The ever-expanding role of asymmetric covalent organocatalysis in scalable, natural product synthesis-Reference-Cited by-同舟云学术

The ever-expanding role of asymmetric covalent organocatalysis in scalable, natural product synthesis

Published:2014 Issue:10 Volume:31 Page:1318-1327
ISSN:0265-0568
Container-title:Nat. Prod. Rep.
language:en
Short-container-title:Nat. Prod. Rep.

Author:

Abbasov Mikail E.¹²³,Romo Daniel¹²³

Affiliation:

1. Department of Chemistry

2. Texas A&M University

3. College Station, United States

Abstract

This Highlight provides a brief overview of covalent, asymmetric modes of organocatalysis and applications of scalable versions of these methods applied to the total synthesis of natural products.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/NP/C4NP00025K

Reference155 articles.

1. Ueber die Bildung des Oxamids aus Cyan

2. Über die Beschleunigung von Aldol‐Kondensationen durch Amino‐säuren

3. Über Aldehyd‐Kondensationen mit sekundären Aminen (Knoevenagel‐Reaktion)

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