ARYLOLEFINS IN MODIFIED PRINS REACTION

DOI: 10.1007/BF00950021

Source and publish data:

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science p. 792 - 794 (1982)

Update date:2022-08-04

Topics:

Authors:

Safarov, M. G.

Nigmatullin, N. G.

Ibatullin, U. G.

Rafikov,S. R.

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

Article abstract of DOI:10.1007/BF00950021

Full text of DOI:10.1007/BF00950021

Products guided by the article

Product name:1,3-Dioxane, 4-methyl-2-(1-methylethyl)-4-phenyl-

Cas No:64820-72-0

R&D Labs maybe for 64820-72-0

Jiaxing Carry Bio-Chem Technology Co.,Ltd

website:http://www.carrybiotech.com

Contact:0573-82788958

Address:Add.Fl 3th, Pharm Vally,Kaichuang Rd, Xiuzhou District, Jiaxing, Zhejiang,314031,China
Chongqing Werlchem Fine Chemical Co. Ltd

Contact:+86-23-67521957

Address:NO.15,Fortune Road,Yubei District,401121,Chongqing,China
suzhou chukai pharmateach co,.ltd

Contact:86-512-88812511

Address:Building 3, Wujiang Scientific Innovation Park, 2358 Changan Rd, Wujiang 215200, Jiangsu Province, P. R. China
RongCheng Tianyu Technology Co.,Ltd.

Contact:86-631-7519595

Address:220Ping Donghai Road RongChengCity,ShangDong Province China
Zibo Kunran Enterprises Co. LTD

website:http://www.kunranchem.com

Contact:0086 533 5200669

Address:No. 96 Jinjing Avenue, Zibo, Shandong, China

Relevant to this article

Doi:10.1007/BF00480973
()
An efficient method for the synthesis of 2-pyridones: Via C-H bond functionalization

Doi:10.1039/d0cc06834a
(2020)
Aromatic sigmatropic hydrogen-shifts in 2-vinyl and 2-allyl-phenols

Doi:10.1002/hlca.19770600624
(1977)
4-Fluorinated L-lysine analogs as selective i-NOS inhibitors: Methodology for introducing fluorine into the lysine side chain

Doi:10.1039/b307563j
(2003)
RAPID PREPARATION OF HEXANUCLEOTIDE TRIESTER BLOCKS FOR USE IN POLYDEOXYRIBONUCLEOTIDE SYNTHESIS

Doi:10.1016/S0040-4039(00)87636-4
(1982)
Palladium-catalyzed ring-closing reaction via C-N bond metathesis for rapid construction of saturated N-heterocycles

Doi:10.1021/jacs.0c10615
(2020)

Article Doi