Literature DB >> 11667272

Synthesis of Unsymmetrical Tetrathiafulvalene Derivatives via Me(3)Al-Promoted Reactions of Organotin Compounds with Esters.

Shyûji Satoki, Sachinori Mishima, Nobutaka Akashi, Kouhei Takahashi, Nobuyuki Masuda, Yasushi Nishimoto, Satoshi Takasaki, Hiroyuki Anzai.   

Abstract

Efficient synthetic methods for the construction of a wide variety of unsymmetrical tetrathiafulvalenes (TTFs) via the Me(3)Al-promoted reactions of organotin thiolates or selenolates with esters are described. Reaction of tin thiolates (3a-c and 10) and selenolates (3d, 5, and 7) with esters (11a,b) in the presence of Me(3)Al as a Lewis acid gave dihydrotetrathiafulvalene derivatives (12, 14, 15, and 17-20) and 1,3-dithiane derivatives (13 and 16). In addition, the synthesis of diselenadithiafulvalene derivatives (25-28) could be accomplished by Me(3)Al-mediated reaction of tin thiolate (2a) or selenolates (3d and 5) with esters (22a, 22d, and 24). Furthermore, the application of the Me(3)Al-promoted reaction of tin thiolate (34) with esters (11a-b, 22a-d, and 35a-b) for the synthesis of unsymmetrical TTFs-fused donors enabled us to obtain various TTFs-fused systems (29-33) in short steps.

Entities:  

Year:  1996        PMID: 11667272     DOI: 10.1021/jo952255e

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

Review 1.  Tetrathiapentalene-based organic conductors.

Authors:  Yohji Misaki
Journal:  Sci Technol Adv Mater       Date:  2009-07-06       Impact factor: 8.090

2.  An unsymmetrical tetrathiafulvalene with a fused 1,2,5-thiadiazole ring and methylthio groups.

Authors:  Masaaki Tomura; Yoshiro Yamashita
Journal:  Molecules       Date:  2009-10-23       Impact factor: 4.411

  2 in total

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