Enantioselective Total Syntheses of Allopumiliotoxins 267A, 323B‘, and 339A. Application of Iodide-Promoted Iminium Ion−Alkyne Cyclizations for Forming Allopumiliotoxin A Alkaloids-Reference-Cited by-同舟云学术

Enantioselective Total Syntheses of Allopumiliotoxins 267A, 323B‘, and 339A. Application of Iodide-Promoted Iminium Ion−Alkyne Cyclizations for Forming Allopumiliotoxin A Alkaloids

Published:1996-01-01 Issue:38 Volume:118 Page:9073-9082
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Caderas Christian¹,Lett Renee¹,Overman Larry E.¹,Rabinowitz Michael H.¹,Robinson Leslie A.¹,Sharp Matthew J.¹,Zablocki Jeffery¹

Affiliation:

1. Contribution from the Department of Chemistry, University of California, Irvine, California 92717-2025

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja961640y

Reference33 articles.

1. (b) NIH NRSA Postdoctoral fellow (GM 09850); current address: DuPont Agricultural Products Division, Elkton Rd., Newark, DE 19714.

2. Toxicity of Panamanian Poison Frogs ( Dendrobates ): Some Biological and Chemical Aspects

3. pumiliotoxins: magnetic resonance spectral assignments and structural definition of pumiliotoxins A and B and related allopumiliotoxins

4. Enantioselective total synthesis of allopumiliotoxin A alkaloids 267A and 339B

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