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Bryostatins : the asymmetric synthesis of the C17-C27 fragment

(1994) SYNLETT. p.231-232
Author
Organization
Abstract
Disconnection at C20-C21 leads to two fragments. The C21-C27 fragment is constructed from D-isobutyl lactate via chelation-controlled allylation. The C17-C20 fragment is obtained from D-pantolactone.
Keywords
BRYOSTATINS, MARINE NATURAL PRODUCTS, D-ISOBUTYL LACTATE, DIASTEREOSELECTIVE ALLYLATION, DIMETHYL DIAZOMETHYL PHOSPHONATE, LEWIS ACID, ALDEHYDES, CONSTRUCTION, CONVENIENT, SYNTHONS, PRODUCTS, REAGENT, ESTERS, C1-C9

Citation

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Chicago
De Brabander, Jef, and Maurits Vandewalle. 1994. “Bryostatins : the Asymmetric Synthesis of the C17-C27 Fragment.” Synlett (4): 231–232.
APA
De Brabander, J., & Vandewalle, M. (1994). Bryostatins : the asymmetric synthesis of the C17-C27 fragment. SYNLETT, (4), 231–232.
Vancouver
1.
De Brabander J, Vandewalle M. Bryostatins : the asymmetric synthesis of the C17-C27 fragment. SYNLETT. 1994;(4):231–2.
MLA
De Brabander, Jef, and Maurits Vandewalle. “Bryostatins : the Asymmetric Synthesis of the C17-C27 Fragment.” SYNLETT 4 (1994): 231–232. Print.
@article{198230,
  abstract     = {Disconnection at C20-C21 leads to two fragments. The C21-C27 fragment is constructed from D-isobutyl lactate via chelation-controlled allylation. The C17-C20 fragment is obtained from D-pantolactone.},
  author       = {De Brabander, Jef and Vandewalle, Maurits},
  issn         = {0936-5214},
  journal      = {SYNLETT},
  keyword      = {BRYOSTATINS,MARINE NATURAL PRODUCTS,D-ISOBUTYL LACTATE,DIASTEREOSELECTIVE ALLYLATION,DIMETHYL DIAZOMETHYL PHOSPHONATE,LEWIS ACID,ALDEHYDES,CONSTRUCTION,CONVENIENT,SYNTHONS,PRODUCTS,REAGENT,ESTERS,C1-C9},
  language     = {eng},
  number       = {4},
  pages        = {231--232},
  title        = {Bryostatins : the asymmetric synthesis of the C17-C27 fragment},
  year         = {1994},
}