Studies on the Synthesis of Stemona Alkaloids; Stereoselective Preparation of the Hydroindole Ring System by Oxidative Cyclization of Tyrosine

DOI: 10.1016/S0040-4039(00)61121-8

Source and publish data:

Tetrahedron Letters p. 5477 - 5480 (1992)

Update date:2022-08-04

Topics:

Authors:

Wipf, Peter

Kim, Yuntae

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

Article abstract of DOI:10.1016/S0040-4039(00)61121-8

The core hydroindole ring system of the Stemona alkaloids was prepared by oxidation of tyrosine with a hypervalent iodine reagent followed by a diastereotopic group-selective intramolecular conjugate addition.Further transformations illustrate the versati

Full text of DOI:10.1016/S0040-4039(00)61121-8

Products guided by the article

Product name:(2S,7aR)-6-Oxo-2,6,7,7a-tetrahydro-indole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester

Cas No:144534-51-0

R&D Labs maybe for 144534-51-0

Cangzhou Senary Chemical Science-tech Co., Ltd

Contact:+86-317-3563899, 3563699

Address:168 Jinde Road, Cangzhou, Hebei, China
RongCheng Tianyu Technology Co.,Ltd.

Contact:86-631-7519595

Address:220Ping Donghai Road RongChengCity,ShangDong Province China
NINGXIA DARONG CHEMICALS & METALLURGY CO.,LTD.

Contact:86-952-2179751

Address:Darong Road, Dawukou, Shizuishan, Ningxia 753001, China
Shanghai ZaiQi Bio-Tech Co., Ltd.,

Contact:+86-21-5482 4098

Address:Bldg. No.7, No.201 MinYi Rd，Songjiang CaoHeJing High-Tech Park Shanghai 201516 P,R,China
Hangzhou Yingshanhua Pigment Chemicals Co.,Ltd.

Contact:+86-0150-58101658

Address:Nanyang Economic DevelopmentZong,Xiaoshan,Hangzhou,China

Relevant to this article

Facile Synthesis of Highly Efficient Lepidine-Based Phosphorescent Iridium(III) Complexes for Yellow and White Organic Light-Emitting Diodes

Doi:10.1002/adfm.201503826
(2016)
One-pot synthesis of N-heterocycles by tandem carbamoylation-oxidative bromolactamization of ω-alkenylmagnesium bromide

Doi:10.1016/j.tetlet.2013.06.002
(2013)
A New Xanthone Synthesis from the Diels-Alder Reaction between 2-Vinylchromen-4-ones and Cyclopentanone Enamine

Doi:10.1039/c39920001310
(1992)
Doi:10.1021/ja01505a023
(1960)
Influenza antiviral activity of F- and OH-containing isopulegol-derived octahydro-2H-chromenes

Doi:10.1016/j.bmcl.2020.127677
(2021)
Asymmetric cascade annulation based on enantioselective oxa-diels-alder cycloaddition of in situ generated isochromenyliums by cooperative binary catalysis of Pd(OAc)₂ and (S)-trip

Doi:10.1021/ja405764p
(2013)

Article Doi