New developments in the chemistry of N-acyliminium ions and related intermediates

WN Speckamp, MJ Moolenaar - Tetrahedron, 2000 - Elsevier
Reactions between N-acyliminium ions and nucleophiles–also described as
amidoalkylation or Mannich type condensations–have been frequently utilized to introduce …

Asymmetric domino reactions. Part A: Reactions based on the use of chiral auxiliaries

H Pellissier - Tetrahedron, 2006 - Elsevier
Conclusions The first part of this review clearly demonstrates the diversity and power of
asymmetric domino reactions based on the use of chiral auxiliaries in the field of synthetic …

Enantioselective synthesis of steroids

AS Chapelon, D Moraléda, R Rodriguez, C Ollivier… - Tetrahedron, 2007 - Elsevier
1. Introduction....................................................................... 11512 2. Chemical resolution of chiral
synthetic intermediates.................................... 11515 2.1. By recrystallization of diastereomeric …

D iels‐A lder Reactions of Imino Dienophiles

GR Heintzelman, IR Meigh, YR Mahajan… - Organic …, 2004 - Wiley Online Library
In comparison to all carbon [4+ 2] cycloadditions, Diesl‐Alder reactions are still in their
infancy. The last four decades, however, have seen intensive research in this area. The …

Selective non-steroidal inhibitors of 5α-reductase type 1

EG Occhiato, A Guarna, G Danza, M Serio - The Journal of steroid …, 2004 - Elsevier
The enzyme 5α-reductase (5αR) catalyses the reduction of testosterone (T) into the more
potent androgen dihydrotestosterone (DHT). The abnormal production of DHT is associated …

Efficient microbial synthesis of key steroidal intermediates from bio-renewable phytosterols by genetically modified Mycobacterium fortuitum strains

N Liu, J Feng, R Zhang, X Chen, X Li, P Yao, Q Wu… - Green …, 2019 - pubs.rsc.org
3aα-H-4α-(3′-Propionic acid)-5α-hydroxy-7aβ-methylhexahydro-1-indanone-δ-lactone
(sitolactone, or HIL) and 3aα-H-4α-(3′-propionic acid)-7aβ-methylhexahydro-1, 5 …

Studies on chromium (0)-promoted higher-order cycloaddition-based benzannulation. Total synthesis of (+)-estradiol

JH Rigby, NC Warshakoon… - Journal of the American …, 1999 - ACS Publications
A benzannulation sequence featuring [6π+ 4π] cycloaddition of (η6-thiepin 1, 1-dioxide)
tricarbonylchromium (0) complexes with highly substituted dienes followed by Ramberg …

Highly Enantioselective Assembly of Functionalized Tetrahydroquinolines with Creation of an All‐Carbon Quaternary Center

HR Tan, HF Ng, J Chang, J Wang - Chemistry–A European Journal, 2012 - infona.pl
A Mannich–Michael combo: An efficient and highly enantioselective cascade process by H‐
bonding catalysis for the synthesis of functionalized tetrahydroquinolines has been …

Benzo[c]quinolizin-3-ones:  A Novel Class of Potent and Selective Nonsteroidal Inhibitors of Human Steroid 5α-Reductase 1

A Guarna, F Machetti, EG Occhiato… - Journal of medicinal …, 2000 - ACS Publications
The synthesis and biological evaluation of a series of novel, selective inhibitors of
isoenzyme 1 of human 5α-reductase (5αR)(EC 1.3. 99.5) are reported. The inhibitors are 4a …

Effect of C-ring modifications in benzo [c] quinolizin-3-ones, new selective inhibitors of human 5α-reductase 1

A Guarna, EG Occhiato, F Machetti, A Trabocchi… - Bioorganic & medicinal …, 2001 - Elsevier
The synthesis and the inhibition potency of octahydro-and decahydrobenzo [c] quinolizin-3-
one derivatives 3–7, as new non-steroidal selective inhibitors of human enzyme 5α …