Reactions of allylmagnesium reagents with carbonyl compounds and compounds with C═ N double bonds: their diastereoselectivities generally cannot be analyzed …

ND Bartolo, JA Read, EM Valentín… - Chemical reviews, 2020 - ACS Publications
This review describes the additions of allylmagnesium reagents to carbonyl compounds and
to imines, focusing on the differences in reactivity between allylmagnesium halides and …

Open-chain steroidal glycosides, a diverse class of plant saponins

VL Challinor, JJ De Voss - Natural Product Reports, 2013 - pubs.rsc.org
Covering: up to September 2012 Saponins are an important class of plant natural products
that consist of a triterpenoid or steroidal skeleton that is glycosylated by varying numbers of …

Steroidal saponins with cytotoxic effects from the rhizomes of Asparagus cochinchinensis

B Liu, B Li, D Zhou, X Wen, Y Wang, G Chen, N Li - Bioorganic Chemistry, 2021 - Elsevier
In the ongoing research on potent antitumor agents from the rhizomes of Asparagus
cochinchinensis, seven undescribed steroidal saponins asparagusoside A–G (1–7), along …

Caco-2 Monolayer Permeability and Stability of Chamaelirium luteum (False Unicorn) Open-Chain Steroidal Saponins

TP Stockdale, VL Challinor, RP Lehmann… - ACS …, 2019 - ACS Publications
Herbal medicines, although significant components of health care for much of the global
populace, are still far less stringently regulated than conventional pharmaceuticals. Safety …

Direct organocatalytic stereoselective transfer hydrogenation of conjugated olefins of steroids

DB Ramachary, R Sakthidevi, PS Reddy - RSC advances, 2013 - pubs.rsc.org
Kinetically controlled and organocatalytic syn-selective transfer hydrogenation has been
successfully demonstrated for the reduction of the enone functional group of various …

A concise account of various approaches for stereoselective construction of the C-20 (H) stereogenic center in steroid side chain

BB Shingate, BG Hazra - Chemical Reviews, 2014 - ACS Publications
Sterols are compounds containing a perhydro-1, 2-cyclopentenophenanthrene ring system
and are found in a variety of different marine, terrestrial, and synthetic sources. The vast …

Structure and Bioactivity of Steroidal Saponins Isolated from the Roots of Chamaelirium luteum (False Unicorn)

VL Challinor, JMU Stuthe, PG Parsons… - Journal of Natural …, 2012 - ACS Publications
Phytochemical investigation of Chamaelirium luteum (“false unicorn”) resulted in the
isolation of 15 steroidal glycosides. Twelve of these (1, 2, 4–9, 11–13, and 15) are …

Structure and Absolute Configuration of Methyl (3R)-Malonyl-(13S)-hydroxycheilanth-17-en-19-oate, a Sesterterpene Derivative from the Roots of Aletris farinosa

VL Challinor, S Chap, RP Lehmann… - Journal of natural …, 2013 - ACS Publications
We report the isolation and structure elucidation of a new cheilanthane sesterterpene from
the roots of Aletris farinosa that possesses an unusual malonate half-ester functional group …

[HTML][HTML] Biosynthetic insights provided by unusual sesterterpenes from the medicinal herb Aletris farinosa

VL Challinor, RC Johnston, PV Bernhardt… - Chemical …, 2015 - pubs.rsc.org
A series of novel sesterterpenes (2–6) have been isolated from the roots of Aletris farinosa
and structurally characterized by MS, NMR, and X-ray crystallography in conjunction with …

Structure and Absolute Configuration of Helosides A and B, New Saponins from Chamaelirium luteum

VL Challinor, JMU Stuthe, PV Bernhardt… - Journal of natural …, 2011 - ACS Publications
Investigation of Chamaelirium luteum roots led to the isolation of two new steroidal
saponins, helosides A (1) and B (2), that contain a previously unreported aglycone …