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ChemInform Abstract: Synthetic Studies on Manzamine A: Construction of the Tricyclic ABC Ring Subunit I.

✍ Scribed by S. LI; S. OHBA; S. KOSEMURA; S. YAMAMURA

Publisher: John Wiley and Sons
Year: 2010
Weight: 29 KB
Volume: 28
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199702184

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ChemInform Abstract: Synthetic Studies o

ChemInform Abstract: Synthetic Studies on Manzamine A: Construction of the Tetracyclic ABCE Ring Substructure.

✍ S. LI; S. YAMAMURA; H. HOSOMI; S. OHBA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 2 views

Synthetic Studies on Manzamine A: Construction of the Tetracyclic ABCE Ring Substructure. -A completely different route to the tetracyclic ABCE ring substructure (V) of manzamine A is described. Beginning with an advanced intermediate (I) the procedure is characterized by the formation of the A rin

ChemInform Abstract: Synthesis of the Tr

ChemInform Abstract: Synthesis of the Tricyclic ABC Ring Subunit of Mazamine A.

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ChemInform Abstract: Synthesis of the Te

ChemInform Abstract: Synthesis of the Tetracyclic ABCE Ring Subunit I, Bearing the 13-Membered Azacycle, of Manzamine A.

✍ S. LI; S. YAMAMURA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 46 KB 👁 2 views

ChemInform Abstract: Synthetic Studies o

ChemInform Abstract: Synthetic Studies on Manzamine A: An Efficient Synthesis of the Bicyclic Compound Leading to the Formation of the Tetracyclic ABCE Ring Subunit. Part 1.

✍ S. LI; S. YAMAMURA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 2 views

ChemInform Abstract: Stereoselective Syn

ChemInform Abstract: Stereoselective Synthesis of the Tricyclic Core ABC-Rings (I) and (II) of Nakadomarin and Manzamine from a Common Intermediate.

✍ Philip Magnus; Mark R. Fielding; Charles Wells; Vince Lynch 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 1 views

ChemInform Abstract: A New Synthetic App

ChemInform Abstract: A New Synthetic Approach to Forskolin: Construction of the ABC Ring System from D-Galactose.

✍ I. HANNA; P. WLODYKA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 37 KB 👁 2 views

The functionalized tricyclic framework (XI) of the diterpene forskolin is synthesized by an intramolecular Diels-Alder reaction of the dienyne (VII), which is obtained by stereoselective introduction of the C side chains at C-1 and C-2 of tri-O-acetyl-D-galactal (I) via C-Ferrier and Claisen-Ireland