A fully synthetic route to hikosamine

DOI: 10.1021/ja00311a090

Source and publish data:

Journal of the American Chemical Society p. 7762 - 7764 (1985)

Update date:2022-08-05

Topics:

Authors:

Danishefsky

Maring Maring

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

Article abstract of DOI:10.1021/ja00311a090

Full text of DOI:10.1021/ja00311a090

Products guided by the article

Product name:C₂₃H₂₀O₈

Cas No:118920-26-6

R&D Labs maybe for 118920-26-6

Synchemie Co., Ltd.

website:http://www.synchemie.com/

Contact:+86-574-87642758

Address:Room 901, Yinyi Bund Building， 132 Renmin Road
Liaoyang Xinyou Chemical Products Co.,Ltd.

Contact:+86-419-5165433 13604191870

Address:Huishang Road6-1, Hongwei District, Liaoyang, Liaoning, China
Richest Group Ltd.

Contact:+86 21 5017 5386

Address:No 999,Jiangyue Rd, Minhang Dist ,201114,Shanghai ,China
shanghai jiuling chemical co.,ltd.

Contact:+86-21-50387295

Address:Zaozhuang Road, Pudong, Shanghai City. China
Chongqing KonAo Health Co.,Ltd

Contact:13687578375

Address:wuhan hubei china

Relevant to this article

Multiple reactivities of dithranol towards 1-alkynyl Fischer carbene complexes (CO)₅M{double bond, long}C(OEt)C{triple bond, long}CPh (M = Cr, W) - Efficient chemical synthesis of aromatic polyketides

Doi:10.1016/j.jorganchem.2009.05.029
(2009)
Direct synthesis of functionalized unsymmetrical β-sulfonamido disulfides by tetrathiomolybdate mediated aziridine ring-opening reactions

Doi:10.1021/jo901528e
(2009)
Synthesis of a ketomethylene isostere of the fibrillating peptide SNNFGAILSS

Doi:10.1021/jo901466b
(2009)
Antileishmanial thioureas: Synthesis, biological activity and in Silico evaluations of new promising derivatives

Doi:10.1248/cpb.c17-00293
(2017)
Phenanthroline ligands with divergent pyridine units

Doi:10.3184/030823409X401817
(2009)
Asymmetrie intermodular Pauson-Khand reaction of symmetrically substituted alkynes

Doi:10.1021/ol901728r
(2009)

Article Doi