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The following term was not found in PubMed: -6-aminocyclohex-3-ene-1-carboxylic
Page 1
Conversion of the Enzymatically Derived (1S,2S)-3-Bromocyclohexa-3,5-diene-1,2-diol into Enantiomerically Pure Compounds Embodying the Pentacyclic Framework of Vindoline.
White LV, Banwell MG. White LV, et al. J Org Chem. 2016 Feb 19;81(4):1617-26. doi: 10.1021/acs.joc.5b02788. Epub 2016 Feb 3. J Org Chem. 2016. PMID: 26788805
This work sets the stage for effecting the conversion of the related metabolite (1S,6R)-5-ethyl-1,6-dihydroxycyclohexa-2,4-diene-1-carboxylic acid (4) into compound 3, the latter being a biogenetic precursor to the clinically significant anticancer agents vin …
This work sets the stage for effecting the conversion of the related metabolite (1S,6R)-5-ethyl-1,6-dihydroxycyclohexa-2,4-die …
Design of chiral bis-phosphoric acid catalyst derived from (R)-3,3'-di(2-hydroxy-3-arylphenyl)binaphthol: catalytic enantioselective Diels-Alder reaction of alpha,beta-unsaturated aldehydes with amidodienes.
Momiyama N, Konno T, Furiya Y, Iwamoto T, Terada M. Momiyama N, et al. J Am Chem Soc. 2011 Dec 7;133(48):19294-7. doi: 10.1021/ja2081444. Epub 2011 Nov 11. J Am Chem Soc. 2011. PMID: 22066907
Chiral bis-phosphoric acid 1 was designed to identify a new class of structural features in chiral Bronsted acid catalysts. ...After systematic variation of the catalyst substituents, as well as the N-acyl substituents of 1,3-butadiene, the use of an N-Cbz amidodien …
Chiral bis-phosphoric acid 1 was designed to identify a new class of structural features in chiral Bronsted acid catalysts. .. …
Constructing conformationally constrained macrobicyclic musks.
Kraft P, Cadalbert R. Kraft P, et al. Chemistry. 2001 Aug 3;7(15):3254-62. doi: 10.1002/1521-3765(20010803)7:15<3254::aid-chem3254>3.0.co;2-#. Chemistry. 2001. PMID: 11531111
These [7.5.1]- and [8.4.1]-macrobicycles were synthesized starting from bicyclo[5.3.1]undec-8-en-9-one (3) and bicyclo[4.3.1]dec-7-en-8-one (8), respectively, by a sequence consisting of catalytic hydrogenation, alpha-alkylation with a TBS-protected (tert-butyldimethylsilyl) hydr …
These [7.5.1]- and [8.4.1]-macrobicycles were synthesized starting from bicyclo[5.3.1]undec-8-en-9-one (3) and bicyclo[4.3.1]dec-7-en-8-one …
Synthesis of the enantiomers of 6-epicastanospermine and 1,6-diepicastanospermine from D- and L-gulonolactone.
Fleet GW, Ramsden NG, Nash RJ, Fellows LE, Jacob GS, Molyneux RJ, di Bello IC, Winchester B. Fleet GW, et al. Carbohydr Res. 1990 Sep 19;205:269-82. doi: 10.1016/0008-6215(90)80146-t. Carbohydr Res. 1990. PMID: 2276139
The synthesis of the enantiomers of 6-epicastanospermine and of 1,6-diepicastanospermine from the enantiomeric gulonolactones is reported and the structure of the former is established as (1S,6R,7R,8R,8aR)-1,6,7,8-tetrahydroxyoctahydroindolizine. The inhibitory acti …
The synthesis of the enantiomers of 6-epicastanospermine and of 1,6-diepicastanospermine from the enantiomeric gulonolactones is reported an …