Unprecedented One-Pot, Domino Tertiary Alcohol Protection–Michael Type Addition of Halides to Morita–Baylis–Hillman Adduct of Isatin with RCOX/K2CO3: Diastereoselective Synthesis of Oxindole Appended β-Halo Esters-Reference-Cited by-同舟云学术

Unprecedented One-Pot, Domino Tertiary Alcohol Protection–Michael Type Addition of Halides to Morita–Baylis–Hillman Adduct of Isatin with RCOX/K2CO3: Diastereoselective Synthesis of Oxindole Appended β-Halo Esters

Published:2013-03-05 Issue:6 Volume:15 Page:1186-1189
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Solaiselvi Rajarethinam¹,Shanmugam Ponnusamy¹,Mandal Asit Baran¹

Affiliation:

1. Council of Scientific and Industrial Research (CSIR)-Central Leather Research Institute (CLRI), Organic Chemistry Division, Chemical Laboratory, Adyar, Chennai-600020, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol303554c

Reference51 articles.

1. Pyrrolidinyl-Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents

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

3. Stereoselective Synthesis of Spirocyclic Oxindoles via Prins Cyclizations

4. Domino reactions in the synthesis of heterocyclic natural products and analogs

5. Stereocontrolled synthesis of spirocyclics

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