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Merck
  • Caesium fluoride-promoted Stille coupling reaction: an efficient synthesis of 9Z-retinoic acid and its analogues using a practical building block.

Caesium fluoride-promoted Stille coupling reaction: an efficient synthesis of 9Z-retinoic acid and its analogues using a practical building block.

Chemical communications (Cambridge, England) (2008-12-03)
Takashi Okitsu, Kinya Iwatsuka, Akimori Wada
摘要

A highly efficient and rapid total synthesis of 9Z-retinoic acid was accomplished by caesium fluoride-promoted Stille coupling reaction; using a common building block, 9Z-retinoic acid analogues were also prepared by the same method without isomerisation of the Z-double bond.

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Sigma-Aldrich
氟化铯, 99%
Sigma-Aldrich
氟化铯, 99.9% trace metals basis
Sigma-Aldrich
氟化铯, purum p.a., ≥98.0%
Sigma-Aldrich
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Sigma-Aldrich
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