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Synthesis of stereochemically defined (E)-cinnamyl alcohol derivatives from the Baylis–Hillman adducts

✍ Scribed by Hyoung Shik Kim; Tae Yi Kim; Ka Young Lee; Yun Mi Chung; Hong Jung Lee; Jae Nyoung Kim

Book ID
104210097
Publisher
Elsevier Science
Year
2000
Tongue
French
Weight
131 KB
Volume
41
Category
Article
ISSN
0040-4039

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✦ Synopsis

The reaction of the Baylis-Hillman adducts 1a-g and trifluoroacetic acid at 30-70°C gave the rearranged cinnamyl alcohols 2a-g stereoselectively in moderate yields.

📜 SIMILAR VOLUMES

ChemInform Abstract: Synthesis of Cinnam
ChemInform Abstract: Synthesis of Cinnamyl Amines from the Baylis—Hillman Adducts: Transformation of Allylic Alcohols to Allylic Amines.
✍ Hong Jung Lee; Yun Mi Chung; Ka Young Lee; Jae Nyoung Kim 📂 Article 📅 2001 🏛 John Wiley and Sons ⚖ 28 KB 👁 2 views

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