Enantioselective Iridium‐Catalyzed Allylation of Acetylenic Ketones via 2‐Propanol‐Mediated Reductive Coupling of Allyl Acetate: C14‐C23 of Pladienolide D-Reference-Cited by-同舟云学术

Enantioselective Iridium‐Catalyzed Allylation of Acetylenic Ketones via 2‐Propanol‐Mediated Reductive Coupling of Allyl Acetate: C14‐C23 of Pladienolide D

Published:2019-11-07 Issue:52 Volume:58 Page:18803-18807
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angewandte Chemie Intl Edit

Author:

Brito Gilmar A.¹,Jung Woo‐Ok¹,Yoo Minjin¹,Krische Michael J.¹^ORCID

Affiliation:

1. University of Texas at Austin Department of Chemistry 105 E 24th St. (A5300) Austin TX 78712-1167 USA

Funder

Welch Foundation

National Institute of General Medical Sciences

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201908939

Reference80 articles.

1. For selected reviews on catalytic enantioselective ketone addition see:

2. Chiral Tertiary Alcohols Made By Catalytic Enantioselective Addition of Unreactive Zinc Reagents to Poorly Electrophilic Ketones?

3. Chirale tertiäre Alkohole durch katalytische enantioselektive Addition von unreaktiven Zinkreagentien an schwach elektrophile Ketone?

4. Asymmetric Addition to Ketones: Enantioselective Formation of Tertiary Alcohols

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