## Abstract A biogenetic‐type total synthesis of(±)‐2‐deoxystemodinone (**1**), by solvolytic rearrangement of the 1‐methyl[2.2.2]oct‐2‐yl methanesulphonate **4**, is described.
A Highly Convergent Total Synthesis of (+)-Myxovirescine M2. Preliminary Communication
✍ Scribed by Dieter Seebach; Miguel A. Maestro; Michael Sefkow; Axel Neidlein; Francine Sternleld; Geo Adam; Thimo Sommerfeld
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- German
- Weight
- 279 KB
- Volume
- 74
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Prepared from (-)-camphor according to the procedure of Rewald [7]. We are grateful t o Professor F. Santau3 of Palack9 University, Olomouc, Czechoslovakia, for providing us with a sample of natural rhoeadine.
## Abstract The octahydroisoindolone moiety related to proxiphomin **(1)** has been synthesized by condensation of __N__‐benzyloxycarbonyl‐protected D, L‐phenylalaninal **(7)** with methyl‐(4‐methyl‐sorbyl)‐malonate **(11)** to yield the branched ethylene derivative **12**. Consecutive intramolecul
## Abstract A stereoselective four‐step synthesis of racemic patchouli alcohol starting from the known 2,6,6‐trimethyl‐2,4‐cyclohexadien‐1‐one [1] and 3‐methylpent‐4‐en‐1‐ol [2] is described.
## Abstract The synthesis of the bromoallenyl‐substituted epoxide derivative **34** related to cepacin A (**1**) starting from D‐arabinose as a chiral pool is reported.