Results 131 to 140 of about 174 (166)
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Total synthesis of the indole alkaloids ngouniensine and epingouniensine

Tetrahedron Letters, 1987
Abstract The first total synthesis of ngouniensine and epingouniensine, by cyclization of a suitable 1-(3-indolylethyl)piperidine-2-carboxylic acid followed by the elaboration of the exocyclic methylene group, is reported.
Joan Bosch   +4 more
openaire   +1 more source

Intramolecular Larock Indole Synthesis: Preparation of 3,4‐Fused Tricyclic Indoles and Total Synthesis of Fargesine

Angewandte Chemie International Edition, 2013
A variety of common, medium, and large ring fused tricyclic indoles including the fargesine precursor (XIV) are prepared from o-iodoaniline substrates under optimized conditions A).
Dong, Shan, Yan, Gao, Yanxing, Jia
openaire   +2 more sources

Total Syntheses of the Monoterpenoid Indole Alkaloids (±)‐Alstoscholarisine B and C

Angewandte Chemie, 2017
AbstractTotal syntheses of the monoterpenoid indole alkaloids (±)‐alstoscholarisine B and C were accomplished starting from a readily available indole‐2‐acetic ester and an α,β‐unsaturated N‐sulfonyllactam.
Jeremy D. Mason, Steven M. Weinreb
openaire   +2 more sources

Metamorphosis of cycloalkenes for the divergent total synthesis of polycyclic indole alkaloids

Chemical Society Reviews, 2018
This review summarizes the divergent synthesis of monoterpene indole alkaloids using cycloalkene as the turning point of structural diversity.
Zhengren Xu, Qian Wang, Jieping Zhu
openaire   +4 more sources

Total Synthesis of the Indole Alkaloid (±)‐ and (+)‐Methyl N‐Decarbomethoxychanofruticosinate

Angewandte Chemie International Edition, 2013
All caged up: The first total synthesis of N-decarbomethoxychanofruticosinate is achieved by using a SmI2 -mediated intramolecular Reformatsky-like reaction to create the seven-membered ring, and an intramolecular oxidative coupling to install the caged and strained ring system.
Yi, Wei, Duo, Zhao, Dawei, Ma
openaire   +2 more sources

Hexacyclic indole alkaloids. A highly convergent total synthesis of cuanzine

The Journal of Organic Chemistry, 1991
A novel route to the hexacyclic indole alkaloid cuanzine 1 has been developed. Key synthetic steps include the cyclocondensation of the imine 8 with the dihydrofuran 10 followed by homogeneous-catalyzed hydrogenation, wherein to COOMe group at C(20) serves as a diastereocontrol element in establishing the C(15) stereogenicity.
G. PALMISANO   +4 more
openaire   +2 more sources

Direct approaches to annulated indoles. A formal total synthesis of 0231B

Tetrahedron, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
George A. Kraus, Tao Wu
openaire   +1 more source

Directed Fischer Indolization as an Approach to the Total Syntheses of (+)-Aspidospermidine and (−)-Tabersonine

Organic Letters, 2017
A conceptually new synthetic approach that provides general access to the aspidosperma alkaloids (+)-aspidospermidine and (-)-tabersonine was developed. This method is based on the regioselective indolization of an ene-hydrazide, which was obtained via a base-catalyzed intramolecular aza-Michael reaction, in situ trapping of the resulting enolate, and ...
Joo-Young Kim   +3 more
openaire   +2 more sources

General Approach for the Synthesis of Sarpagine/Macroline Indole Alkaloids. Enantiospecific Total Synthesis of the Indole Alkaloid Trinervine

Organic Letters, 2001
[structure: see text] The total synthesis of the indole alkaloid trinervine 1 was accomplished in enantiospecific fashion in an overall yield of 20% (from the tetracyclic ketone 8) in 10 reaction vessels (12.5% from tryptophan methyl ester). The synthesis of the N(a)-H substituted macroline equivalent 2 was also completed in high yield via the same ...
X, Liu, J M, Cook
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Total Synthesis of the Tremorgenic Indole Diterpene Paspalinine

Angewandte Chemie International Edition, 2012
Masaru, Enomoto   +2 more
openaire   +2 more sources

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