NMR Spectroscopic Investigations of Mixed Aggregates Underlying Highly Enantioselective 1,2-Additions of Lithium Cyclopropylacetylide to Quinazolinones-Reference-Cited by-同舟云学术

NMR Spectroscopic Investigations of Mixed Aggregates Underlying Highly Enantioselective 1,2-Additions of Lithium Cyclopropylacetylide to Quinazolinones

Published:2001-08-22 Issue:37 Volume:123 Page:9135-9143
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Parsons, Rodney L.¹,Fortunak Joseph M.¹,Dorow Roberta L.¹,Harris Gregory D.¹,Kauffman Goss S.¹,Nugent William A.¹,Winemiller Mark D.¹,Briggs Timothy F.¹,Xiang Bosong¹,Collum David B.¹

Affiliation:

1. Contribution from DuPont Pharmaceuticals, Chemical Process Research and Development, Chambersworks, PRF-112, Deepwater, New Jersey 08023, and Department of Chemistry and Chemical Biology, Baker Laboratory, Cornell University, Ithaca, New York 14853-1301

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0105616

Reference35 articles.

1. L-743, 726 (DMP-266): a novel, highly potent nonnucleoside inhibitor of the human immunodeficiency virus type 1 reverse transcriptase

2. Practical Asymmetric Synthesis of Efavirenz (DMP 266), an HIV-1 Reverse Transcriptase Inhibitor

3. A Novel, Highly Enantioselective Ketone Alkynylation Reaction Mediated by Chiral Zinc Aminoalkoxides

4. Synthesis of a Series of 4-(Arylethynyl)-6-chloro-4-cyclopropyl-3,4-dihydroquinazolin-2(1H)-ones as Novel Non-nucleoside HIV-1 Reverse Transcriptase Inhibitors

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