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

NEM CHEMICAL CO.，LTD

website:http://www.NEM.COM.CN

Contact:+86-393-4411771

Address:The west section of shengli Road,Puyang,Henan Province,China
Tomo Pharma Chem Co., Limited

Contact:+86-158-05817090

Address:ROOM 9F, FLAT 2, GUODU DEVELOPING BLDG, No.182, ZHAOHUI ROAD
Shao Xing Empire Import&Export CO.,ltd

Contact:86-575-82127757

Address:11#, Weiwu Road, Shangyu Industrial Park, Hangzhou Bay, Hangzhou, Zhejiang Province, China
Suzhou CarbonWell Pharma-Tech Co., Ltd

Contact:Tel: + 86 (0)512-8898-1216; + 86-18606258602

Address:2358 Changan Road, Wujiang Scientific Innovation Park, Wujiang, Jiangsu Province, P. R. China 215200
Phantom-pharma

Contact:

Address:

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