An important application of the 1,8-diketone ring formation reaction: A concise synthesis of 5,6-diphenyl[1,3]dithiolo[4,5-b][1,4]dithiine-2-thione and its coupling product

E. Ertas; T. Ozturk

doi:10.1039/b003714l

An important application of the 1,8-diketone ring formation reaction: A concise synthesis of 5,6-diphenyl[1,3]dithiolo[4,5-b][1,4]dithiine-2-thione and its coupling product

E. Ertas
, T. Ozturk^*

^*Bu çalışma için yazışmadan sorumlu yazar

Scientific and Technological Research Council of Turkey

Araştırma sonucu: Dergiye katkı › Makale › bilirkişi

18 Atıf (Scopus)

Özet

Syntheses of fully unsaturated 5,6-diphenyl[1,3]dithiolo[4,5b][1,4]dithiine-2-thione and its coupling product, a fully unsaturated analogue of BEDT-TTF, have been achieved by a 1,8-diketone ring formation reaction.

Orijinal dil	İngilizce
Sayfa (başlangıç-bitiş)	2039-2040
Sayfa sayısı	2
Dergi	Chemical Communications
Basın numarası	20
DOI'lar	https://doi.org/10.1039/b003714l
Yayın durumu	Yayınlandı - 21 Eki 2000
Harici olarak yayınlandı	Evet

Belgeye Erişim

10.1039/b003714l

Diğer Dosyalar ve Linkler

Link to publication in Scopus

Alıntı Yap

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title = "An important application of the 1,8-diketone ring formation reaction: A concise synthesis of 5,6-diphenyl[1,3]dithiolo[4,5-b][1,4]dithiine-2-thione and its coupling product",

abstract = "Syntheses of fully unsaturated 5,6-diphenyl[1,3]dithiolo[4,5b][1,4]dithiine-2-thione and its coupling product, a fully unsaturated analogue of BEDT-TTF, have been achieved by a 1,8-diketone ring formation reaction.",

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T2 - A concise synthesis of 5,6-diphenyl[1,3]dithiolo[4,5-b][1,4]dithiine-2-thione and its coupling product

AU - Ertas, E.

AU - Ozturk, T.

PY - 2000/10/21

Y1 - 2000/10/21

N2 - Syntheses of fully unsaturated 5,6-diphenyl[1,3]dithiolo[4,5b][1,4]dithiine-2-thione and its coupling product, a fully unsaturated analogue of BEDT-TTF, have been achieved by a 1,8-diketone ring formation reaction.

AB - Syntheses of fully unsaturated 5,6-diphenyl[1,3]dithiolo[4,5b][1,4]dithiine-2-thione and its coupling product, a fully unsaturated analogue of BEDT-TTF, have been achieved by a 1,8-diketone ring formation reaction.

UR - https://www.scopus.com/pages/publications/0034699901

U2 - 10.1039/b003714l

DO - 10.1039/b003714l

M3 - Article

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JO - Chemical Communications

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ER -

An important application of the 1,8-diketone ring formation reaction: A concise synthesis of 5,6-diphenyl[1,3]dithiolo[4,5-b][1,4]dithiine-2-thione and its coupling product

Özet

Belgeye Erişim

Diğer Dosyalar ve Linkler

Parmak izi

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