOCHEMISTRY;

STEREOSELECTIVITY;

PASSIFLORICIN A; PYRONE DERIVATIVE;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; STEREOISOMERISM; SYNTHESIS;

CATALYSIS; MOLECULAR STRUCTURE; PYRONES; STEREOISOMERISM;

EID: 84857216714     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c2ob06711k     Document Type: Article

References (43)

1. S. D. Rychnovsky Chem. Rev. 1995 95 2021
2. J. Jodynis-Liebert M. Murias E. Bloszyk Planta Med. 2000 66 199
3. S. E. Drewes B. M. Schlapelo Horn R. Scott-Shaw O. Sandor Phytochemistry 1995 38 1427
4. F. Echeverri V. Arango W. Quiñones F. Torres G. Escobar Y. Rosero R. Archbold Phytochemistry 2001 56 881
5. W. Cardona W. Quinones F. Echeverri Molecules 2004 9 666
6. J. Murga J. Garcia-Fortanet M. Carda J. A. Marco Tetrahedron Lett. 2003 44 7909
7. J. Garcia-Fortanet J. Murga M. Carda J. A. Marco Org. Lett. 2003 5 1447
8. J. Cossy S. BouzBouz M. C. R. Popkin C. R. Chim. 2003 6 547
9. S. BouzBouz J. Cossy Tetrahedron Lett. 2003 44 4471
10. J. Murga J. García-Fortanet M. Carda J. A. Marco J. Org. Chem. 2004 69 7277
11. S. Chandrasekhar C. H. Rambabu A. S. Reddy Tetrahedron Lett. 2008 49 4476
12. D. A. Evans J. A. Gauchet-Prunet J. Org. Chem. 1993 58 2446
13. T. J. Hunter G. A. O'Doherty Org. Lett. 2001 3 1049
14. Y. Wang Y. Xing Q. Zhang G. A. O'Doherty Chem. Commun. 2011 47 8493
15. G. Sabitha M. N. Prasad K. Shankaraiah M. N. Reddy J. S. Yadav Synthesis 2010 22 3891
16. P. I. Dalko, Enantioselective Organocatalysis: Reactions and Experimental Procedures Wiley, Weinheim, 2007
17. A. Dondoni A. Massi Angew. Chem., Int. Ed. 2008 47 4638
18. D. W. C. MacMillian Nature 2008 455 304
19. J. Casas M. Engqvist I. Ibrahem B. Kaynak A. Cordova Angew. Chem., Int. Ed. 2005 44 1343
20. D. B. Ramachary N. S. Chowdari C. F. Barbas Synlett 2003 1910
21. M. T. Hechavarria Fonseca B. List Angew. Chem., Int. Ed. 2004 43 3958
22. J. Franzen M. Marigo D. Fielenbach T. C. Wabnitz A. Kjærsgaard K. A. Jørgensen J. Am. Chem. Soc. 2005 127 18296
23. P. Merino T. Tejero Angew. Chem., Int. Ed. 2004 43 2995
24. B. List J. Am. Chem. Soc. 2002 124 5656
25. G. Zhong Y. Yu Org. Lett. 2004 6 1637
26. M. Lu D. Zhu Y. Lu Y. Hou B. Tan G. Zhong Angew. Chem., Int. Ed. 2008 47 10187
27. B. List Tetrahedron 2002 58 5573
28. D. Enders C. Grondal M. R. M. Hüttl Angew. Chem., Int. Ed. 2007 46 1570
29. X. Yu W. Wang Org. Biomol. Chem. 2008 6 2037
30. A. M. Walji D. W. C. MacMillan Synlett 2007 1477
31. N. B. Kondekar P. Kumar Org. Lett. 2009 11 2611
32. P. Kumar S. V. Naidu P. Gupta J. Org. Chem. 2005 70 2843
33. P. Kumar S. V. Naidu J. Org. Chem. 2005 70 4207
34. P. Gupta S. V. Naidu P. Kumar Tetrahedron Lett. 2005 46 6571
35. P. Kumar P. Gupta S. V. Naidu Chem.-Eur. J. 2006 12 1397
36. P. Kumar S. V. Naidu J. Org. Chem. 2006 71 3935
37. P. Gupta P. Kumar Eur. J. Org. Chem. 2008 1195
38. S. K Pandey M. Pandey P. Kumar Tetrahedron Lett. 2008 49 3297
39. P. S. Chowdhury P. Gupta P. Kumar Tetrahedron Lett. 2009 50 7018
40. P. Kumar M. Pandey P. Gupta S. V. Naidu D. D. Dhavale Eur. J. Org. Chem. 2010 36 6993
41. L. Fitjer U. Quabeck Synth. Commun. 1985 15 855
42. R. H. Grubbs S. Chang Tetrahedron 1998 54 4413
43. J. Prunet Angew. Chem., Int. Ed. 2003 42 2826