Synthesis of enantiomerically pure bay-region 3,4-diol 1,2-epoxide diastereomers and other derivatives of the potent carcinogen dibenz[c,h]acridine

1985 ◽  
Vol 50 (1) ◽  
pp. 98-107 ◽  
Author(s):  
Roland E. Lehr ◽  
Subodh Kumar ◽  
Naohiro Shirai ◽  
Donald M. Jerina
Keyword(s):  
Enantiomerically Pure ◽  
Potent Carcinogen ◽  
Derivatives Of

scholarly journals Enzymatic Approach to the Synthesis of Enantiomerically Pure Hydroxy Derivatives of 1,3,5-Triaza-7-phosphaadamantane

2021 ◽  
Author(s):  
Małgorzata Kwiatkowska ◽  
Jarosław Błaszczyk ◽  
Lesław Sieroń ◽  
Piotr Kiełbasiński
Keyword(s):  
Enantiomerically Pure ◽  
Derivatives Of

scholarly journals Straightforward synthesis of enantiomerically pure 1,2,3-triazoles derived from amino esters

2018 ◽  
Vol 16 (17) ◽  
pp. 3168-3176 ◽  
Author(s):  
Gastón Silveira-Dorta ◽  
Sampad Jana ◽  
Lucie Borkova ◽  
Joice Thomas ◽  
Wim Dehaen
Keyword(s):  
Amino Acids ◽  
Enantiomerically Pure ◽  
Triazole Derivatives ◽  
Amino Esters ◽  
Good Yielding ◽  
Derivatives Of

An easy, good-yielding access to functionalized enantiomerically pure 1,2,3-triazole derivatives of amino acids using commercially available ketones and amino esters is described.

ChemInform Abstract: Synthesis of Two Useful, Enantiomerically Pure Derivatives of (S)-4-Hydroxy-2-cyclohexenone.

ChemInform ◽  
1990 ◽  
Vol 21 (1) ◽  
Author(s):  
J. E. AUDIA ◽  
L. BOISVERT ◽  
A. D. PATTEN ◽  
A. VILLALOBOS ◽  
S. J. DANISHEFSKY
Keyword(s):  
Enantiomerically Pure ◽  
Derivatives Of

Synthesis of two useful, enantiomerically pure derivatives of (S)-4-hydroxy-2-cyclohexenone

1989 ◽  
Vol 54 (15) ◽  
pp. 3738-3740 ◽  
Author(s):  
James E. Audia ◽  
Louise Boisvert ◽  
Arthur D. Patten ◽  
Anabella Villalobos ◽  
Samuel J. Danishefsky
Keyword(s):  
Enantiomerically Pure ◽  
Derivatives Of

Competitive Intramolecular Diels - Alder Reactions of bis-α,β-Unsaturated Ester Derivatives of Enzymatically Derived and Enantiopure cis-1,2-Dihydrocatechols. Enantiodivergent Synthesis of Monochiral Bicyclo[2.2.2]oct-2-enes

2003 ◽  
Vol 56 (9) ◽  
pp. 861 ◽  
Author(s):  
Martin G. Banwell ◽  
Cai Chun ◽  
Alison J. Edwards ◽  
Markus M. Vögtle
Keyword(s):  
Natural Products ◽  
Single Crystal ◽  
Building Blocks ◽  
Diels Alder ◽  
Unsaturated Ester ◽  
Enantiomerically Pure ◽  
X Ray ◽  
Derivatives Of ◽  
Natural Products Synthesis

bis-Crotonate and related α,β-unsaturated ester derivatives of readily available and enantiomerically pure cis-1,2-dihydrocatechols engage, upon heating in refluxing toluene, in two competitive intramolecular Diels–Alder reactions to give varying mixtures of chromatographically separable and pseudo-enantiomeric bicyclo[2.2.2]oct-2-enes. Such adducts, many of which have been characterized by single-crystal X-ray analysis, are likely to serve as useful building blocks in natural products synthesis.

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