Studies on the alkaloids of the calycanthaceae and their syntheses. (Q38425885)

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scientific article published on 15 April 2015

Language	Label	Description	Also known as
English	Studies on the alkaloids of the calycanthaceae and their syntheses.	scientific article published on 15 April 2015

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25884552%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

2 references

Europe PubMed Central

6 July 2022

Studies on the alkaloids of the calycanthaceae and their syntheses (English)

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25884552%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

1 reference

13 September 2020

1 reference

PubMed publication ID

2

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25884552%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

author name string

Jin-Biao Xu

1

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25884552%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

language of work or name

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publication date

15 April 2015

3 references

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25884552%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

13 September 2020

6 July 2022

2 references

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25884552%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

13 September 2020

20

1 reference

Europe PubMed Central

PMC publication ID

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5 March 2020

4

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25884552%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

6715-6738

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25884552%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

copyright license

Creative Commons Attribution

2 references

13 September 2020

6 July 2022

copyright status

0 references

Molecular phylogeny and intra- and intercontinental biogeography of Calycanthaceae

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES20046715

21 January 2018

Chimonanthus nitens var. salicifolius Aqueous Extract Protects against 5-Fluorouracil Induced Gastrointestinal Mucositis in a Mouse Model

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES20046715

21 January 2018

Two new coumarin glycosides from Chimonanthus nitens

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES20046715

21 January 2018

New 29-nor-cycloartanes with a 3,4-seco- and a novel 2,3-seco-structure from the leaves of Sinocalycanthus chinensis

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES20046715

21 January 2018

Essential leaf oils in Calycanthus Floridus

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES20046715

21 January 2018

Enantioselective Construction of Vicinal Stereogenic Quaternary Centers by Dialkylation: Practical Total Syntheses of (+)- and meso-Chimonanthine.

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES20046715

21 January 2018

Idiospermuline, a Trimeric Pyrrolidinoindoline Alkaloid from the Seed of Idiospermum australiense

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES20046715

21 January 2018

Antifungal activity of alkaloids from the seeds of Chimonanthus praecox.

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES20046715

21 January 2018

Dimeric pyrrolidinoindoline-type alkaloids with melanogenesis inhibitory activity in flower buds of Chimonanthus praecox.

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES20046715

21 January 2018

Convulsant actions of calycanthine

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES20046715

21 January 2018

Antinociceptive profile of hodgkinsine

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES20046715

21 January 2018

Synthesis and antinociceptive activity of chimonanthines and pyrrolidinoindoline-type alkaloids

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES20046715

21 January 2018

Application of diazene-directed fragment assembly to the total synthesis and stereochemical assignment of (+)-desmethyl-meso-chimonanthine and related heterodimeric alkaloids

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES20046715

21 January 2018

Directed heterodimerization: stereocontrolled assembly via solvent-caged unsymmetrical diazene fragmentation

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES20046715

21 January 2018

A versatile synthesis of unsymmetrical 3,3'-bioxindoles: stereoselective Mukaiyama aldol reactions of 2-siloxyindoles with isatins.

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES20046715

21 January 2018

Enantioselective total syntheses of the cyclotryptamine alkaloids hodgkinsine and hodgkinsine B.

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES20046715

21 January 2018

The asymmetric intramolecular Heck reaction in natural product total synthesis

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES20046715

21 January 2018

Simple indole alkaloids and those with a non-rearranged monoterpenoid unit

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES20046715

21 January 2018

Concise synthesis of the (±)-Nb-desmethyl-meso-chimonanthine

1 reference

https://pubmed.ncbi.nlm.nih.gov/25884552

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid determination of volatile compounds emitted from Chimonanthus praecox flowers by HS-SPME-GC-MS.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25884552

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Core-structure-oriented asymmetric organocatalytic substitution of 3-hydroxyoxindoles: application in the enantioselective total synthesis of (+)-folicanthine

1 reference

https://pubmed.ncbi.nlm.nih.gov/25884552

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catalytic asymmetric total synthesis of chimonanthine, folicanthine, and calycanthine through double Michael reaction of bisoxindole

1 reference

https://pubmed.ncbi.nlm.nih.gov/25884552

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biogenetic-type synthesis of the Calycanthaceous alkaloids

1 reference

https://pubmed.ncbi.nlm.nih.gov/25884552

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enantioselective total synthesis of the cyclotryptamine alkaloid idiospermuline

1 reference

https://pubmed.ncbi.nlm.nih.gov/25884552

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chemical constituents of chloroform fraction from leaves of Chimonanthus salicifolius

1 reference

https://pubmed.ncbi.nlm.nih.gov/25884552

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Action of calycanthine on nervous transmission in cockroach central nervous system.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25884552

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Iodine-mediated regioselective C2-amination of indoles and a concise total synthesis of (±)-folicanthine

1 reference

https://pubmed.ncbi.nlm.nih.gov/25884552

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chemical composition, antioxidant and antimicrobial activity of the extracts of the flowers of the Chinese plant Chimonanthus praecox

1 reference

https://pubmed.ncbi.nlm.nih.gov/25884552

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Concise total synthesis of (-)-calycanthine, (+)-chimonanthine, and (+)-folicanthine

1 reference

https://pubmed.ncbi.nlm.nih.gov/25884552

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.3390/MOLECULES20046715

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25884552%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25884552%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25884552%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

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