Two-directional synthesis and biological evaluation of alkaloid 5-epi-cis-275B'.

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Two-directional synthesis and biological evaluation of alkaloid 5-epi-cis-275B'.

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2014 nî lūn-bûn

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2014年の論文

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年學術文章

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2014年學術文章

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2014年學術文章

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Two-directional synthesis and biological evaluation of alkaloid 5-epi-cis-275B'.

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label

Two-directional synthesis and biological evaluation of alkaloid 5-epi-cis-275B'.

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Two-directional synthesis and biological evaluation of alkaloid 5-epi-cis-275B'.

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P1476

Two-directional synthesis and biological evaluation of alkaloid 5-epi-cis-275B'

@en

P2093

Annabella F Newton

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David Richards

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Gareth Harbottle

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Ian R Mellor

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Pooja Aggarwal

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P2860

Alkaloids from amphibian skin: a tabulation of over eight-hundred compounds.

Cascade reactions in total synthesis.

Occurrence and significance of decahydroquinolines from dendrobatid poison frogs and a myrmicine ant: use of 1H and 13C NMR in their conformational analysis

A two-directional approach to pyrrolizidines: total syntheses and biological evaluation of alkaloid cis-223B and (±)-xenovenine.

Two-directional synthesis as a tool for diversity-oriented synthesis: Synthesis of alkaloid scaffolds.

Decahydroquinoline alkaloids: noncompetitive blockers for nicotinic acetylcholine receptor-channels in pheochromocytoma cells and Torpedo electroplax.

Biomimetic construction of the hydroquinoline ring system. Diastereodivergent enantioselective synthesis of 2,5-disubstituted cis-decahydroquinolines.

Spatial and temporal patterns of alkaloid variation in the poison frog Oophaga pumilio in Costa Rica and Panama over 30 years.

Tandem reactions, cascade sequences, and biomimetic strategies in total synthesis.

A general synthetic route to enantiopure 5-substituted cis-decahydroquinolines.

P304

15355-15357

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P31

scholarly article

P356

10.1039/C4CC07287A

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P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

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P50

Robert Stockman

George Procopiou

P577

2014-10-28T00:00:00Z

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P698

25348081

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