Total synthesis of (+)-decursivine.Org Lett. 2011 Oct 07; 13(19):5302-5.OL
Abstract
The first asymmetric synthesis of natural indole alkaloid (+)-decursivine was accomplished. The key step involves the PIFA-mediated intramolecular [3 + 2] cycloaddition of 5-hydroxytryptophan with a substituted cinnamamide in a highly diastereoselective manner.
Links
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
21916429
Citation
Sun, Deqian, et al. "Total Synthesis of (+)-decursivine." Organic Letters, vol. 13, no. 19, 2011, pp. 5302-5.
Sun D, Zhao Q, Li C. Total synthesis of (+)-decursivine. Org Lett. 2011;13(19):5302-5.
Sun, D., Zhao, Q., & Li, C. (2011). Total synthesis of (+)-decursivine. Organic Letters, 13(19), 5302-5. https://doi.org/10.1021/ol2021669
Sun D, Zhao Q, Li C. Total Synthesis of (+)-decursivine. Org Lett. 2011 Oct 7;13(19):5302-5. PubMed PMID: 21916429.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Total synthesis of (+)-decursivine.
AU - Sun,Deqian,
AU - Zhao,Qiwu,
AU - Li,Chaozhong,
Y1 - 2011/09/14/
PY - 2011/9/16/entrez
PY - 2011/9/16/pubmed
PY - 2012/1/18/medline
SP - 5302
EP - 5
JF - Organic letters
JO - Org Lett
VL - 13
IS - 19
N2 - The first asymmetric synthesis of natural indole alkaloid (+)-decursivine was accomplished. The key step involves the PIFA-mediated intramolecular [3 + 2] cycloaddition of 5-hydroxytryptophan with a substituted cinnamamide in a highly diastereoselective manner.
SN - 1523-7052
UR - https://www.unboundmedicine.com/medline/citation/21916429/Total_synthesis_of__+__decursivine_
L2 - https://doi.org/10.1021/ol2021669
DB - PRIME
DP - Unbound Medicine
ER -