Annulation of Thioimidates and Vinyl Carbodiimides to Prepare 2-Aminopyrimidines, Competent Nucleophiles for Intramolecular Alkyne Hydroamination. Synthesis of (−)-Crambidine-Reference-Cited by-同舟云学术

Annulation of Thioimidates and Vinyl Carbodiimides to Prepare 2-Aminopyrimidines, Competent Nucleophiles for Intramolecular Alkyne Hydroamination. Synthesis of (−)-Crambidine

Published:2010-01-22 Issue:6 Volume:132 Page:1802-1803
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Perl Nicholas R.¹,Ide Nathan D.¹,Prajapati Sudeep¹,Perfect Hahdi H.¹,Durón Sergio G.¹,Gin David Y.¹

Affiliation:

1. Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, New York 10065, and the Department of Chemistry, University of Illinois, Urbana, Illinois 61801

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja910831k

Reference21 articles.

1. The guanidine metabolites of Ptilocaulis spiculifer and related compounds; isolation and synthesis

2. Crambescidins: new antiviral and cytotoxic compounds from the sponge Crambe crambe

3. Structure and chemical properties of ptilomycalin A

4. Polycyclic Guanidine Alkaloids from the Marine Sponge Crambe crambe and Ca++ Channel Blocker Activity of Crambescidin 816

5. Polycyclic guanidine-containing compounds from the Mediterranean sponge Crambe crambe: the structure of 13,14,15-isocrambescidin 800 and the absolute stereochemistry of the pentacyclic guanidine moieties of the crambescidins

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