Unexpected highly chemoselective deprotection of the acetals from aldehydes and not ketones: TESOTf-2,6-lutidine combination

Journal of the American Chemical Society

Volumn 126, Issue 38, 2004, Pages 11800-11801

  Fujioka, Hiromichi ^a   Sawama, Yoshinari ^a   Murata, Nobutaka ^a   Okitsu, Takashi ^a   Kubo, Ozora ^a   Matsuda, Satoshi ^a   Kita, Yasuyuki ^a  

^a OSAKA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ACETAL; ALDEHYDE; KETONE; REAGENT; TRIETHYLSILYLTRIFLATE 2,6 LUTIDINE; TRIFLUOROMETHANESULFONIC ACID; TRIMETHYLSILYLTRIFLATE 2,6 LUTIDINE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 4644323241     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja046103p     Document Type: Article

References (21)

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21. Total synthesis of scyphostatin is in progress, and the preparation of 11 will be presented soon. Compare Fujioka, H.; Kotoku, N.; Sawama, Y.; Nagatomi, Y.; Kita, Y. Tetrahedron Lett. 2002, 43, 4825.