Efficient Synthesis of (+)-MK7607 and its C-1 Epimer via the Stereoselective Transposition of a Tertiary Allylic Alcohol-Reference-Cited by-同舟云学术

Efficient Synthesis of (+)-MK7607 and its C-1 Epimer via the Stereoselective Transposition of a Tertiary Allylic Alcohol

Published:2009-05-21 Issue:12 Volume:11 Page:2583-2586
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Lim Chaemin¹,Baek Dong Jae¹,Kim Deukjoon¹,Youn So Won¹,Kim Sanghee¹

Affiliation:

1. College of Pharmacy, Seoul National University, Seoul 151-742, Korea, and Department of Chemistry, Pukyong National University, Busan 608-737, Korea

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol9008987

Reference39 articles.

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2. Carbohydrate Mimetics: A New Strategy for Tackling the Problem of Carbohydrate-Mediated Biological Recognition

3. Synthesis and Conformational and Biological Aspects of Carbasugars

4. A norbornyl route to cyclohexitols: stereoselective synthesis of conduritol-E, allo-inositol, MK 7607 and gabosines

5. Syntheses of (-)-MK7607 and Other Carbasugars from (-)-Shikimic Acid

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