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Mo-katalysierte Hydrostannylierungen
Formal
total synthesis of (±)-herbertene-1,13-diol
and (±)-α-herbertenol
via Ireland ester Claisen rearrangement and RCM reaction sequence, A. Srikrishna
and B. Vasantha Lakshmi, Synlett, 2005,
1173.
Construction
of vicinal quaternary carbon atoms by Ireland ester Claisen rearrangement. Total
synthesis of (±)-herbertenolide,
(±)-herberteneacetal,
(±)-herbertene-1,14-diol
and (±)-herbertene-1,15-diol,
A. Srikrishna and B. Vasantha Lakshmi, Tetrahedron Lett.,
2005, 46, 4879.
The first
total synthesis of a bioactive metabolite, a spirobenzofuran isolated from the
fungi Acremonium sp. HKI 0230, A. Srikrishna and B. Vasantha Lakshmi,
Tetrahedron Lett., 2005, 46, 7029.
The first
total synthesis of (±)-lagopodin A, A. Srikrishna, B. Vasantha Lakshmi
and P. C. Ravikumar, Tetrahedron Lett., 2006, 47,
1277.
Construction
of spiro[5.5]undecanes containing a quaternary carbon atom adjacent to a
spirocentre via an Ireland ester Claisen rearrangement and RCM reaction
sequence. Total syntheses of (±)-α-chamigrene,
(±)-β-chamigrene
and (±)-laurencenone C, A. Srikrishna, B. Vasantha Lakshmi and
M. Mathews, Tetrahedron Lett., 2006, 47,
2103.
Pyridinium Chlorochromate mediated oxidative cyclisation of sterically crowded γ-δ-unsaturated alcohols, A. Srikrishna, B. Vasantha Lakshmi and A.V.S. Sudhakar, Tetrahedron Lett., 2007, 48, 7610.
B. V. Lakshmi, U. Kazmaier “A straightforward approach towards substituted Morita-Baylis-Hillman (MBH) products via hydrostannation of acetylenic ketones”, Synlett, 2010, 407-410.
B. V. Lakshmi, U. K. Wefelscheid, U. Kazmaier, “Synthesis of
Arylstannanes from Silyl Triflates via Aryne Intermediates”,
Synlett,
2011, 345–348.