d5-Reactions of Doubly Deprotonated γ,δ-Unsaturated Carbonyl Derivatives with Electrophiles. A Novel Approach to the Synthesis of Tetrahydrofuran and Tetrahydropyran Derivatives

DOI: 10.1002/hlca.19820650202

Source and publish data:

Helvetica Chimica Acta p. 419 - 450 (1982)

Update date:2022-08-04

Topics:

Authors:

Seebach, Dieter

Pohmakotr, Manat

Schregenberger, Christian

Weidmann, Beat

Mali, Raghao S.

Pohmakotr, Srisuke

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

Article abstract of DOI:10.1002/hlca.19820650202

The dienone-dianion derivatives 1 react with all types of electrophiles tested (alkyl halide, silyl chloride, ester, ketone, aldehyde, epoxide) to give β,υ-unsaturated carbonyl compounds of type A (see Formulae 2-6, 13, 14 and Tables 1-5).The α- and β-hyd

Full text of DOI:10.1002/hlca.19820650202

Products guided by the article

Product name:2-Octenoic acid, 7-hydroxy-, (E)-

Cas No:80736-31-8

R&D Labs maybe for 80736-31-8

ZHUHAI HAIRUIDE BIOSCIENCE AND TECHNOLOGY CO.,LTD

website:http://www.zhhairuide.com

Contact:+8613326687259/+86-756-7789199

Address:No.10 Yonghui Road
Lonwin Chemical Group Limited

website:http://www.lonwinchem.com

Contact:Tel: 86-21-59858395

Address:No#966,Huaxu Road,Shanghai 201702,P.R.China
Longhui qunfeng Chemical Co., Ltd

Contact:86-731-82173407

Address:South-east Industrial Park, Longhui County, Hunan Province, China
Changsha Easchem Co.,Limited

website:http://www.easchem.com

Contact:+86-731-89722861 89722891

Address:2/F-4/Bld Colorful Palace, No.605 Changsha Ave, Yuhua Area Changsha Hunan China.
TIANJIN GST CHEMICAL TECHNOLOGY CO., LTD

Contact:+86-22-25210964

Address:Room. 208, No. -12-C, No. 13, Xinbei Road, Tanggu District, New Haixin Area, Tianjin City, China

Relevant to this article

Doi:10.1139/v67-245
(1967)
Kinetics of Monomerization or Polymerization Reaction for Bis(N-phenyl-salicylideneaminato)nickel(II) and Bis(N-methylsalicylideneaminato)nickel(II) in Solid Phase

Doi:10.1246/bcsj.54.3361
(1981)
Synthesis of phenyl α- and β-L-arabinofuranoside

Doi:10.1016/S0008-6215(00)80806-X
(1982)
The chemistry of indoles. XVI. A convenient synthesis of substituted indoles carrying a hydroxy group, a halogeno group, or a carbon side chain at the 4-position via 4-indolediazonium salts and a total synthesis of (±)-6,7-secoagroclavine

Doi:10.1248/cpb.29.3145
(1981)
Investigations of β-sultones, V: On the reaction of vicinal polycarbonyl compounds with alkanesulfonyl halides and triethylamine, Part 2.

Doi:10.1002/ardp.19823150114
(1982)
Synthesis of highly selective lysosomal markers by coupling 2-(2′-hydroxyphenyl)benzothiazole (HBT) with benzothiazolium cyanine (Cy): the impact of substituents on selectivity and optical properties

Doi:10.1039/c9tb01672d
(2019)

Article Doi