Synthesis of the brominated marine alkaloids (±)-arborescidine A, B and C

DOI: 10.1016/S0040-4020(98)00306-8

Source and publish data:

Tetrahedron p. 6135 - 6146 (1998)

Update date:2022-08-03

Topics:

Authors:

Burm, Brigitte E.A.

Meijler, Michael M.

Korver, Jacco

Wanner, Martin J.

Koomen, Gerrit-Jan

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

Article abstract of DOI:10.1016/S0040-4020(98)00306-8

A straightforward synthesis of the brominated marine alkaloids arborescidine A (1), B (2) and C (3), starting from 6-bromo-(N-methyl) trypatamine is described. An equilibrium, under both basic and acidic conditions was found to exist between the trans- and cis-isomers 3 and 4. Spectral data indicated that the structure of isomer 4 does not correspond with the compound identified as arborescidine D recently isolated from the marine tunicate Pseudodistoma arborescens.

Full text of DOI:10.1016/S0040-4020(98)00306-8

Products guided by the article

Product name:Carbamic acid, [2-(6-bromo-1H-indol-3-yl)ethyl]-, 1,1-dimethylethyl ester

Cas No:209168-88-7

R&D Labs maybe for 209168-88-7

Binzhou Holly Pharmaceutical Co.,Ltd.

Contact:74517

Address:No.15 Dapu Road,Huangpu District Shanghai,P.R.China
Ningbo Huajia Chemicals

Contact:+86-574-87065746

Address:10th Floor, No.787 Baizhang East Road,
Shreeji pharma international

Contact:0091-265-2313036

Address:311, ATLANTIS HEIGHTS SARABHAI MAIN ROAD,VADIWADI ,VADODARA
Exploiter Molybdenum Co.,Ltd

Contact:86-379-63338609

Address:Jiudian Village,Deting Town,Song County,Luoyang
Qingdao S. H. Huanyu Imp. & Exp. Co., Ltd.

Contact:86-532-88250866

Address:Room 615, World Trade Centre Building B, Hongkong Middle Roda 6#, Qingdao, Shandong, China

Relevant to this article

Synthesis, X-ray Structure, Spectroscopic Characterization, and Theoretical Prediction of the Structure and Electronic Spectrum of Eu(btfa)₃·bipy and an Assessment of the Effect of Fluorine as a β-Diketone Substituent on the Ligand-Metal Energy Transfer Process

Doi:10.1021/ic971602v
(1998)
Chiral dienolate-based remote asymmetric induction: The asymmetric α- oxylation/Pd(0)-catalyzed allylic substitution sequence leading to γ-chiral α,β-unsaturated acid derivatives

Doi:10.1016/S0040-4039(98)00770-9
(1998)
Elimination of the 4-hydroxyl group of the alkaloids related to morphine. XI. Synthesis of (minus)-14 hydroxy-3-methoxy-N-methylmorphinan derivatives.

Doi:10.1016/S0040-4020(01)96351-3
(1968)
Imidovanadium(v) complexes as reaction partners for kinetically stabilized phosphaalkynes: Synthesis of 1,2,4-azaphosphavanada(v)-cyclobutenes, 1,3,5-triphosphabenzenes, and 1H-1,2,4-azadiphospholes

Doi:10.1002/1521-3765(20001215)6:24<4558::AID-CHEM4558>3.0.CO;2-6
(2000)
Rearrangement of derivatives of 1,3-dithian-5-amine into bicyclic 2-thiazolidines. Crystal structures of cis- and trans-1-(2-aryl-1,3-dithian-5-yl)-2-thioureas and cis- and trans-5-aryl-3-imino-7,7a-dihydro-1H,3H,5H-thiazolo[3,4-c]thiazoles

Doi:10.1002/hlca.19840670720
(1984)
Synthesis and antibacterial activity of [6,5,5] and [6,6,5] tricyclic fused oxazolidinones

Doi:10.1016/S0960-894X(98)00194-2
(1998)

Article Doi