CONVENIENT SYNTHESIS OF (TRIPHENYL)GERMYL AND (TRIPHENYL)STANNYL SUBSTITUTED ALLENES

DOI: 10.1016/0022-328X(84)80703-2

Source and publish data:

Journal of Organometallic Chemistry p. 227 - 234 (1984)

Update date:2022-08-03

Topics:

Authors:

Ruitenberg, K.

Westmijze, H.

Kleijn, H.

Vermeer, P.

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

Article abstract of DOI:10.1016/0022-328X(84)80703-2

Allenyl-germanes and -stannanes, Ph3MC(R)=C=CR'R" (M = Ge, Sn) can be obtained, generally in excellent yield, through alkylcopper(I)-induced 1,3-substitution of the propargylic chlorides Ph3MC<*>CCR'R"Cl.In the tin series, however transmetallation is the

Full text of DOI:10.1016/0022-328X(84)80703-2

Products guided by the article

Product name:Stannane, [1-(1,1-dimethylethyl)-1,2-butadienyl]triphenyl-

Cas No:92753-06-5

R&D Labs maybe for 92753-06-5

HUNAN OUYA BIOLOGICAL CO.,LTD

Contact:+8613400661290

Address:No 908,Kangwan Rd, Liuyang Economic
Suzhou Lixin Pharmaceutical Co., Ltd.

Contact:86-512-88169812

Address:21 Tangxi Road, Suzhou New District, Suzhou 215151
Jiaxing Taixin Pharmaceutical Chemical Co., Ltd

Contact:0573-82613601

Address:Chemical Park, Jiaxing, Zhejiang, China
Hubei Xinghuo Chemical Co., Ltd.,

Contact:13925817279 13907299441

Address:Xinghuo Fine Chemistry Industrial Park, Xiaochang County, Hubei Province, China
Beyond Pharmaceutical Co., Ltd

Contact:+86-571-8195-3185

Address:No. 13-1, Liansheng Road, Yuhang District

Relevant to this article

Iron-Catalyzed Thiocyclization for the Synthesis of Trifluoro-methylated Benzothiophenes by C-H Functionalization of Aryl Disulfides

Doi:10.1055/s-0036-1588923
(2017)
Synthesis of the 4,10-dihydro-3H-pyridazino[1,6-b]isoquinolin-10-one system by a furan recyclization reaction

Doi:10.1055/s-2007-983764
(2007)
Synthesis of pyrroloisoquinolines from papaverine

Doi:10.1134/S1070428006040154
(2006)
Asymmetric organocatalytic β-hydroxylation of α,β- unsaturated aldehydes

Doi:10.1021/ja068908y
(2007)
Microwave assisted synthesis of n-substituted-7-hydroxy-4-methyl-2- oxoquinolines as anticonvulsant agents

Doi:10.1155/2011/121476
(2011)
Doi:10.1039/jr9640005110
(1964)

Article Doi