Reduction of an Enaminone: Synthesis of the Diamino Alcohol Core of Ritonavir-Reference-Cited by-同舟云学术

Reduction of an Enaminone: Synthesis of the Diamino Alcohol Core of Ritonavir

Published:1999-01-08 Issue:2 Volume:3 Page:94-100
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Haight Anthony R.¹,Stuk Timothy L.¹,Allen Michael S.¹,Bhagavatula Lakshmi¹,Fitzgerald Michael¹,Hannick Steven M.¹,Kerdesky Francis A. J.¹,Menzia Jerome A.¹,Parekh Shyamal I.¹,Robbins Timothy A.¹,Scarpetti David¹,Tien Jien-Heh J.¹

Affiliation:

1. Chemical Process Research, D54P, and Process Research, D45L, Abbott Laboratories, 1401 Sheridan Road, North Chicago, Illinois 60064

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/op9802071

Reference18 articles.

1. Enaminones

2. Reduction of enaminones in the preparation of 3-aminocyclohexanols; a novel preparation of tetronic acid

3. Ketenes. VIII. Some Reactions of 1-(Dimethylamino)-4-methyl-1-penten-3-one1

4. Enantioselective synthesis of indolizine derivatives by rearrangement-cyclization of isoxazoline-5-spirocyclopropanes

5. Acylation of Enamines. III. Reduction of Protonated Enaminones with Sodium Borohydride. Synthesis of alpha,beta-Unsaturated Ketones.

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