1‐Hydroxymethyl‐7‐oxabicyclo[2.2.1]hept‐2‐ene skeleton in enantiopure form through enzymatic kinetic resolution-Reference-Cited by-同舟云学术

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1‐Hydroxymethyl‐7‐oxabicyclo[2.2.1]hept‐2‐ene skeleton in enantiopure form through enzymatic kinetic resolution

Published:2019-02-12 Issue:4 Volume:31 Page:336-347
ISSN:0899-0042
Container-title:Chirality
language:en
Short-container-title:Chirality

Author:

Reddy U. Chandrasekhar¹,Manheri Muraleedharan K.¹^ORCID

Affiliation:

1. Department of ChemistryIndian Institute of Technology Madras Chennai India

Funder

Department of Science and Technology

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chir.23060

Reference81 articles.

1. Derivatives of 7-oxabicyclo[2.2.1]heptane in nature and as useful synthetic intermediates

2. Rapid formation of complexity in the total synthesis of natural products enabled by oxabicyclo[2.2.1]heptene building blocks

3. Total synthesis of (+)-pinitol

4. Toward the total synthesis of tetrodotoxin: stereoselective construction of the 7-oxanorbornane intermediate

5. Intramolecular Alkylative Arylation of Oxabicylic Alkene: A Potential Diene Approach for the Synthesis of Estrone and Analogous Steroid Structures

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