The Experts below are selected from a list of 158823 Experts worldwide ranked by ideXlab platform
Eietsu Hasegawa - One of the best experts on this subject based on the ideXlab platform.
-
a Formal Method for the de n n dialkylation of sommelet hauser rearrangement products
ChemInform, 2012Co-Authors: Eiji Tayama, Ryota Sato, Keisuke Takedachi, Hajime Iwamoto, Eietsu HasegawaAbstract:The present Method furnishes valuable intermediates for preparation of α-aryl-α-amino or α-aryl-β-amino carboxylic acid derivatives.
-
a Formal Method for the de n n dialkylation of sommelet hauser rearrangement products
Tetrahedron, 2012Co-Authors: Eiji Tayama, Ryota Sato, Keisuke Takedachi, Hajime Iwamoto, Eietsu HasegawaAbstract:Abstract Selective amine de-alkylation enables the conversion of Sommelet–Hauser rearrangement products into 2-aryl-2-bromoacetic acid derivatives. These compounds are valuable synthetic intermediates in the synthesis of α-aryl-α-amino or α-aryl-β-amino acid derivatives. The Method presented herein is a Formal de-N,N-dialkylation of Sommelet–Hauser rearrangement products.
Eiji Tayama - One of the best experts on this subject based on the ideXlab platform.
-
a Formal Method for the de n n dialkylation of sommelet hauser rearrangement products
ChemInform, 2012Co-Authors: Eiji Tayama, Ryota Sato, Keisuke Takedachi, Hajime Iwamoto, Eietsu HasegawaAbstract:The present Method furnishes valuable intermediates for preparation of α-aryl-α-amino or α-aryl-β-amino carboxylic acid derivatives.
-
a Formal Method for the de n n dialkylation of sommelet hauser rearrangement products
Tetrahedron, 2012Co-Authors: Eiji Tayama, Ryota Sato, Keisuke Takedachi, Hajime Iwamoto, Eietsu HasegawaAbstract:Abstract Selective amine de-alkylation enables the conversion of Sommelet–Hauser rearrangement products into 2-aryl-2-bromoacetic acid derivatives. These compounds are valuable synthetic intermediates in the synthesis of α-aryl-α-amino or α-aryl-β-amino acid derivatives. The Method presented herein is a Formal de-N,N-dialkylation of Sommelet–Hauser rearrangement products.
Hajime Iwamoto - One of the best experts on this subject based on the ideXlab platform.
-
a Formal Method for the de n n dialkylation of sommelet hauser rearrangement products
ChemInform, 2012Co-Authors: Eiji Tayama, Ryota Sato, Keisuke Takedachi, Hajime Iwamoto, Eietsu HasegawaAbstract:The present Method furnishes valuable intermediates for preparation of α-aryl-α-amino or α-aryl-β-amino carboxylic acid derivatives.
-
a Formal Method for the de n n dialkylation of sommelet hauser rearrangement products
Tetrahedron, 2012Co-Authors: Eiji Tayama, Ryota Sato, Keisuke Takedachi, Hajime Iwamoto, Eietsu HasegawaAbstract:Abstract Selective amine de-alkylation enables the conversion of Sommelet–Hauser rearrangement products into 2-aryl-2-bromoacetic acid derivatives. These compounds are valuable synthetic intermediates in the synthesis of α-aryl-α-amino or α-aryl-β-amino acid derivatives. The Method presented herein is a Formal de-N,N-dialkylation of Sommelet–Hauser rearrangement products.
Keisuke Takedachi - One of the best experts on this subject based on the ideXlab platform.
-
a Formal Method for the de n n dialkylation of sommelet hauser rearrangement products
ChemInform, 2012Co-Authors: Eiji Tayama, Ryota Sato, Keisuke Takedachi, Hajime Iwamoto, Eietsu HasegawaAbstract:The present Method furnishes valuable intermediates for preparation of α-aryl-α-amino or α-aryl-β-amino carboxylic acid derivatives.
-
a Formal Method for the de n n dialkylation of sommelet hauser rearrangement products
Tetrahedron, 2012Co-Authors: Eiji Tayama, Ryota Sato, Keisuke Takedachi, Hajime Iwamoto, Eietsu HasegawaAbstract:Abstract Selective amine de-alkylation enables the conversion of Sommelet–Hauser rearrangement products into 2-aryl-2-bromoacetic acid derivatives. These compounds are valuable synthetic intermediates in the synthesis of α-aryl-α-amino or α-aryl-β-amino acid derivatives. The Method presented herein is a Formal de-N,N-dialkylation of Sommelet–Hauser rearrangement products.
Ryota Sato - One of the best experts on this subject based on the ideXlab platform.
-
a Formal Method for the de n n dialkylation of sommelet hauser rearrangement products
ChemInform, 2012Co-Authors: Eiji Tayama, Ryota Sato, Keisuke Takedachi, Hajime Iwamoto, Eietsu HasegawaAbstract:The present Method furnishes valuable intermediates for preparation of α-aryl-α-amino or α-aryl-β-amino carboxylic acid derivatives.
-
a Formal Method for the de n n dialkylation of sommelet hauser rearrangement products
Tetrahedron, 2012Co-Authors: Eiji Tayama, Ryota Sato, Keisuke Takedachi, Hajime Iwamoto, Eietsu HasegawaAbstract:Abstract Selective amine de-alkylation enables the conversion of Sommelet–Hauser rearrangement products into 2-aryl-2-bromoacetic acid derivatives. These compounds are valuable synthetic intermediates in the synthesis of α-aryl-α-amino or α-aryl-β-amino acid derivatives. The Method presented herein is a Formal de-N,N-dialkylation of Sommelet–Hauser rearrangement products.
