Convenient one-pot synthesis of symmetrical xanthenes

DOI: 10.1055/s-1995-3979

Source and publish data:

Synthesis p. 693 - 698 (1995)

Update date:2022-08-04

Topics:

Authors:

Novak Novak

Kovacs Kovacs

Pirok Pirok

Kolonits

Szabo Szabo

Fekete Fekete

Weiszfeiler

Szantay Szantay

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

Article abstract of DOI:10.1055/s-1995-3979

A new method is described for the preparation of symmetrically substituted xanthenes 12. They were obtained by consecutive rearrangements and intramolecular cyclizations of allyl aryl ethers 3 formed in situ from hydroquinone derivatives 1 and methallyl a

Full text of DOI:10.1055/s-1995-3979

Products guided by the article

Product name:2-(1-hydroxy-2-methylpropyl)-3,5,6-trimethyl<1,4>benzoquinone

Cas No:169771-51-1

R&D Labs maybe for 169771-51-1

Changzhou Sunsheng Chem Co., Ltd

Contact:+1-(989)-854-0648

Address:No. 28 Yinshan Rd., Xixiashu Industrial Park
Hubei Xinghuo Chemical Co., Ltd.,

Contact:13925817279 13907299441

Address:Xinghuo Fine Chemistry Industrial Park, Xiaochang County, Hubei Province, China
Taizhou KEDE Chemical.Co.,Ltd.

Contact:86-576-84613060

Address:Jiangkou Chemical Zoon
Shandong Shouguang Songchuan Industrial Additives Co.,Ltd

Contact:+86-536-8566856

Address:Shouguang,Shandong,China
Hangzhou jls Flame Retardants Chemical Co.,Ltd

Contact:+86-571-87250387/87250386

Address:MOGANSHAN RODA 1418# SHANGCHENG INDUSTRIAL PARK

Relevant to this article

Nickel-Catalyzed Decarbonylation of Acylsilanes

Doi:10.1021/acs.joc.0c00772
(2020)
Development of methionyl-trna synthetase inhibitors as antibiotics for gram-positive bacterial infections

Doi:10.1128/AAC.00999-17
(2017)
Addition of molecular fluorine to azlactones: General synthetic method of erythro-β-fluorinated α-amino acids

Doi:10.1248/cpb.43.760
(1995)
Synthetic lipidation of peptides and amino acids: Monolayer structure and properties

Doi:10.1021/ja00142a019
(1995)
Synthesis, crystal structure, deoxyribose nucleic acid interaction and antitumor activity of some thiosemicarbazonatomolybdenum(VI)

Doi:10.1016/j.ica.2014.04.005
(2014)
Doi:10.1139/v57-041
(1957)

Article Doi