Finkelstein Reaction

This step is from the synthesis of Strychnine by Larry E. Overman. Show me the full synthesis.

LiCl

RT

This step is from the synthesis of Cristatic Acid, Methyl Ester by Alois Fürstner. Show me the full synthesis.

MsCl, LiBr, Et₃N

CH₂Cl₂, THF
0 °C, 3 h
76 %

This step is from the synthesis of Taxol by Paul A. Wender. Show me the full synthesis.

LiBr

Acetone
RT, 72 h
73 %

This step is from the synthesis of Aspidofractinine by Claude Spino. Show me the full synthesis.

NaI

Acetone
Reflux, 3 h

This step is from the synthesis of Cyanocobalamin by Robert B. Woodward. Show me the full synthesis.

LiBr

DMF

This step is from the synthesis of Aigialomycin D by Joanne E. Harvey. Show me the full synthesis.

NaI

MEK
Reflux, 24 h
99 %

This step is from the synthesis of Stigmatellin A by Dieter Enders. Show me the full synthesis.

NaI

Acetone
Reflux, 5 d
83 %

This step is from the synthesis of Doliculide by Arun K. Ghosh. Show me the full synthesis.

NaI

MEK
85 °C, 15 h

This step is from the synthesis of Reserpine by Stephen Hanessian. Show me the full synthesis.

NaI
3 Å MS

MeCN
RT, 18 h
97 %

This step is from the synthesis of Quadrone by Samuel J. Danishefsky. Show me the full synthesis.

LiBr

Acetone
Reflux, 6 h

This step is from the synthesis of Quadrone by Samuel J. Danishefsky. Show me the full synthesis.

NaI, Pyr

Acetone
Reflux, 15 h

This step is from the synthesis of Strychnine by Christopher D. Vanderwal. Show me the full synthesis.

MsCl, Et₃N, LiBr

THF
-25 °C to RT, 5 h

This step is from the synthesis of Cyclophellitol by Ken-Ichi Sato. Show me the full synthesis.

NaI

Acetone
Reflux

This step is from the synthesis of Hirsutene by Dennis P. Curran. Show me the full synthesis.

n-Bu₄N⁺ I^-

PhH
Reflux, 2 h
75 %

This step is from the synthesis of Epibatidine by David A. Evans. Show me the full synthesis.

LiBr

THF
Reflux, 36 h
84 %