Synthesis of 1,2-Diamino Acid Derivatives Utilizing Diastereoselective Tandem N-Alkylation/Homo- and Cross-Addition Reaction of $$\alpha $$ α -Aldimino Thioesters-Reference-Cited by-同舟云学术

Synthesis of 1,2-Diamino Acid Derivatives Utilizing Diastereoselective Tandem N-Alkylation/Homo- and Cross-Addition Reaction of $$\alpha $$ α -Aldimino Thioesters

Published:2017-05-30 Issue:10 Volume:42 Page:4249-4261
ISSN:2193-567X
Container-title:Arabian Journal for Science and Engineering
language:en
Short-container-title:Arab J Sci Eng

Author:

Mizota Isao,Nakajima Yuji,Higashino Asako,Shimizu Makoto

Funder

Japan Society for the Promotion of Science (JP)

MEXT

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://link.springer.com/article/10.1007/s13369-017-2615-y/fulltext.html

Reference64 articles.

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2. De Parrodi, C.A.; Juaristi, E.: Chiral 1,2-amino alcohols and 1,2-diamines derived from cyclohexene oxide: recent applications in asymmetric synthesis. Synlett 2699–2715 (2006). doi: 10.1055/s-2006-950259

3. Kizirian, J.C.: Chiral tertiary diamines in asymmetric synthesis. Chem. Rev. 108, 140–205 (2008)

4. Nakayama, K.; Maruoka, K.: Complete Switch of product selectivity in asymmetric direct aldol reaction with two different chiral organocatalysts from a common chiral source. J. Am. Chem. Soc. 130, 17666–17667 (2008)

5. Cimarelli, C.; Fratoni, D.; Palmieri, G.: Complete Switch of product selectivity in asymmetric direct aldol reaction with two different chiral organocatalysts from a common chiral source. Tetrahedron Asymmetry 20, 2234–2239 (2009)

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