Total Synthesis of (+/−)-Frondosin B and (+/−)-5-epi-Liphagal by Using a Concise (4+3) Cycloaddition Approach

Collective Total Synthesis of Englerin A and B, Orientalol E and F, and Oxyphyllol: Application of the Organocatalytic [4+3] Cycloaddition Reaction

(2013) Jie Wang et al.   CHEMISTRY-A EUROPEAN JOURNAL

Regio- and Stereoselective[4+3] Cycloaddition Towards Fused 5,7,6-Tricyclic Skeletons

(2013) Wanchun Gong et al.   Chemistry-An Asian Journal

Recent Synthetic Strategies to Access Seven-Membered Carbocycles in Natural Product Synthesis

(2013) Dieter Enders et al.   SYNTHESIS-STUTTGART

Gallium(III)-Catalyzed Three-Component (4+3) Cycloaddition Reactions

(2012) Xinping Han et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

A Novel, Facile Approach to Frondosin B and 5-epi-Liphagal via a New [4 + 3]-Cycloaddition

(2012) Jie Zhang et al.   ORGANIC LETTERS

Elaboration of the carbocyclic ring systems in plumarellide and rameswaralide using a coordinated intramolecular cycloaddition approach, based on a common biosynthesis model

(2012) Matthew J. Palframan et al.   TETRAHEDRON LETTERS

Lewis Acid-Catalyzed [3+4] Annulation of 2-(Heteroaryl)- cyclopropane-1,1-dicarboxylates with Cyclopentadiene

(2011) Olga A. Ivanova et al.   ADVANCED SYNTHESIS & CATALYSIS

The Catalytic Enantioselective Total Synthesis of (+)-Liphagal

(2011) Joshua J. Day et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Scope and Mechanism of the (4+3) Cycloaddition Reaction of Furfuryl Cations

(2011) Johan M. Winne et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Total Synthesis of (±)-Cortistatin J from Furan

(2011) Mark G. Nilson et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

The (4+3)-cycloaddition reaction: heteroatom-substituted allylic cations as dienophiles

(2010) Michael Harmata   CHEMICAL COMMUNICATIONS

The (4+3)-cycloaddition reaction: simple allylic cations as dienophiles

(2010) Michael Harmata   CHEMICAL COMMUNICATIONS

An efficient synthesis of (±)-frondosin B using a Stille–Heck reaction sequence

(2010) Kye-Simeon Masters et al.   ORGANIC & BIOMOLECULAR CHEMISTRY

Enantioselective Total Synthesis of the Selective PI3 Kinase Inhibitor Liphagal

(2010) Enrique Alvarez-Manzaneda et al.   ORGANIC LETTERS

Enantiospecific, Biosynthetically Inspired Formal Total Synthesis of (+)-Liphagal

(2010) Jonathan H. George et al.   ORGANIC LETTERS

Synthesis of (±)-Nosyberkol (Isotuberculosinol, Revised Structure of Edaxadiene) and (±)-Tuberculosinol

(2010) Nathan Maugel et al.   ORGANIC LETTERS

The organocatalytic three-step total synthesis of (+)-frondosin B

(2010) Maud Reiter et al.   Chemical Science

Asymmetric Synthesis of Seven-Membered Carbocyclic Rings via a Sequential Oxyanionic 5-Exo-Dig Cyclization/Claisen Rearrangement Process. Total Synthesis of (−)-Frondosin B

(2009) Timo V. Ovaska et al.   ORGANIC LETTERS

A concise synthesis of the bioactive meroterpenoid natural product (±)-liphagal, a potent PI3K inhibitor

(2009) Goverdhan Mehta et al.   TETRAHEDRON LETTERS

An intramolecular [4+3]-cycloaddition approach to rameswaralide inspired by biosynthesis speculation

(2009) Gerald Pattenden et al.   TETRAHEDRON LETTERS

Asymmetric [4 + 3] Cycloadditions between Benzofuranyldiazoacetates and Dienes:  Formal Synthesis of (+)-Frondosin B

(2008) Jeremy P. Olson et al.   ORGANIC LETTERS

A total synthesis of (±)-frondosins A and B

(2008) Goverdhan Mehta et al.   TETRAHEDRON LETTERS