Catalytic asymmetric total synthesis of tangutorine.Org Lett. 2010 Feb 19; 12(4):872-5.OL
Abstract
The first enantioselective total synthesis of tangutorine has been achieved, wherein a Pd-catalyzed asymmetric allylic amination using a chiral diaminophosphine oxide (DIAPHOX) preligand was the key step.
Links
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
20092264
Citation
Nemoto, Tetsuhiro, et al. "Catalytic Asymmetric Total Synthesis of Tangutorine." Organic Letters, vol. 12, no. 4, 2010, pp. 872-5.
Nemoto T, Yamamoto E, Franzén R, et al. Catalytic asymmetric total synthesis of tangutorine. Org Lett. 2010;12(4):872-5.
Nemoto, T., Yamamoto, E., Franzén, R., Fukuyama, T., Wu, R., Fukamachi, T., Kobayashi, H., & Hamada, Y. (2010). Catalytic asymmetric total synthesis of tangutorine. Organic Letters, 12(4), 872-5. https://doi.org/10.1021/ol902929a
Nemoto T, et al. Catalytic Asymmetric Total Synthesis of Tangutorine. Org Lett. 2010 Feb 19;12(4):872-5. PubMed PMID: 20092264.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Catalytic asymmetric total synthesis of tangutorine.
AU - Nemoto,Tetsuhiro,
AU - Yamamoto,Eri,
AU - Franzén,Robert,
AU - Fukuyama,Takashi,
AU - Wu,Riliga,
AU - Fukamachi,Toshihiko,
AU - Kobayashi,Hiroshi,
AU - Hamada,Yasumasa,
PY - 2010/1/23/entrez
PY - 2010/1/23/pubmed
PY - 2010/3/12/medline
SP - 872
EP - 5
JF - Organic letters
JO - Org Lett
VL - 12
IS - 4
N2 - The first enantioselective total synthesis of tangutorine has been achieved, wherein a Pd-catalyzed asymmetric allylic amination using a chiral diaminophosphine oxide (DIAPHOX) preligand was the key step.
SN - 1523-7052
UR - https://www.unboundmedicine.com/medline/citation/20092264/Catalytic_asymmetric_total_synthesis_of_tangutorine_
DB - PRIME
DP - Unbound Medicine
ER -