Mechanism of Acylation of Lithium Phenylacetylide with a Weinreb Amide-Reference-Cited by-同舟云学术

Mechanism of Acylation of Lithium Phenylacetylide with a Weinreb Amide

Published:2006-08-02 Issue:18 Volume:71 Page:7117-7119
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Qu Bo¹,Collum David B.¹

Affiliation:

1. Contribution from the Department of Chemistry and Chemical Biology, Baker Laboratory, Cornell University, Ithaca, New York 14853-1301 %dbc6@cornell.edu

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo061223w

Reference19 articles.

1. Tetrahedral intermediates in reactions of carboxylic acid derivatives with nucleophiles

2. N-methoxy-n-methylamides as effective acylating agents

3. The Growing Synthetic Utility of Weinreb′s Amide

4. One-Pot Multistep Bohlmann−Rahtz Heteroannulation Reactions: Synthesis of Dimethyl Sulfomycinamate

5. The total synthesis of the polyether antibiotic X-206

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