Synthetic approaches to the alkaloids of the ancistrocladaceae: control of the diastereoisomer excess in the synthesis of axially chiral biaryls: a synthesis of (–)-ancistrocladinine-Reference-Cited by-同舟云学术

Synthetic approaches to the alkaloids of the ancistrocladaceae: control of the diastereoisomer excess in the synthesis of axially chiral biaryls: a synthesis of (–)-ancistrocladinine

Published:1991 Issue:5 Volume: Page:278-280
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Rizzacasa Mark A.,Sargent Melvyn V.

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1991/C3/C39910000278

Reference9 articles.

1. Facile Synthesis of 1,1′-Binaphthyl-2-carboxylates via Nucleophilic Aromatic Substitution of 1-Methoxy-2-naphthoic Esters by 1-Naphthyl Grignard Reagents

2. Asymmetric synthesis of (-)-steganone. Further application of chiral biaryl syntheses

3. First total synthesis of (−)-dioncophylline A (“Triphyophylline”) and of selected stereoisomers: Complete (revised) stereostructure

4. Synthetic approaches to the alkaloids of the ancistrocladaceae: (–)-O-methylancistrocladine and (+)-O-methylhamatine

5. Enantioselective synthesis of binaphthyls via nucleophilic aromatic substitution on chiral oxazolines

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