Prop-2-ynyl- and Propadienyl-lithium Reagents. Regiocontrolled Synthesis of Allenic Compounds

DOI: 10.1039/c39830001133

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1133 - 1134 (1983)

Update date:2022-08-05

Topics:

Authors:

Huynh, Chanh

Linstrumelle, Gerard

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

Article abstract of DOI:10.1039/c39830001133

Direct proof for the rearrangement of the prop-2-ynyl-lithium (2) into the propadienyl-lithium (4) is provided by the formation of the 1,3-disubstituted allenic compounds (7).

Full text of DOI:10.1039/c39830001133

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:1,2-Undecadiene, 3-methyl-

Cas No:59409-51-7

R&D Labs maybe for 59409-51-7

Zhuhai Rundu Pharmaceutical co.,Ltd

Contact:+86-756-7630755

Address:No.6,North Airport Road,Sanzao Town,Jinwan District
HAORUI ENTERPRISES LLC

Contact:(1) 206-3550089

Address:5115 NE 8TH PL, Renton, WA 98059 USA
Shenyang Mole pharmaceutical Technology Development Co.,Ltd

Contact:+86-24-31204918/13889278616

Address:No.44, wanliutang road, shenhe District of Shenyang
Shandong Xingshun New Material Co., Ltd.

website:http://www.sd-xingshun.com

Contact:+86-519-86461196

Address:Middle of Luhua East Road, Dingtao District
Basilea Pharmaceutica China Ltd.

Contact:+86-513-82198075

Address:No.638 Xiushan Road(East),Haimen, Jiangsu 226100, P.R.China

Relevant to this article

Structure-activity relationships of 2-chloro-N⁶-substituted- 4′-thioadenosine-5′-uronamides as highly potent and selective agonists at the human A₃ adenosine receptor

Doi:10.1021/jm050595e
(2006)
Identification of sucrose diesters of aryldihydronaphthalene-type lignans from Trigonotis peduncularis and the nature of their fluorescence

Doi:10.1021/np800071r
(2008)
Doi:10.1007/BF00480439
()
A biological comparison of benzene with thiophene in condensed ring systems

Doi:10.1007/BF00909106
(1976)
Synthesis of benzoxepins via rearrangement of dihydrofurans derived from carbonyl ylide [3+2] cycloaddition

Doi:10.1016/S0040-4039(03)01193-6
(2003)
Doi:10.1016/S0022-328X(00)89366-3
(1976)

Article Doi