Stereoselective synthesis of spirocyclic oxindoles based on a one-pot Ullmann coupling/Claisen rearrangement and its application to the synthesis of a hexahydropyrrolo[2,3-b]indole alkaloid-Reference-Cited by-同舟云学术

Stereoselective synthesis of spirocyclic oxindoles based on a one-pot Ullmann coupling/Claisen rearrangement and its application to the synthesis of a hexahydropyrrolo[2,3-b]indole alkaloid

Published:2013-11 Issue:45 Volume:69 Page:9481-9493
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Miyamoto Hiroshi,Hirano Tomohiro,Okawa Yoichiro,Nakazaki Atsuo,Kobayashi Susumu

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference111 articles.

1. Strategies for the enantioselective synthesis of spirooxindoles

2. Recent advances in organocatalytic methods for the synthesis of disubstituted 2- and 3-indolinones

3. Catalytic Asymmetric Synthesis of Oxindoles Bearing a Tetrasubstituted Stereocenter at the C-3 Position

4. Asymmetric Syntheses of Oxindole and Indole Spirocyclic Alkaloid Natural Products

5. Construction of Spiro[pyrrolidine‐3,3′‐oxindoles] − Recent Applications to the Synthesis of Oxindole Alkaloids

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