- Horner–Wadsworth–Emmons/Heck
procedures for the
preparation of 3-alkenyl-
oxindoles: The
synthesis of
Semaxanib and GW441756". Tetrahedron. 66 (33): 6606–6612...
- The
Hinsberg oxindole synthesis is a
method of
preparing oxindoles from the
bisulfite additions of glyoxal. It is
named after its
inventor Oscar Hinsberg...
- (1973). "Use of halogen-sulfide
complexes in the
synthesis of indoles,
oxindoles, and
alkylated aromatic amines". J. Am. Chem. Soc. 95 (19): 6508. doi:10...
- Tsuneoka, Kazuko; Nakagawa, Masako; Akaboshi,
Sanya (1969). "Thiation of
Oxindoles".
Chemical and
Pharmaceutical Bulletin. 17 (3): 550–558. doi:10.1248/cpb...
- Acid-Catalyzed Hofmann–Martius
Rearrangement of 3-N-Aryl-2-
oxindoles into 3-(Arylamino)-2-
oxindoles".
Organic Letters. 8 (16): 3497–9. doi:10.1021/ol061191z...
- Horner–Wadsworth–Emmons/Heck
procedures for the
preparation of 3-alkenyl-
oxindoles: The
synthesis of
Semaxanib and GW441756". Tetrahedron. 66 (33): 6606–6612...
- M., Edgar, J. A., Flower, K., Vit, I., Willing, R. I. (June 1998). "
Oxindoles from
Phalaris coerulescens". Phytochemistry. 48 (3): 437–439. Bibcode:1998PChem...
- The Stollé
synthesis is a
series of
chemical reactions that
produce oxindoles from
anilines and α-haloacid
chlorides (or
oxalyl chloride). The
first step...
-
Indigo can be
converted to
isatin and then to
oxindole. Then, in 1866,
Adolf von
Baeyer reduced oxindole to
indole using zinc dust. In 1869, he proposed...
- Mitraphylline, an
oxindole derivative, is an
active alkaloid in the
leaves of the tree
Mitragyna speciosa,
commonly known as kratom. As a non-narcotic...
