Hydrostannation and Hydrogermylation of Allenes

DOI: 10.1246/bcsj.61.2693

Source and publish data:

Bulletin of the Chemical Society of Japan p. 2693 - 2695 (1988)

Update date:2022-08-03

Topics:

Authors:

Ichinose, Yoshifumi

Oshima, Koichiro

Utimoto, Kiitiro

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

Article abstract of DOI:10.1246/bcsj.61.2693

Treatment of allenes with Ph3SnH or Ph3GeH in the presence of Pd(PPh3)4 catalyst provides the corresponding allylic stannanes or allylic germanes in good yields.Et3B induced radical addition of Ph3SnH or Ph3GeH to allenes are also described.

Full text of DOI:10.1246/bcsj.61.2693

Products guided by the article

Product name:1-dimethylphenylsilyl-2-triphenylstannyl-1-propene

Cas No:120978-56-5

R&D Labs maybe for 120978-56-5

Shaanxi Lighte Optoelectronics Material Co., Ltd.

Contact:+86-29-88320728-622/619/620

Address:No.55 INDUSTRY ROAD 2,XI'AN NATIONAL CIVIL AEROSPACE INDUSTRIAL PARK.XI'AN China 710065.
Zhuhai Rundu Pharmaceutical co.,Ltd

Contact:+86-756-7630755

Address:No.6,North Airport Road,Sanzao Town,Jinwan District
wuxi huabin bio-tech Co.,Ltd(expird)

Contact:86-0510-85133006

Address:hubin road NO157
Shandong Zhongcheng Barium Salt Co., Ltd

Contact:+86-15725732638

Address:No.29 baoxi road, hi-tech zone, zibo, shandong
Kunshan Yalong Trading Co,.Ltd

Contact:86-512-57621185

Address:805-807 Room Hongqiao Mansion ,1088 West Qianjin Road, Kunshan, Jiangsu，China

Relevant to this article

Design and synthesis of indole derivatives of adenophostin A. A entry into subtype-selective IP₃ receptor ligands

Doi:10.1016/j.tetlet.2009.12.045
(2010)
Oxygenation of Substituted Vinylcyclopropanes: Preparative and Mechanistic Studies

Doi:10.1021/ja00195a047
(1989)
Reciprocal Tests of Steric Opposition to Down-Disrotatory Thermal Decyclization of <3.2.1> Propellanes. The Cycloreversion Stereochemistry of the 6,7,8-Trimethyltricyclo<3.2.1.0^1,5>octanes

Doi:10.1016/S0040-4039(00)80621-8
(1988)
Thromboxane A₂ receptor antagonists. I. Synthesis and pharmacological activity of 7-oxabicyclo[2.2.1]heptane derivatives with the benzenesulfonylamino group

Doi:10.1248/cpb.37.327
(1989)
SYNTHESIS, ANALGESIC, AND CEREBROVASCULAR ACTIVITY OF N-AMINOACETYL DERIVATIVES OF PYROLLIDONE-2

Doi:10.1007/BF00758415
(1989)
Iodine : A versatile reagent in carbohydrate chemistry IV. Per-O-Acetylation, regioselective acylation and acetolysis

Doi:10.1016/S0040-4020(97)00742-4
(1997)

Article Doi