2015
DOI: 10.1080/00397911.2015.1121280
|View full text |Cite
|
Sign up to set email alerts
|

Facile green synthesis of 16-dehydropregnenolone acetate (16-DPA) from diosgenin

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
3
0

Year Published

2018
2018
2023
2023

Publication Types

Select...
4
1

Relationship

0
5

Authors

Journals

citations
Cited by 5 publications
(3 citation statements)
references
References 15 publications
0
3
0
Order By: Relevance
“…The process is still used and subject to further optimization. 34 Of course, no one is infallible, and Marker was no exception: e.g. Longwell and Wintersteiner suspected 35 and finally Gallagher has proven 36 that the structure of Marker-Lawson acid 37 was incorrect; Wall et al 38 also pointed out that the natural or artefact status of the sapogenin texogenin isolated by Marker et al 39 is unclear.…”
Section: Early Years and Educationmentioning
confidence: 99%
“…The process is still used and subject to further optimization. 34 Of course, no one is infallible, and Marker was no exception: e.g. Longwell and Wintersteiner suspected 35 and finally Gallagher has proven 36 that the structure of Marker-Lawson acid 37 was incorrect; Wall et al 38 also pointed out that the natural or artefact status of the sapogenin texogenin isolated by Marker et al 39 is unclear.…”
Section: Early Years and Educationmentioning
confidence: 99%
“…In today's era, the field of chemistry has achieved remarkable feats. The advent of green synthesis methods has significantly alleviated environmental burdens while presenting novel methods for more efficient separation and purification of reaction products to achieve high reaction yields [24][25][26][27]. During the 1980s, the microbial transformation of sterols, which are by-products of mainly soy and paper production, gained rapid development and application, offering the advantages of reduced waste and increased productivity.…”
Section: Introductionmentioning
confidence: 99%
“…The main raw materials for chemical conversion are diosgenin, a key raw material extracted from Dioscorea species , and the chemically produced 16-dehydropregnenolone acetate (Fig. 1 B), as the central intermediates for the synthesis of a large number of steroidal drugs (Baruah et al 2015 ; Herraiz 2017 ) (Fig. 1 C).…”
Section: Introductionmentioning
confidence: 99%