Novel addition of 5H-benzo[f]-1,2,3,4-tetrathiepin and 6H-benzo[g]- 1,2,3,4,5-pentathiocin to alkenes in the presence of BF3·OEt2
✍ Scribed by Shin-ichi Satoh; Ryu Sato
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- French
- Weight
- 275 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
The treatment of SH-benzo[f+l,2,3,4+enathiepin ( B'lTP ) or 6H-benzo[g]-l,2,3,4,5-pentathiocin ( BFTC ) with alkenes in the presence of BF3aEt2 afforded trclns adducts, 2,3disubstituted ben~l, (1). which further reacted with alkenes to give cis adducts, 2,3disubstituted benz~l.4ditbiepanes
(2).
📜 SIMILAR VOLUMES
## Abstract Four previously unknown polycyclic heterocyclic ring systems, namely, benzo[__h__]thieno[3′,2′:4,5]‐thieno[2,3‐__c__]quinoline (6), benzo[__h__]thieno[3′,2′:4,5]thieno[2,3‐__c__]quinoline (11), benzo[__f__]thieno‐[3′,2′:4,5]thieno[2,3‐__c__]tetrazolo[1,5‐__a__]quinoline (12) and benzo[_
## Abstract via reaction of o‐phenylenediamine (I) with 1,3,5‐oxadiazin‐2‐ones (II)