Dyotropic Rearrangement Facilitated Proximal Functionalization and Oxidative Removal of Angular Methyl Groups: Efficient Syntheses of 23‘-Deoxy Cephalostatin 1 Analogues-Reference-Cited by-同舟云学术

Dyotropic Rearrangement Facilitated Proximal Functionalization and Oxidative Removal of Angular Methyl Groups: Efficient Syntheses of 23‘-Deoxy Cephalostatin 1 Analogues

Published:2002-04-05 Issue:17 Volume:124 Page:4548-4549
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Li Wei¹,LaCour Thomas G.¹,Fuchs P. L.¹

Affiliation:

1. Department of Chemistry, Purdue University, West Lafayette, Indiana 47907

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja017323v

Reference15 articles.

1. The First Total Synthesis of (Corrected) Ritterazine M

2. Interphylal Product Splicing: The First Total Syntheses of Cephalostatin 1, the North Hemisphere of Ritterazine G, and the Highly Active Hybrid Analogue, Ritterostatin GN1N1

3. An Efficient Protocol for the Synthesis of Unsymmetrical Pyrazines. Total Synthesis of Dihydrocephalostatin 11

4. Synthesis of a C14',15' dihydro derivative of the south hexacyclic steroid unit of cephalostatin 1. Part II: Spiroketal synthesis and stereochemical assignment by nmr spectroscopy

5. Biomimetic Total Syntheses of (+)-Cephalostatin 7, (+)-Cephalostatin 12, and (+)-Ritterazine K

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