Asymmetric induction using chiral 1,2,4-triazole arad benzimidazole derivatives

DOI: 10.1016/S0957-4166(97)00155-9

Source and publish data:

Tetrahedron Asymmetry p. 1491 - 1500 (1997)

Update date:2022-07-29

Topics:

Authors:

Katritzky, Alan R.

Aslan, Diana C.

Leeming, Peter

Steel, Peter J.

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

Article abstract of DOI:10.1016/S0957-4166(97)00155-9

Lithiated N-substituted 1,2,4-triazoles 3 and 8 and benzimidazole 11 reacted with (1R)-fenchone to give derivatives 5c, 9 and 12 in good yields as single diastereoisomers, (S)-Lactic acid 16 reacted with o-phenylenediamine 15 to give optically pure (S)-2-

Full text of DOI:10.1016/S0957-4166(97)00155-9

Products guided by the article

Product name:1H-1,2,4-Triazole, 1-(methoxyphenylmethyl)-

Cas No:105873-94-7

R&D Labs maybe for 105873-94-7

Shandong Xinke Petrochemical Co., Ltd.

Contact:+86-546-7277016

Address:Gudao Industrial Park, Hekou District, Dongying, Shandong Province, China
jiangsu haian chemical co.,ltd.

Contact:86-513-15851283853

Address:No.99,Changjiang West Road,Haian County,Jiangsu Province,China
ShangHai BMG Chemical Co., Ltd

Contact:+86-13524845543

Address:Room 602, no 291 sikai road shanghai
Suqian Ruixing Chemical Co., Ltd.

Contact:+86-527-80805666（总机）;84836008(销售)

Address:3 Jingsilu, Zone north, Hubin Xincheng Development Park, Suqian, China
KAIYUAN CHEMICAL COMPANY LIMITED.

website:http://www.kaiyuanchem.com

Contact:+86-22-59891255/66/77

Address:B-2205, Kuangshi International Building, Yingbin Road, XiangLuo Bay Business District, Binhai New area, Tianjin, China.

Relevant to this article

A homogeneous catalyst for reduction of optically active esters to the corresponding chiral alcohols without loss of optical purities

Doi:10.1002/adsc.200900114
(2010)
Synthesis of biologically active tetraacetyl-3-deoxy-D-manno-2-octulosonic acid(KDO)-(α2→6)-D)-glucosamine analogs of lipid A

Doi:10.1248/cpb.34.2302
(1986)
Substrate modification as a means of enhancing the enantioselectivity of microbial reductions of β-keto esters. An (R)- or (S )-1,3,5-trihydroxypentane synthon

Doi:10.1021/jo00378a007
(1987)
Synthesis and insecticidal activity of novel benzothiazole derivatives containing the coumarin moiety

Doi:10.24820/ark.5550190.p010.664
(2018)
Fast and efficient preparation of an α-fucosyl building block by reductive 1,2-benzylidene ring-opening reaction

Doi:10.1055/s-2008-1077961
(2008)
A 1,10-phenanthroline-containing ring connected to a porphyrin by a rigid aromatic spacer and its copper-complexed pseudorotaxane

Doi:10.1002/ejic.200700177
(2007)

Article Doi