✦ LIBER ✦

ChemInform Abstract: Highly Enantioselective Synthesis of Spiro[cyclohexanone-oxindoles] and Spiro[cyclohexanone-pyrazolones] by Asymmetric Cascade [5 + 1] Double Michael Reactions.

✍ Scribed by Bin Wu; Jian Chen; Mei-Qiu Li; Jin-Xin Zhang; Xiao-Ping Xu; Shun-Jun Ji; Xing-Wang Wang

Book ID: 112046505
Publisher: John Wiley and Sons
Year: 2012
Weight: 39 KB
Volume: 43
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.201228108

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Highly Enantioselective Synthesis of Spi

Highly Enantioselective Synthesis of Spiro[cyclohexanone-oxindoles] and Spiro[cyclohexanone-pyrazolones] by Asymmetric Cascade [5+1] Double Michael Reactions

✍ Bin Wu; Jian Chen; Mei-Qiu Li; Jin-Xin Zhang; Xiao-Ping Xu; Shun-Jun Ji; Xing-Wa 📂 Article 📅 2012 🏛 John Wiley and Sons 🌐 English ⚖ 475 KB

ChemInform Abstract: Direct Catalytic As

ChemInform Abstract: Direct Catalytic Asymmetric Synthesis of Highly Functionalized Tetronic Acids/Tetrahydro-isobenzofuran-1,5-diones via Combination of Cascade Three-Component Reductive Alkylations and Michael-Aldol Reactions.

✍ Dhevalapally B. Ramachary; Mamillapalli Kishor 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 71 KB

ChemInform Abstract: Facile Construction

ChemInform Abstract: Facile Construction of the Tricyclo[5.2.1.01,5]decane Ring System by Intramolecular Double Michael Reaction: Highly Stereocontrolled Total Synthesis of (.+-.)-8,14-Cedranediol and (.+-.)-8,14-Cedranoxide.

✍ Masataka Ihara; Kei Makita; Kiyosei Takasu 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 KB 👁 1 views

Facile Construction of the Tricyclo[5.2.1.0 1,5 ]decane Ring System by Intramolecular Double Michael Reaction: Highly Stereocontrolled Total Synthesis of (±)-8,14-Cedranediol and (±)-8,14-Cedranoxide. -Intramolecular double Michael reaction of cyclopentenone (I) is the key step in the synthesis of r