نتایج جستجو برای: indolizidine

تعداد نتایج: 138  

2017
Ari M.P. Koskinen Oili A. Kallatsa Maija Nissinen

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Journal: :iranian journal of chemistry and chemical engineering (ijcce) 2006
ghodsi mohammadi ziarani r. chenevert ali reza badiei

(-)-gephyrotoxin-223 was formally synthesized from chiral synthon 1 which has been chemoenzymatically synthesized  in the presence  of candida antartica lipase.

2005
Brendon S. Gourlay Peter P. Molesworth John H. Ryan Jason A. Smith

An investigation of the reaction requirements to effect the Clauson-Kaas pyrrole synthesis led to the formulation of a new procedure that avoids the contact of pyrroles to heat or strongly acidic conditions that cause decomposition of the desired products. The procedure involves mild hydrolysis of 2,5-dimethoxytetrahydrofuran in water to the activated species 2,5-dihydroxytetrahydrofuran that r...

Journal: :Organic letters 2016
Suet-Pick Wong Kam-Weng Chong Kuan-Hon Lim Siew-Huah Lim Yun-Yee Low Toh-Seok Kam

Two new monoterpene indole alkaloids, characterized by previously unencountered natural product skeletons, viz., arborisidine (1), incorporating indolizidine and cyclohexanone moieties fused to an indole unit, and arbornamine (2), incorporating an unprecedented 6/5/6/5/6 "arbornane" skeleton (distinct from the eburnan or tacaman skeleton), were isolated from a Malayan Kopsia arborea. The struct...

Journal: :The Journal of organic chemistry 1999
Kim M. Werner Jesus M. de Los Santos Steven M. Weinreb Maoyu Shang

The marine ascidian Clavelina cylindrica produces a series of interesting tricyclic quinolizidine and indolizidine alkaloids that show toxicity in a brine shrimp assay.1 Cylindricines A (1), C (2), D (3), E (4), and F (5) differ only in the functionality of the methylene substituent in the fivemembered ring. Interestingly, cylindricines A and B (7) interconvert simply upon standing in solution,...

Journal: :Beilstein Journal of Organic Chemistry 2008
Angela Nelson H Martin Garraffo Thomas F Spande John W Daly Paul J Stevenson

A short synthesis of the postulated structure for indolizidine alkaloid 259B with the hydrogens at C5 and C9 entgegen has been achieved with complete control of stereochemistry at C5. Both diastereoisomers at C8 were obtained, but neither proved to be the natural product. The comparison of the mass and FTIR spectral properties of the synthetic compounds to those of the natural material strongly...

Journal: :Organic & biomolecular chemistry 2010
Vincenzo Zambrano Gloria Rassu Annamaria Roggio Luigi Pinna Franca Zanardi Claudio Curti Giovanni Casiraghi Lucia Battistini

An efficient, stereocontrolled synthesis of (6S,7S,8S,8aR)-6,7,8-trihydroxyindolizidine (alias 1-deoxy-7,8-di-epi-castanospermine) (14) has been developed, which exploits an asymmetric vinylogous Mukaiyama aldol reaction (VMAR) between N-(tert-butoxycarbonyl)-2-(tert-butyldimethylsilyloxy)pyrrole (1) and 2,3-O-isopropylidene-D-glyceraldehyde (2) to construct the initial pyrrolidine building blo...

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