Synthesis of (−)-Agelastatin A by [3.3] Sigmatropic Rearrangement of Allyl Cyanate

2007 ◽  
Vol 9 (16) ◽  
pp. 2989-2992 ◽  
Author(s):  
Yoshiyasu Ichikawa ◽  
Tomonori Yamaoka ◽  
Keiji Nakano ◽  
Hiyoshizo Kotsuki
Keyword(s):  
Sigmatropic Rearrangement ◽  
Agelastatin A

Total Synthesis of (−)-Agelastatin A: The Application of a Sequential Sigmatropic Rearrangement

2009 ◽  
Vol 11 (12) ◽  
pp. 2687-2690 ◽  
Author(s):  
Naoto Hama ◽  
Tomoki Matsuda ◽  
Takaaki Sato ◽  
Noritaka Chida
Keyword(s):  
Total Synthesis ◽  
Sigmatropic Rearrangement ◽  
Agelastatin A

Synthesis of (-)-Agelastatin A by [3.3] Sigmatropic Rearrangement of Allyl Cyanate.

ChemInform ◽  
2007 ◽  
Vol 38 (48) ◽  
Author(s):  
Yoshiyasu Ichikawa ◽  
Tomonori Yamaoka ◽  
Keiji Nakano ◽  
Hiyoshizo Kotsuki
Keyword(s):  
Sigmatropic Rearrangement ◽  
Agelastatin A

scholarly journals Copper-Catalyzed Synthesis of Axially Chiral Biaryls with Diaryliodonium Salts as Arylation Reagents

Molecules ◽  
2021 ◽  
Vol 26 (11) ◽  
pp. 3223
Author(s):  
Ji-Wei Zhang ◽  
Shao-Hua Xiang ◽  
Shaoyu Li ◽  
Bin Tan
Keyword(s):  
Amino Alcohols ◽  
Sigmatropic Rearrangement ◽  
Synthetic Route ◽  
Mild Conditions ◽  
Good Substrate ◽  
Diaryliodonium Salts ◽  
Axially Chiral

NOBIN and BINAM derivatives harboring biaryl frameworks are recognized as a class of important atropisomers with versatile applications. Here, we present an efficient synthetic route to access such compounds through copper-catalyzed domino arylation of N-arylhydroxylamines or N-arylhydrazines with diaryliodonium salts and [3,3]-sigmatropic rearrangement. This reaction features mild conditions, good substrate compatibility, and excellent efficiency. The practicality of this protocol was further extended by the synthesis of biaryl amino alcohols.

An Umpolung Oxa-[2,3] Sigmatropic Rearrangement Employing Arynes for the Synthesis of Functionalized Enol Ethers

2021 ◽  
Author(s):  
Rahul N. Gaykar ◽  
Malini George ◽  
Avishek Guin ◽  
Subrata Bhattacharjee ◽  
Akkattu T. Biju
Keyword(s):  
Sigmatropic Rearrangement ◽  
Enol Ethers

scholarly journals Imino‐λ 3 ‐iodane and Catalytic Amount of I 2 ‐Mediated Synthesis of N ‐Allylsulfenamides via [2,3]‐Sigmatropic Rearrangement

2020 ◽  
Vol 2020 (41) ◽  
pp. 6433-6439
Author(s):  
Cody L. Makitalo ◽  
Akira Yoshimura ◽  
Gregory T. Rohde ◽  
Irina A. Mironova ◽  
Rosa Y. Yusubova ◽  
...  
Keyword(s):  
Catalytic Amount ◽  
Sigmatropic Rearrangement

Catalyst-Free [2,3]-Sigmatropic Rearrangement Reactions of Photochemically Generated Ammonium Ylides

Synthesis ◽  
2019 ◽  
Vol 51 (23) ◽  
pp. 4348-4358 ◽  
Author(s):  
Fang Li ◽  
Feifei He ◽  
Rene M. Koenigs
Keyword(s):  
Visible Light ◽  
Sigmatropic Rearrangement ◽  
Tertiary Amines ◽  
Amino Esters ◽  
Catalyst Free ◽  
Rearrangement Reaction ◽  
Rearrangement Reactions ◽  
Free Ammonium

The rearrangement reaction of ammonium ylides furnishes valuable α,α-disubstituted amino esters. In this work, we describe the visible-light photolysis reaction of aryldiazoacetates in the presence of tertiary amines that react via a free ammonium ylide in a sigmatropic rearrangement reaction to provide amino esters in moderate to very good yields (33 examples, up to 97% yield).

ChemInform Abstract: Selenoxide Elimination and [2,3]-Sigmatropic Rearrangement

ChemInform ◽  
2010 ◽  
Vol 31 (29) ◽  
pp. no-no
Author(s):  
Yoshiaki Nishibayashi ◽  
Sakae Uemura
Keyword(s):  
Sigmatropic Rearrangement
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