𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthetic Studies Toward Sarain A (I). Formation of the Western Macrocyclic Ring.

✍ Scribed by Moo Je Sung; Hyoung Ik Lee; Hee Bong Lee; Jin Kun Cha

Publisher
John Wiley and Sons
Year
2003
Weight
56 KB
Volume
34
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Studies towards the synthesis of neopelt
Studies towards the synthesis of neopeltolide: synthesis of a ring-closing metathesis macrocyclization precursor
✍ Gordon J. Florence; Romain F. Cadou πŸ“‚ Article πŸ“… 2010 πŸ› Elsevier Science 🌐 French βš– 445 KB

An advanced ring-closing metathesis precursor for the synthesis of the marine macrolide neopeltolide is prepared in a stereocontrolled manner by the coupling of the C2-C10 and C11-C16 subunits. The metathesis reaction of 4 with Grubbs' II or Nolan's indenylidene catalyst led to the unexpected format

A general synthetic route towards bastad
A general synthetic route towards bastadins. Part 2: Synthesis of the western part of bastadins 4–16, and fully functionalized macrocycle of bastadin 12
✍ Elias A. Couladouros; Vassilios I. Moutsos πŸ“‚ Article πŸ“… 1999 πŸ› Elsevier Science 🌐 French βš– 215 KB

A general synthetic route for the construction of the western part of the macrocyclic bastadins 4-16 is presented. The western and the eastern segments were coupled using the imidazolide of the corresponding acid. The bromine at position y2 may be added at this advanced step regiospecifically, stren

Studies on the Synthetic Usefulness of t
Studies on the Synthetic Usefulness of the Nitro Function. Part I. A Novel Cyclopentenone Ring Annelation
✍ Yoshihiko Nakashita; Toshio Watanabe; Erwin Benkert; Annalaura Lorenzi-Riatsch; πŸ“‚ Article πŸ“… 1984 πŸ› John Wiley and Sons 🌐 German βš– 184 KB

## Abstract A novel cyclopentenone ring annelation reaction is described. The treatment of the nitro compound **13** with aqueous sodium hydroxide in the presence of a phase‐transfer catalyst furnished **14a** in one step. Similar treatment of **7** led to **8**, the reaction of which with __t__‐Bu