Diastereoselective Synthesis of Terminal Bromo-Substituted Propargylamines via Generation of Lithium Bromoacetylide and Addition to Chiral N-tert-Butanesulfinyl Aldimines-Reference-Cited by-同舟云学术

Diastereoselective Synthesis of Terminal Bromo-Substituted Propargylamines via Generation of Lithium Bromoacetylide and Addition to Chiral N-tert-Butanesulfinyl Aldimines

Published:2021-01-15 Issue:3 Volume:86 Page:2667-2681
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Jolly Charles S.¹,Kochanowski Emma¹,Dodd Cayden J.¹,Post Savannah J.¹,Hill Harrison M.¹,Turlington Mark¹^ORCID

Affiliation:

1. Department of Chemistry & Biochemistry, Berry College, Mount Berry, Georgia 30149, United States

Funder

Berry College

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.0c02697

Reference22 articles.

1. Universal Peptidomimetics

2. One-Pot, Three-Aryne Cascade Strategy for Naphthalene Formation from 1,3-Diynes and 1,2-Benzdiyne Equivalents

3. Optimization of LpxC Inhibitor Lead Compounds Focusing on Efficacy and Formulation for High Dose Intravenous Administration

4. The Bromopentadienyl Acrylate Approach to Himbacine

5. Diastereoselective Syntheses of Functionalized Five-Membered Carbocycles and Heterocycles by a SmI2-Promoted Intramolecular Coupling of Bromoalkynes and α,β-Unsaturated Esters

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