Transformation of β-Nitro Alcohols to the Corresponding Nitro Imines with Lithium Hexamethyldisilazide (LHMDS) via Sequential Retro Nitro-Aldol–Nitro-Mannich Reaction-Reference-Cited by-同舟云学术

Transformation of β-Nitro Alcohols to the Corresponding Nitro Imines with Lithium Hexamethyldisilazide (LHMDS) via Sequential Retro Nitro-Aldol–Nitro-Mannich Reaction

Published:2009-01-29 Issue:5 Volume:39 Page:868-874
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Tanaka Seiji¹,Kochi Kazuhiro¹,Ito Hiroyuki¹,Mukawa Jun¹,Kishikawa Keiki¹,Yamamoto Makoto¹,Kohmoto Shigeo¹

Affiliation:

1. a Department of Applied Chemistry and Biotechnology, Faculty of Engineering , Chiba University , Chiba, Japan

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397910802432188

Reference9 articles.

1. Double nitro-Mannich reaction utilizing in situ generated N-trimethylsilylaldimines: novel four-component one-pot synthesis of nitroimines

2. syn-Selective Catalytic Asymmetric Nitro-Mannich Reactions Using a Heterobimetallic Cu−Sm−Schiff Base Complex

3. Mixed La−Li Heterobimetallic Complexes for Tertiary Nitroaldol Resolution

4. Facile synthesis of 2-nitroalkanols by tetramethylguanidine (TMG)-catalyzed addition of primary nitroalkanes to aldehydes and alicyclic ketones

5. Highly enantioselective nitroaldol reaction catalyzed by new chiral copper complexes

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