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Asymmetric Total Synthesis of Erythromycin. 1. Synthesis of an Erythronolide A Seco Acid Derivative via Asymmetric Induction

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TLDR
The specific incorporation per C4 unit, 3.3%, calculated from 13C NMR data (Table I), is identical with that obtained from I4C radioactivity measurements.
Abstract
3210-3213 The specific incorporation per C4 unit, 3.3%, calculated from 13C NMR data (Table I), is identical with that obtained from I4C radioactivity measurements. The signals due to the I3C-enriched carbon atoms in the proton decoupled I3C NMR spectrum of labeled retronecine appear as multiplets (Table

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Journal ArticleDOI

C-H bond functionalization: emerging synthetic tools for natural products and pharmaceuticals

TL;DR: This Review provides an overview of C-H bond functionalization strategies for the rapid synthesis of biologically active compounds such as natural products and pharmaceutical targets.
Journal ArticleDOI

Asymmetric catalysis by chiral hydrogen-bond donors.

TL;DR: This review documents the structural and mechanistic features that contribute to high enantioselectivity in hydrogen-bond-mediated catalytic processes in small-molecule, synthetic catalyst systems.
Journal ArticleDOI

Double Asymmetric Synthesis and a New Strategy for Stereochemical Control in Organic Synthesis

TL;DR: In this article, it is shown that double asymmetric induction can be analyzed in terms of the single asymmetric reactions of each of the two chiral reactants, and a new strategy based on this rule for the predictable creation of new chiral centers is discussed and the use of this strategy for the synthesis of sugars and macrolides is presented.
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