N-Carbamate α-aminoalkyl-p-tolylsulfones—convenient substrates in the nitro-Mannich synthesis of secondary N-carbamate protected syn-2-amino-1-nitroalkanephosphonates-Reference-Cited by-同舟云学术

N-Carbamate α-aminoalkyl-p-tolylsulfones—convenient substrates in the nitro-Mannich synthesis of secondary N-carbamate protected syn-2-amino-1-nitroalkanephosphonates

Published:2010-12 Issue:52 Volume:66 Page:9840-9848
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Błaszczyk Roman,Gajda Anna,Zawadzki Stefan,Czubacka Ewelina,Gajda Tadeusz

Funder

Ministry of Education and Science

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference115 articles.

1. For recent reviews, see:

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3. Asymmetric Catalytic Aza-Henry Reactions Leading to 1,2-Diamines and 1,2-Diaminocarboxylic Acids

4. Recent Advances in Catalytic Asymmetric Addition to Imines and Related C=N Systems

5. Recent Advances in Stereoselective Syntheses Using N-Acylimines

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