Isolable Analogues of the Breslow Intermediate Derived from Chiral Triazolylidene Carbenes

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DiRocco, Daniel A.; Oberg, Kevin M.; Rovis, Tomislav;
(2012)
  • Publisher: Figshare
  • Related identifiers: doi: 10.1021/ja302031v.s003, doi: 10.1021/ja302031v.s002
  • Subject: thiamine mode | acyl carbanion | azolylidene catalysis | homoenolate processes | Isolable Analogues | Ecology | triazolylidene carbenes | nitrogen analogues | acyl carbanion processes | Biochemistry | Breslow Intermediate Derived | model system | Science Policy
    • FOR: 69999 Biological Sciences not elsewhere classified | 39999 Chemical Sciences not elsewhere classified

Since Breslow’s initial report on the thiamine mode of action, the study of catalytic acyl carbanion processes has been an area of immense interest. With the advent of azolylidene catalysis, a plethora of reactivtiy has been harnessed, but the crucial nucleo... View more
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