Scholarly article on La(C2H4)(1+) 128058-65-1 from Journal of the American Chemical Society p. 4434 - 4435

DOI: 10.1021/ja00221a065

Source and publish data:

Journal of the American Chemical Society p. 4434 - 4435 (1988)

Update date:2022-08-06

Topics:

Authors:

Huang, Yongqing

Freiser, Ben. S.

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

Article abstract of DOI:10.1021/ja00221a065

Full text of DOI:10.1021/ja00221a065

Products guided by the article

Product name:La(C₂H₄)⁽¹⁺⁾

Cas No:128058-65-1

R&D Labs maybe for 128058-65-1

HANGZHOU ZHONGCHANG SCIENTIFIC CO.,LTD

Contact:+86-571-88932183

Address:Hangzhou
Changzhou Ruiping Chemical Co., Ltd

website:http://www.wishchem.com

Contact:+86-519-82324280

Address:No.288-1 Huacheng Road, Jintan
FOSHAN NANHAI ZHONGNAN PHARMACEUTICAL FACTORY

Contact:0086-0757-85609331

Address:XIAHENGTIAN INDUSTRIAL ZONE,SHAYONG VILLAGE,LISHUI TOWN
Shanghai Potomer International Trade CO., LTD

Contact:+86-21-61397128

Address:Room 304,No.505 ,Caoyang Road.Shanghai,China
LIAOYANG TENGYUAN FOOD ADDITIVE FACTORY

Contact:+86-419-5807666

Address:Haodianzi village,Hanling Town,Liaoyang county

Relevant to this article

Behavior of 3(2-pyridinylmethylene)-5-aryl-2(3H)-furanones and 3(3-pyridinylmethylene)-5-aryl-2(3H)-furanones as alkylating agents: A comparative study

Doi:10.1002/jhet.709
(2011)
An approach to mimicking the sesquiterpene cyclase phase by nickel-promoted diene/alkyne cooligomerization

Doi:10.1021/jo202314a
(2012)
N-Alkenyl Acylketene S,N-Acetals from 2,3-Dihydro-1,3-benzothiazoles and Carboxylic Anhydrides. X-Ray Molecular Structure of 2-(Butyrylmethylene)-N-(cyclohex-1-enyl)-2,3-dihydro-1,3-benzothiazole

Doi:10.1039/P19910001505
(1991)
GE-180: A novel fluorine-18 labelled PET tracer for imaging Translocator protein 18 kDa (TSPO)

Doi:10.1016/j.bmcl.2011.12.084
(2012)
Assembled structures and magnetic properties of viologen-[M(mnt) ₂] charge-transfer salts (mnt = maleonitriledithiolate; M = Cu, Ni, Pt)

Doi:10.1016/j.ica.2011.11.043
(2012)
Toward the development of a general chiral auxiliary. A remarkable, highly diastereoselective, auxiliary-mediated substitution: Application to an enantioselective synthesis of the cyclohexene subunit of (+)-tetronolide

Doi:10.1021/jo961585b
(1996)

Article Doi

DOI: 10.1021/ja00221a065

Source and publish data: