INFLUENCE DE LA NATURE DU LIGAND AROMATIQUE SUR L'INDUCTION ASYMETRIQUE OBSERVEE LORS DE L'ADDITION D'ARYLMETHYLSULFOXYDES SUR DES CARBONYLES

DOI: 10.1016/S0040-4039(01)90195-9

Source and publish data:

Tetrahedron Letters p. 4113 - 4116 (1984)

Update date:2022-08-04

Topics:

Authors:

Demailly, Gilles

Greck, Christine

Solladie, Guy

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

Article abstract of DOI:10.1016/S0040-4039(01)90195-9

The presence of an orthopyridyl substituent instead of a p-Tolyl on a chiral sulfoxide group increased drastically the asymmetric induction observed during the addition of arylmethylsulfoxide on carbonyl compounds.

Full text of DOI:10.1016/S0040-4039(01)90195-9

Products guided by the article

Product name:2-((R)-2-Methoxy-benzenesulfinyl)-1-phenyl-ethanol

Cas No:93300-85-7

R&D Labs maybe for 93300-85-7

Shandong Jiulong Hisince Pharmaceutical Co.,Ltd.

Contact:--

Address:Huadian Pioneer Park, Huadian Township, Qihe County, Dezhou City, Shandong, P.R.China
Taizhou Huading Chemical Co.,Ltd(expird)

Contact:+86-576-88583898

Address:Economic&Technology development zone,Taizhou City,Zhejiang Province,China
Zhejiang Tianyu Pharmaceutical Co., Ltd.

Contact:+86-576-84177669, 89189665,89189688,84168770

Address:Jiangkou Development Zone, Huangyan, Taizhou City, Zhejiang
Chengdu Yunyi International Trade Co., Ltd

Contact:

Address:china
Chengdu Green technology Co.,Ltd.

Contact:86-28-82608355

Address:C9 ,Economic Headquarters, Economic Development Zone, Chengdu.

Relevant to this article

A Sigmatropic Rearrangement Involving Dimethyl Sulfoxide during an Oxidation of a Carbohydrate Derivative

Doi:10.1021/jo00203a018
(1985)
Doi:10.1039/jr9530001398
(1953)
Doi:10.1021/jo01089a016
(1959)
Synthesis of Ethyl (2RS,3SR)-1-Tosyl-3-vinylazetidine-2-carboxylate and Ethyl (2RS,E)-3-Ethylidene-1-tosylazetidine-2-carboxylate (=rac-Ethyl N-Tosylpolyoximate)

Doi:10.1002/hlca.19880710513
(1988)
Conversion of Olefins into Ketones by an Iron-Catalyzed Wacker-type Oxidation Using Oxygen as the Sole Oxidant

Doi:10.1002/anie.201710370
(2018)
Selective Isotope Labelling of Leucine Residues by Using α-Ketoacid Precursor Compounds

Doi:10.1002/cbic.201200737
(2013)

Article Doi