An unusual reaction of Lawesson's reagent with 1,8-diketones: A synthesis of fused 1,4-dithiins and thiophenes

Turan Ozturk

doi:10.1016/0040-4039(96)00396-6

An unusual reaction of Lawesson's reagent with 1,8-diketones: A synthesis of fused 1,4-dithiins and thiophenes

Turan Ozturk^*

^*Bu çalışma için yazışmadan sorumlu yazar

University of Kent

Araştırma çıktısı: Dergi yayını › Makale › Hakem

55 Atıf (Scopus)

Özet

Reaction of 1,8-diketones 3 with Lawesson's reagent 8 resulted in the formation of five and six-membered rings 5-7, 18, depending on the nature of the substituents. Product 6 is converted in two steps to the unsymmetric 'ET' analogue 20, containing an extra double bond.

Orijinal dil	İngilizce
Sayfa (başlangıç-bitiş)	2821-2824
Sayfa sayısı	4
Dergi	Tetrahedron Letters
Hacim	37
Basın numarası	16
DOI'lar	https://doi.org/10.1016/0040-4039(96)00396-6
Yayın durumu	Yayınlandı - 15 Nis 1996
Harici olarak yayınlandı	Evet

Belgeye Erişim

10.1016/0040-4039(96)00396-6

Diğer Dosyalar ve Linkler

Link to publication in Scopus

Alıntı Yap

@article{7b4463c6a09c41fbb99238d13d87a25f,

title = "An unusual reaction of Lawesson's reagent with 1,8-diketones: A synthesis of fused 1,4-dithiins and thiophenes",

abstract = "Reaction of 1,8-diketones 3 with Lawesson's reagent 8 resulted in the formation of five and six-membered rings 5-7, 18, depending on the nature of the substituents. Product 6 is converted in two steps to the unsymmetric 'ET' analogue 20, containing an extra double bond.",

author = "Turan Ozturk",

year = "1996",

month = apr,

day = "15",

doi = "10.1016/0040-4039(96)00396-6",

language = "English",

volume = "37",

pages = "2821--2824",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd",

number = "16",

}

TY - JOUR

T1 - An unusual reaction of Lawesson's reagent with 1,8-diketones

T2 - A synthesis of fused 1,4-dithiins and thiophenes

AU - Ozturk, Turan

PY - 1996/4/15

Y1 - 1996/4/15

N2 - Reaction of 1,8-diketones 3 with Lawesson's reagent 8 resulted in the formation of five and six-membered rings 5-7, 18, depending on the nature of the substituents. Product 6 is converted in two steps to the unsymmetric 'ET' analogue 20, containing an extra double bond.

AB - Reaction of 1,8-diketones 3 with Lawesson's reagent 8 resulted in the formation of five and six-membered rings 5-7, 18, depending on the nature of the substituents. Product 6 is converted in two steps to the unsymmetric 'ET' analogue 20, containing an extra double bond.

UR - https://www.scopus.com/pages/publications/0029979203

U2 - 10.1016/0040-4039(96)00396-6

DO - 10.1016/0040-4039(96)00396-6

M3 - Article

AN - SCOPUS:0029979203

SN - 0040-4039

VL - 37

SP - 2821

EP - 2824

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 16

ER -

An unusual reaction of Lawesson's reagent with 1,8-diketones: A synthesis of fused 1,4-dithiins and thiophenes

Özet

Belgeye Erişim

Diğer Dosyalar ve Linkler

Parmak izi

Alıntı Yap