The isolation of flueggenines A and B by Yue and co-workers in 2006 has triggered a burst of isolation reports of dimeric and oligomeric securinega alkaloid natural products. The compelling molecular structures of these compounds with various modes of connection between monomeric securinega units have posed intriguing challenges to the synthetic organic community. Herein, we have categorized high-order securinega alkaloids based on their biosynthetic mode of dimerization or oligomerization. We then have compiled all reported syntheses of dimeric securinega alkaloids based on our classification. 1 Introduction 2 Categorization of High-Order Securinega Alkaloid Natural Products 3 Syntheses of Type I Dimeric Securinega Alkaloids 4 Syntheses of...
Chapter 1 presents a flexible synthesis of (-)-securinine in 18 steps and 16% overall isolated yield...
From \(Securinega\) \(suffruticosa\) (Pall.) Rehd (Fam. Euphorbiaceae), grown in Rongo, North Bengal...
Part one of this dissertation describes the synthesis of novel polycyclic natural product-like compo...
We describe different modes of dimerization of various α′,γ-dioxyenone derivatives with potential ap...
The Securinega alkaloids feature a compact tetracyclic structural framework and can be divided into ...
The first total synthesis of dimeric securinega alkaloid (-)-flueggenine C is completed via an accel...
Flueggeacosines A–C (1–3), three dimeric securinine-type alkaloid analogues with unprecedented skele...
The first total synthesis of dimeric securinega alkaloid (−)-flueggenine C is completed via an accel...
Abstract: The Securinega alkaloids are a family of approximately 20 tetracyclic compounds isolated f...
The synthesis of the Securinega alkaloid secu’amamine E (ent–virosine A) has been accomplished for t...
We describe different modes of dimerization of various α′,γ-dioxyenone derivatives with potential ap...
ABSTRACT: Although dimeric natural products can often be synthesized in the laboratory by directly m...
The synthesis of the <i>Securinega</i> alkaloid secu’amamine E (<i>ent</i>-virosine A) has been acco...
textHerein is described our synthetic studies towards the synthesis of secu'amamine A, a member of t...
Phytochemical investigation on the fruits of Flueggea suffruticosa resulted in the isolation of thre...
Chapter 1 presents a flexible synthesis of (-)-securinine in 18 steps and 16% overall isolated yield...
From \(Securinega\) \(suffruticosa\) (Pall.) Rehd (Fam. Euphorbiaceae), grown in Rongo, North Bengal...
Part one of this dissertation describes the synthesis of novel polycyclic natural product-like compo...
We describe different modes of dimerization of various α′,γ-dioxyenone derivatives with potential ap...
The Securinega alkaloids feature a compact tetracyclic structural framework and can be divided into ...
The first total synthesis of dimeric securinega alkaloid (-)-flueggenine C is completed via an accel...
Flueggeacosines A–C (1–3), three dimeric securinine-type alkaloid analogues with unprecedented skele...
The first total synthesis of dimeric securinega alkaloid (−)-flueggenine C is completed via an accel...
Abstract: The Securinega alkaloids are a family of approximately 20 tetracyclic compounds isolated f...
The synthesis of the Securinega alkaloid secu’amamine E (ent–virosine A) has been accomplished for t...
We describe different modes of dimerization of various α′,γ-dioxyenone derivatives with potential ap...
ABSTRACT: Although dimeric natural products can often be synthesized in the laboratory by directly m...
The synthesis of the <i>Securinega</i> alkaloid secu’amamine E (<i>ent</i>-virosine A) has been acco...
textHerein is described our synthetic studies towards the synthesis of secu'amamine A, a member of t...
Phytochemical investigation on the fruits of Flueggea suffruticosa resulted in the isolation of thre...
Chapter 1 presents a flexible synthesis of (-)-securinine in 18 steps and 16% overall isolated yield...
From \(Securinega\) \(suffruticosa\) (Pall.) Rehd (Fam. Euphorbiaceae), grown in Rongo, North Bengal...
Part one of this dissertation describes the synthesis of novel polycyclic natural product-like compo...