1,2-Dimethoxy-4,5-dimethylene: a new protecting group for acyclic amino acid derivatives prepared by Stevens rearrangement-Reference-Cited by-同舟云学术

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1,2-Dimethoxy-4,5-dimethylene: a new protecting group for acyclic amino acid derivatives prepared by Stevens rearrangement

Published:2012-03 Issue:11 Volume:53 Page:1373-1375
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Tayama Eiji,Takedachi Keisuke,Iwamoto Hajime,Hasegawa Eietsu

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

1. Sigmatropic rearrangements of ‘onium’ ylids

2. Nitrogen, Oxygen, and Sulfur Ylide Chemistry,2002

3. Green’s Protective Groups in Organic Synthesis;Wuts,2006

4. Asymmetric [2,3]-Rearrangement of Glycine-Derived Allyl Ammonium Ylids

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1. Base-induced Sommelet–Hauser rearrangement of N-(pyridinylmethyl) tetraalkylammonium salts;Tetrahedron;2022-04

2. 40.1.1.4.3 Synthesis of Amines by Rearrangement (Update 2020);Knowledge Updates 2020/2;2020

3. Selective Ring-Opening of N-Alkyl Pyrrolidines with Chloroformates to 4-Chlorobutyl Carbamates;The Journal of Organic Chemistry;2017-06-15

4. Recent Advances in the Base-Induced Sommelet-Hauser Rearrangement of Amino Acid Derived Ammonium Ylides;The Chemical Record;2015-07-14

5. Protection for the Amino Group;Greene's Protective Groups in Organic Synthesis;2014-08-11

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