Synthesis of the orienticin C M(2-4) macrocycle utilizing a nucleophilic aromatic substitution strategy

DOI: 10.1016/0040-4039(96)00582-5

Source and publish data:

Tetrahedron Letters p. 3251 - 3254 (1996)

Update date:2022-07-29

Topics:

Authors:

Evans, David A.

Watson, Paul S.

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

Article abstract of DOI:10.1016/0040-4039(96)00582-5

The synthesis of the fully functionalized M(2-4) macrocyclic orienticin C subunit 5 is described utilizing an intramolecular nucleophilic aromatic substitution reaction.

Full text of DOI:10.1016/0040-4039(96)00582-5

Products guided by the article

Product name:(S)-2-Benzyloxycarbonylamino-N-[bis-(4-methoxy-phenyl)-methyl]-succinamic acid 2-trimethylsilanyl-ethyl ester

Cas No:189007-62-3

R&D Labs maybe for 189007-62-3

Ji'nan Orgachem Pharmaceutical Co.,Ltd

Contact:+86-531-82687810

Address:Jinan
KindChem Co.,Ltd,

Contact:+86-25-85281586

Address:13F,Bld2#,South of Longpan Road
SuZhou Ascepion Pharmaceuticals, Inc.(expird)

Contact:0512-86881668

Address:Building C,68Xingqing Road,Suzhou,China.
STAR SYNTHESIS CO.,LIMITED

Contact:+(852) 301-98033

Address:Flat C, 23/F, Lucky Plaza, 315-321 Lockhart Road, Wan Chai, Hong Kong
Shandong Xingshun New Material Co., Ltd.

website:http://www.sd-xingshun.com

Contact:+86-519-86461196

Address:Middle of Luhua East Road, Dingtao District

Relevant to this article

1-(2-alkanamidoethyl)-6-methoxyindole derivatives: A new class of potent indole melatonin analogues

Doi:10.1021/jm960653j
(1997)
Doi:10.1016/S0040-4039(01)99932-0
()
Copper-Catalyzed Difunctionalization of Terminal Alkynes with Diazo Esters and Amines to Construct β-Enamino Esters

Doi:10.1002/adsc.201600883
(2016)
Coumarin sulfonamides derivatives as potent and selective COX-2 inhibitors with efficacy in suppressing cancer proliferation and metastasis

Doi:10.1016/j.bmcl.2016.06.037
(2016)
Ruthenium-catalyzed oxidative homocoupling of arylboronic acids in water: Ligand tuned reactivity and mechanistic study

Doi:10.1021/acs.inorgchem.6b01115
(2016)
Doi:10.1021/ja00489a014
(1978)

Article Doi