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Studies Toward the Synthesis of Spirolide C: Exploration Into the Formation of the 23-Membered All-Carbon Macrocyclic Framework

Organic Letters - United States

doi 10.1021/ol203342e

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January 19, 2012

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American Chemical Society (ACS)

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Studies Toward the Synthesis of Spirolide C: Exploration Into the Formation of the 23-Membered All-Carbon Macrocyclic Framework

Organic Letters - United States

doi 10.1021/ol203342e

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

Studies Toward the Synthesis of (−)-Zampanolide: Preparation of the Macrocyclic Core

Studies Toward the Synthesis of Phomactin A. An Approach to the Macrocyclic Core

Studies Toward the Synthesis of Maoecrystal V

Total Synthesis of Gymnorrhizol, an Unprecedented 15-Membered Macrocyclic Polydisulfide From the Chinese Mangrove Bruguiera Gymnorrhiza

Studies Directed Toward the Synthesis of Methyllycaconitine

Studies on the Transannular Diels–Alder Reaction of 15-Membered Macrocyclic Trienes Containing Atrans-Transdiene. Part I: Synthesis and Isomerization of Various Model Cyclopentadecatrienes

Progress Toward the Total Synthesis of Frondosin C

Synthetic Studies Toward the Total Synthesis of Aeroplysinin

Facile Formation of Chiral Calixarene Analogs Incorporating Cystine Peptide Into the Macrocyclic Ring