Enantioselective Synthesis of Altohyrtin C (Spongistatin 2): Synthesis of the EF-Bis(pyran) Subunit

DOI: 10.1002/anie.199727411

Source and publish data:

Angewandte Chemie - International Edition in English p. 2741 - 2744 (1997)

Update date:2022-08-03

Topics:

Authors:

Evans, David A.

Trotter, B. Wesley

Cote, Bernard

Coleman, Paul J.

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

Article abstract of DOI:10.1002/anie.199727411

Keywords: altohyrtin; antitumor agents; natural products; spongistatin; total synthesis

Full text of DOI:10.1002/anie.199727411

Products guided by the article

Product name:(2S,3R)-4-Benzyloxy-2-methyl-3-triethylsilanyloxy-butyraldehyde

Cas No:203515-62-2

R&D Labs maybe for 203515-62-2

shijiazhuang baisheng chem co.; ltd

Contact:86-0311-80790826

Address:shijiazhuang hebei
Hisyntech Corporation Limited

Contact:0086-22-23410962

Address:17-201, Ningfuli, Shuishanggongyuandong road,Nankai district, Tianjin, China
Nanjing Fayekong Chemcial Co.,Ltd(expird)

Contact:86-25-58813444

Address:Rm 1503, Unit 1, Building 5, Zijinnanyuan, Nanjing, Jiangsu, China
Beijing Green Guardee Technology CO,.LTD

Contact:+86-10-69706062

Address:F2 BLdj,5 No.37 Chaoqian Road
Shanghai FWD Chemicals ltd

website:http://www.fwdchem.com

Contact:86-21-54450828

Address:Room 802,Lotus Tower ,159 Tianzhou Road,Xuhui District,Shanghai

Relevant to this article

Thermal Rearrangement of 5,6-Benzotricyclo<3.2.0.0^2,7>hept-5-ene into 2-Vinylindene via an Intramolecular Retro-Diels-Alder Reaction

Doi:10.1021/jo01309a020
(1980)
Doi:10.1021/ja01371a053
(1930)
Phosphine oxides as stabilizing ligands for the palladium-catalyzed cross-coupling of potassium aryldimethylsilanolates

Doi:10.1016/j.tet.2007.02.017
(2007)
A Highly Reactive Oxoiron(IV) Complex Supported by a Bioinspired N₃O Macrocyclic Ligand

Doi:10.1002/anie.201707872
(2017)
Creation of hoop- and bowl-shaped benzenoid systems by selective detraction of [60]fullerene conjugation. [10]Cyclophenacene and fused corannulene derivatives

Doi:10.1021/ja048683w
(2004)
Doi:10.1021/ja01246a019
(1943)

Article Doi