Sm or Zn-induced coupling reactions. A facile route to 1,2-diketones

DOI: 10.1016/S0040-4039(97)01804-2

Source and publish data:

Tetrahedron Letters p. 7603 - 7604 (1997)

Update date:2022-08-17

Topics:

Authors:

Baruah, Bipul

Boruah, Anima

Prajapati, Dipak

Sandhu, Jagir S

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/S0040-4039(97)01804-2

Coupling of keto cyanides 1 into 1,2-diketones 2 has been performed by the action of SmI₂ or ZnI₂ in tetrahydrofuran at ambient temperature in high yields.

Full text of DOI:10.1016/S0040-4039(97)01804-2

Products guided by the article

Product name:4,4'-DIMETHOXYBENZIL

Cas No:1226-42-2

R&D Labs maybe for 1226-42-2

CHEMINN LTD.

website:http://www.cheminn.com/

Contact:86-531-67875205

Address:No.9-2,South of Shanda Road, Jinan ,China
Shanghai Sharing technologies Co., Ltd.

Contact:86-021-66787223

Address:No11, Lane 225, Jinxiang Road,Pudong district
Hangzhou Zhenghan Biological Technology Co., Ltd.

Contact:86-571-88781753

Address:liangzhu yuhang hangzhou city
Engineering Research Center of Pesticide, Heilongjiang Province

Contact:+86-451-86609001

Address:No.74 of Xuefu Road, Nangang District,
JiYi Chemical (Beijing) Co., Ltd.

Contact:+86-10-89385733

Address:Shilou Town of Fangshan District， Beijing

Relevant to this article

Efficient synthesis of the cholinephosphate phospholipid headgroup

Doi:10.1016/S0009-3084(00)00224-3
(2001)
Access to 1-indolyltetrahydro-β-carbolines: via metal-free cross-dehydrogenative coupling: The total synthesis of eudistomin U, isoeudistomin U and 19-bromoisoeudistomin U

Doi:10.1039/d0cc06958b
(2021)
9-Sulfonyl-9(H)-Purine Derivatives Inhibit HCV Replication Via their Degradation Species

Doi:10.1007/s11094-021-02369-1
(2021)
Doi:10.1021/ja00477a035
(1978)
Synthesis of fused pyridopyrrolidine dione derivatives using hetero Diels-Alder reactions

Doi:10.1016/S0040-4039(01)02000-7
(2001)
A short water-soluble self-assembling peptide forms amyloid-like fibrils

Doi:10.1039/b607657b
(2006)

Article Doi