General synthesis of side-chain derivatives of cannabinoids

1979 ◽  
Vol 44 (5) ◽  
pp. 677-683 ◽  
Author(s):  
Colin G. Pitt ◽  
Herbert H. Seltzman ◽  
Yousry Sayed ◽  
Charles E. Twine ◽  
David L. Williams
Keyword(s):  
Side Chain ◽  
Derivatives Of ◽  
General Synthesis

ChemInform Abstract: A GENERAL SYNTHESIS OF SIDE CHAIN DERIVATIVES OF Δ9-THC

1978 ◽  
Vol 9 (12) ◽  
Author(s):  
C. G. PITT ◽  
H. H. SELTZMAN ◽  
Y. SAYED ◽  
C. E. JUN. TWINE ◽  
D. L. WILLIAMS
Keyword(s):  
Side Chain ◽  
Derivatives Of ◽  
General Synthesis

A general synthesis of side chain derivatives of Δ9-thc

1978 ◽  
Vol 19 (1) ◽  
pp. 37-40 ◽  
Author(s):  
Colin G. Pitt ◽  
Herbert H. Seltzman ◽  
Yousry Sayed ◽  
Charles E. Twine ◽  
David L. Williams
Keyword(s):  
Side Chain ◽  
Derivatives Of ◽  
General Synthesis

ChemInform Abstract: GENERAL SYNTHESIS OF SIDE-CHAIN DERIVATIVES OF CANNABINOIDS

1979 ◽  
Vol 10 (28) ◽  
Author(s):  
C. G. PITT ◽  
H. H. SELTZMAN ◽  
Y. SAYED ◽  
C. E. JUN. TWINE ◽  
D. L. WILLIAMS
Keyword(s):  
Side Chain ◽  
Derivatives Of ◽  
General Synthesis

Absolute configuration at C(20) of the derivatives of 21-nor-5α-cholane-20,24-diol

1980 ◽  
Vol 45 (9) ◽  
pp. 2443-2451
Author(s):  
Vladimír Pouzar ◽  
Miroslav Havel
Keyword(s):  
Absolute Configuration ◽  
Side Chain ◽  
Chemical Correlation ◽  
The Absolute ◽  
Derivatives Of

Derivatives of 21-nor-5α-cholane-20,24-diol XI and XIX were prepared by stepwise construction of the side-chain in the position 17β. Their absolute configuration at C(20) was determined on the basis of chemical correlation with the derivatives of 21-nor-5α-cholan-20-ol, XVI and XXIV. The absolute configuration of alcohols XVI and XXIV was determined from the ratio of the yields in which they are formed during the reduction of ketone X and using the benzoate rule. To compounds XI-XVIII the configuration 20R and to compounds XIX-XXVI the configuration 20S has been assigned.

scholarly journals Synthesis of New Derivatives of BEDT-TTF: Installation of Alkyl, Ethynyl, and Metal-Binding Side Chains and Formation of Tris(BEDT-TTF) Systems

2021 ◽  
Vol 7 (8) ◽  
pp. 110
Author(s):  
Songjie Yang ◽  
Matteo Zecchini ◽  
Andrew Brooks ◽  
Sara Krivickas ◽  
Desiree Dalligos ◽  
...  
Keyword(s):  
Metal Binding ◽  
Tricarboxylic Acid ◽  
Metal Salts ◽  
Side Chain ◽  
Side Chains ◽  
Ethynyl Group ◽  
X Ray ◽  
Transition Metal Salts ◽  
Alkyl Side Chains ◽  
Derivatives Of

The syntheses of new BEDT-TTF derivatives are described. These comprise BEDT-TTF with one ethynyl group (HC≡C-), with two (n-heptyl) or four (n-butyl) alkyl side chains, with two trans acetal (-CH(OMe)2) groups, with two trans aminomethyl (-CH2NH2) groups, and with an iminodiacetate (-CH2N(CH2CO2−)2 side chain. Three transition metal salts have been prepared from the latter donor, and their magnetic properties are reported. Three tris-donor systems are reported bearing three BEDT-TTF derivatives with ester links to a core derived from benzene-1,3,5-tricarboxylic acid. The stereochemistry and molecular structure of the donors are discussed. X-ray crystal structures of two BEDT-TTF donors are reported: one with two CH(OMe)2 groups and with one a -CH2N(CH2CO2Me)2 side chain.

Novel Pentaheterocycles. First General Synthesis Entry to Functionalized Derivatives of Pyrido[2,3-f:6,5-f?]di[1,2,4]triazolo[4,3-a] pyrimidin-5(1H)-ones

2004 ◽  
Vol 135 (2) ◽  
pp. 211-222 ◽  
Author(s):  
Magda A. Abdallah ◽  
Ahmad S. Shawali ◽  
Thoraya A. Farghaly ◽  
Mosselhi A. N. Mosselhi
Keyword(s):  
Derivatives Of ◽  
General Synthesis

New 4-Hydroxypyridine and 4-Hydroxyquinoline Derivatives as Inhibitors of NADH-ubiquinone Reductase in the Respiratory Chain

1989 ◽  
Vol 44 (7-8) ◽  
pp. 609-616 ◽  
Author(s):  
Kun Hoe Chung ◽  
Kwang Yun Cho ◽  
Yasuko Asami ◽  
Nobutaka Takahashi ◽  
Shigeo Yoshida
Keyword(s):  
Electron Transport ◽  
Respiratory Chain ◽  
Side Chain ◽  
Pyridine Derivatives ◽  
Transport Function ◽  
Optimal Length ◽  
Structure Activity ◽  
Membrane Effect ◽  
Relationship Of ◽  
Derivatives Of

Many derivatives of 2,3-dim ethoxy-4-hydroxypyridine, which were designed from examination of the structure-activity relationship of piericidins, were tested for inhibition of NADH-UQ reductase. The lipophilic side chain of those compounds was indicated to be a key part for activity and its optimal length was conjectured. By the use of two different phases of assay material, intact mitochondria and submitochondria, the size of a membrane effect was shown to depend on the structure of the side chain. 4-Hydroxyquinoline derivatives were also tested for an analogous role in relation to the electron transport function of menaquinone, and they were proven to be inhibitors of NADH-UQ reductase as good as the pyridine derivatives.

New N.alpha.-Guanidinobenzoyl Derivatives of Hirudin-54-65 Containing Stabilized Carboxyl or Phosphoryl Groups on the Side Chain of Phenylalanine-63

1994 ◽  
Vol 37 (5) ◽  
pp. 625-629 ◽  
Author(s):  
Christophe Thurieau ◽  
Serge Simonet ◽  
Joseph Paladino ◽  
Jean-Francois Prost ◽  
Tony Verbeuren ◽  
...  
Keyword(s):  
Side Chain ◽  
Phosphoryl Groups ◽  
Derivatives Of

A Simple Method to Generate Side-Chain Derivatives of Regioregular Polythiophene via the GRIM Metathesis and Post-polymerization Functionalization

2003 ◽  
Vol 36 (1) ◽  
pp. 61-64 ◽  
Author(s):  
Lei Zhai ◽  
Richard L. Pilston ◽  
Karen L. Zaiger ◽  
Kristoffer K. Stokes ◽  
Richard D. McCullough
Keyword(s):  
Side Chain ◽  
Simple Method ◽  
Derivatives Of
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