Journal ArticleDOI
Enantioselective total synthesis of marine alkaloids, manzamine A and related compounds
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TLDR
A review of studies toward the enantioselective total synthesis of ircinal A, manzamine A and related compounds is presented in detail in this paper, where a review of their work is presented.About:
This article is published in Journal of Heterocyclic Chemistry.The article was published on 2000-05-01. It has received 27 citations till now. The article focuses on the topics: Total synthesis.read more
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Simple indole alkaloids and those with a nonrearranged monoterpenoid unit
Satoshi Hibino,Tominari Choshi +1 more
TL;DR: This review covers the literature on simple indole alkaloid and those with a nonrearranged monoterpenoid unit from the beginning of 2012 up to the end of 2013, which includes newly isolated alkaloids, structure determinations, total syntheses and biological activities.
Journal ArticleDOI
Arylglyoxals in synthesis of heterocyclic compounds.
Journal ArticleDOI
The First Total Synthesis of Nakadomarin A
TL;DR: The first total synthesis of (+)-nakadomarin A, an enantiomer of natural product, has been accomplished from stereochemically defined 4-oxopiperidin-3-carboxylic acid derivative.
Journal ArticleDOI
Synthesis of β- and γ-Carbolines by the Palladium/Copper-Catalyzed Coupling and Cyclization of Terminal Acetylenes
Haiming Zhang,Richard C. Larock +1 more
TL;DR: In this article, a variety of 3-substituted β- and γ-carbolines have been synthesized from 3-iodoindole-2-carboxaldehydes and 2-bromoindoles-3-carboardaldehyde, respectively, using PdCl2(PPh3)/CuI as the catalyst.
Journal ArticleDOI
New Route to the Synthesis of the Isocryptolepine Alkaloid and Its Related Skeletons Using a Modified Pictet–Spengler Reaction†
TL;DR: In this article, a new route to the synthesis of the isocryptolepine alkaloid with antimalarial activity using a modified Pictet-Spengler reaction has been devised.
References
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Journal ArticleDOI
Manzamine A, a novel antitumor alkaloid from a sponge
Journal ArticleDOI
Regioselective synthesis of β-ketoesters from lithium enolates and methyl cyanoformate
Lewis N. Mander,S.Paul Sethi +1 more
TL;DR: C-acylation of lithium enolates by methyl cyanoformate provides high yields of β-keto esters under mild conditions and with 100% regioselectivity as mentioned in this paper.
Journal ArticleDOI
Smooth and efficient deoxygenation of secondary alcohols. A general procedure for the conversion of ribonucleosides to 2'-deoxynucleosides
Morris J. Robins,John S. Wilson +1 more
Journal Article
3,5-ジメチルピラゾールでのアリル酸化反応 三酸化クロム錯体 ステロイド性δ 5 -7-ケトン
Salmond W G,Barta M A,Havens J L +2 more