Scholarly article on 13151-04-7 44652-54-2 from Journal of the American Chemical Society p. 1806 - 1812

DOI: 10.1021/ja00895a025

Source and publish data:

Journal of the American Chemical Society p. 1806 - 1812 (1963)

Update date:2022-07-28

Topics:

Authors:

Schechter,H.

Brain,D.K.

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

Article abstract of DOI:10.1021/ja00895a025

Full text of DOI:10.1021/ja00895a025

Products guided by the article

Product name:13151-04-7

Cas No:44652-54-2

R&D Labs maybe for 44652-54-2

Anhui Xinyuan Technology Co.,Ltd

Contact:0086-559-3515800

Address:No.16 Zijin Rd, Circular Economic Zone, Huizhou District, Huangshan Anhui China
Chameleon Specialty Chemicals

Contact:+44 7958 511245

Address:PO Box 469, Manchester, UK
NEW FORTUNE INDUSTRIAL CO.,LTD.

website:http://newfortune.lookchem.com/

Contact:+86-25-8645-9456

Address:C4-105 GREEN ISLAND FLOWER TOWN
Beijing Mesochem Technology Co.,LTD

website:http://www.mesochem.com

Contact:0086-10-57862036

Address:2301, Floor 23, Building 9 Lippo Plaza, Yard 8 Ronghua Middle Road, ETDZ, Beijing, China
Shanghai Yuantai Chemical Products Co., Ltd

Contact:021--66129803

Address:Chengyin Road,Shanghai,China

Relevant to this article

A Cycloaddition Cascade Approach to the Total Synthesis of (-)-FR182877

Doi:10.1021/ja037643+
(2003)
Highly enantioselective Darzens reaction of a camphor-derived sulfonium amide to give glycidic amides and their applications in synthesis

Doi:10.1021/ja0272540
(2002)
Stereoselective Preparation of Dienyl Zirconocene Complexes via a Tandem Allylic C-H Bond Activation-Elimination Sequence

Doi:10.1021/ja036751t
(2003)
Synthesis and adrenergic β-blocking activity of some propanolamine derivatives

Doi:10.1248/cpb.26.1443
(1978)
Doi:10.1002/hlca.19650480722
(1965)
A straightforward enantioselective route to dialkyl sulfoxides based upon two carbon-for-carbon substitution reactions on the sulfinyl group

Doi:10.1021/jo025974j
(2002)

Article Doi

DOI: 10.1021/ja00895a025