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-Hisashi Yamamoto Researcher Activity Profile

Research Author Detailed Information 

Are you HISASHI YAMAMOTO?? Join now for FREE! You can update this page and your profile image by registering at Molecular Stationhisashi yamamoto

Hisashi Yamamoto Publication Rate By Year

Hisashi Yamamoto has published 2 paper(s) in 2003, 6 paper(s) in 2004, 4 paper(s) in 2005, 4 paper(s) in 2006, 5 paper(s) in 2007, 3 paper(s) in 2008, for a total of 24 research publications in total.

hisashi yamamoto researcher

Hisashi H Yamamoto Author Information

LAST NAME: yamamoto

FIRST NAME: hisashi

INITIALS: H

AFFILIATION:

Papers

Hisashi Yamamoto's Publication Record

  1. Diastereo- and enantioselective synthesis of nitroso Diels-Alder-type bicycloketones using dienamine: mechanistic insight into sequential nitroso Aldol/Michael reaction and application for optically pure 1-amino-3,4-diol synthesis. Year Published: 2007
  2. Department of Chemistry, University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637, USA.
  3. Enantioselective route to platensimycin: an intramolecular Robinson annulation approach. Year Published: 2007
  4. Department of Chemistry, The University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637, USA.
  5. Reversible acute renal failure associated with clomipramine-induced interstitial nephritis. Year Published: 2007
  6. Division of Nephrology, Department of Medicine, Jichi Medical University, 3311-1 Yakushiji, Shimotsuke-shi, Tochigi 329-0498, Japan.
  7. Reversible acute renal failure associated with clomipramine-induced interstitial nephritis. Year Published: 2007
  8. Division of Nephrology, Department of Medicine, Jichi Medical University, 3311-1 Yakushiji, Shimotsuke-shi, Tochigi 329-0498, Japan.
  9. Ketone super silyl enol ethers in sequential reactions: diastereoselective generation of tertiary carbinols in one pot. Year Published: 2008
  10. Department of Chemistry, The University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637, and Department of Chemistry, Aichi University of Education, Igaya-cho, Kariya 448-8542, Japan.
  11. Year Published: 2003
  12. Graduate School of Engineering, Nagoya University, SORST, Japan Science and Technology Corporation (JST), Furo-cho, Chikusa, Nagoya 464-8603, Japan.
  13. Catalytic enantioselective synthesis of alpha-aminooxy and alpha-hydroxy ketone using nitrosobenzene. Year Published: 2003
  14. Department of Chemistry, University of Chicago, 5735 South Ellis Avenue, Illinois 60637, USA.
  15. Catalytic, highly enantio, and diastereoselective nitroso diels-alder reaction. Year Published: 2004
  16. Department of Chemistry, The University of Chicago, Illinois, USA. yamamoto@uchicago.edu
  17. Enantioselective O- and N-nitroso aldol synthesis of tin enolates. Isolation of three BINAP-silver complexes and their role in regio- and enantioselectivity. Year Published: 2004
  18. Department of Chemistry, The University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637, USA.
  19. Enantioselective tandem O-nitroso Aldol/Michael reaction. Year Published: 2004
  20. Department of Chemistry, The University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637, USA.
  21. A new artificial cyclase for polyprenoids: enantioselective total synthesis of (-)-chromazonarol, (+)-8-epi-puupehedione, and (-)-11'-deoxytaondiol methyl ether. Year Published: 2004
  22. Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa, Nagoya 464-8603, Japan.
  23. Catalytic, highly enantio- and diastereoselective pinacol coupling reaction with a new tethered bis(8-quinolinolato) ligand. Year Published: 2004
  24. Department of Chemistry, The University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637, USA.
  25. Lewis acid-mediated selective chlorinations of silyl enolate. Year Published: 2004
  26. Department of Chemistry, University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637, USA.
  27. Bronsted acid catalysis of achiral enamine for regio- and enantioselective nitroso aldol synthesis. Year Published: 2005
  28. Department of Chemistry, The University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637, USA.
  29. Axially chiral biaryl diols catalyze highly enantioselective hetero-Diels-Alder reactions through hydrogen bonding. Year Published: 2005
  30. Department of Chemistry, The University of Chicago, 5735 South Ellis Avenue, Chicago, IL 60637, USA.
  31. Cyanuric chloride as a mild and active Beckmann rearrangement catalyst. Year Published: 2005
  32. Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa, Nagoya 464-8603, Japan.
  33. Silver-catalyzed asymmetric Sakurai-Hosomi allylation of ketones. Year Published: 2005
  34. Department of Chemistry, The University of Chicago, Illinois 60637, USA.
  35. Tris(trimethylsilyl)silyl-governed aldehyde cross-aldol cascade reaction. Year Published: 2006
  36. Department of Chemistry, The University of Chicago, 5735 South Ellis Avenue, Chicago, IL 60637, USA.
  37. Catalytic enantioselective Nozaki-Hiyama allylation reaction with tethered bis(8-quinolinolato) (TBOx) chromium complex. Year Published: 2006
  38. Department of Chemistry, The University of Chicago, Illinois 60637, USA.
  39. Year Published: 2006
  40. Department of Chemistry, University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637, USA.
  41. Catalytic enantioselective hetero-Diels-Alder reactions of an azo compound. Year Published: 2006
  42. Department of Chemistry, University of Chicago, 5735 South Ellis Avenue, Chicago, IL 60637, USA.
  43. Super silyl group for a sequential diastereoselective aldol-polyhalomethyllithium addition reaction. Year Published: 2008
  44. Department of Chemistry, The University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637.
  45. Ketone super silyl enol ethers in sequential reactions: diastereoselective generation of tertiary carbinols in one pot. Year Published: 2008
  46. Department of Chemistry, The University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637, USA.
  47. Triflimide (HNTf2)-catalyzed aldehyde cross-aldol reaction using "super silyl" enol ethers. Year Published: 2007
  48. Department of Chemistry, The University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637, USA.
 

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