Total Synthesis and Stereochemical Revision of Acortatarins A and B
Author:
Affiliation:
1. Organic Chemistry Division-II and Center for Nuclear Magnetic Resonance, CSIR-Indian Institute of Chemical Technology, Hyderabad-500 607, India
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol202121k
Reference29 articles.
1. Acortatarins A and B, Two Novel Antioxidative Spiroalkaloids with a Naturally Unusual Morpholine Motif from Acorus tatarinowii
2. Acortatarins A and B, Two Novel Antioxidative Spiroalkaloids with a Naturally Unusual Morpholine Motif from Acorus tatarinowii
3. A Facile Route to Tripyrrane from 2,5-Bis(hydroxymethyl)pyrrole and the Improved Synthesis of Porphine by the "3 + 1" Approach
4. The first isolation of unsubstituted porphyrinogen and unsubstituted 21-oxaporphyrinogen by the ‘3+1’ approach from 2,5-bis(hydroxymethyl)pyrrole and tripyrrane derivatives
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