๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

A formal convergent synthesis of (+)-trans-solamin

โœ Scribed by Sadagopan Raghavan; S. Ganapathy Subramanian; K.A. Tony


Publisher
Elsevier Science
Year
2008
Tongue
French
Weight
126 KB
Volume
49
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

โœฆ Synopsis


A formal convergent synthesis of solamin is disclosed. The synthetic strategy exploits the potential of the sulfinyl group as an auxiliary, nucleophile and in C-C bond formation. The synthetic route can be adapted to the synthesis of stereoisomers of solamin, analogs with variable carbon side chains, and other members of mono-THF acetogenins.


๐Ÿ“œ SIMILAR VOLUMES


A formal total synthesis of erythromycin
โœ Tadashi Nakata; Mineo Fukui; Takeshi Oishi ๐Ÿ“‚ Article ๐Ÿ“… 1988 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 264 KB

In the preceding paper. the syntheses of the optically active two segments (+)-2 and (-)-2 having most of chiral centers involved in erythronolide A were reported. In this report, coupling reaction of these two segments and the subsequent elaboration leading to carbamate 1. a key intermediate in W

A simple convergent synthesis of trans-f
โœ Yuji Mori; Shinjiro Mitsuoka; Hiroshi Furukawa ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 160 KB

A highly convergent method for the synthesis of trans-fused polytetrahydropyrans was developed, which involves: (i) coupling of cyclic triflate with an acetylene unit; (ii) oxidation of acetylene to 1,2-diketone; (iii) formation of a trans-fused cyclic dihemiacetal; (iv) O-methylation of the dihemia